BIOL 171 CH15 Flashcards
Recombination between linked genes comes about for what reason?
A) Mutation on one homolog is different from that on the other homolog.
B) Independent assortment sometimes fails because Mendel had not calculated appropriately.
C) When genes are linked they always “travel” together at anaphase.
D) Crossovers between these genes result in chromosomal exchange.
E) Nonrecombinant chromosomes break and then re-join with one another.
D
Three genes at three loci are being mapped in a particular species. Each has two phenotypes, one of which is markedly different from the wild type. The unusual allele of the first gene is inherited with either of the others about 50% of the time. However, the unusual alleles of the other two genes are inherited together 14.4% of the time. Which of the following describes what is happening?
A) The genes are showing independent assortment.
B) The three genes are linked.
C) The first gene is linked but the other two are not.
D) The first gene is assorting independently from the other two that are linked.
E) The first gene is located 14.4 units apart from the other two.
D
In birds, sex is determined by a ZW chromosome scheme. Males are ZZ and females are ZW. A recessive lethal allele that causes death of the embryo is sometimes present on the Z chromosome in pigeons. What would be the sex ratio in the offspring of a cross between a male that is heterozygous for the lethal allele and a normal female?
A) 2:1 male to female B) 1:2 male to female C) 1:1 male to female D) 4:3 male to female E) 3:1 male to female
A
Z superscript d w kills off one so there are 2 males and one female remaining
Duchenne muscular dystrophy (DMD) is caused by a gene on the human X chromosome. The patients have muscles that weaken over time because they have absent or decreased dystrophin, a muscle protein. They rarely live past their 20s. How likely is it for a woman to have this condition?
A) Women can never have this condition.
B) One-half of the daughters of an affected man could have this condition.
C) One-fourth of the children of an affected father and a carrier mother could have this condition.
D) Very rarely would a woman have this condition; the condition would be due to a chromosome error.
E) Only if a woman is XXX could she have this condition.
D
In humans, clear gender differentiation occurs, not at fertilization, but after the second month of gestation. What is the first event of this differentiation?
A) formation of testosterone in male embryos
B) formation of estrogens in female embryos
C) anatomical differentiation of a penis in male embryos
D) activation of SRY in male embryos and masculinization of the gonads
E) activation of SRY in females and feminization of the gonads
D
Which of the following statements is true of linkage?
A) The closer two genes are on a chromosome, the lower the probability that a crossover will occur between them.
B) The observed frequency of recombination of two genes that are far apart from each other has a maximum value of 100%.
C) All of the traits that Mendel studied–seed color, pod shape, flower color, and others–are due to genes linked on the same chromosome.
D) Linked genes are found on different chromosomes.
E) Crossing over occurs during prophase II of meiosis.
A
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 on the Y chromosome.
B) The gene involved is on the X chromosome.
C) The gene involved is on an autosome, but only in males.
D) Other male-specific factors influence eye color in flies.
E) Other female-specific factors influence eye color in flies.
B
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) excessive emotional instability D) normal female E) sterile female
D
In humans, male-pattern baldness is controlled by an autosomal gene that occurs in two allelic forms. Allele Hn determines nonbaldness, and allele Hb determines pattern baldness. In males, because of the presence of testosterone, allele Hb is dominant over Hn. If a man and woman both with genotype HnHb have a son, what is the chance that he will eventually be bald?
E
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 their 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
B
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
A
Sex determination in mammals is due to the SRY region of 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 SRY 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
E) Down syndrome, 46, XX
B
The centimorgan (cM) is a unit named in honor of Thomas Hunt Morgan. To what is it equal?
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
B
Which of the following two genes are closest on a genetic map of Drosophila? A) b and vg B) vg and cn C) rb and cn D) cn and b E) b and rb
E
Thomas Hunt Morgan’s choice of Drosophila melanogaster has been proven to be useful even today. Which of the following has/have continued to make it a most useful species?
I. its four pairs of chromosomes
II. a very large number of visible as well as biochemically mutant phenotypes
III. easy and inexpensive maintenance
IV. short generation time and large number of offspring
A) I and IV only B) II and III only C) I, II, and III only D) II, III, and IV only E) I, II, III, IV, and VE
E
