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At what point in cell division is a chromosome lost so that, after fertilization with a normal gamete, the result is an embryo with 45,X?


A) after an error occurring in anaphase I or anaphase II
B) after an error occurring in anaphase I only
C) after an error occurring in anaphase II only
D) after an error occurring in prophase I only
E) after an error occurring in metaphase II only

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Cinnabar eyes is a sex-linked recessive characteristic in fruit flies. If a female having cinnabar eyes is crossed with a wild-type male, what percentage of the F1 males will have cinnabar eyes?


A) 0%
B) 25%
C) 50%
D) 75%
E) 100%

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One possible result of chromosomal breakage is for a fragment to join a nonhomologous chromosome. What is this alteration called?


A) deletion
B) transversion
C) inversion
D) translocation
E) duplication

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D

Why does recombination between linked genes continue to occur?


A) Recombination is a requirement for independent assortment.
B) Recombination must occur or genes will not assort independently.
C) New allele combinations are acted upon by natural selection.
D) Without recombination there would be an insufficient number of gametes.

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Sex determination in mammals is due to the SRY gene on the Y chromosome. An abnormality of this region could allow which of the following to have a male phenotype?


A) Turner syndrome, 45,X
B) translocation of the SRY gene to an autosome of a 46,XX individual
C) a person with an extra X chromosome
D) a person with one normal and one shortened (deleted) X

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B

How would one 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.

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Which of the following statements correctly describes aneuploid conditions?


A) A monosomy is more frequent than a trisomy.
B) Monosomy X is the only known viable human monosomy.
C) Of all human aneuploidies, only Down syndrome is associated with mental retardation.
D) An aneuploidy resulting in the deletion of a chromosome segment is less serious than a duplication.

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A woman is found to have 47 chromosomes, including three X chromosomes. Which of the following describes her expected phenotype?


A) masculine characteristics such as facial hair
B) enlarged genital structures
C) healthy female of slightly above-average height
D) sterile female

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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 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) death of the cancer cells in the tumor

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Sturtevant provided genetic evidence for the existence of four pairs of chromosomes in Drosophila in which of the following ways?


A) There are four major functional classes of genes in Drosophila.
B) Drosophila genes cluster into four distinct groups of linked genes.
C) The overall number of genes in Drosophila is a multiple of four.
D) The entire Drosophila genome has approximately 400 map units.
E) Drosophila genes have, on average, four different alleles.

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Please use the following information to answer the question(s) below. A man who is an achondroplastic dwarf with normal vision marries a color-blind woman of normal height. The man's father was 6 feet tall, and both the woman's parents were of average height. Achondroplastic dwarfism is autosomal dominant, and red-green color blindness is X-linked recessive. -What proportion of their sons would be color-blind and of normal height?


A) none
B) half
C) one out of four
D) three out of four
E) all

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Of the following human aneuploidies, which is the one that generally has the most severe impact on the health of the individual?


A) 47,+21
B) 47,XXY
C) 47,XXX
D) 47,XYY
E) 45,X

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  Figure 12.2 In a series of mapping experiments, the recombination frequencies for four different linked genes of Drosophila were determined as shown in Figure 12.2. What is the order of these genes on a chromosome map? A)  rb-cn-vg-b B)  vg-b-rb-cn C)  cn-rb-b-vg D)  b-rb-cn-vg E)  vg-cn-b-rb Figure 12.2 In a series of mapping experiments, the recombination frequencies for four different linked genes of Drosophila were determined as shown in Figure 12.2. What is the order of these genes on a chromosome map?


A) rb-cn-vg-b
B) vg-b-rb-cn
C) cn-rb-b-vg
D) b-rb-cn-vg
E) vg-cn-b-rb

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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) XNXn and XNY

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Which of the following statements best describes the SRY gene?


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

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Please use the following information to answer the question(s) below. A man who is an achondroplastic dwarf with normal vision marries a color-blind woman of normal height. The man's father was 6 feet tall, and both the woman's parents were of average height. Achondroplastic dwarfism is autosomal dominant, and red-green color blindness is X-linked recessive. -How many of the couple's daughters might be expected to be color-blind dwarfs?


A) all
B) none
C) half
D) one out of four
E) three out of four

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B

Which of the following events causes recombination between linked genes to occur?


A) Mutation on one homolog is different from that on the other homolog.
B) When genes are linked they always "travel" together at anaphase.
C) Crossovers between these genes result in chromosomal exchange.
D) Nonrecombinant chromosomes break and then re-join with one another.

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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 that has been exchanged with a portion of his chromosome 12. Although he is normal because 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-fourth will be normal, 1/4 will have the translocation, and 1/2 will have duplications and deletions.
B) All will carry the same translocation as the father.
C) None will carry the translocation because abnormal sperm will die.
D) His sperm will be sterile so the couple might consider adoption.
E) One-half will be normal and the rest will have the father's translocation.

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Please use the following information to answer the question(s) below. 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 did a testcross with an organism that had been found to be heterozygous for the three recessive traits and was able to identify progeny of the phenotypic distribution (+ = wild type) shown in Figure 12.3. Please use the following information to answer the question(s)  below. 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 did a testcross with an organism that had been found to be heterozygous for the three recessive traits and was able to identify progeny of the phenotypic distribution (+ = wild type)  shown in Figure 12.3.   Figure 12.3 -If recombination frequency is equal to distance in map units, what is the approximate distance between genes A and B? A)  1.5 map units B)  3 map units C)  6 map units D)  15 map units E)  30 map units Figure 12.3 -If recombination frequency is equal to distance in map units, what is the approximate distance between genes A and B?


A) 1.5 map units
B) 3 map units
C) 6 map units
D) 15 map units
E) 30 map units

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One map unit is equivalent to which of the following values?


A) the physical distance between two linked genes
B) 1% frequency of recombination between two genes
C) 1 nanometer of distance between two genes
D) the distance between a pair of homologous chromosomes
E) the recombination frequency between two genes assorting independently

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