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Topic 3: Genetics
Description
Overview of the essential ideas for this topic.
3.1: Every living organism inherits a blueprint for life from its parents.
3.2: Chromosomes carry genes in a linear sequence that is shared by members of a species.
3.3: Alleles segregate during meiosis allowing new combinations to be formed by the fusion of gametes.
3.4: The inheritance of genes follows patterns.
3.5: Biologists have developed techniques for artificial manipulation of DNA, cells and organisms.
Directly related questions
- 17N.1.SL.TZ0.15: HindIII is an endonuclease that recognizes the sequence A A G C T T, cutting between the two...
- 17N.1.SL.TZ0.15: HindIII is an endonuclease that recognizes the sequence A A G C T T, cutting between the two...
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17N.3.HL.TZ0.03b:
Some regions of DNA act as telomeres or produce tRNA. State one other function of DNA sequences that do not code for protein.
- 17N.1.SL.TZ0.16: An allele for lactase persistence allows humans to digest milk as adults. People who lack this...
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17N.3.HL.TZ0.03b:
Some regions of DNA act as telomeres or produce tRNA. State one other function of DNA sequences that do not code for protein.
-
17N.3.HL.TZ0.b:
Some regions of DNA act as telomeres or produce tRNA. State one other function of DNA sequences that do not code for protein.
- 17N.2.SL.TZ0.02c: State an application of plasmids in biotechnology.
- 17N.1.SL.TZ0.16: An allele for lactase persistence allows humans to digest milk as adults. People who lack this...
- 17N.2.SL.TZ0.02c: State an application of plasmids in biotechnology.
- 17N.2.SL.TZ0.c: State an application of plasmids in biotechnology.
- 18M.1.SL.TZ1.14: What is the same in all parts of homologous chromosomes? A. Base pair sequence B. Alleles C....
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17N.1.HL.TZ0.10:
The image shows a karyogram.
[Source: https://commons.wikimedia.org/wiki/File:Karyotype_of_sheep_(Ovis_aries).png, by M. Singh, X. Ma, E. Amoah and G. Kannan]
What information can be determined from this karyogram?
A. The sex is female.
B. The haploid number is 54.
C. Disjunction occurred during meiosis.
D. The species is not human.
-
17N.1.HL.TZ0.10:
The image shows a karyogram.
[Source: https://commons.wikimedia.org/wiki/File:Karyotype_of_sheep_(Ovis_aries).png, by M. Singh, X. Ma, E. Amoah and G. Kannan]
What information can be determined from this karyogram?
A. The sex is female.
B. The haploid number is 54.
C. Disjunction occurred during meiosis.
D. The species is not human.
- 18M.1.SL.TZ1.14: What is the same in all parts of homologous chromosomes? A. Base pair sequence B. Alleles C....
- 17N.1.HL.TZ0.12: A dominant autosomal allele for lactase persistence allows humans to digest milk as adults....
- 17N.1.HL.TZ0.12: A dominant autosomal allele for lactase persistence allows humans to digest milk as adults....
- 17N.2.SL.TZ0.06c: Outline natural methods of cloning in some eukaryotes.
- 17N.2.SL.TZ0.06c: Outline natural methods of cloning in some eukaryotes.
- 17N.2.SL.TZ0.c: Outline natural methods of cloning in some eukaryotes.
- 18M.1.SL.TZ1.15: What helps make the genome of each human unique?
- 18M.1.HL.TZ1.35: What forms when two different chromatids of the same homologous pair cross over? A. Daughter...
- 18M.1.SL.TZ1.15: What helps make the genome of each human unique?
- 18M.1.SL.TZ1.21: What explains the presence in living humans of DNA sections which are identical to DNA found in...
- 18M.1.HL.TZ1.35: What forms when two different chromatids of the same homologous pair cross over? A. Daughter...
- 18M.2.SL.TZ1.3a: Using the Punnett grid, explain how two parents can have children with any of the different ABO...
- 18M.1.SL.TZ1.21: What explains the presence in living humans of DNA sections which are identical to DNA found in...
- 18M.1.HL.TZ1.40: What contributes to the total DNA content of a zygote?
-
18M.2.HL.TZ1.3b.i:
Distinguish between sex-linked genes and genes with linked loci.
- 18M.1.HL.TZ1.40: What contributes to the total DNA content of a zygote?
- 18M.2.SL.TZ1.3a: Using the Punnett grid, explain how two parents can have children with any of the different ABO...
- 18M.2.SL.TZ1.a: Using the Punnett grid, explain how two parents can have children with any of the different ABO...
-
18M.2.HL.TZ1.3b.i:
Distinguish between sex-linked genes and genes with linked loci.
- 18M.2.SL.TZ2.2b.ii: Distinguish between the chromosomes of eukaryotic cells and prokaryotic cells.
-
18M.2.HL.TZ1.b.i:
Distinguish between sex-linked genes and genes with linked loci.
-
18M.2.HL.TZ1.3b.ii:
Outline how it can be shown that the genes for shell base colour (Cc) and presence or absence of bands (Bb) are linked.
-
18M.2.HL.TZ1.3b.ii:
Outline how it can be shown that the genes for shell base colour (Cc) and presence or absence of bands (Bb) are linked.
-
18M.2.HL.TZ1.b.ii:
Outline how it can be shown that the genes for shell base colour (Cc) and presence or absence of bands (Bb) are linked.
- 18M.2.HL.TZ1.4a: Sickle cell anemia is due to a single base substitution in DNA. Using the diagram, outline how...
-
18M.2.SL.TZ2.6c:
Explain the process of genetically modifying bacteria.
-
18M.2.SL.TZ2.6c:
Explain the process of genetically modifying bacteria.
-
18M.2.SL.TZ2.c:
Explain the process of genetically modifying bacteria.
- 18M.2.HL.TZ1.4a: Sickle cell anemia is due to a single base substitution in DNA. Using the diagram, outline how...
- 18M.2.HL.TZ2.3a.i: The micrograph shows a plant cell of Lilium grandiflorum during meiosis. Identify, giving...
- 18M.2.HL.TZ1.a: Sickle cell anemia is due to a single base substitution in DNA. Using the diagram, outline how...
- 18M.1.HL.TZ2.16: For what purpose is a karyogram used? A. To identify gene loci in a species B. To identify...
- 18M.2.HL.TZ2.3a.i: The micrograph shows a plant cell of Lilium grandiflorum during meiosis. Identify, giving...
- 18M.2.HL.TZ2.a.i: The micrograph shows a plant cell of Lilium grandiflorum during meiosis. Identify, giving...
-
18M.2.HL.TZ2.3b:
The genes for cystic fibrosis and blood group are not linked. Two parents are heterozygous for cystic fibrosis. One parent has blood group O and the other has blood group AB. Using a Punnett square, determine the probability that their child will have both cystic fibrosis and blood group A.
-
18M.2.HL.TZ2.3b:
The genes for cystic fibrosis and blood group are not linked. Two parents are heterozygous for cystic fibrosis. One parent has blood group O and the other has blood group AB. Using a Punnett square, determine the probability that their child will have both cystic fibrosis and blood group A.
-
18M.2.HL.TZ2.b:
The genes for cystic fibrosis and blood group are not linked. Two parents are heterozygous for cystic fibrosis. One parent has blood group O and the other has blood group AB. Using a Punnett square, determine the probability that their child will have both cystic fibrosis and blood group A.
- 18M.2.SL.TZ2.2b.ii: Distinguish between the chromosomes of eukaryotic cells and prokaryotic cells.
- 18M.2.SL.TZ2.b.ii: Distinguish between the chromosomes of eukaryotic cells and prokaryotic cells.
- 18M.1.SL.TZ2.12: Some yeast genes can be replaced by human genes that then continue to produce the same human...
- 18M.1.HL.TZ2.16: For what purpose is a karyogram used? A. To identify gene loci in a species B. To identify...
- 18M.1.HL.TZ2.17: Which process could cause non-disjunction if it occurred during meiosis? A. Sister chromatids do...
- 18M.1.SL.TZ2.12: Some yeast genes can be replaced by human genes that then continue to produce the same human...
- 18N.1.SL.TZ0.12: The image shows the chromosomes in four cells of an insect at the end of meiosis. What is the...
- 18N.1.SL.TZ0.12: The image shows the chromosomes in four cells of an insect at the end of meiosis. What is the...
- 18M.1.HL.TZ2.17: Which process could cause non-disjunction if it occurred during meiosis? A. Sister chromatids do...
- 18N.1.SL.TZ0.14: A human gene has two alleles. One allele, P, is dominant over the recessive allele p. Embryos...
- 18M.1.SL.TZ2.13: What determines the genomic size of a species? A. The total amount of DNA B. The total number...
- 18M.1.HL.TZ2.19: Which technique is used to amplify very small samples of DNA? A. Cloning B. Gel...
- 18M.1.SL.TZ2.13: What determines the genomic size of a species? A. The total amount of DNA B. The total number...
- 18N.1.SL.TZ0.14: A human gene has two alleles. One allele, P, is dominant over the recessive allele p. Embryos...
- 18M.1.HL.TZ2.19: Which technique is used to amplify very small samples of DNA? A. Cloning B. Gel...
- 18N.1.SL.TZ0.15: In cats, black coat colour is dominant over gray. A female black cat, whose mother is gray, mates...
- 18M.1.SL.TZ2.14: What happens during meiosis I and meiosis II?
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18M.1.HL.TZ2.20:
Nail patella syndrome is a rare disease that causes abnormalities of the nails and some bones. Its alleles are linked to the blood group alleles on the same chromosome. The pedigree chart shows the inheritance of these two characteristics over three generations.
[Source: Copyright © 1998. Phillip McClean]
Which descendant represents a recombinant phenotype?
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18M.1.HL.TZ2.20:
Nail patella syndrome is a rare disease that causes abnormalities of the nails and some bones. Its alleles are linked to the blood group alleles on the same chromosome. The pedigree chart shows the inheritance of these two characteristics over three generations.
[Source: Copyright © 1998. Phillip McClean]
Which descendant represents a recombinant phenotype?
- 18M.1.SL.TZ2.14: What happens during meiosis I and meiosis II?
- 18N.1.SL.TZ0.15: In cats, black coat colour is dominant over gray. A female black cat, whose mother is gray, mates...
-
18N.1.HL.TZ0.11:
The image shows chromosomes from an insect (2 n = 8).
Which pair of chromosomes are the sex chromosomes of this insect species?
A. c and e
B. a and h
C. f and h
D. a and e
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18N.1.SL.TZ0.16:
The image shows the results of Griffith’s experiment with S and R strains of Streptococcus pneumoniae in mice (Mus musculus).
What is an explanation for the results?
A. Mice vary in their resistance to bacteria.
B. The R strain and S strain mated.
C. R strain bacteria are more heat-stable than S strain.
D. DNA was transferred from heat-killed S cells to R cells.
-
18N.1.SL.TZ0.16:
The image shows the results of Griffith’s experiment with S and R strains of Streptococcus pneumoniae in mice (Mus musculus).
What is an explanation for the results?
A. Mice vary in their resistance to bacteria.
B. The R strain and S strain mated.
C. R strain bacteria are more heat-stable than S strain.
D. DNA was transferred from heat-killed S cells to R cells.
- 18M.1.SL.TZ2.15: What is the percentage risk of a child inheriting Huntington’s disease if only one parent has the...
-
18N.1.HL.TZ0.11:
The image shows chromosomes from an insect (2 n = 8).
Which pair of chromosomes are the sex chromosomes of this insect species?
A. c and e
B. a and h
C. f and h
D. a and e
- 18M.1.SL.TZ2.15: What is the percentage risk of a child inheriting Huntington’s disease if only one parent has the...
- 18M.1.SL.TZ2.16: Which technique is used to amplify very small samples of DNA? A. Cloning B. Gel...
-
18N.1.HL.TZ0.14:
Ampicillin (Amp) is an antibiotic. A plasmid carrying a gene for Amp resistance was used to transform bacteria in a tube of broth. A control tube without plasmid was also produced. The results were plated as shown. Which plate has only colonies of transformed bacteria?
-
18N.1.HL.TZ0.14:
Ampicillin (Amp) is an antibiotic. A plasmid carrying a gene for Amp resistance was used to transform bacteria in a tube of broth. A control tube without plasmid was also produced. The results were plated as shown. Which plate has only colonies of transformed bacteria?
- 18M.1.SL.TZ2.16: Which technique is used to amplify very small samples of DNA? A. Cloning B. Gel...
- 18N.2.SL.TZ0.6a: Isolated communities in rural Finland, Hungary and some of the Scottish islands have a high...
- 18N.1.HL.TZ0.27: Sanger developed a method for determining DNA base sequences using terminating nucleotides called...
- 18N.1.HL.TZ0.27: Sanger developed a method for determining DNA base sequences using terminating nucleotides called...
- 19M.2.SL.TZ1.6a: Identify, with a reason, the sex of this individual.
- 18N.2.SL.TZ0.6a: Isolated communities in rural Finland, Hungary and some of the Scottish islands have a high...
- 18N.2.SL.TZ0.a: Isolated communities in rural Finland, Hungary and some of the Scottish islands have a high...
-
19M.2.SL.TZ2.1i:
Outline the conclusions that can be drawn from the data in the graph for the group of aphids fed for three generations on transgenic thale cress plants (T).
- 18N.2.HL.TZ0.7a: Isolated communities in rural Finland, Hungary and some of the Scottish islands have a high...
- 18N.2.HL.TZ0.7a: Isolated communities in rural Finland, Hungary and some of the Scottish islands have a high...
- 18N.2.HL.TZ0.a: Isolated communities in rural Finland, Hungary and some of the Scottish islands have a high...
-
19M.1.SL.TZ1.13:
The system of sex determination in chimpanzees (Pan troglodytes) is the same as in other mammals. A chimpanzee has 48 chromosomes in the nuclei of its body cells.
What can be deduced from this information?
A. The sex of the chimpanzee
B. The number of genes in each chromosome
C. Whether non-disjunction has occurred
D. The number of autosomes in a diploid cell
- 19M.2.SL.TZ1.6a: Identify, with a reason, the sex of this individual.
-
19M.1.SL.TZ1.13:
The system of sex determination in chimpanzees (Pan troglodytes) is the same as in other mammals. A chimpanzee has 48 chromosomes in the nuclei of its body cells.
What can be deduced from this information?
A. The sex of the chimpanzee
B. The number of genes in each chromosome
C. Whether non-disjunction has occurred
D. The number of autosomes in a diploid cell
-
19M.2.SL.TZ2.1i:
Outline the conclusions that can be drawn from the data in the graph for the group of aphids fed for three generations on transgenic thale cress plants (T).
-
19M.2.SL.TZ2.i:
Outline the conclusions that can be drawn from the data in the graph for the group of aphids fed for three generations on transgenic thale cress plants (T).
- 19M.2.SL.TZ1.a: Identify, with a reason, the sex of this individual.
- 19M.2.SL.TZ1.6b: Identify the chromosome that is affected by a trisomy in this individual, naming the condition...
- 19M.2.SL.TZ2.1j: Discuss whether natural selection would favour the transgenic EBF-producing thale cress plants if...
- 19M.2.SL.TZ2.1j: Discuss whether natural selection would favour the transgenic EBF-producing thale cress plants if...
- 19M.2.SL.TZ2.j: Discuss whether natural selection would favour the transgenic EBF-producing thale cress plants if...
-
19M.1.SL.TZ1.14:
At which stage of meiosis are bivalents formed?
A. Interphase
B. Prophase I
C. Prophase II
D. Metaphase II
- 19M.2.SL.TZ1.6b: Identify the chromosome that is affected by a trisomy in this individual, naming the condition...
-
19M.1.SL.TZ1.14:
At which stage of meiosis are bivalents formed?
A. Interphase
B. Prophase I
C. Prophase II
D. Metaphase II
-
19M.1.SL.TZ1.15:
Creeper in chickens is a condition in which the chickens are born with very short legs. The creeper allele (C) is dominant over the normal allele (c). Embryos which are homozygous for the dominant allele fail to develop into viable chickens and die before they hatch. What phenotypic ratio would you expect in the live offspring of a cross between two creeper chickens?
A. All creeper
B. 1 creeper; 2 normal
C. 2 creeper; 1 normal
D. 3 creeper; 1 normal
- 19M.2.SL.TZ1.b: Identify the chromosome that is affected by a trisomy in this individual, naming the condition...
-
19M.1.SL.TZ2.8:
Which statement correctly describes genome and proteome?
A. Only the genome but not the proteome can be analysed using gel electrophoresis.
B. The genome and the proteome are the same in all tissues in an organism.
C. In cells of different tissues, the genome is the same while the proteome varies.
D. Only mutations in the proteome but not in the genome cause any variability.
- 19M.2.SL.TZ2.2b: Outline the use of a karyogram during pregnancy.
-
19M.1.SL.TZ2.8:
Which statement correctly describes genome and proteome?
A. Only the genome but not the proteome can be analysed using gel electrophoresis.
B. The genome and the proteome are the same in all tissues in an organism.
C. In cells of different tissues, the genome is the same while the proteome varies.
D. Only mutations in the proteome but not in the genome cause any variability.
- 19M.2.SL.TZ2.2b: Outline the use of a karyogram during pregnancy.
- 19M.2.SL.TZ2.b: Outline the use of a karyogram during pregnancy.
- 19M.2.SL.TZ2.4b: Explain one cause of mutation.
-
19M.1.SL.TZ1.15:
Creeper in chickens is a condition in which the chickens are born with very short legs. The creeper allele (C) is dominant over the normal allele (c). Embryos which are homozygous for the dominant allele fail to develop into viable chickens and die before they hatch. What phenotypic ratio would you expect in the live offspring of a cross between two creeper chickens?
A. All creeper
B. 1 creeper; 2 normal
C. 2 creeper; 1 normal
D. 3 creeper; 1 normal
-
19M.1.SL.TZ1.16:
Which pedigree chart is consistent with the inheritance of red-green colour blindness?
[Source: © International Baccalaureate Organization 2019]
-
19M.1.SL.TZ1.16:
Which pedigree chart is consistent with the inheritance of red-green colour blindness?
[Source: © International Baccalaureate Organization 2019]
- 19M.1.HL.TZ1.11: What technique was used by John Cairns to measure the length of the DNA molecule in Escherichia...
-
19M.1.SL.TZ2.13:
The graph shows the incidence of trisomy resulting from non-disjunction in pregnancies at different maternal ages.
[Source: Center for Disease Control]
What can be inferred from the graph?
A. The incidence of three copies of a chromosome increases directly in proportion with the age of the mother.
B. The incidence of three sets of chromosomes increases from age 20.
C. The incidence of three copies of a chromosome increases the most from age 35.
D. The incidence of three sets of chromosomes increases the most from age 30.
- 19M.1.HL.TZ1.11: What technique was used by John Cairns to measure the length of the DNA molecule in Escherichia...
- 19M.2.SL.TZ2.4b: Explain one cause of mutation.
- 19M.2.SL.TZ2.b: Explain one cause of mutation.
-
19M.1.HL.TZ2.22:
Two restriction endonucleases (EcoRI and BamHI) were used to cut a DNA sample into smaller fragments. These were then subjected to gel electrophoresis and the results are shown. The lengths of the DNA fragments are measured in kilobases (kb). One kilobase is 1000 DNA bases.
[Source: © International Baccalaureate Organization 2019]
Which statement is supported by the data?
A. The DNA sample is approximately 16 kb in size.
B. Each endonuclease produces a 2 kb fragment.
C. Both endonucleases produce the same number of fragments.
D. The fragments produced using both endonucleases are all different from those produced by the individual endonucleases.
-
19M.1.SL.TZ2.13:
The graph shows the incidence of trisomy resulting from non-disjunction in pregnancies at different maternal ages.
[Source: Center for Disease Control]
What can be inferred from the graph?
A. The incidence of three copies of a chromosome increases directly in proportion with the age of the mother.
B. The incidence of three sets of chromosomes increases from age 20.
C. The incidence of three copies of a chromosome increases the most from age 35.
D. The incidence of three sets of chromosomes increases the most from age 30.
-
19M.1.HL.TZ2.22:
Two restriction endonucleases (EcoRI and BamHI) were used to cut a DNA sample into smaller fragments. These were then subjected to gel electrophoresis and the results are shown. The lengths of the DNA fragments are measured in kilobases (kb). One kilobase is 1000 DNA bases.
[Source: © International Baccalaureate Organization 2019]
Which statement is supported by the data?
A. The DNA sample is approximately 16 kb in size.
B. Each endonuclease produces a 2 kb fragment.
C. Both endonucleases produce the same number of fragments.
D. The fragments produced using both endonucleases are all different from those produced by the individual endonucleases.
-
19M.1.SL.TZ2.14:
The pedigree chart shows a family affected by cystic fibrosis.
[Source: © International Baccalaureate Organization 2019]
What is the genotype of the affected boy’s father?
A. AA only
B. Either AA or Aa
C. Aa only
D. aa only
-
19M.1.SL.TZ2.14:
The pedigree chart shows a family affected by cystic fibrosis.
[Source: © International Baccalaureate Organization 2019]
What is the genotype of the affected boy’s father?
A. AA only
B. Either AA or Aa
C. Aa only
D. aa only
- 19M.2.HL.TZ2.1a: Distinguish between the data for the leaves infested with the armyworm and the leaves infested...
- 19M.2.HL.TZ1.2a: Distinguish between the structure of the chromosomes of prokaryotes and eukaryotes.
- 19M.1.SL.TZ2.15: The children in a family have blood groups A, B and O. What are the genotypes of their...
- 19M.2.HL.TZ1.2a: Distinguish between the structure of the chromosomes of prokaryotes and eukaryotes.
- 19M.2.HL.TZ1.a: Distinguish between the structure of the chromosomes of prokaryotes and eukaryotes.
- 19M.2.HL.TZ2.1a: Distinguish between the data for the leaves infested with the armyworm and the leaves infested...
- 19M.2.HL.TZ2.a: Distinguish between the data for the leaves infested with the armyworm and the leaves infested...
- 19M.1.SL.TZ2.15: The children in a family have blood groups A, B and O. What are the genotypes of their...
- 19M.2.HL.TZ2.1b: Compare and contrast the effects of treatment of the leaves using C1 and C2 with the effects of...
- 19M.2.HL.TZ2.1b: Compare and contrast the effects of treatment of the leaves using C1 and C2 with the effects of...
- 19M.2.HL.TZ2.b: Compare and contrast the effects of treatment of the leaves using C1 and C2 with the effects of...
-
19M.1.SL.TZ2.16:
Genetically modified maize, called Bt maize, is thought to be affecting the monarch butterfly (Danaus plexippus) in the USA. What is the reason for this?
A. The monarch butterfly feeds on maize nectar, which contains Bt toxin.
B. The monarch caterpillar feeds on maize leaves, which contain Bt toxin.
C. Bt toxin kills the plants that the monarch caterpillar usually eats.
D. Bt toxin is in maize pollen, which blows on to plants that the monarch caterpillar eats.
- 19M.2.HL.TZ2.1c: Identify the process that was used to amplify the targeted genes.
- 19M.2.HL.TZ2.1c: Identify the process that was used to amplify the targeted genes.
- 19M.2.HL.TZ2.c: Identify the process that was used to amplify the targeted genes.
- 19M.2.HL.TZ1.2b: Outline the causes of sickle cell anemia.
-
19M.1.SL.TZ2.16:
Genetically modified maize, called Bt maize, is thought to be affecting the monarch butterfly (Danaus plexippus) in the USA. What is the reason for this?
A. The monarch butterfly feeds on maize nectar, which contains Bt toxin.
B. The monarch caterpillar feeds on maize leaves, which contain Bt toxin.
C. Bt toxin kills the plants that the monarch caterpillar usually eats.
D. Bt toxin is in maize pollen, which blows on to plants that the monarch caterpillar eats.
- 19M.2.HL.TZ1.2b: Outline the causes of sickle cell anemia.
- 19M.2.HL.TZ1.b: Outline the causes of sickle cell anemia.
- 19M.2.HL.TZ2.1d: Deduce, with a reason, which gene is first transcribed when exposed to C2.
- 19M.2.HL.TZ2.1d: Deduce, with a reason, which gene is first transcribed when exposed to C2.
- 19M.2.HL.TZ2.d: Deduce, with a reason, which gene is first transcribed when exposed to C2.
- 19M.2.SL.TZ2.1h: Identify, with a reason, the aphids that were most strongly repelled by EBF.
-
19M.2.HL.TZ2.1e:
Each gene is activated by one or more of the treatments. From the gel electrophoresis data, discuss the impact of the herbivorous mite infestation on gene activation compared to treatment with C1 and C2.
-
19M.2.HL.TZ2.1e:
Each gene is activated by one or more of the treatments. From the gel electrophoresis data, discuss the impact of the herbivorous mite infestation on gene activation compared to treatment with C1 and C2.
-
19M.2.HL.TZ2.e:
Each gene is activated by one or more of the treatments. From the gel electrophoresis data, discuss the impact of the herbivorous mite infestation on gene activation compared to treatment with C1 and C2.
- 19M.2.HL.TZ2.1f: Using the gene activation data, deduce, giving two reasons, whether the armyworm or the...
- 19M.2.HL.TZ1.2c.i: Identify, with a reason, the sex of this individual.
- 19M.2.SL.TZ2.1h: Identify, with a reason, the aphids that were most strongly repelled by EBF.
- 19M.2.HL.TZ1.2c.i: Identify, with a reason, the sex of this individual.
- 19M.2.HL.TZ1.c.i: Identify, with a reason, the sex of this individual.
- 19M.2.HL.TZ2.1f: Using the gene activation data, deduce, giving two reasons, whether the armyworm or the...
- 19M.2.HL.TZ2.f: Using the gene activation data, deduce, giving two reasons, whether the armyworm or the...
- 19M.2.SL.TZ2.h: Identify, with a reason, the aphids that were most strongly repelled by EBF.
- 19M.3.SL.TZ2.2a: Estimate the length of the molecule of DNA shown in the autoradiogram between the two...
- 19M.2.HL.TZ1.2c.ii: State the haploid number for this nucleus.
- 19M.3.SL.TZ2.2a: Estimate the length of the molecule of DNA shown in the autoradiogram between the two...
- 19M.2.HL.TZ2.7b: Mendel found the same pattern of inheritance in all the crosses that he performed. Outline, with...
- 19M.3.SL.TZ2.a: Estimate the length of the molecule of DNA shown in the autoradiogram between the two...
- 19M.3.SL.TZ2.2b: Determine, with a reason, the nucleotide base that was marked with...
- 19M.2.HL.TZ1.2c.ii: State the haploid number for this nucleus.
- 19M.2.HL.TZ1.c.ii: State the haploid number for this nucleus.
- 19M.3.SL.TZ2.2b: Determine, with a reason, the nucleotide base that was marked with...
- 19M.3.SL.TZ2.b: Determine, with a reason, the nucleotide base that was marked with...
- 19M.2.HL.TZ2.7b: Mendel found the same pattern of inheritance in all the crosses that he performed. Outline, with...
- 19M.2.HL.TZ2.b: Mendel found the same pattern of inheritance in all the crosses that he performed. Outline, with...
- 19N.2.SL.TZ0.3c: List three characteristics of eukaryotic homologous chromosomes.
- 19M.2.HL.TZ2.7c: Explain the cause of sickle cell anemia and how this disease affects humans.
- 19M.2.HL.TZ2.7c: Explain the cause of sickle cell anemia and how this disease affects humans.
- 19M.2.HL.TZ2.c: Explain the cause of sickle cell anemia and how this disease affects humans.
- 19N.2.HL.TZ0.2a: State the type of inheritance shown.
-
19N.2.SL.TZ0.1d:
State the proportion of the ancestral allele for the gene GS3 in the O. rufipogon-III population.
-
19N.2.SL.TZ0.1d:
State the proportion of the ancestral allele for the gene GS3 in the O. rufipogon-III population.
-
19N.2.SL.TZ0.d:
State the proportion of the ancestral allele for the gene GS3 in the O. rufipogon-III population.
- 19N.2.SL.TZ0.3c: List three characteristics of eukaryotic homologous chromosomes.
- 19N.2.SL.TZ0.1e: Distinguish between the proportion of ancestral and derived alleles for all three genes in O....
- 19N.2.SL.TZ0.1e: Distinguish between the proportion of ancestral and derived alleles for all three genes in O....
- 19N.2.SL.TZ0.e: Distinguish between the proportion of ancestral and derived alleles for all three genes in O....
- 19N.2.SL.TZ0.1f: State one reason for having a control group.
- 19N.2.HL.TZ0.2a: State the type of inheritance shown.
- 19N.2.HL.TZ0.a: State the type of inheritance shown.
- 19N.2.HL.TZ0.6b: Outline the structural and genetic characteristics of eukaryotic chromosomes.
- 19N.2.SL.TZ0.c: List three characteristics of eukaryotic homologous chromosomes.
- 19N.2.SL.TZ0.6b: Outline how two parents could have a child with any of the four ABO blood groups.
- 19N.2.HL.TZ0.6b: Outline the structural and genetic characteristics of eukaryotic chromosomes.
- 19N.2.HL.TZ0.b: Outline the structural and genetic characteristics of eukaryotic chromosomes.
- 19N.2.SL.TZ0.1f: State one reason for having a control group.
- 19N.2.SL.TZ0.f: State one reason for having a control group.
- 19N.2.SL.TZ0.6b: Outline how two parents could have a child with any of the four ABO blood groups.
- 19N.2.HL.TZ0.7b: Outline how two parents could have a child with any of the four ABO blood groups.
- 19N.2.SL.TZ0.b: Outline how two parents could have a child with any of the four ABO blood groups.
-
19N.1.SL.TZ0.14:
A pregnant woman had fetal cells removed by chorionic villus sampling and tested. The following karyogram was produced.
[Source: Mediscan / Alamy Stock Photo]
What does this show?
A. The child is female with Down syndrome.
B. The child is female without Down syndrome.
C. The child is male with Down syndrome.
D. The child is male without Down syndrome.
- 19N.2.HL.TZ0.7b: Outline how two parents could have a child with any of the four ABO blood groups.
- 19N.2.HL.TZ0.b: Outline how two parents could have a child with any of the four ABO blood groups.
- 19N.1.HL.TZ0.10: Which statements are characteristics of alleles? I. Alleles differ significantly in number of...
-
19N.1.SL.TZ0.14:
A pregnant woman had fetal cells removed by chorionic villus sampling and tested. The following karyogram was produced.
[Source: Mediscan / Alamy Stock Photo]
What does this show?
A. The child is female with Down syndrome.
B. The child is female without Down syndrome.
C. The child is male with Down syndrome.
D. The child is male without Down syndrome.
- 19N.1.HL.TZ0.10: Which statements are characteristics of alleles? I. Alleles differ significantly in number of...
- 19N.1.SL.TZ0.15: A variety of Pelargonium has yellow leaves. When plants of this variety are crossed, the...
-
19N.1.HL.TZ0.12:
The pedigree chart shows the inheritance of hemophilia in some of the descendants of Queen Victoria. Which letter points to a family member certain to be heterozygous?
[Source: © International Baccalaureate Organization 2019]
- 19N.1.SL.TZ0.15: A variety of Pelargonium has yellow leaves. When plants of this variety are crossed, the...
-
19N.1.HL.TZ0.12:
The pedigree chart shows the inheritance of hemophilia in some of the descendants of Queen Victoria. Which letter points to a family member certain to be heterozygous?
[Source: © International Baccalaureate Organization 2019]
-
19N.1.SL.TZ0.16:
A pair of alleles controls the secretion of antigens corresponding to blood group in saliva. Examine the pedigree chart.
[Source: © International Baccalaureate Organization 2019]
Based on this pedigree chart, which best describes the allele conferring antigen secretion in saliva?
A. Dominant
B. Recessive
C. Sex-linked
D. Co-dominant
-
19N.1.SL.TZ0.16:
A pair of alleles controls the secretion of antigens corresponding to blood group in saliva. Examine the pedigree chart.
[Source: © International Baccalaureate Organization 2019]
Based on this pedigree chart, which best describes the allele conferring antigen secretion in saliva?
A. Dominant
B. Recessive
C. Sex-linked
D. Co-dominant
- 19N.1.SL.TZ0.17: What is PCR used for? A. Separate fragments of DNA by size B. Amplify small amounts of DNA C....
- 20N.1.SL.TZ0.13: In the pedigree chart, individuals affected by a genetic disease are shown as shaded symbols....
- 19N.1.SL.TZ0.17: What is PCR used for? A. Separate fragments of DNA by size B. Amplify small amounts of DNA C....
-
20N.1.HL.TZ0.12:
In DNA profiling, short tandem repeats (STRs) of DNA are used, as these vary a great deal between individuals. Some skin cells were retrieved from a crime scene. Three STR sections of the DNA from these cells, from the victim and from a suspect, were analysed and the results are shown in the table.
What can be concluded from the gel electrophoresis data?
A. The suspect was at the crime scene.
B. The victim has the band moving the least distance.
C. The suspect and the victim have bands moving the same distance.
D. The skin cells have the band moving the greatest distance.
- 20N.1.SL.TZ0.13: In the pedigree chart, individuals affected by a genetic disease are shown as shaded symbols....
- 20N.1.SL.TZ0.14: Tall heterozygous pea plants were crossed and the resulting seeds grown. Out of 360 plants, 270...
- 20N.2.SL.TZ0.4b.i: Define mutation.
-
20N.1.HL.TZ0.12:
In DNA profiling, short tandem repeats (STRs) of DNA are used, as these vary a great deal between individuals. Some skin cells were retrieved from a crime scene. Three STR sections of the DNA from these cells, from the victim and from a suspect, were analysed and the results are shown in the table.
What can be concluded from the gel electrophoresis data?
A. The suspect was at the crime scene.
B. The victim has the band moving the least distance.
C. The suspect and the victim have bands moving the same distance.
D. The skin cells have the band moving the greatest distance.
-
20N.1.HL.TZ0.13:
Testing the chromosomes of a girl with Turner syndrome produced the following karyogram.
[Source: Turner’s syndrome karyotype 45,XO. This female lacks the second X chromosome present in the
normal karyotype. Symptoms include short stature, neck webbing, elbow deformity, widely spaced nipples with shield chest, primary amenorrhea, sexual infantilism and sterility. The ovaries are reduced to fibrous streaks. Also known as XO syndrome or ovarian short-stature syndrome. Credit: Wessex Reg. Genetics Centre. Attribution 4.0 International (CC BY 4.0).]The condition can result from non-disjunction occurring in anaphase I of meiosis in an egg cell. Two cells result from the first division, one of which would lead to Turner syndrome. Which chromosomes will be in the other cell (polar body) at the end of meiosis I?
A. 44 autosomes and X
B. 44 autosomes and XX
C. 22 autosomes and X
D. 22 autosomes and XX
-
20N.1.HL.TZ0.13:
Testing the chromosomes of a girl with Turner syndrome produced the following karyogram.
[Source: Turner’s syndrome karyotype 45,XO. This female lacks the second X chromosome present in the
normal karyotype. Symptoms include short stature, neck webbing, elbow deformity, widely spaced nipples with shield chest, primary amenorrhea, sexual infantilism and sterility. The ovaries are reduced to fibrous streaks. Also known as XO syndrome or ovarian short-stature syndrome. Credit: Wessex Reg. Genetics Centre. Attribution 4.0 International (CC BY 4.0).]The condition can result from non-disjunction occurring in anaphase I of meiosis in an egg cell. Two cells result from the first division, one of which would lead to Turner syndrome. Which chromosomes will be in the other cell (polar body) at the end of meiosis I?
A. 44 autosomes and X
B. 44 autosomes and XX
C. 22 autosomes and X
D. 22 autosomes and XX
- 20N.2.SL.TZ0.4b.i: Define mutation.
- 20N.2.SL.TZ0.b.i: Define mutation.
- 20N.1.SL.TZ0.14: Tall heterozygous pea plants were crossed and the resulting seeds grown. Out of 360 plants, 270...
- 20N.1.SL.TZ0.15: What are all the possible phenotypes of children born to a mother with blood group AB and a...
-
21M.2.HL.TZ1.7a:
Outline the inheritance of blood types in the ABO blood system in humans.
- 20N.1.SL.TZ0.15: What are all the possible phenotypes of children born to a mother with blood group AB and a...
-
21M.1.SL.TZ1.17:
A two-cell sea urchin (Echinoidea) embryo was physically separated by scientists into two cells. Each cell, through further embryonic development, became an adult sea urchin.
[Source: Clker-Free-Vector-Images/Pixabay.]
What is the relationship between the two adult sea urchins?
A. They are equivalent to non-identical twins.
B. Half of the genes would be the same.
C. Both adults would have haploid cells.
D. They are clones.
-
20N.2.SL.TZ0.6b:
Outline what occurs in cells in the first division of meiosis.
-
20N.2.SL.TZ0.6b:
Outline what occurs in cells in the first division of meiosis.
-
20N.2.SL.TZ0.b:
Outline what occurs in cells in the first division of meiosis.
-
21M.2.HL.TZ1.7a:
Outline the inheritance of blood types in the ABO blood system in humans.
-
20N.2.HL.TZ0.8c:
Discuss the process, including potential risks and benefits, of using bacteria to genetically modify plant crop species.
-
21M.1.SL.TZ1.17:
A two-cell sea urchin (Echinoidea) embryo was physically separated by scientists into two cells. Each cell, through further embryonic development, became an adult sea urchin.
[Source: Clker-Free-Vector-Images/Pixabay.]
What is the relationship between the two adult sea urchins?
A. They are equivalent to non-identical twins.
B. Half of the genes would be the same.
C. Both adults would have haploid cells.
D. They are clones.
-
21M.2.HL.TZ1.a:
Outline the inheritance of blood types in the ABO blood system in humans.
-
21M.2.HL.TZ1.8a:
Outline the process of DNA profiling.
- 21M.1.SL.TZ1.18: Which genotype would be normally found in a gamete? A. Rr B. RS C. rStt D. TUt
- 21M.1.SL.TZ1.18: Which genotype would be normally found in a gamete? A. Rr B. RS C. rStt D. TUt
-
20N.2.HL.TZ0.8c:
Discuss the process, including potential risks and benefits, of using bacteria to genetically modify plant crop species.
-
20N.2.HL.TZ0.c:
Discuss the process, including potential risks and benefits, of using bacteria to genetically modify plant crop species.
-
21M.2.HL.TZ1.8a:
Outline the process of DNA profiling.
- 21M.1.SL.TZ1.19: Which statement applies to meiosis and mitosis? A. Meiosis occurs in a greater number of...
-
21M.2.HL.TZ1.a:
Outline the process of DNA profiling.
-
21M.2.HL.TZ2.5b:
Outline how sperm are produced from diploid cells in the testis and how this production can be sustained over many decades of adult life.
- 21M.1.SL.TZ1.19: Which statement applies to meiosis and mitosis? A. Meiosis occurs in a greater number of...
-
21M.2.SL.TZ2.2c:
Distinguish between the outcomes of a cell dividing either by mitosis or meiosis.
-
21M.2.SL.TZ2.2c:
Distinguish between the outcomes of a cell dividing either by mitosis or meiosis.
-
21M.2.SL.TZ2.c:
Distinguish between the outcomes of a cell dividing either by mitosis or meiosis.
-
21M.2.HL.TZ2.5b:
Outline how sperm are produced from diploid cells in the testis and how this production can be sustained over many decades of adult life.
-
21M.1.SL.TZ2.13:
The electron micrograph shows a section through a plant cell.
[Source: Photo © E. Newcomb.]
In which structure(s) is the genome of the cell contained?
A. Z only
B. X, Y and Z only
C. W and X only
D. X and Y only
-
21M.2.HL.TZ2.b:
Outline how sperm are produced from diploid cells in the testis and how this production can be sustained over many decades of adult life.
-
21M.2.HL.TZ2.7a:
Describe the structure of the DNA molecule.
-
21M.1.SL.TZ2.13:
The electron micrograph shows a section through a plant cell.
[Source: Photo © E. Newcomb.]
In which structure(s) is the genome of the cell contained?
A. Z only
B. X, Y and Z only
C. W and X only
D. X and Y only
-
21M.2.HL.TZ2.7a:
Describe the structure of the DNA molecule.
- 21M.1.SL.TZ2.14: What feature of eukaryotic chromosomes distinguishes them from the chromosomes of...
-
21M.2.HL.TZ2.a:
Describe the structure of the DNA molecule.
- 21M.1.HL.TZ2.10: What is a feature of the human genome? A. Plasmids B. Messenger RNA C. Transfer RNA D....
- 21M.1.HL.TZ2.10: What is a feature of the human genome? A. Plasmids B. Messenger RNA C. Transfer RNA D....
- 21M.1.SL.TZ2.14: What feature of eukaryotic chromosomes distinguishes them from the chromosomes of...
- 21M.1.SL.TZ2.15: A woman with blood type A has three children with a man who has blood type AB. The first child...
- 21M.1.HL.TZ2.11: What feature of eukaryotic chromosomes distinguishes them from the chromosomes of...
- 21M.1.HL.TZ2.11: What feature of eukaryotic chromosomes distinguishes them from the chromosomes of...
- 21M.1.SL.TZ2.15: A woman with blood type A has three children with a man who has blood type AB. The first child...
-
21M.1.HL.TZ2.12:
The image shows tetrads in the anther of a lily. A tetrad is a group of four cells, produced when one mother cell divides by meiosis. The tetrad indicated by the arrow contains a total of 48 chromosomes.
[Source: [Tetrad], 2012. [image online] Available at: https://www.iasprr.org/old/iasprr-pix/lily/tetrad.jpg [accessed: 4 April 2019]. Photo courtesy of Professor Scott D. Russell.]
What is the diploid number of the plant?
A. 12
B. 24
C. 48
D. 96
- 21M.1.SL.TZ2.16: What benefit is derived from the use of Bt crops? A. It can lead to an increase in genetic...
-
21M.1.HL.TZ2.12:
The image shows tetrads in the anther of a lily. A tetrad is a group of four cells, produced when one mother cell divides by meiosis. The tetrad indicated by the arrow contains a total of 48 chromosomes.
[Source: [Tetrad], 2012. [image online] Available at: https://www.iasprr.org/old/iasprr-pix/lily/tetrad.jpg [accessed: 4 April 2019]. Photo courtesy of Professor Scott D. Russell.]
What is the diploid number of the plant?
A. 12
B. 24
C. 48
D. 96
- 21M.1.SL.TZ2.16: What benefit is derived from the use of Bt crops? A. It can lead to an increase in genetic...
-
21N.1.SL.TZ0.13:
John Cairns used the technique of autoradiography to produce photographs of DNA from the bacterium E. coli.
[Source: © Cold Spring Harbor Laboratory Press. Autoradiography of bacterium E. coli DNA - micrograph, The Chromosome of
Escherichia coli Cairns, J.P., 1963. Cold Spring Harbor Symposia, Quantitative Biology, 28(44).]Which conclusion was drawn from his experiments?
A. The DNA in all organisms is circular.
B. DNA in E. coli naturally contains thymidine.
C. DNA replication is conservative.
D. The DNA in E. coli is 900 μm in length.
-
21N.1.SL.TZ0.13:
John Cairns used the technique of autoradiography to produce photographs of DNA from the bacterium E. coli.
[Source: © Cold Spring Harbor Laboratory Press. Autoradiography of bacterium E. coli DNA - micrograph, The Chromosome of
Escherichia coli Cairns, J.P., 1963. Cold Spring Harbor Symposia, Quantitative Biology, 28(44).]Which conclusion was drawn from his experiments?
A. The DNA in all organisms is circular.
B. DNA in E. coli naturally contains thymidine.
C. DNA replication is conservative.
D. The DNA in E. coli is 900 μm in length.
- 21N.1.SL.TZ0.14: Down syndrome can be detected before birth by chorionic villus sampling. From where are the cells...
- 21N.1.SL.TZ0.14: Down syndrome can be detected before birth by chorionic villus sampling. From where are the cells...
-
21N.2.SL.TZ0.6b:
Explain the need for halving the chromosome number during a sexual life cycle and how this is done.
- 21N.1.SL.TZ0.15: In humans, male pattern baldness is caused by a recessive sex-linked gene found only on the X...
- 21N.1.SL.TZ0.15: In humans, male pattern baldness is caused by a recessive sex-linked gene found only on the X...
-
21N.2.SL.TZ0.6b:
Explain the need for halving the chromosome number during a sexual life cycle and how this is done.
-
21N.2.SL.TZ0.b:
Explain the need for halving the chromosome number during a sexual life cycle and how this is done.
- 21N.1.SL.TZ0.16: The image shows the result of DNA profiling of a mother, a child and four men. Which man is most...
- 21N.1.SL.TZ0.16: The image shows the result of DNA profiling of a mother, a child and four men. Which man is most...
-
21N.2.HL.TZ0.2a.i:
Draw a Punnett square to show all the possible genotypes of Queen Victoria’s children.
- 22M.1.SL.TZ1.13: The table shows the estimated total number of genes in several organisms. What can be deduced...
- 21N.1.HL.TZ1.12: Huntington’s disease can develop in middle age and leads to death of brain cells. It is carried...
- 21N.1.HL.TZ1.12: Huntington’s disease can develop in middle age and leads to death of brain cells. It is carried...
- 22M.1.SL.TZ1.13: The table shows the estimated total number of genes in several organisms. What can be deduced...
-
21N.2.HL.TZ0.2a.i:
Draw a Punnett square to show all the possible genotypes of Queen Victoria’s children.
-
21N.2.HL.TZ0.a.i:
Draw a Punnett square to show all the possible genotypes of Queen Victoria’s children.
-
21N.1.HL.TZ1.13:
A nucleus was removed from a cell of sheep P and fused with a denucleated egg cell of sheep Q. This was transplanted into the uterus of sheep R, which gave birth to Dolly.
[Source: Photo courtesy of The Roslin Institute, The University of Edinburgh, Roslin, Scotland, UK, n.d. Dolly the Sheep
in a field at The Roslin Institute. [image online] Available at: https://www.livescience.com/57961-dolly-the-sheepannouncement-
20-year-anniversary.html [Accessed 23 March 2020].]Which describes Dolly?
A. A clone of sheep P, because Dolly was formed from the nucleus of its udder cell
B. A clone of sheep Q, because Dolly was formed from one of its egg cells
C. A clone of sheep R, because Dolly developed in its uterus
D. Not a proper clone, as more than one sheep was involved in the development
- 21N.2.HL.TZ0.2a.ii: Deduce the genotype of Queen Victoria’s daughter Alice.
-
21N.1.HL.TZ1.13:
A nucleus was removed from a cell of sheep P and fused with a denucleated egg cell of sheep Q. This was transplanted into the uterus of sheep R, which gave birth to Dolly.
[Source: Photo courtesy of The Roslin Institute, The University of Edinburgh, Roslin, Scotland, UK, n.d. Dolly the Sheep
in a field at The Roslin Institute. [image online] Available at: https://www.livescience.com/57961-dolly-the-sheepannouncement-
20-year-anniversary.html [Accessed 23 March 2020].]Which describes Dolly?
A. A clone of sheep P, because Dolly was formed from the nucleus of its udder cell
B. A clone of sheep Q, because Dolly was formed from one of its egg cells
C. A clone of sheep R, because Dolly developed in its uterus
D. Not a proper clone, as more than one sheep was involved in the development
- 21N.2.HL.TZ0.2a.ii: Deduce the genotype of Queen Victoria’s daughter Alice.
- 21N.2.HL.TZ0.a.ii: Deduce the genotype of Queen Victoria’s daughter Alice.
- 22M.1.SL.TZ1.14: Chromosome numbers vary between species. Which statement refers to humans? A. An egg cell has 22...
-
22M.2.SL.TZ2.7c:
Suggest possible benefits and risks of using genetic modification to develop varieties of crop plant with traits such as drought resistance.
- 22M.1.SL.TZ1.14: Chromosome numbers vary between species. Which statement refers to humans? A. An egg cell has 22...
- 22M.1.SL.TZ1.15: What is produced by meiosis in a cell of a male animal? A. Four gametes, each with the same...
- 22M.2.SL.TZ1.4a: State the probability that Edward had hemophilia.
-
22M.2.SL.TZ2.7c:
Suggest possible benefits and risks of using genetic modification to develop varieties of crop plant with traits such as drought resistance.
- 22M.2.SL.TZ1.4a: State the probability that Edward had hemophilia.
- 22M.2.SL.TZ1.a: State the probability that Edward had hemophilia.
-
22M.2.SL.TZ1.4b:
Explain the reasons for none of the females in the pedigree chart having hemophilia.
- 22M.1.SL.TZ1.15: What is produced by meiosis in a cell of a male animal? A. Four gametes, each with the same...
-
22M.2.SL.TZ2.c:
Suggest possible benefits and risks of using genetic modification to develop varieties of crop plant with traits such as drought resistance.
- 22M.1.SL.TZ2.13: Which statement defines alleles? A. They are the different forms of a gene that have the same...
- 22M.1.SL.TZ1.16: Huntington’s disease is an autosomal dominant genetic disease. What are the chances of two...
-
22M.2.SL.TZ1.4b:
Explain the reasons for none of the females in the pedigree chart having hemophilia.
-
22M.2.SL.TZ1.b:
Explain the reasons for none of the females in the pedigree chart having hemophilia.
- 22M.1.SL.TZ2.13: Which statement defines alleles? A. They are the different forms of a gene that have the same...
- 22M.1.SL.TZ1.16: Huntington’s disease is an autosomal dominant genetic disease. What are the chances of two...
-
22M.1.SL.TZ2.14:
The karyogram shown belongs to a human being.
[Source: Reproduced from Tennakoon J, Kandasamy Y, Alcock G, Koh TH. Edwards syndrome with double trisomy. Singapore Med J. 2008 Jul;49(7):e190-1. PMID: 18695855.]
What can be deduced from this karyogram?
A. The person is a male with Down syndrome.
B. The person is a female with Down syndrome.
C. The person is a male with a genetic disorder.
D. The person is a female with a missing chromosome.
-
22M.1.SL.TZ2.14:
The karyogram shown belongs to a human being.
[Source: Reproduced from Tennakoon J, Kandasamy Y, Alcock G, Koh TH. Edwards syndrome with double trisomy. Singapore Med J. 2008 Jul;49(7):e190-1. PMID: 18695855.]
What can be deduced from this karyogram?
A. The person is a male with Down syndrome.
B. The person is a female with Down syndrome.
C. The person is a male with a genetic disorder.
D. The person is a female with a missing chromosome.
- 22M.1.HL.TZ1.12: Which process occurs in meiosis but not in mitosis? A. Attachment of spindle fibres to the...
- 22M.1.HL.TZ1.12: Which process occurs in meiosis but not in mitosis? A. Attachment of spindle fibres to the...
- 22M.2.SL.TZ1.7b: Distinguish between the processes of meiosis and mitosis.
- 22M.1.SL.TZ2.15: The pedigree chart shows the inheritance of hemochromatosis, a genetic disease which causes an...
- 22M.2.SL.TZ1.7b: Distinguish between the processes of meiosis and mitosis.
- 22M.2.SL.TZ1.b: Distinguish between the processes of meiosis and mitosis.
- 22M.1.HL.TZ2.10: Where can the entire genome of an organism be found? A. In the DNA present in plasmids of a...
- 22M.1.SL.TZ2.15: The pedigree chart shows the inheritance of hemochromatosis, a genetic disease which causes an...
- 22M.1.HL.TZ2.10: Where can the entire genome of an organism be found? A. In the DNA present in plasmids of a...
-
22M.1.SL.TZ2.16:
A cloning method used for livestock involves in vitro fertilization (IVF) with selected male and female gametes. The diagram shows the steps followed after in vitro fertilization.
[Source: Aldona Griskeviciene / Shutterstock.com.]
What does X represent?
A. A group of eggs
B. An embryo
C. A follicle
D. A group of zygotes
- 22M.2.HL.TZ1.4a: State the level of protein structure at which the polypeptide chains of hemoglobin are combined.
-
22M.2.SL.TZ2.6b:
A family has a history of hemophilia that is caused by a sex-linked recessive allele. A woman from this family is a carrier and marries a man who does not have the allele. Showing your working, determine the probability of their children having the disease.
-
22M.1.SL.TZ2.16:
A cloning method used for livestock involves in vitro fertilization (IVF) with selected male and female gametes. The diagram shows the steps followed after in vitro fertilization.
[Source: Aldona Griskeviciene / Shutterstock.com.]
What does X represent?
A. A group of eggs
B. An embryo
C. A follicle
D. A group of zygotes
- 22M.2.HL.TZ1.4a: State the level of protein structure at which the polypeptide chains of hemoglobin are combined.
- 22M.2.HL.TZ1.a: State the level of protein structure at which the polypeptide chains of hemoglobin are combined.
-
22M.2.SL.TZ2.6b:
A family has a history of hemophilia that is caused by a sex-linked recessive allele. A woman from this family is a carrier and marries a man who does not have the allele. Showing your working, determine the probability of their children having the disease.
-
22M.2.SL.TZ2.b:
A family has a history of hemophilia that is caused by a sex-linked recessive allele. A woman from this family is a carrier and marries a man who does not have the allele. Showing your working, determine the probability of their children having the disease.
- 22M.1.SL.TZ2.17: A group of students used quadrat sampling to gather data on the presence of two plant species in...
-
22M.2.HL.TZ1.4c:
Outline the role of tRNA in hemoglobin synthesis.
- 22M.1.SL.TZ2.17: A group of students used quadrat sampling to gather data on the presence of two plant species in...
-
22M.2.HL.TZ1.4c:
Outline the role of tRNA in hemoglobin synthesis.
-
22M.2.HL.TZ1.c:
Outline the role of tRNA in hemoglobin synthesis.
-
22N.2.SL.TZ0.4a:
Draw the symbol for individual X on the diagram.
- 22N.1.SL.TZ0.13: What is a difference between two alleles of a gene? A. Their positions on homologous...
-
22M.2.HL.TZ1.8b:
Describe how DNA profiling can be used to establish paternity.
-
22M.2.HL.TZ1.8b:
Describe how DNA profiling can be used to establish paternity.
-
22M.2.HL.TZ1.b:
Describe how DNA profiling can be used to establish paternity.
-
22M.2.HL.TZ2.2b.ii:
Explain Cairns’s technique to measure the length of the DNA molecule.
-
22M.2.HL.TZ2.2b.ii:
Explain Cairns’s technique to measure the length of the DNA molecule.
-
22M.2.HL.TZ2.b.ii:
Explain Cairns’s technique to measure the length of the DNA molecule.
-
22N.2.SL.TZ0.4a:
Draw the symbol for individual X on the diagram.
-
22N.1.HL.TZ0.13:
Amniocentesis and chorionic villus sampling (CVS) are used to test for fetal abnormalities. Which statement is a valid comparison between the two tests?
A. CVS is performed later in pregnancy but has more risk of miscarriage than amniocentesis.
B. Amniocentesis is performed earlier in pregnancy but has more risk of miscarriage than CVS.
C. CVS is performed earlier in pregnancy but has more risk of miscarriage than amniocentesis.
D. Amniocentesis is performed later in pregnancy but has more risk of miscarriage than CVS.
-
22N.2.SL.TZ0.a:
Draw the symbol for individual X on the diagram.
-
22N.2.SL.TZ0.4b:
Calculate the probability of male Y having an allele for the disorder.
-
22N.2.SL.TZ0.4b:
Calculate the probability of male Y having an allele for the disorder.
-
22N.1.HL.TZ0.13:
Amniocentesis and chorionic villus sampling (CVS) are used to test for fetal abnormalities. Which statement is a valid comparison between the two tests?
A. CVS is performed later in pregnancy but has more risk of miscarriage than amniocentesis.
B. Amniocentesis is performed earlier in pregnancy but has more risk of miscarriage than CVS.
C. CVS is performed earlier in pregnancy but has more risk of miscarriage than amniocentesis.
D. Amniocentesis is performed later in pregnancy but has more risk of miscarriage than CVS.
- 22N.1.SL.TZ0.13: What is a difference between two alleles of a gene? A. Their positions on homologous...
- 22N.1.SL.TZ0.14: Which event occurs in the first division of meiosis? A. Synthesis of DNA B. Pulling apart of...
-
22N.2.SL.TZ0.b:
Calculate the probability of male Y having an allele for the disorder.
- 22N.2.SL.TZ0.4c: Explain how the information in the box labelled B indicates that the gene is not sex-linked.
- 22N.2.SL.TZ0.4c: Explain how the information in the box labelled B indicates that the gene is not sex-linked.
- 22N.1.SL.TZ0.14: Which event occurs in the first division of meiosis? A. Synthesis of DNA B. Pulling apart of...
- 22N.2.SL.TZ0.c: Explain how the information in the box labelled B indicates that the gene is not sex-linked.
-
22N.2.SL.TZ0.4d:
Explain how a single base substitution mutation in DNA can cause a change to a protein.
-
22N.1.SL.TZ0.15:
A couple have four children whose blood groups are A, B and AB. What is the likely combination of the parents’ genotypes?
A. IAi and IBi
B. IAi and IBIB
C. IAIB and ii
D. IAIA and IBIB
-
22N.2.SL.TZ0.4d:
Explain how a single base substitution mutation in DNA can cause a change to a protein.
-
22N.2.SL.TZ0.d:
Explain how a single base substitution mutation in DNA can cause a change to a protein.
-
22N.2.HL.TZ0.2a:
Identify the stage of meiosis shown where exchange of genetic material occurs.
-
22N.1.SL.TZ0.15:
A couple have four children whose blood groups are A, B and AB. What is the likely combination of the parents’ genotypes?
A. IAi and IBi
B. IAi and IBIB
C. IAIB and ii
D. IAIA and IBIB
- 22N.1.SL.TZ0.16: A process for genetically modifying a plant is shown. What is the name of enzyme II and the...
-
22N.2.HL.TZ0.2a:
Identify the stage of meiosis shown where exchange of genetic material occurs.
-
22N.2.HL.TZ0.a:
Identify the stage of meiosis shown where exchange of genetic material occurs.
-
23M.1.HL.TZ1.34:
A total of 271 164 people were tested for blood groups in Mexico. The pie chart summarizes the ABO blood group distribution.
[Source: Canizalez-Román, A. et al., 2018. Blood Groups Distribution and Gene Diversity
of the ABO and Rh (D) Loci in the Mexican Population.
BioMed Research International, (Article ID 1925619).
http://dx.doi.org/10.1155/2018/1925619. Public domain.]What can be concluded from the ABO blood group distribution in Mexico?
A. Allele frequencies are not the same for all blood group alleles.
B. The majority of the Mexican population shows a co-dominant phenotype.
C. Most of the Mexican population can receive blood from all blood groups.
D. Only 2 % of the Mexican population have a heterozygous genotype for blood groups.
- 22N.1.SL.TZ0.16: A process for genetically modifying a plant is shown. What is the name of enzyme II and the...
-
22N.1.SL.TZ0.24:
A short sequence of amino acids (represented by letters) in cytochrome c is shown for six vertebrates. Letters in bold indicate identical amino acids for all species.
Which statement refers to this section of cytochrome c?
A. The DNA base sequences for human and rhesus monkey are different.
B. The most DNA base changes are between humans and snapping turtles.
C. The largest number of amino acid differences is two.
D. The amino acid at position 32 is the most variable.
-
22N.1.SL.TZ0.24:
A short sequence of amino acids (represented by letters) in cytochrome c is shown for six vertebrates. Letters in bold indicate identical amino acids for all species.
Which statement refers to this section of cytochrome c?
A. The DNA base sequences for human and rhesus monkey are different.
B. The most DNA base changes are between humans and snapping turtles.
C. The largest number of amino acid differences is two.
D. The amino acid at position 32 is the most variable.
-
23M.2.HL.TZ1.5a:
Explain the conclusion that can be drawn from Cross 1.
-
23M.2.SL.TZ1.5a:
Explain the conclusion that can be drawn from Cross 1.
-
23M.1.HL.TZ1.34:
A total of 271 164 people were tested for blood groups in Mexico. The pie chart summarizes the ABO blood group distribution.
[Source: Canizalez-Román, A. et al., 2018. Blood Groups Distribution and Gene Diversity
of the ABO and Rh (D) Loci in the Mexican Population.
BioMed Research International, (Article ID 1925619).
http://dx.doi.org/10.1155/2018/1925619. Public domain.]What can be concluded from the ABO blood group distribution in Mexico?
A. Allele frequencies are not the same for all blood group alleles.
B. The majority of the Mexican population shows a co-dominant phenotype.
C. Most of the Mexican population can receive blood from all blood groups.
D. Only 2 % of the Mexican population have a heterozygous genotype for blood groups.
-
23M.2.HL.TZ1.5a:
Explain the conclusion that can be drawn from Cross 1.
-
23M.2.HL.TZ1.a:
Explain the conclusion that can be drawn from Cross 1.
-
23M.2.SL.TZ1.5a:
Explain the conclusion that can be drawn from Cross 1.
-
23M.2.SL.TZ1.a:
Explain the conclusion that can be drawn from Cross 1.
-
23M.1.HL.TZ2.13:
The pedigree chart shows the inheritance of three generations of Duane syndrome, a condition caused by a dominant allele that affects alignment of the eyes.
[Source: Yang, M.-M., Ho, M. et al., 2013. Pedigree of a Chinese family with Duane retraction syndrome. [diagram online]
Available at: https://www.researchgate.net/figure/Pedigree-of-a-Chinese-family-with-Duane-retraction-syndrome-
Squares-men-circles_fig1_236921765 [Accessed 5 October 2021]. Public domain.]If individuals II:1 and II:2 had a third child, what is the probability that the child would have Duane syndrome?
A. 25 %
B. 50 %
C. 75 %
D. 100 %
- 23M.2.HL.TZ2.4ai: State with a reason whether pangolins are autotrophic or heterotrophic.
- 23M.2.HL.TZ2.4ai: State with a reason whether pangolins are autotrophic or heterotrophic.
- 23M.2.HL.TZ2.i: State with a reason whether pangolins are autotrophic or heterotrophic.
-
23M.1.SL.TZ2.16:
The pedigree chart shows the inheritance of three generations of Duane syndrome, a condition caused by a dominant allele that affects alignment of the eyes.
[Source: Yang, M.-M., Ho, M. et al., 2013. Pedigree of a Chinese family with Duane retraction syndrome. [diagram online]
Available at: https://www.researchgate.net/figure/Pedigree-of-a-Chinese-family-with-Duane-retraction-syndrome-
Squares-men-circles_fig1_236921765 [Accessed 5 October 2021]. Public domain.]If individuals II:1 and II:2 had a third child, what is the probability that the child would have Duane syndrome?
A. 25 %
B. 50 %
C. 75 %
D. 100 %
-
23M.1.SL.TZ2.16:
The pedigree chart shows the inheritance of three generations of Duane syndrome, a condition caused by a dominant allele that affects alignment of the eyes.
[Source: Yang, M.-M., Ho, M. et al., 2013. Pedigree of a Chinese family with Duane retraction syndrome. [diagram online]
Available at: https://www.researchgate.net/figure/Pedigree-of-a-Chinese-family-with-Duane-retraction-syndrome-
Squares-men-circles_fig1_236921765 [Accessed 5 October 2021]. Public domain.]If individuals II:1 and II:2 had a third child, what is the probability that the child would have Duane syndrome?
A. 25 %
B. 50 %
C. 75 %
D. 100 %
-
23M.1.HL.TZ2.13:
The pedigree chart shows the inheritance of three generations of Duane syndrome, a condition caused by a dominant allele that affects alignment of the eyes.
[Source: Yang, M.-M., Ho, M. et al., 2013. Pedigree of a Chinese family with Duane retraction syndrome. [diagram online]
Available at: https://www.researchgate.net/figure/Pedigree-of-a-Chinese-family-with-Duane-retraction-syndrome-
Squares-men-circles_fig1_236921765 [Accessed 5 October 2021]. Public domain.]If individuals II:1 and II:2 had a third child, what is the probability that the child would have Duane syndrome?
A. 25 %
B. 50 %
C. 75 %
D. 100 %
- 23M.1.HL.TZ2.31: What is a result of crossing over in meiosis? A. Gene linkage B. Non-disjunction C. Haploid...
- 23M.1.HL.TZ1.1: The micrograph shows two types of blood cell. What determines the differences between the two...
- 23M.1.SL.TZ1.1: The micrograph shows two types of blood cell. What determines the differences between the two...
- 23M.1.HL.TZ2.31: What is a result of crossing over in meiosis? A. Gene linkage B. Non-disjunction C. Haploid...
- 23M.1.HL.TZ2.32: In the fruit fly Drosophila, the alleles for red eyes and brown bodies are dominant to the...
- 23M.1.HL.TZ2.32: In the fruit fly Drosophila, the alleles for red eyes and brown bodies are dominant to the...
-
23M.2.SL.TZ2.2a:
State how many chromosomes there would be in male or female gametes of L. purpureus.
-
23M.2.SL.TZ2.2a:
State how many chromosomes there would be in male or female gametes of L. purpureus.
- 23M.1.HL.TZ1.1: The micrograph shows two types of blood cell. What determines the differences between the two...
- 23M.1.SL.TZ1.1: The micrograph shows two types of blood cell. What determines the differences between the two...
-
23M.2.SL.TZ2.a:
State how many chromosomes there would be in male or female gametes of L. purpureus.
-
23M.2.SL.TZ1.6a:
Outline the sequence of events that occurs during mitosis.
-
23M.1.HL.TZ1.10:
Scientists sequenced the genes in each chromosome of chimpanzees (Pan troglodytes) and humans (Homo sapiens). The graph shows the mean divergence between the genes of these species by chromosome.
[Source: Material from: Mikkelsen, T.S. et al, Initial sequence of the chimpanzee genome and
comparison with the human genome, 2005 Nature, reproduced with permission of SNCSC.]
What can be deduced from this data?
A. Autosomes are more similar than Y chromosomes.B. There is the same number of chromosomes in humans and chimpanzees.
C. Humans are more closely related to chimpanzees than to other species.
D. Smaller chromosomes are more similar than larger chromosomes.
-
23M.1.SL.TZ1.14:
Scientists sequenced the genes in each chromosome of chimpanzees (Pan troglodytes) and humans (Homo sapiens). The graph shows the mean divergence between the genes of these species by chromosome.
[Source: Material from: Mikkelsen, T.S. et al, Initial sequence of the chimpanzee genome and
comparison with the human genome, 2005 Nature, reproduced with permission of SNCSC.]
What can be deduced from this data?
A. Autosomes are more similar than Y chromosomes.B. There is the same number of chromosomes in humans and chimpanzees.
C. Humans are more closely related to chimpanzees than to other species.
D. Smaller chromosomes are more similar than larger chromosomes.
-
23M.2.SL.TZ1.6a:
Outline the sequence of events that occurs during mitosis.
-
23M.2.SL.TZ1.a:
Outline the sequence of events that occurs during mitosis.
-
23M.1.SL.TZ1.14:
Scientists sequenced the genes in each chromosome of chimpanzees (Pan troglodytes) and humans (Homo sapiens). The graph shows the mean divergence between the genes of these species by chromosome.
[Source: Material from: Mikkelsen, T.S. et al, Initial sequence of the chimpanzee genome and
comparison with the human genome, 2005 Nature, reproduced with permission of SNCSC.]
What can be deduced from this data?
A. Autosomes are more similar than Y chromosomes.B. There is the same number of chromosomes in humans and chimpanzees.
C. Humans are more closely related to chimpanzees than to other species.
D. Smaller chromosomes are more similar than larger chromosomes.
-
23M.1.HL.TZ1.10:
Scientists sequenced the genes in each chromosome of chimpanzees (Pan troglodytes) and humans (Homo sapiens). The graph shows the mean divergence between the genes of these species by chromosome.
[Source: Material from: Mikkelsen, T.S. et al, Initial sequence of the chimpanzee genome and
comparison with the human genome, 2005 Nature, reproduced with permission of SNCSC.]
What can be deduced from this data?
A. Autosomes are more similar than Y chromosomes.B. There is the same number of chromosomes in humans and chimpanzees.
C. Humans are more closely related to chimpanzees than to other species.
D. Smaller chromosomes are more similar than larger chromosomes.
-
23M.1.HL.TZ1.11:
The micrograph shows a cross section of a lily (Lilium longiflorum) anther.
[Source: Sinhyu / iStock.]
What can be found in X?
A. Haploid nuclei produced by meiosis
B. Diploid nuclei produced by fertilization
C. Haploid nuclei produced by mitosis
D. Diploid nuclei produced by pollination
-
23M.1.HL.TZ1.11:
The micrograph shows a cross section of a lily (Lilium longiflorum) anther.
[Source: Sinhyu / iStock.]
What can be found in X?
A. Haploid nuclei produced by meiosis
B. Diploid nuclei produced by fertilization
C. Haploid nuclei produced by mitosis
D. Diploid nuclei produced by pollination
-
23M.1.HL.TZ1.26:
DNA methylation profiles in zebrafish (Danio rerio) gametes were determined. The methylated areas were divided into three groups according to the amount of methylation: high, medium and low methylation.
[Source: Potok, M.E., Nix, D.A., Parnell, T.J. and Cairns, B.R., 2013.
Reprogramming the Maternal Zebrafish Genome afterFertilization to
Match the Paternal Methylation Pattern.
Cell, [e-journal] 153(4), pp. 759–772. http://dx.doi.org/10.1016/j.
cell.2013.04.030.]Methylation of DNA in sperm and egg is removed immediately after fertilization. What is the reason for this?
A. Methylation allows RNA polymerase to join the promoter.B. It is needed to form homologous pairs of chromosomes.
C. It allows expression of genes linked to early development.
D. Transcription of promoters only occurs in methylated genes.
-
23M.1.HL.TZ1.26:
DNA methylation profiles in zebrafish (Danio rerio) gametes were determined. The methylated areas were divided into three groups according to the amount of methylation: high, medium and low methylation.
[Source: Potok, M.E., Nix, D.A., Parnell, T.J. and Cairns, B.R., 2013.
Reprogramming the Maternal Zebrafish Genome afterFertilization to
Match the Paternal Methylation Pattern.
Cell, [e-journal] 153(4), pp. 759–772. http://dx.doi.org/10.1016/j.
cell.2013.04.030.]Methylation of DNA in sperm and egg is removed immediately after fertilization. What is the reason for this?
A. Methylation allows RNA polymerase to join the promoter.B. It is needed to form homologous pairs of chromosomes.
C. It allows expression of genes linked to early development.
D. Transcription of promoters only occurs in methylated genes.
Sub sections and their related questions
3.1 Genes
-
17N.3.HL.TZ0.03b:
Some regions of DNA act as telomeres or produce tRNA. State one other function of DNA sequences that do not code for protein.
- 18M.2.HL.TZ1.4a: Sickle cell anemia is due to a single base substitution in DNA. Using the diagram, outline how...
- 18M.1.SL.TZ2.12: Some yeast genes can be replaced by human genes that then continue to produce the same human...
- 18M.1.SL.TZ2.13: What determines the genomic size of a species? A. The total amount of DNA B. The total number...
-
19M.1.SL.TZ1.13:
The system of sex determination in chimpanzees (Pan troglodytes) is the same as in other mammals. A chimpanzee has 48 chromosomes in the nuclei of its body cells.
What can be deduced from this information?
A. The sex of the chimpanzee
B. The number of genes in each chromosome
C. Whether non-disjunction has occurred
D. The number of autosomes in a diploid cell
-
19M.1.SL.TZ2.8:
Which statement correctly describes genome and proteome?
A. Only the genome but not the proteome can be analysed using gel electrophoresis.
B. The genome and the proteome are the same in all tissues in an organism.
C. In cells of different tissues, the genome is the same while the proteome varies.
D. Only mutations in the proteome but not in the genome cause any variability.
- 19M.2.HL.TZ1.2b: Outline the causes of sickle cell anemia.
- 19M.2.HL.TZ2.7c: Explain the cause of sickle cell anemia and how this disease affects humans.
-
19N.2.SL.TZ0.1d:
State the proportion of the ancestral allele for the gene GS3 in the O. rufipogon-III population.
- 19N.2.SL.TZ0.1e: Distinguish between the proportion of ancestral and derived alleles for all three genes in O....
- 19N.2.SL.TZ0.1f: State one reason for having a control group.
- 19N.1.HL.TZ0.10: Which statements are characteristics of alleles? I. Alleles differ significantly in number of...
- 20N.2.SL.TZ0.4b.i: Define mutation.
-
21M.1.SL.TZ2.13:
The electron micrograph shows a section through a plant cell.
[Source: Photo © E. Newcomb.]
In which structure(s) is the genome of the cell contained?
A. Z only
B. X, Y and Z only
C. W and X only
D. X and Y only
- 21M.1.HL.TZ2.10: What is a feature of the human genome? A. Plasmids B. Messenger RNA C. Transfer RNA D....
- 22M.1.SL.TZ1.13: The table shows the estimated total number of genes in several organisms. What can be deduced...
- 22M.1.SL.TZ2.13: Which statement defines alleles? A. They are the different forms of a gene that have the same...
- 22M.2.HL.TZ1.4a: State the level of protein structure at which the polypeptide chains of hemoglobin are combined.
-
22M.2.HL.TZ1.4c:
Outline the role of tRNA in hemoglobin synthesis.
-
22N.2.SL.TZ0.4d:
Explain how a single base substitution mutation in DNA can cause a change to a protein.
- 22N.1.SL.TZ0.13: What is a difference between two alleles of a gene? A. Their positions on homologous...
-
22N.1.SL.TZ0.24:
A short sequence of amino acids (represented by letters) in cytochrome c is shown for six vertebrates. Letters in bold indicate identical amino acids for all species.
Which statement refers to this section of cytochrome c?
A. The DNA base sequences for human and rhesus monkey are different.
B. The most DNA base changes are between humans and snapping turtles.
C. The largest number of amino acid differences is two.
D. The amino acid at position 32 is the most variable.
- 23M.1.HL.TZ1.1: The micrograph shows two types of blood cell. What determines the differences between the two...
- 23M.1.SL.TZ1.1: The micrograph shows two types of blood cell. What determines the differences between the two...
-
19N.2.SL.TZ0.1d:
State the proportion of the ancestral allele for the gene GS3 in the O. rufipogon-III population.
- 19N.2.SL.TZ0.1e: Distinguish between the proportion of ancestral and derived alleles for all three genes in O....
- 19N.2.SL.TZ0.1f: State one reason for having a control group.
-
19N.2.SL.TZ0.d:
State the proportion of the ancestral allele for the gene GS3 in the O. rufipogon-III population.
- 19N.2.SL.TZ0.e: Distinguish between the proportion of ancestral and derived alleles for all three genes in O....
- 19N.2.SL.TZ0.f: State one reason for having a control group.
- 19N.1.HL.TZ0.10: Which statements are characteristics of alleles? I. Alleles differ significantly in number of...
- 20N.2.SL.TZ0.4b.i: Define mutation.
- 20N.2.SL.TZ0.b.i: Define mutation.
-
21M.1.SL.TZ2.13:
The electron micrograph shows a section through a plant cell.
[Source: Photo © E. Newcomb.]
In which structure(s) is the genome of the cell contained?
A. Z only
B. X, Y and Z only
C. W and X only
D. X and Y only
- 21M.1.HL.TZ2.10: What is a feature of the human genome? A. Plasmids B. Messenger RNA C. Transfer RNA D....
- 22M.1.SL.TZ1.13: The table shows the estimated total number of genes in several organisms. What can be deduced...
- 22M.1.SL.TZ2.13: Which statement defines alleles? A. They are the different forms of a gene that have the same...
- 22M.2.HL.TZ1.4a: State the level of protein structure at which the polypeptide chains of hemoglobin are combined.
-
22M.2.HL.TZ1.4c:
Outline the role of tRNA in hemoglobin synthesis.
- 22M.2.HL.TZ1.a: State the level of protein structure at which the polypeptide chains of hemoglobin are combined.
-
22M.2.HL.TZ1.c:
Outline the role of tRNA in hemoglobin synthesis.
-
22N.2.SL.TZ0.4d:
Explain how a single base substitution mutation in DNA can cause a change to a protein.
-
22N.2.SL.TZ0.d:
Explain how a single base substitution mutation in DNA can cause a change to a protein.
- 22N.1.SL.TZ0.13: What is a difference between two alleles of a gene? A. Their positions on homologous...
-
22N.1.SL.TZ0.24:
A short sequence of amino acids (represented by letters) in cytochrome c is shown for six vertebrates. Letters in bold indicate identical amino acids for all species.
Which statement refers to this section of cytochrome c?
A. The DNA base sequences for human and rhesus monkey are different.
B. The most DNA base changes are between humans and snapping turtles.
C. The largest number of amino acid differences is two.
D. The amino acid at position 32 is the most variable.
-
17N.3.HL.TZ0.03b:
Some regions of DNA act as telomeres or produce tRNA. State one other function of DNA sequences that do not code for protein.
-
17N.3.HL.TZ0.b:
Some regions of DNA act as telomeres or produce tRNA. State one other function of DNA sequences that do not code for protein.
- 23M.1.HL.TZ1.1: The micrograph shows two types of blood cell. What determines the differences between the two...
- 23M.1.SL.TZ1.1: The micrograph shows two types of blood cell. What determines the differences between the two...
- 18M.2.HL.TZ1.4a: Sickle cell anemia is due to a single base substitution in DNA. Using the diagram, outline how...
- 18M.2.HL.TZ1.a: Sickle cell anemia is due to a single base substitution in DNA. Using the diagram, outline how...
- 18M.1.SL.TZ2.12: Some yeast genes can be replaced by human genes that then continue to produce the same human...
- 18M.1.SL.TZ2.13: What determines the genomic size of a species? A. The total amount of DNA B. The total number...
-
19M.1.SL.TZ1.13:
The system of sex determination in chimpanzees (Pan troglodytes) is the same as in other mammals. A chimpanzee has 48 chromosomes in the nuclei of its body cells.
What can be deduced from this information?
A. The sex of the chimpanzee
B. The number of genes in each chromosome
C. Whether non-disjunction has occurred
D. The number of autosomes in a diploid cell
-
19M.1.SL.TZ2.8:
Which statement correctly describes genome and proteome?
A. Only the genome but not the proteome can be analysed using gel electrophoresis.
B. The genome and the proteome are the same in all tissues in an organism.
C. In cells of different tissues, the genome is the same while the proteome varies.
D. Only mutations in the proteome but not in the genome cause any variability.
- 19M.2.HL.TZ1.2b: Outline the causes of sickle cell anemia.
- 19M.2.HL.TZ1.b: Outline the causes of sickle cell anemia.
- 19M.2.HL.TZ2.7c: Explain the cause of sickle cell anemia and how this disease affects humans.
- 19M.2.HL.TZ2.c: Explain the cause of sickle cell anemia and how this disease affects humans.
3.2 Chromosomes
-
17N.1.HL.TZ0.10:
The image shows a karyogram.
[Source: https://commons.wikimedia.org/wiki/File:Karyotype_of_sheep_(Ovis_aries).png, by M. Singh, X. Ma, E. Amoah and G. Kannan]
What information can be determined from this karyogram?
A. The sex is female.
B. The haploid number is 54.
C. Disjunction occurred during meiosis.
D. The species is not human.
- 18M.1.SL.TZ1.14: What is the same in all parts of homologous chromosomes? A. Base pair sequence B. Alleles C....
- 18M.2.SL.TZ2.2b.ii: Distinguish between the chromosomes of eukaryotic cells and prokaryotic cells.
- 18M.1.HL.TZ2.16: For what purpose is a karyogram used? A. To identify gene loci in a species B. To identify...
-
18N.1.HL.TZ0.11:
The image shows chromosomes from an insect (2 n = 8).
Which pair of chromosomes are the sex chromosomes of this insect species?
A. c and e
B. a and h
C. f and h
D. a and e
- 19M.1.HL.TZ1.11: What technique was used by John Cairns to measure the length of the DNA molecule in Escherichia...
- 19M.2.SL.TZ1.6a: Identify, with a reason, the sex of this individual.
- 19M.2.SL.TZ1.6b: Identify the chromosome that is affected by a trisomy in this individual, naming the condition...
- 19M.2.SL.TZ2.2b: Outline the use of a karyogram during pregnancy.
- 19M.2.HL.TZ1.2a: Distinguish between the structure of the chromosomes of prokaryotes and eukaryotes.
- 19M.2.HL.TZ1.2c.i: Identify, with a reason, the sex of this individual.
- 19M.3.SL.TZ2.2a: Estimate the length of the molecule of DNA shown in the autoradiogram between the two...
- 19M.3.SL.TZ2.2b: Determine, with a reason, the nucleotide base that was marked with...
- 19N.2.SL.TZ0.3c: List three characteristics of eukaryotic homologous chromosomes.
-
19N.1.SL.TZ0.14:
A pregnant woman had fetal cells removed by chorionic villus sampling and tested. The following karyogram was produced.
[Source: Mediscan / Alamy Stock Photo]
What does this show?
A. The child is female with Down syndrome.
B. The child is female without Down syndrome.
C. The child is male with Down syndrome.
D. The child is male without Down syndrome.
- 19N.2.HL.TZ0.6b: Outline the structural and genetic characteristics of eukaryotic chromosomes.
-
20N.1.HL.TZ0.13:
Testing the chromosomes of a girl with Turner syndrome produced the following karyogram.
[Source: Turner’s syndrome karyotype 45,XO. This female lacks the second X chromosome present in the
normal karyotype. Symptoms include short stature, neck webbing, elbow deformity, widely spaced nipples with shield chest, primary amenorrhea, sexual infantilism and sterility. The ovaries are reduced to fibrous streaks. Also known as XO syndrome or ovarian short-stature syndrome. Credit: Wessex Reg. Genetics Centre. Attribution 4.0 International (CC BY 4.0).]The condition can result from non-disjunction occurring in anaphase I of meiosis in an egg cell. Two cells result from the first division, one of which would lead to Turner syndrome. Which chromosomes will be in the other cell (polar body) at the end of meiosis I?
A. 44 autosomes and X
B. 44 autosomes and XX
C. 22 autosomes and X
D. 22 autosomes and XX
-
21M.1.SL.TZ1.17:
A two-cell sea urchin (Echinoidea) embryo was physically separated by scientists into two cells. Each cell, through further embryonic development, became an adult sea urchin.
[Source: Clker-Free-Vector-Images/Pixabay.]
What is the relationship between the two adult sea urchins?
A. They are equivalent to non-identical twins.
B. Half of the genes would be the same.
C. Both adults would have haploid cells.
D. They are clones.
- 21M.1.SL.TZ2.14: What feature of eukaryotic chromosomes distinguishes them from the chromosomes of...
-
21M.2.HL.TZ2.7a:
Describe the structure of the DNA molecule.
- 21M.1.HL.TZ2.11: What feature of eukaryotic chromosomes distinguishes them from the chromosomes of...
-
21M.1.HL.TZ2.12:
The image shows tetrads in the anther of a lily. A tetrad is a group of four cells, produced when one mother cell divides by meiosis. The tetrad indicated by the arrow contains a total of 48 chromosomes.
[Source: [Tetrad], 2012. [image online] Available at: https://www.iasprr.org/old/iasprr-pix/lily/tetrad.jpg [accessed: 4 April 2019]. Photo courtesy of Professor Scott D. Russell.]
What is the diploid number of the plant?
A. 12
B. 24
C. 48
D. 96
-
21N.1.SL.TZ0.13:
John Cairns used the technique of autoradiography to produce photographs of DNA from the bacterium E. coli.
[Source: © Cold Spring Harbor Laboratory Press. Autoradiography of bacterium E. coli DNA - micrograph, The Chromosome of
Escherichia coli Cairns, J.P., 1963. Cold Spring Harbor Symposia, Quantitative Biology, 28(44).]Which conclusion was drawn from his experiments?
A. The DNA in all organisms is circular.
B. DNA in E. coli naturally contains thymidine.
C. DNA replication is conservative.
D. The DNA in E. coli is 900 μm in length.
- 22M.1.SL.TZ1.14: Chromosome numbers vary between species. Which statement refers to humans? A. An egg cell has 22...
-
22M.1.SL.TZ2.14:
The karyogram shown belongs to a human being.
[Source: Reproduced from Tennakoon J, Kandasamy Y, Alcock G, Koh TH. Edwards syndrome with double trisomy. Singapore Med J. 2008 Jul;49(7):e190-1. PMID: 18695855.]
What can be deduced from this karyogram?
A. The person is a male with Down syndrome.
B. The person is a female with Down syndrome.
C. The person is a male with a genetic disorder.
D. The person is a female with a missing chromosome.
- 22M.1.HL.TZ2.10: Where can the entire genome of an organism be found? A. In the DNA present in plasmids of a...
-
22M.2.HL.TZ2.2b.ii:
Explain Cairns’s technique to measure the length of the DNA molecule.
- 19N.2.SL.TZ0.3c: List three characteristics of eukaryotic homologous chromosomes.
- 19N.2.SL.TZ0.c: List three characteristics of eukaryotic homologous chromosomes.
-
19N.1.SL.TZ0.14:
A pregnant woman had fetal cells removed by chorionic villus sampling and tested. The following karyogram was produced.
[Source: Mediscan / Alamy Stock Photo]
What does this show?
A. The child is female with Down syndrome.
B. The child is female without Down syndrome.
C. The child is male with Down syndrome.
D. The child is male without Down syndrome.
- 19N.2.HL.TZ0.6b: Outline the structural and genetic characteristics of eukaryotic chromosomes.
- 19N.2.HL.TZ0.b: Outline the structural and genetic characteristics of eukaryotic chromosomes.
-
20N.1.HL.TZ0.13:
Testing the chromosomes of a girl with Turner syndrome produced the following karyogram.
[Source: Turner’s syndrome karyotype 45,XO. This female lacks the second X chromosome present in the
normal karyotype. Symptoms include short stature, neck webbing, elbow deformity, widely spaced nipples with shield chest, primary amenorrhea, sexual infantilism and sterility. The ovaries are reduced to fibrous streaks. Also known as XO syndrome or ovarian short-stature syndrome. Credit: Wessex Reg. Genetics Centre. Attribution 4.0 International (CC BY 4.0).]The condition can result from non-disjunction occurring in anaphase I of meiosis in an egg cell. Two cells result from the first division, one of which would lead to Turner syndrome. Which chromosomes will be in the other cell (polar body) at the end of meiosis I?
A. 44 autosomes and X
B. 44 autosomes and XX
C. 22 autosomes and X
D. 22 autosomes and XX
-
21M.1.SL.TZ1.17:
A two-cell sea urchin (Echinoidea) embryo was physically separated by scientists into two cells. Each cell, through further embryonic development, became an adult sea urchin.
[Source: Clker-Free-Vector-Images/Pixabay.]
What is the relationship between the two adult sea urchins?
A. They are equivalent to non-identical twins.
B. Half of the genes would be the same.
C. Both adults would have haploid cells.
D. They are clones.
- 21M.1.SL.TZ2.14: What feature of eukaryotic chromosomes distinguishes them from the chromosomes of...
-
21M.2.HL.TZ2.7a:
Describe the structure of the DNA molecule.
-
21M.2.HL.TZ2.a:
Describe the structure of the DNA molecule.
- 21M.1.HL.TZ2.11: What feature of eukaryotic chromosomes distinguishes them from the chromosomes of...
-
21M.1.HL.TZ2.12:
The image shows tetrads in the anther of a lily. A tetrad is a group of four cells, produced when one mother cell divides by meiosis. The tetrad indicated by the arrow contains a total of 48 chromosomes.
[Source: [Tetrad], 2012. [image online] Available at: https://www.iasprr.org/old/iasprr-pix/lily/tetrad.jpg [accessed: 4 April 2019]. Photo courtesy of Professor Scott D. Russell.]
What is the diploid number of the plant?
A. 12
B. 24
C. 48
D. 96
-
21N.1.SL.TZ0.13:
John Cairns used the technique of autoradiography to produce photographs of DNA from the bacterium E. coli.
[Source: © Cold Spring Harbor Laboratory Press. Autoradiography of bacterium E. coli DNA - micrograph, The Chromosome of
Escherichia coli Cairns, J.P., 1963. Cold Spring Harbor Symposia, Quantitative Biology, 28(44).]Which conclusion was drawn from his experiments?
A. The DNA in all organisms is circular.
B. DNA in E. coli naturally contains thymidine.
C. DNA replication is conservative.
D. The DNA in E. coli is 900 μm in length.
- 22M.1.SL.TZ1.14: Chromosome numbers vary between species. Which statement refers to humans? A. An egg cell has 22...
-
22M.1.SL.TZ2.14:
The karyogram shown belongs to a human being.
[Source: Reproduced from Tennakoon J, Kandasamy Y, Alcock G, Koh TH. Edwards syndrome with double trisomy. Singapore Med J. 2008 Jul;49(7):e190-1. PMID: 18695855.]
What can be deduced from this karyogram?
A. The person is a male with Down syndrome.
B. The person is a female with Down syndrome.
C. The person is a male with a genetic disorder.
D. The person is a female with a missing chromosome.
- 22M.1.HL.TZ2.10: Where can the entire genome of an organism be found? A. In the DNA present in plasmids of a...
-
22M.2.HL.TZ2.2b.ii:
Explain Cairns’s technique to measure the length of the DNA molecule.
-
22M.2.HL.TZ2.b.ii:
Explain Cairns’s technique to measure the length of the DNA molecule.
-
17N.1.HL.TZ0.10:
The image shows a karyogram.
[Source: https://commons.wikimedia.org/wiki/File:Karyotype_of_sheep_(Ovis_aries).png, by M. Singh, X. Ma, E. Amoah and G. Kannan]
What information can be determined from this karyogram?
A. The sex is female.
B. The haploid number is 54.
C. Disjunction occurred during meiosis.
D. The species is not human.
- 18M.1.SL.TZ1.14: What is the same in all parts of homologous chromosomes? A. Base pair sequence B. Alleles C....
- 18M.2.SL.TZ2.2b.ii: Distinguish between the chromosomes of eukaryotic cells and prokaryotic cells.
- 18M.2.SL.TZ2.b.ii: Distinguish between the chromosomes of eukaryotic cells and prokaryotic cells.
- 18M.1.HL.TZ2.16: For what purpose is a karyogram used? A. To identify gene loci in a species B. To identify...
-
18N.1.HL.TZ0.11:
The image shows chromosomes from an insect (2 n = 8).
Which pair of chromosomes are the sex chromosomes of this insect species?
A. c and e
B. a and h
C. f and h
D. a and e
- 19M.1.HL.TZ1.11: What technique was used by John Cairns to measure the length of the DNA molecule in Escherichia...
- 19M.2.SL.TZ1.6a: Identify, with a reason, the sex of this individual.
- 19M.2.SL.TZ1.6b: Identify the chromosome that is affected by a trisomy in this individual, naming the condition...
- 19M.2.SL.TZ1.a: Identify, with a reason, the sex of this individual.
- 19M.2.SL.TZ1.b: Identify the chromosome that is affected by a trisomy in this individual, naming the condition...
- 19M.2.SL.TZ2.2b: Outline the use of a karyogram during pregnancy.
- 19M.2.SL.TZ2.b: Outline the use of a karyogram during pregnancy.
- 19M.2.HL.TZ1.2a: Distinguish between the structure of the chromosomes of prokaryotes and eukaryotes.
- 19M.2.HL.TZ1.2c.i: Identify, with a reason, the sex of this individual.
- 19M.2.HL.TZ1.a: Distinguish between the structure of the chromosomes of prokaryotes and eukaryotes.
- 19M.2.HL.TZ1.c.i: Identify, with a reason, the sex of this individual.
- 19M.3.SL.TZ2.2a: Estimate the length of the molecule of DNA shown in the autoradiogram between the two...
- 19M.3.SL.TZ2.2b: Determine, with a reason, the nucleotide base that was marked with...
- 19M.3.SL.TZ2.a: Estimate the length of the molecule of DNA shown in the autoradiogram between the two...
- 19M.3.SL.TZ2.b: Determine, with a reason, the nucleotide base that was marked with...
3.3 Meiosis
- 18M.1.SL.TZ1.15: What helps make the genome of each human unique?
- 18M.1.HL.TZ1.35: What forms when two different chromatids of the same homologous pair cross over? A. Daughter...
- 18M.2.HL.TZ2.3a.i: The micrograph shows a plant cell of Lilium grandiflorum during meiosis. Identify, giving...
- 18M.1.SL.TZ2.14: What happens during meiosis I and meiosis II?
- 18M.1.HL.TZ2.17: Which process could cause non-disjunction if it occurred during meiosis? A. Sister chromatids do...
-
19M.1.SL.TZ1.14:
At which stage of meiosis are bivalents formed?
A. Interphase
B. Prophase I
C. Prophase II
D. Metaphase II
-
19M.1.SL.TZ2.13:
The graph shows the incidence of trisomy resulting from non-disjunction in pregnancies at different maternal ages.
[Source: Center for Disease Control]
What can be inferred from the graph?
A. The incidence of three copies of a chromosome increases directly in proportion with the age of the mother.
B. The incidence of three sets of chromosomes increases from age 20.
C. The incidence of three copies of a chromosome increases the most from age 35.
D. The incidence of three sets of chromosomes increases the most from age 30.
- 19M.2.HL.TZ1.2c.ii: State the haploid number for this nucleus.
-
20N.2.SL.TZ0.6b:
Outline what occurs in cells in the first division of meiosis.
- 21M.1.SL.TZ1.19: Which statement applies to meiosis and mitosis? A. Meiosis occurs in a greater number of...
-
21M.2.SL.TZ2.2c:
Distinguish between the outcomes of a cell dividing either by mitosis or meiosis.
- 21N.1.SL.TZ0.14: Down syndrome can be detected before birth by chorionic villus sampling. From where are the cells...
-
21N.2.SL.TZ0.6b:
Explain the need for halving the chromosome number during a sexual life cycle and how this is done.
- 22M.1.SL.TZ1.15: What is produced by meiosis in a cell of a male animal? A. Four gametes, each with the same...
- 22M.2.SL.TZ1.7b: Distinguish between the processes of meiosis and mitosis.
- 22M.1.HL.TZ1.12: Which process occurs in meiosis but not in mitosis? A. Attachment of spindle fibres to the...
-
22N.2.HL.TZ0.2a:
Identify the stage of meiosis shown where exchange of genetic material occurs.
- 22N.1.SL.TZ0.14: Which event occurs in the first division of meiosis? A. Synthesis of DNA B. Pulling apart of...
-
22N.1.HL.TZ0.13:
Amniocentesis and chorionic villus sampling (CVS) are used to test for fetal abnormalities. Which statement is a valid comparison between the two tests?
A. CVS is performed later in pregnancy but has more risk of miscarriage than amniocentesis.
B. Amniocentesis is performed earlier in pregnancy but has more risk of miscarriage than CVS.
C. CVS is performed earlier in pregnancy but has more risk of miscarriage than amniocentesis.
D. Amniocentesis is performed later in pregnancy but has more risk of miscarriage than CVS.
-
23M.1.HL.TZ1.11:
The micrograph shows a cross section of a lily (Lilium longiflorum) anther.
[Source: Sinhyu / iStock.]
What can be found in X?
A. Haploid nuclei produced by meiosis
B. Diploid nuclei produced by fertilization
C. Haploid nuclei produced by mitosis
D. Diploid nuclei produced by pollination
- 23M.1.HL.TZ2.31: What is a result of crossing over in meiosis? A. Gene linkage B. Non-disjunction C. Haploid...
-
20N.2.SL.TZ0.6b:
Outline what occurs in cells in the first division of meiosis.
-
20N.2.SL.TZ0.b:
Outline what occurs in cells in the first division of meiosis.
- 21M.1.SL.TZ1.19: Which statement applies to meiosis and mitosis? A. Meiosis occurs in a greater number of...
-
21M.2.SL.TZ2.2c:
Distinguish between the outcomes of a cell dividing either by mitosis or meiosis.
-
21M.2.SL.TZ2.c:
Distinguish between the outcomes of a cell dividing either by mitosis or meiosis.
- 21N.1.SL.TZ0.14: Down syndrome can be detected before birth by chorionic villus sampling. From where are the cells...
-
21N.2.SL.TZ0.6b:
Explain the need for halving the chromosome number during a sexual life cycle and how this is done.
-
21N.2.SL.TZ0.b:
Explain the need for halving the chromosome number during a sexual life cycle and how this is done.
- 22M.1.SL.TZ1.15: What is produced by meiosis in a cell of a male animal? A. Four gametes, each with the same...
- 22M.2.SL.TZ1.7b: Distinguish between the processes of meiosis and mitosis.
- 22M.2.SL.TZ1.b: Distinguish between the processes of meiosis and mitosis.
- 22M.1.HL.TZ1.12: Which process occurs in meiosis but not in mitosis? A. Attachment of spindle fibres to the...
-
22N.2.HL.TZ0.2a:
Identify the stage of meiosis shown where exchange of genetic material occurs.
-
22N.2.HL.TZ0.a:
Identify the stage of meiosis shown where exchange of genetic material occurs.
- 22N.1.SL.TZ0.14: Which event occurs in the first division of meiosis? A. Synthesis of DNA B. Pulling apart of...
-
22N.1.HL.TZ0.13:
Amniocentesis and chorionic villus sampling (CVS) are used to test for fetal abnormalities. Which statement is a valid comparison between the two tests?
A. CVS is performed later in pregnancy but has more risk of miscarriage than amniocentesis.
B. Amniocentesis is performed earlier in pregnancy but has more risk of miscarriage than CVS.
C. CVS is performed earlier in pregnancy but has more risk of miscarriage than amniocentesis.
D. Amniocentesis is performed later in pregnancy but has more risk of miscarriage than CVS.
- 18M.1.SL.TZ1.15: What helps make the genome of each human unique?
-
23M.1.HL.TZ1.11:
The micrograph shows a cross section of a lily (Lilium longiflorum) anther.
[Source: Sinhyu / iStock.]
What can be found in X?
A. Haploid nuclei produced by meiosis
B. Diploid nuclei produced by fertilization
C. Haploid nuclei produced by mitosis
D. Diploid nuclei produced by pollination
- 23M.1.HL.TZ2.31: What is a result of crossing over in meiosis? A. Gene linkage B. Non-disjunction C. Haploid...
- 18M.1.HL.TZ1.35: What forms when two different chromatids of the same homologous pair cross over? A. Daughter...
- 18M.2.HL.TZ2.3a.i: The micrograph shows a plant cell of Lilium grandiflorum during meiosis. Identify, giving...
- 18M.2.HL.TZ2.a.i: The micrograph shows a plant cell of Lilium grandiflorum during meiosis. Identify, giving...
- 18M.1.SL.TZ2.14: What happens during meiosis I and meiosis II?
- 18M.1.HL.TZ2.17: Which process could cause non-disjunction if it occurred during meiosis? A. Sister chromatids do...
-
19M.1.SL.TZ1.14:
At which stage of meiosis are bivalents formed?
A. Interphase
B. Prophase I
C. Prophase II
D. Metaphase II
-
19M.1.SL.TZ2.13:
The graph shows the incidence of trisomy resulting from non-disjunction in pregnancies at different maternal ages.
[Source: Center for Disease Control]
What can be inferred from the graph?
A. The incidence of three copies of a chromosome increases directly in proportion with the age of the mother.
B. The incidence of three sets of chromosomes increases from age 20.
C. The incidence of three copies of a chromosome increases the most from age 35.
D. The incidence of three sets of chromosomes increases the most from age 30.
- 19M.2.HL.TZ1.2c.ii: State the haploid number for this nucleus.
- 19M.2.HL.TZ1.c.ii: State the haploid number for this nucleus.
3.4 Inheritance
- 17N.1.SL.TZ0.16: An allele for lactase persistence allows humans to digest milk as adults. People who lack this...
- 17N.1.HL.TZ0.12: A dominant autosomal allele for lactase persistence allows humans to digest milk as adults....
- 18M.1.SL.TZ1.21: What explains the presence in living humans of DNA sections which are identical to DNA found in...
- 18M.1.HL.TZ1.40: What contributes to the total DNA content of a zygote?
- 18M.2.SL.TZ1.3a: Using the Punnett grid, explain how two parents can have children with any of the different ABO...
-
18M.2.HL.TZ1.3b.i:
Distinguish between sex-linked genes and genes with linked loci.
-
18M.2.HL.TZ1.3b.ii:
Outline how it can be shown that the genes for shell base colour (Cc) and presence or absence of bands (Bb) are linked.
-
18M.2.HL.TZ2.3b:
The genes for cystic fibrosis and blood group are not linked. Two parents are heterozygous for cystic fibrosis. One parent has blood group O and the other has blood group AB. Using a Punnett square, determine the probability that their child will have both cystic fibrosis and blood group A.
- 18M.1.SL.TZ2.15: What is the percentage risk of a child inheriting Huntington’s disease if only one parent has the...
-
18M.1.HL.TZ2.20:
Nail patella syndrome is a rare disease that causes abnormalities of the nails and some bones. Its alleles are linked to the blood group alleles on the same chromosome. The pedigree chart shows the inheritance of these two characteristics over three generations.
[Source: Copyright © 1998. Phillip McClean]
Which descendant represents a recombinant phenotype?
- 18N.1.SL.TZ0.12: The image shows the chromosomes in four cells of an insect at the end of meiosis. What is the...
- 18N.1.SL.TZ0.14: A human gene has two alleles. One allele, P, is dominant over the recessive allele p. Embryos...
- 18N.1.SL.TZ0.15: In cats, black coat colour is dominant over gray. A female black cat, whose mother is gray, mates...
- 18N.2.SL.TZ0.6a: Isolated communities in rural Finland, Hungary and some of the Scottish islands have a high...
- 18N.2.HL.TZ0.7a: Isolated communities in rural Finland, Hungary and some of the Scottish islands have a high...
-
19M.1.SL.TZ1.15:
Creeper in chickens is a condition in which the chickens are born with very short legs. The creeper allele (C) is dominant over the normal allele (c). Embryos which are homozygous for the dominant allele fail to develop into viable chickens and die before they hatch. What phenotypic ratio would you expect in the live offspring of a cross between two creeper chickens?
A. All creeper
B. 1 creeper; 2 normal
C. 2 creeper; 1 normal
D. 3 creeper; 1 normal
-
19M.1.SL.TZ1.16:
Which pedigree chart is consistent with the inheritance of red-green colour blindness?
[Source: © International Baccalaureate Organization 2019]
-
19M.1.SL.TZ2.14:
The pedigree chart shows a family affected by cystic fibrosis.
[Source: © International Baccalaureate Organization 2019]
What is the genotype of the affected boy’s father?
A. AA only
B. Either AA or Aa
C. Aa only
D. aa only
- 19M.1.SL.TZ2.15: The children in a family have blood groups A, B and O. What are the genotypes of their...
- 19M.2.SL.TZ2.4b: Explain one cause of mutation.
- 19M.2.HL.TZ2.7b: Mendel found the same pattern of inheritance in all the crosses that he performed. Outline, with...
- 19N.2.SL.TZ0.6b: Outline how two parents could have a child with any of the four ABO blood groups.
- 19N.1.SL.TZ0.15: A variety of Pelargonium has yellow leaves. When plants of this variety are crossed, the...
-
19N.1.SL.TZ0.16:
A pair of alleles controls the secretion of antigens corresponding to blood group in saliva. Examine the pedigree chart.
[Source: © International Baccalaureate Organization 2019]
Based on this pedigree chart, which best describes the allele conferring antigen secretion in saliva?
A. Dominant
B. Recessive
C. Sex-linked
D. Co-dominant
- 19N.2.HL.TZ0.2a: State the type of inheritance shown.
- 19N.2.HL.TZ0.7b: Outline how two parents could have a child with any of the four ABO blood groups.
-
19N.1.HL.TZ0.12:
The pedigree chart shows the inheritance of hemophilia in some of the descendants of Queen Victoria. Which letter points to a family member certain to be heterozygous?
[Source: © International Baccalaureate Organization 2019]
- 20N.1.SL.TZ0.13: In the pedigree chart, individuals affected by a genetic disease are shown as shaded symbols....
- 20N.1.SL.TZ0.14: Tall heterozygous pea plants were crossed and the resulting seeds grown. Out of 360 plants, 270...
- 20N.1.SL.TZ0.15: What are all the possible phenotypes of children born to a mother with blood group AB and a...
- 21M.1.SL.TZ1.18: Which genotype would be normally found in a gamete? A. Rr B. RS C. rStt D. TUt
-
21M.2.HL.TZ1.7a:
Outline the inheritance of blood types in the ABO blood system in humans.
- 21M.1.SL.TZ2.15: A woman with blood type A has three children with a man who has blood type AB. The first child...
-
21M.2.HL.TZ2.5b:
Outline how sperm are produced from diploid cells in the testis and how this production can be sustained over many decades of adult life.
- 21N.1.SL.TZ0.15: In humans, male pattern baldness is caused by a recessive sex-linked gene found only on the X...
- 21N.1.HL.TZ1.12: Huntington’s disease can develop in middle age and leads to death of brain cells. It is carried...
-
21N.2.HL.TZ0.2a.i:
Draw a Punnett square to show all the possible genotypes of Queen Victoria’s children.
- 21N.2.HL.TZ0.2a.ii: Deduce the genotype of Queen Victoria’s daughter Alice.
- 22M.1.SL.TZ1.16: Huntington’s disease is an autosomal dominant genetic disease. What are the chances of two...
- 22M.2.SL.TZ1.4a: State the probability that Edward had hemophilia.
-
22M.2.SL.TZ1.4b:
Explain the reasons for none of the females in the pedigree chart having hemophilia.
-
22M.2.SL.TZ2.6b:
A family has a history of hemophilia that is caused by a sex-linked recessive allele. A woman from this family is a carrier and marries a man who does not have the allele. Showing your working, determine the probability of their children having the disease.
- 22M.1.SL.TZ2.15: The pedigree chart shows the inheritance of hemochromatosis, a genetic disease which causes an...
- 22M.1.SL.TZ2.17: A group of students used quadrat sampling to gather data on the presence of two plant species in...
-
22N.2.SL.TZ0.4a:
Draw the symbol for individual X on the diagram.
-
22N.2.SL.TZ0.4b:
Calculate the probability of male Y having an allele for the disorder.
- 22N.2.SL.TZ0.4c: Explain how the information in the box labelled B indicates that the gene is not sex-linked.
-
22N.1.SL.TZ0.15:
A couple have four children whose blood groups are A, B and AB. What is the likely combination of the parents’ genotypes?
A. IAi and IBi
B. IAi and IBIB
C. IAIB and ii
D. IAIA and IBIB
-
23M.2.HL.TZ1.5a:
Explain the conclusion that can be drawn from Cross 1.
- 23M.2.HL.TZ2.4ai: State with a reason whether pangolins are autotrophic or heterotrophic.
-
23M.1.HL.TZ1.10:
Scientists sequenced the genes in each chromosome of chimpanzees (Pan troglodytes) and humans (Homo sapiens). The graph shows the mean divergence between the genes of these species by chromosome.
[Source: Material from: Mikkelsen, T.S. et al, Initial sequence of the chimpanzee genome and
comparison with the human genome, 2005 Nature, reproduced with permission of SNCSC.]
What can be deduced from this data?
A. Autosomes are more similar than Y chromosomes.B. There is the same number of chromosomes in humans and chimpanzees.
C. Humans are more closely related to chimpanzees than to other species.
D. Smaller chromosomes are more similar than larger chromosomes.
-
23M.1.HL.TZ1.34:
A total of 271 164 people were tested for blood groups in Mexico. The pie chart summarizes the ABO blood group distribution.
[Source: Canizalez-Román, A. et al., 2018. Blood Groups Distribution and Gene Diversity
of the ABO and Rh (D) Loci in the Mexican Population.
BioMed Research International, (Article ID 1925619).
http://dx.doi.org/10.1155/2018/1925619. Public domain.]What can be concluded from the ABO blood group distribution in Mexico?
A. Allele frequencies are not the same for all blood group alleles.
B. The majority of the Mexican population shows a co-dominant phenotype.
C. Most of the Mexican population can receive blood from all blood groups.
D. Only 2 % of the Mexican population have a heterozygous genotype for blood groups.
-
23M.1.HL.TZ2.13:
The pedigree chart shows the inheritance of three generations of Duane syndrome, a condition caused by a dominant allele that affects alignment of the eyes.
[Source: Yang, M.-M., Ho, M. et al., 2013. Pedigree of a Chinese family with Duane retraction syndrome. [diagram online]
Available at: https://www.researchgate.net/figure/Pedigree-of-a-Chinese-family-with-Duane-retraction-syndrome-
Squares-men-circles_fig1_236921765 [Accessed 5 October 2021]. Public domain.]If individuals II:1 and II:2 had a third child, what is the probability that the child would have Duane syndrome?
A. 25 %
B. 50 %
C. 75 %
D. 100 %
- 23M.1.HL.TZ2.32: In the fruit fly Drosophila, the alleles for red eyes and brown bodies are dominant to the...
-
23M.2.SL.TZ2.2a:
State how many chromosomes there would be in male or female gametes of L. purpureus.
-
23M.2.SL.TZ1.5a:
Explain the conclusion that can be drawn from Cross 1.
-
23M.2.SL.TZ1.6a:
Outline the sequence of events that occurs during mitosis.
-
23M.1.SL.TZ1.14:
Scientists sequenced the genes in each chromosome of chimpanzees (Pan troglodytes) and humans (Homo sapiens). The graph shows the mean divergence between the genes of these species by chromosome.
[Source: Material from: Mikkelsen, T.S. et al, Initial sequence of the chimpanzee genome and
comparison with the human genome, 2005 Nature, reproduced with permission of SNCSC.]
What can be deduced from this data?
A. Autosomes are more similar than Y chromosomes.B. There is the same number of chromosomes in humans and chimpanzees.
C. Humans are more closely related to chimpanzees than to other species.
D. Smaller chromosomes are more similar than larger chromosomes.
-
23M.1.SL.TZ2.16:
The pedigree chart shows the inheritance of three generations of Duane syndrome, a condition caused by a dominant allele that affects alignment of the eyes.
[Source: Yang, M.-M., Ho, M. et al., 2013. Pedigree of a Chinese family with Duane retraction syndrome. [diagram online]
Available at: https://www.researchgate.net/figure/Pedigree-of-a-Chinese-family-with-Duane-retraction-syndrome-
Squares-men-circles_fig1_236921765 [Accessed 5 October 2021]. Public domain.]If individuals II:1 and II:2 had a third child, what is the probability that the child would have Duane syndrome?
A. 25 %
B. 50 %
C. 75 %
D. 100 %
- 19N.2.SL.TZ0.6b: Outline how two parents could have a child with any of the four ABO blood groups.
- 19N.2.SL.TZ0.b: Outline how two parents could have a child with any of the four ABO blood groups.
- 19N.1.SL.TZ0.15: A variety of Pelargonium has yellow leaves. When plants of this variety are crossed, the...
-
19N.1.SL.TZ0.16:
A pair of alleles controls the secretion of antigens corresponding to blood group in saliva. Examine the pedigree chart.
[Source: © International Baccalaureate Organization 2019]
Based on this pedigree chart, which best describes the allele conferring antigen secretion in saliva?
A. Dominant
B. Recessive
C. Sex-linked
D. Co-dominant
- 19N.2.HL.TZ0.2a: State the type of inheritance shown.
- 19N.2.HL.TZ0.a: State the type of inheritance shown.
- 19N.2.HL.TZ0.7b: Outline how two parents could have a child with any of the four ABO blood groups.
- 19N.2.HL.TZ0.b: Outline how two parents could have a child with any of the four ABO blood groups.
-
19N.1.HL.TZ0.12:
The pedigree chart shows the inheritance of hemophilia in some of the descendants of Queen Victoria. Which letter points to a family member certain to be heterozygous?
[Source: © International Baccalaureate Organization 2019]
- 20N.1.SL.TZ0.13: In the pedigree chart, individuals affected by a genetic disease are shown as shaded symbols....
- 20N.1.SL.TZ0.14: Tall heterozygous pea plants were crossed and the resulting seeds grown. Out of 360 plants, 270...
- 20N.1.SL.TZ0.15: What are all the possible phenotypes of children born to a mother with blood group AB and a...
- 21M.1.SL.TZ1.18: Which genotype would be normally found in a gamete? A. Rr B. RS C. rStt D. TUt
-
21M.2.HL.TZ1.7a:
Outline the inheritance of blood types in the ABO blood system in humans.
-
21M.2.HL.TZ1.a:
Outline the inheritance of blood types in the ABO blood system in humans.
- 21M.1.SL.TZ2.15: A woman with blood type A has three children with a man who has blood type AB. The first child...
-
21M.2.HL.TZ2.5b:
Outline how sperm are produced from diploid cells in the testis and how this production can be sustained over many decades of adult life.
-
21M.2.HL.TZ2.b:
Outline how sperm are produced from diploid cells in the testis and how this production can be sustained over many decades of adult life.
- 21N.1.SL.TZ0.15: In humans, male pattern baldness is caused by a recessive sex-linked gene found only on the X...
- 21N.1.HL.TZ1.12: Huntington’s disease can develop in middle age and leads to death of brain cells. It is carried...
-
21N.2.HL.TZ0.2a.i:
Draw a Punnett square to show all the possible genotypes of Queen Victoria’s children.
- 21N.2.HL.TZ0.2a.ii: Deduce the genotype of Queen Victoria’s daughter Alice.
-
21N.2.HL.TZ0.a.i:
Draw a Punnett square to show all the possible genotypes of Queen Victoria’s children.
- 21N.2.HL.TZ0.a.ii: Deduce the genotype of Queen Victoria’s daughter Alice.
- 22M.1.SL.TZ1.16: Huntington’s disease is an autosomal dominant genetic disease. What are the chances of two...
- 22M.2.SL.TZ1.4a: State the probability that Edward had hemophilia.
-
22M.2.SL.TZ1.4b:
Explain the reasons for none of the females in the pedigree chart having hemophilia.
- 22M.2.SL.TZ1.a: State the probability that Edward had hemophilia.
-
22M.2.SL.TZ1.b:
Explain the reasons for none of the females in the pedigree chart having hemophilia.
-
22M.2.SL.TZ2.6b:
A family has a history of hemophilia that is caused by a sex-linked recessive allele. A woman from this family is a carrier and marries a man who does not have the allele. Showing your working, determine the probability of their children having the disease.
-
22M.2.SL.TZ2.b:
A family has a history of hemophilia that is caused by a sex-linked recessive allele. A woman from this family is a carrier and marries a man who does not have the allele. Showing your working, determine the probability of their children having the disease.
- 22M.1.SL.TZ2.15: The pedigree chart shows the inheritance of hemochromatosis, a genetic disease which causes an...
- 22M.1.SL.TZ2.17: A group of students used quadrat sampling to gather data on the presence of two plant species in...
-
22N.2.SL.TZ0.4a:
Draw the symbol for individual X on the diagram.
-
22N.2.SL.TZ0.4b:
Calculate the probability of male Y having an allele for the disorder.
- 22N.2.SL.TZ0.4c: Explain how the information in the box labelled B indicates that the gene is not sex-linked.
-
22N.2.SL.TZ0.a:
Draw the symbol for individual X on the diagram.
-
22N.2.SL.TZ0.b:
Calculate the probability of male Y having an allele for the disorder.
- 22N.2.SL.TZ0.c: Explain how the information in the box labelled B indicates that the gene is not sex-linked.
-
22N.1.SL.TZ0.15:
A couple have four children whose blood groups are A, B and AB. What is the likely combination of the parents’ genotypes?
A. IAi and IBi
B. IAi and IBIB
C. IAIB and ii
D. IAIA and IBIB
- 17N.1.SL.TZ0.16: An allele for lactase persistence allows humans to digest milk as adults. People who lack this...
- 17N.1.HL.TZ0.12: A dominant autosomal allele for lactase persistence allows humans to digest milk as adults....
- 18M.1.SL.TZ1.21: What explains the presence in living humans of DNA sections which are identical to DNA found in...
-
23M.2.HL.TZ1.5a:
Explain the conclusion that can be drawn from Cross 1.
-
23M.2.HL.TZ1.a:
Explain the conclusion that can be drawn from Cross 1.
- 23M.2.HL.TZ2.4ai: State with a reason whether pangolins are autotrophic or heterotrophic.
- 23M.2.HL.TZ2.i: State with a reason whether pangolins are autotrophic or heterotrophic.
-
23M.1.HL.TZ1.10:
Scientists sequenced the genes in each chromosome of chimpanzees (Pan troglodytes) and humans (Homo sapiens). The graph shows the mean divergence between the genes of these species by chromosome.
[Source: Material from: Mikkelsen, T.S. et al, Initial sequence of the chimpanzee genome and
comparison with the human genome, 2005 Nature, reproduced with permission of SNCSC.]
What can be deduced from this data?
A. Autosomes are more similar than Y chromosomes.B. There is the same number of chromosomes in humans and chimpanzees.
C. Humans are more closely related to chimpanzees than to other species.
D. Smaller chromosomes are more similar than larger chromosomes.
-
23M.1.HL.TZ1.34:
A total of 271 164 people were tested for blood groups in Mexico. The pie chart summarizes the ABO blood group distribution.
[Source: Canizalez-Román, A. et al., 2018. Blood Groups Distribution and Gene Diversity
of the ABO and Rh (D) Loci in the Mexican Population.
BioMed Research International, (Article ID 1925619).
http://dx.doi.org/10.1155/2018/1925619. Public domain.]What can be concluded from the ABO blood group distribution in Mexico?
A. Allele frequencies are not the same for all blood group alleles.
B. The majority of the Mexican population shows a co-dominant phenotype.
C. Most of the Mexican population can receive blood from all blood groups.
D. Only 2 % of the Mexican population have a heterozygous genotype for blood groups.
-
23M.1.HL.TZ2.13:
The pedigree chart shows the inheritance of three generations of Duane syndrome, a condition caused by a dominant allele that affects alignment of the eyes.
[Source: Yang, M.-M., Ho, M. et al., 2013. Pedigree of a Chinese family with Duane retraction syndrome. [diagram online]
Available at: https://www.researchgate.net/figure/Pedigree-of-a-Chinese-family-with-Duane-retraction-syndrome-
Squares-men-circles_fig1_236921765 [Accessed 5 October 2021]. Public domain.]If individuals II:1 and II:2 had a third child, what is the probability that the child would have Duane syndrome?
A. 25 %
B. 50 %
C. 75 %
D. 100 %
- 23M.1.HL.TZ2.32: In the fruit fly Drosophila, the alleles for red eyes and brown bodies are dominant to the...
-
23M.2.SL.TZ2.2a:
State how many chromosomes there would be in male or female gametes of L. purpureus.
-
23M.2.SL.TZ2.a:
State how many chromosomes there would be in male or female gametes of L. purpureus.
-
23M.2.SL.TZ1.5a:
Explain the conclusion that can be drawn from Cross 1.
-
23M.2.SL.TZ1.a:
Explain the conclusion that can be drawn from Cross 1.
-
23M.2.SL.TZ1.6a:
Outline the sequence of events that occurs during mitosis.
-
23M.2.SL.TZ1.a:
Outline the sequence of events that occurs during mitosis.
-
23M.1.SL.TZ1.14:
Scientists sequenced the genes in each chromosome of chimpanzees (Pan troglodytes) and humans (Homo sapiens). The graph shows the mean divergence between the genes of these species by chromosome.
[Source: Material from: Mikkelsen, T.S. et al, Initial sequence of the chimpanzee genome and
comparison with the human genome, 2005 Nature, reproduced with permission of SNCSC.]
What can be deduced from this data?
A. Autosomes are more similar than Y chromosomes.B. There is the same number of chromosomes in humans and chimpanzees.
C. Humans are more closely related to chimpanzees than to other species.
D. Smaller chromosomes are more similar than larger chromosomes.
-
23M.1.SL.TZ2.16:
The pedigree chart shows the inheritance of three generations of Duane syndrome, a condition caused by a dominant allele that affects alignment of the eyes.
[Source: Yang, M.-M., Ho, M. et al., 2013. Pedigree of a Chinese family with Duane retraction syndrome. [diagram online]
Available at: https://www.researchgate.net/figure/Pedigree-of-a-Chinese-family-with-Duane-retraction-syndrome-
Squares-men-circles_fig1_236921765 [Accessed 5 October 2021]. Public domain.]If individuals II:1 and II:2 had a third child, what is the probability that the child would have Duane syndrome?
A. 25 %
B. 50 %
C. 75 %
D. 100 %
- 18M.1.HL.TZ1.40: What contributes to the total DNA content of a zygote?
- 18M.2.SL.TZ1.3a: Using the Punnett grid, explain how two parents can have children with any of the different ABO...
- 18M.2.SL.TZ1.a: Using the Punnett grid, explain how two parents can have children with any of the different ABO...
-
18M.2.HL.TZ1.3b.i:
Distinguish between sex-linked genes and genes with linked loci.
-
18M.2.HL.TZ1.3b.ii:
Outline how it can be shown that the genes for shell base colour (Cc) and presence or absence of bands (Bb) are linked.
-
18M.2.HL.TZ1.b.i:
Distinguish between sex-linked genes and genes with linked loci.
-
18M.2.HL.TZ1.b.ii:
Outline how it can be shown that the genes for shell base colour (Cc) and presence or absence of bands (Bb) are linked.
-
18M.2.HL.TZ2.3b:
The genes for cystic fibrosis and blood group are not linked. Two parents are heterozygous for cystic fibrosis. One parent has blood group O and the other has blood group AB. Using a Punnett square, determine the probability that their child will have both cystic fibrosis and blood group A.
-
18M.2.HL.TZ2.b:
The genes for cystic fibrosis and blood group are not linked. Two parents are heterozygous for cystic fibrosis. One parent has blood group O and the other has blood group AB. Using a Punnett square, determine the probability that their child will have both cystic fibrosis and blood group A.
- 18M.1.SL.TZ2.15: What is the percentage risk of a child inheriting Huntington’s disease if only one parent has the...
-
18M.1.HL.TZ2.20:
Nail patella syndrome is a rare disease that causes abnormalities of the nails and some bones. Its alleles are linked to the blood group alleles on the same chromosome. The pedigree chart shows the inheritance of these two characteristics over three generations.
[Source: Copyright © 1998. Phillip McClean]
Which descendant represents a recombinant phenotype?
- 18N.1.SL.TZ0.12: The image shows the chromosomes in four cells of an insect at the end of meiosis. What is the...
- 18N.1.SL.TZ0.14: A human gene has two alleles. One allele, P, is dominant over the recessive allele p. Embryos...
- 18N.1.SL.TZ0.15: In cats, black coat colour is dominant over gray. A female black cat, whose mother is gray, mates...
- 18N.2.SL.TZ0.6a: Isolated communities in rural Finland, Hungary and some of the Scottish islands have a high...
- 18N.2.SL.TZ0.a: Isolated communities in rural Finland, Hungary and some of the Scottish islands have a high...
- 18N.2.HL.TZ0.7a: Isolated communities in rural Finland, Hungary and some of the Scottish islands have a high...
- 18N.2.HL.TZ0.a: Isolated communities in rural Finland, Hungary and some of the Scottish islands have a high...
-
19M.1.SL.TZ1.15:
Creeper in chickens is a condition in which the chickens are born with very short legs. The creeper allele (C) is dominant over the normal allele (c). Embryos which are homozygous for the dominant allele fail to develop into viable chickens and die before they hatch. What phenotypic ratio would you expect in the live offspring of a cross between two creeper chickens?
A. All creeper
B. 1 creeper; 2 normal
C. 2 creeper; 1 normal
D. 3 creeper; 1 normal
-
19M.1.SL.TZ1.16:
Which pedigree chart is consistent with the inheritance of red-green colour blindness?
[Source: © International Baccalaureate Organization 2019]
-
19M.1.SL.TZ2.14:
The pedigree chart shows a family affected by cystic fibrosis.
[Source: © International Baccalaureate Organization 2019]
What is the genotype of the affected boy’s father?
A. AA only
B. Either AA or Aa
C. Aa only
D. aa only
- 19M.1.SL.TZ2.15: The children in a family have blood groups A, B and O. What are the genotypes of their...
- 19M.2.SL.TZ2.4b: Explain one cause of mutation.
- 19M.2.SL.TZ2.b: Explain one cause of mutation.
- 19M.2.HL.TZ2.7b: Mendel found the same pattern of inheritance in all the crosses that he performed. Outline, with...
- 19M.2.HL.TZ2.b: Mendel found the same pattern of inheritance in all the crosses that he performed. Outline, with...
3.5 Genetic modification and biotechnology
- 17N.1.SL.TZ0.15: HindIII is an endonuclease that recognizes the sequence A A G C T T, cutting between the two...
- 17N.2.SL.TZ0.02c: State an application of plasmids in biotechnology.
- 17N.2.SL.TZ0.06c: Outline natural methods of cloning in some eukaryotes.
-
18M.2.SL.TZ2.6c:
Explain the process of genetically modifying bacteria.
- 18M.1.SL.TZ2.16: Which technique is used to amplify very small samples of DNA? A. Cloning B. Gel...
- 18M.1.HL.TZ2.19: Which technique is used to amplify very small samples of DNA? A. Cloning B. Gel...
-
18N.1.SL.TZ0.16:
The image shows the results of Griffith’s experiment with S and R strains of Streptococcus pneumoniae in mice (Mus musculus).
What is an explanation for the results?
A. Mice vary in their resistance to bacteria.
B. The R strain and S strain mated.
C. R strain bacteria are more heat-stable than S strain.
D. DNA was transferred from heat-killed S cells to R cells.
-
18N.1.HL.TZ0.14:
Ampicillin (Amp) is an antibiotic. A plasmid carrying a gene for Amp resistance was used to transform bacteria in a tube of broth. A control tube without plasmid was also produced. The results were plated as shown. Which plate has only colonies of transformed bacteria?
- 18N.1.HL.TZ0.27: Sanger developed a method for determining DNA base sequences using terminating nucleotides called...
-
19M.1.SL.TZ2.16:
Genetically modified maize, called Bt maize, is thought to be affecting the monarch butterfly (Danaus plexippus) in the USA. What is the reason for this?
A. The monarch butterfly feeds on maize nectar, which contains Bt toxin.
B. The monarch caterpillar feeds on maize leaves, which contain Bt toxin.
C. Bt toxin kills the plants that the monarch caterpillar usually eats.
D. Bt toxin is in maize pollen, which blows on to plants that the monarch caterpillar eats.
- 19M.2.SL.TZ2.1h: Identify, with a reason, the aphids that were most strongly repelled by EBF.
-
19M.2.SL.TZ2.1i:
Outline the conclusions that can be drawn from the data in the graph for the group of aphids fed for three generations on transgenic thale cress plants (T).
- 19M.2.SL.TZ2.1j: Discuss whether natural selection would favour the transgenic EBF-producing thale cress plants if...
-
19M.1.HL.TZ2.22:
Two restriction endonucleases (EcoRI and BamHI) were used to cut a DNA sample into smaller fragments. These were then subjected to gel electrophoresis and the results are shown. The lengths of the DNA fragments are measured in kilobases (kb). One kilobase is 1000 DNA bases.
[Source: © International Baccalaureate Organization 2019]
Which statement is supported by the data?
A. The DNA sample is approximately 16 kb in size.
B. Each endonuclease produces a 2 kb fragment.
C. Both endonucleases produce the same number of fragments.
D. The fragments produced using both endonucleases are all different from those produced by the individual endonucleases.
- 19M.2.HL.TZ2.1a: Distinguish between the data for the leaves infested with the armyworm and the leaves infested...
- 19M.2.HL.TZ2.1b: Compare and contrast the effects of treatment of the leaves using C1 and C2 with the effects of...
- 19M.2.HL.TZ2.1c: Identify the process that was used to amplify the targeted genes.
- 19M.2.HL.TZ2.1d: Deduce, with a reason, which gene is first transcribed when exposed to C2.
-
19M.2.HL.TZ2.1e:
Each gene is activated by one or more of the treatments. From the gel electrophoresis data, discuss the impact of the herbivorous mite infestation on gene activation compared to treatment with C1 and C2.
- 19M.2.HL.TZ2.1f: Using the gene activation data, deduce, giving two reasons, whether the armyworm or the...
- 19N.1.SL.TZ0.17: What is PCR used for? A. Separate fragments of DNA by size B. Amplify small amounts of DNA C....
-
20N.2.HL.TZ0.8c:
Discuss the process, including potential risks and benefits, of using bacteria to genetically modify plant crop species.
-
20N.1.HL.TZ0.12:
In DNA profiling, short tandem repeats (STRs) of DNA are used, as these vary a great deal between individuals. Some skin cells were retrieved from a crime scene. Three STR sections of the DNA from these cells, from the victim and from a suspect, were analysed and the results are shown in the table.
What can be concluded from the gel electrophoresis data?
A. The suspect was at the crime scene.
B. The victim has the band moving the least distance.
C. The suspect and the victim have bands moving the same distance.
D. The skin cells have the band moving the greatest distance.
-
21M.2.HL.TZ1.8a:
Outline the process of DNA profiling.
- 21M.1.SL.TZ2.16: What benefit is derived from the use of Bt crops? A. It can lead to an increase in genetic...
- 21N.1.SL.TZ0.16: The image shows the result of DNA profiling of a mother, a child and four men. Which man is most...
-
21N.1.HL.TZ1.13:
A nucleus was removed from a cell of sheep P and fused with a denucleated egg cell of sheep Q. This was transplanted into the uterus of sheep R, which gave birth to Dolly.
[Source: Photo courtesy of The Roslin Institute, The University of Edinburgh, Roslin, Scotland, UK, n.d. Dolly the Sheep
in a field at The Roslin Institute. [image online] Available at: https://www.livescience.com/57961-dolly-the-sheepannouncement-
20-year-anniversary.html [Accessed 23 March 2020].]Which describes Dolly?
A. A clone of sheep P, because Dolly was formed from the nucleus of its udder cell
B. A clone of sheep Q, because Dolly was formed from one of its egg cells
C. A clone of sheep R, because Dolly developed in its uterus
D. Not a proper clone, as more than one sheep was involved in the development
-
22M.2.SL.TZ2.7c:
Suggest possible benefits and risks of using genetic modification to develop varieties of crop plant with traits such as drought resistance.
-
22M.1.SL.TZ2.16:
A cloning method used for livestock involves in vitro fertilization (IVF) with selected male and female gametes. The diagram shows the steps followed after in vitro fertilization.
[Source: Aldona Griskeviciene / Shutterstock.com.]
What does X represent?
A. A group of eggs
B. An embryo
C. A follicle
D. A group of zygotes
-
22M.2.HL.TZ1.8b:
Describe how DNA profiling can be used to establish paternity.
- 22N.1.SL.TZ0.16: A process for genetically modifying a plant is shown. What is the name of enzyme II and the...
- 19N.1.SL.TZ0.17: What is PCR used for? A. Separate fragments of DNA by size B. Amplify small amounts of DNA C....
-
20N.2.HL.TZ0.8c:
Discuss the process, including potential risks and benefits, of using bacteria to genetically modify plant crop species.
-
20N.2.HL.TZ0.c:
Discuss the process, including potential risks and benefits, of using bacteria to genetically modify plant crop species.
-
20N.1.HL.TZ0.12:
In DNA profiling, short tandem repeats (STRs) of DNA are used, as these vary a great deal between individuals. Some skin cells were retrieved from a crime scene. Three STR sections of the DNA from these cells, from the victim and from a suspect, were analysed and the results are shown in the table.
What can be concluded from the gel electrophoresis data?
A. The suspect was at the crime scene.
B. The victim has the band moving the least distance.
C. The suspect and the victim have bands moving the same distance.
D. The skin cells have the band moving the greatest distance.
-
21M.2.HL.TZ1.8a:
Outline the process of DNA profiling.
-
21M.2.HL.TZ1.a:
Outline the process of DNA profiling.
- 21M.1.SL.TZ2.16: What benefit is derived from the use of Bt crops? A. It can lead to an increase in genetic...
- 21N.1.SL.TZ0.16: The image shows the result of DNA profiling of a mother, a child and four men. Which man is most...
-
21N.1.HL.TZ1.13:
A nucleus was removed from a cell of sheep P and fused with a denucleated egg cell of sheep Q. This was transplanted into the uterus of sheep R, which gave birth to Dolly.
[Source: Photo courtesy of The Roslin Institute, The University of Edinburgh, Roslin, Scotland, UK, n.d. Dolly the Sheep
in a field at The Roslin Institute. [image online] Available at: https://www.livescience.com/57961-dolly-the-sheepannouncement-
20-year-anniversary.html [Accessed 23 March 2020].]Which describes Dolly?
A. A clone of sheep P, because Dolly was formed from the nucleus of its udder cell
B. A clone of sheep Q, because Dolly was formed from one of its egg cells
C. A clone of sheep R, because Dolly developed in its uterus
D. Not a proper clone, as more than one sheep was involved in the development
-
22M.2.SL.TZ2.7c:
Suggest possible benefits and risks of using genetic modification to develop varieties of crop plant with traits such as drought resistance.
-
22M.2.SL.TZ2.c:
Suggest possible benefits and risks of using genetic modification to develop varieties of crop plant with traits such as drought resistance.
-
22M.1.SL.TZ2.16:
A cloning method used for livestock involves in vitro fertilization (IVF) with selected male and female gametes. The diagram shows the steps followed after in vitro fertilization.
[Source: Aldona Griskeviciene / Shutterstock.com.]
What does X represent?
A. A group of eggs
B. An embryo
C. A follicle
D. A group of zygotes
-
22M.2.HL.TZ1.8b:
Describe how DNA profiling can be used to establish paternity.
-
22M.2.HL.TZ1.b:
Describe how DNA profiling can be used to establish paternity.
- 22N.1.SL.TZ0.16: A process for genetically modifying a plant is shown. What is the name of enzyme II and the...
- 17N.1.SL.TZ0.15: HindIII is an endonuclease that recognizes the sequence A A G C T T, cutting between the two...
- 17N.2.SL.TZ0.02c: State an application of plasmids in biotechnology.
- 17N.2.SL.TZ0.c: State an application of plasmids in biotechnology.
- 17N.2.SL.TZ0.06c: Outline natural methods of cloning in some eukaryotes.
- 17N.2.SL.TZ0.c: Outline natural methods of cloning in some eukaryotes.
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18M.2.SL.TZ2.6c:
Explain the process of genetically modifying bacteria.
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18M.2.SL.TZ2.c:
Explain the process of genetically modifying bacteria.
- 18M.1.SL.TZ2.16: Which technique is used to amplify very small samples of DNA? A. Cloning B. Gel...
- 18M.1.HL.TZ2.19: Which technique is used to amplify very small samples of DNA? A. Cloning B. Gel...
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18N.1.SL.TZ0.16:
The image shows the results of Griffith’s experiment with S and R strains of Streptococcus pneumoniae in mice (Mus musculus).
What is an explanation for the results?
A. Mice vary in their resistance to bacteria.
B. The R strain and S strain mated.
C. R strain bacteria are more heat-stable than S strain.
D. DNA was transferred from heat-killed S cells to R cells.
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18N.1.HL.TZ0.14:
Ampicillin (Amp) is an antibiotic. A plasmid carrying a gene for Amp resistance was used to transform bacteria in a tube of broth. A control tube without plasmid was also produced. The results were plated as shown. Which plate has only colonies of transformed bacteria?
- 18N.1.HL.TZ0.27: Sanger developed a method for determining DNA base sequences using terminating nucleotides called...
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19M.1.SL.TZ2.16:
Genetically modified maize, called Bt maize, is thought to be affecting the monarch butterfly (Danaus plexippus) in the USA. What is the reason for this?
A. The monarch butterfly feeds on maize nectar, which contains Bt toxin.
B. The monarch caterpillar feeds on maize leaves, which contain Bt toxin.
C. Bt toxin kills the plants that the monarch caterpillar usually eats.
D. Bt toxin is in maize pollen, which blows on to plants that the monarch caterpillar eats.
- 19M.2.SL.TZ2.1h: Identify, with a reason, the aphids that were most strongly repelled by EBF.
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19M.2.SL.TZ2.1i:
Outline the conclusions that can be drawn from the data in the graph for the group of aphids fed for three generations on transgenic thale cress plants (T).
- 19M.2.SL.TZ2.1j: Discuss whether natural selection would favour the transgenic EBF-producing thale cress plants if...
- 19M.2.SL.TZ2.h: Identify, with a reason, the aphids that were most strongly repelled by EBF.
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19M.2.SL.TZ2.i:
Outline the conclusions that can be drawn from the data in the graph for the group of aphids fed for three generations on transgenic thale cress plants (T).
- 19M.2.SL.TZ2.j: Discuss whether natural selection would favour the transgenic EBF-producing thale cress plants if...
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19M.1.HL.TZ2.22:
Two restriction endonucleases (EcoRI and BamHI) were used to cut a DNA sample into smaller fragments. These were then subjected to gel electrophoresis and the results are shown. The lengths of the DNA fragments are measured in kilobases (kb). One kilobase is 1000 DNA bases.
[Source: © International Baccalaureate Organization 2019]
Which statement is supported by the data?
A. The DNA sample is approximately 16 kb in size.
B. Each endonuclease produces a 2 kb fragment.
C. Both endonucleases produce the same number of fragments.
D. The fragments produced using both endonucleases are all different from those produced by the individual endonucleases.
- 19M.2.HL.TZ2.1a: Distinguish between the data for the leaves infested with the armyworm and the leaves infested...
- 19M.2.HL.TZ2.1b: Compare and contrast the effects of treatment of the leaves using C1 and C2 with the effects of...
- 19M.2.HL.TZ2.1c: Identify the process that was used to amplify the targeted genes.
- 19M.2.HL.TZ2.1d: Deduce, with a reason, which gene is first transcribed when exposed to C2.
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19M.2.HL.TZ2.1e:
Each gene is activated by one or more of the treatments. From the gel electrophoresis data, discuss the impact of the herbivorous mite infestation on gene activation compared to treatment with C1 and C2.
- 19M.2.HL.TZ2.1f: Using the gene activation data, deduce, giving two reasons, whether the armyworm or the...
- 19M.2.HL.TZ2.a: Distinguish between the data for the leaves infested with the armyworm and the leaves infested...
- 19M.2.HL.TZ2.b: Compare and contrast the effects of treatment of the leaves using C1 and C2 with the effects of...
- 19M.2.HL.TZ2.c: Identify the process that was used to amplify the targeted genes.
- 19M.2.HL.TZ2.d: Deduce, with a reason, which gene is first transcribed when exposed to C2.
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19M.2.HL.TZ2.e:
Each gene is activated by one or more of the treatments. From the gel electrophoresis data, discuss the impact of the herbivorous mite infestation on gene activation compared to treatment with C1 and C2.
- 19M.2.HL.TZ2.f: Using the gene activation data, deduce, giving two reasons, whether the armyworm or the...