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Which of the following statements would explain a testcross involving F₁ dihybrid flies in which more parental-type offspring than recombinant-type offspring are produced?


A) The two genes are closely linked on the same chromosome.
B) The two genes are linked but on different chromosomes.
C) Recombination did not occur in the cell during meiosis.
D) Both of the characters are controlled by more than one gene.

E) All of the above
F) A) and D)

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Which of the following correctly describes a Philadelphia chromosome?


A) a human chromosome 22 that has had a specific translocation
B) a human chromosome 9 that is found only in one type of cancer
C) an animal chromosome found primarily in the mid-Atlantic area of the United States
D) a chromosome found only in mitochondria

E) A) and B)
F) All of the above

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Use the following information to answer the question. A plantlike organism on the planet Pandora can have three recessive genetic traits: bluish leaves, due to an allele (a) of gene A; a feathered stem, due to an allele (b) of gene B; and hollow roots due to an allele (c) of gene C. The three genes are linked and recombine. A geneticist performed a testcross with an organism that had been found to be heterozygous for the three recessive traits, and she was able to identify progeny of the following phenotypic distribution (+ = wild type) : Use the following information to answer the question. A plantlike organism on the planet Pandora can have three recessive genetic traits: bluish leaves, due to an allele (a)  of gene A; a feathered stem, due to an allele (b)  of gene B; and hollow roots due to an allele (c)  of gene C. The three genes are linked and recombine. A geneticist performed a testcross with an organism that had been found to be heterozygous for the three recessive traits, and she was able to identify progeny of the following phenotypic distribution (+ = wild type) :   The greatest distance among the three genes is between a and c. What does this mean? A)  Gene c is between a and b. B)  Genes are in the order: a-b-c. C)  Gene a is not recombining with c. D)  Gene a is between b and c. The greatest distance among the three genes is between a and c. What does this mean?


A) Gene c is between a and b.
B) Genes are in the order: a-b-c.
C) Gene a is not recombining with c.
D) Gene a is between b and c.

E) A) and B)
F) A) and C)

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Use the following information to answer the question. A plantlike organism on the planet Pandora can have three recessive genetic traits: bluish leaves, due to an allele (a) of gene A; a feathered stem, due to an allele (b) of gene B; and hollow roots due to an allele (c) of gene C. The three genes are linked and recombine. A geneticist performed a testcross with an organism that had been found to be heterozygous for the three recessive traits, and she was able to identify progeny of the following phenotypic distribution (+ = wild type) : Use the following information to answer the question. A plantlike organism on the planet Pandora can have three recessive genetic traits: bluish leaves, due to an allele (a)  of gene A; a feathered stem, due to an allele (b)  of gene B; and hollow roots due to an allele (c)  of gene C. The three genes are linked and recombine. A geneticist performed a testcross with an organism that had been found to be heterozygous for the three recessive traits, and she was able to identify progeny of the following phenotypic distribution (+ = wild type) :   Which of the progeny phenotypes will require recombination between genes A and B? A)  1, 2, 5, and 6 B)  1, 3, 6, and 7 C)  2, 4, 5, and 8 D)  2, 3, 5, and 7 Which of the progeny phenotypes will require recombination between genes A and B?


A) 1, 2, 5, and 6
B) 1, 3, 6, and 7
C) 2, 4, 5, and 8
D) 2, 3, 5, and 7

E) C) and D)
F) A) and C)

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A phenotypically normal prospective couple seeks genetic counseling because the man knows that he has a translocation of a portion of his chromosome 4, which has been exchanged with a portion of his chromosome 12. Although his translocation is balanced, he and his wife want to know the probability that his sperm will be abnormal. What is your prognosis regarding his sperm?


A) One-quarter will carry the two normal chromosomes, 4 and 12, one-quarter will have only the two translocation chromosomes and no normal chromosomes 4 and 12, and half will have one normal and one translocated chromosome.
B) All will carry the same translocation as the father.
C) None will carry the translocation.
D) Half will be normal, and the rest will have the father's translocation.

E) None of the above
F) B) and C)

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Use the following information to answer the question. A plantlike organism on the planet Pandora can have three recessive genetic traits: bluish leaves, due to an allele (a) of gene A; a feathered stem, due to an allele (b) of gene B; and hollow roots due to an allele (c) of gene C. The three genes are linked and recombine. A geneticist performed a testcross with an organism that had been found to be heterozygous for the three recessive traits, and she was able to identify progeny of the following phenotypic distribution (+ = wild type) : Use the following information to answer the question. A plantlike organism on the planet Pandora can have three recessive genetic traits: bluish leaves, due to an allele (a)  of gene A; a feathered stem, due to an allele (b)  of gene B; and hollow roots due to an allele (c)  of gene C. The three genes are linked and recombine. A geneticist performed a testcross with an organism that had been found to be heterozygous for the three recessive traits, and she was able to identify progeny of the following phenotypic distribution (+ = wild type) :   What is the greatest benefit of having used a testcross for this experiment? A)  The homozygous recessive parents are obvious to the naked eye. B)  The homozygous parents are the only ones whose crossovers make a difference. C)  The phenotypes of the progeny reveal the allelic content of the gamete from the heterozygous parent. D)  All of the progeny will be heterozygous. What is the greatest benefit of having used a testcross for this experiment?


A) The homozygous recessive parents are obvious to the naked eye.
B) The homozygous parents are the only ones whose crossovers make a difference.
C) The phenotypes of the progeny reveal the allelic content of the gamete from the heterozygous parent.
D) All of the progeny will be heterozygous.

E) All of the above
F) A) and B)

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Use the following information to answer the question. Use the following information to answer the question.   In a Drosophila experiment, a cross was made between homozygous wild-type females and yellow-bodied males. All of the resulting F₁s were phenotypically wild type. However, adult flies of the F₂ generation (resulting from matings of the F₁s)  had the characteristics shown in the figure. How is the mutant allele for yellow body inherited? A)  It is not X-linked. B)  It is X-linked. C)  It is inherited by X inactivation. D)  It is Y-linked. In a Drosophila experiment, a cross was made between homozygous wild-type females and yellow-bodied males. All of the resulting F₁s were phenotypically wild type. However, adult flies of the F₂ generation (resulting from matings of the F₁s) had the characteristics shown in the figure. How is the mutant allele for yellow body inherited?


A) It is not X-linked.
B) It is X-linked.
C) It is inherited by X inactivation.
D) It is Y-linked.

E) A) and B)
F) All of the above

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A couple has a child with Down syndrome. The mother is 39 years old at the time of delivery. Which of the following is the most probable cause of the child's condition?


A) The woman inherited this tendency from her parents.
B) The mother had a chromosomal duplication.
C) One member of the couple underwent nondisjunction in somatic cell production.
D) One of the gametes in the mother most likely underwent nondisjunction during meiosis.

E) A) and B)
F) A) and C)

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Which of the following individuals will inherit an X-linked allele from a man who carries it?


A) all of his daughters
B) half of his daughters
C) all of his sons
D) all of his children

E) C) and D)
F) B) and D)

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When Thomas Hunt Morgan crossed his red-eyed F₁ generation flies to each other, the F₂ generation included both red- and white-eyed flies. Remarkably, all the white-eyed flies were male. What was the explanation for this result?


A) The gene involved is located on the Y chromosome.
B) The gene involved is located on the X chromosome.
C) The gene involved is located on an autosome, but only in males.
D) Other male-specific factors influence eye color in flies.

E) None of the above
F) All of the above

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Red-green color blindness is a sex-linked recessive trait in humans. Two people with normal color vision have a color-blind son. What are the genotypes of the parents?


A) XⁿXⁿ and XⁿY
B) XᴺXᴺ and XⁿY
C) XᴺXᴺ and XᴺY
D) XᴺXⁿ and XᴺY

E) C) and D)
F) All of the above

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What is an adaptive advantage of recombination between linked genes?


A) Recombination is required for independent assortment.
B) Recombination must occur or genes will not assort independently.
C) New allele combinations are acted upon by natural selection.
D) The forces on the cell during meiosis II result in recombination.

E) All of the above
F) A) and B)

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Abnormal chromosomes are frequently found in malignant tumors. Errors such as translocations may place a gene in close proximity to different control regions. Which of the following events might then occur to make the cancer worse?


A) an increase in nondisjunction
B) expression of inappropriate gene products
C) a decrease in mitotic frequency
D) failure of the cancer cells to multiply

E) B) and C)
F) None of the above

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Mitochondrial DNA is primarily involved in coding for proteins needed for protein complexes of the electron transport chain and ATP synthase. Therefore, mutations in mitochondrial genes would most affect which of the following processes?


A) DNA synthesis in cells of the immune system
B) the movement of oxygen into erythrocytes
C) generation of ATP in muscle cells
D) the storage of urine in the urinary bladder

E) All of the above
F) A) and B)

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The SRY gene is best described as ________.


A) a gene present on the X chromosome that triggers female development
B) an autosomal gene that is required for the expression of genes on the Y chromosome
C) a gene present on the Y chromosome that triggers male development
D) an autosomal gene that is required for the expression of genes on the X chromosome

E) A) and D)
F) None of the above

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If cell X enters meiosis, and nondisjunction of one chromosome occurs in one of its daughter cells during meiosis II, how will this affect the gametes at the completion of meiosis?


A) All the gametes descended from cell X will be diploid.
B) Half of the gametes descended from cell X will be n + 1, and half will be n - 1.
C) One-quarter of the gametes descended from cell X will be n + 1, one-quarter will be n - 1, and half will be n.
D) Two of the four gametes descended from cell X will be haploid, and two will be diploid.

E) A) and C)
F) B) and C)

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What is a syndrome?


A) a characteristic facial appearance
B) a trait that leads to cancer at some stage in life
C) a group of traits typically found in conjunction with a particular chromosomal aberration or gene mutation
D) a specific characteristic that appears in conjunction with one specific aneuploidy

E) B) and C)
F) B) and D)

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Map units on a linkage map cannot be relied upon to calculate physical distances on a chromosome for which of the following reasons?


A) The frequency of crossing over varies along the length of the chromosome.
B) The relationship between recombination frequency and map units is different in every individual.
C) Physical distances between genes change during the course of the cell cycle.
D) The gene order on the chromosomes is slightly different in every individual.

E) B) and C)
F) All of the above

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Sex determination in mammals is due to the SRY gene found on the Y chromosome. Which of the following situations could allow a person with an XX karyotype to develop a male phenotype?


A) the loss of the SRY gene from an autosome
B) translocation of SRY to an X chromosome
C) the presence of an extra autosomal chromosome
D) the presence of one normal and one shortened (deleted) X

E) B) and C)
F) None of the above

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Pseudohypertrophic muscular dystrophy is a human disorder that causes gradual deterioration of the muscles. Only boys are affected, and they are always born to phenotypically normal parents. Due to the severity of the disease, the boys die in their teens. Is this disorder likely to be caused by a dominant or recessive allele? Is the inheritance of this trait sex-linked or autosomal?


A) dominant, sex-linked
B) recessive, autosomal
C) recessive, sex-linked
D) incomplete dominant, sex-linked

E) A) and D)
F) B) and D)

Correct Answer

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