Chapter 7: Problem 15
What is a Barr body, and where is it found in a cell?
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Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Chapter 7: Problem 15
What is a Barr body, and where is it found in a cell?
These are the key concepts you need to understand to accurately answer the question.
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Get started for freeDescribe how nondisjunction in human female gametes can give rise to Klinefelter and 'Turner syndrome offspring following fertilization by a normal male gamete.
In the wasp Bracon hebetor, a form of parthenogenesis (the development of unfertilized eggs into progeny) resulting in haploid organisms is not uncommon. All haploids are males. When off. spring arise from fertilization, females almost invariably result. P. W. Whiting has shown that an X-linked gene with nine multiple alleles \(\left(X_{a}, X_{b},\) etc.) controls sex determination. Any homozygous \right. or hemizygous condition results in males, and any heterozygous condition results in females, If an \(X_{a} / X_{b}\) female mates with an \(X_{a}\) male and lays 50 percent fertilized and 50 percent unfertilized eggs, what proportion of male and female offspring will result?
In mice, the X-linked dominant mutation Testicular feminization (Tfin) eliminates the normal response to the testicular hormone testosterone during sexual differentiation, An XY mouse bearing the \(\mathrm{T}\) for allele on the \(\mathrm{X}\) chromosome develops testes, but no further male differentiation occurs the external genitalia of such an animal are female. From this information, what might you conclude about the role of the Tfim gene product and the \(X\) and Y chromosomes in sex determination and sexual differentiation in mammals? Can you devise an experiment, assuming you can "genetically engineer" the chromosomes of mice, to test and confirm your explanation?
An attached-X female fly, \(\overline{X X} Y\) (see the "Insights and Solutions" box), expresses the recessive X-linked white-eye mutation. It is crossed to a male fly that expresses the X-linked recessive miniature-wing mutation. Determine the outcome of this cross in terms of sex, eye color, and wing size of the offspring.
The genes encoding the red-and green-color-detecting proteins of the human eye are located next to one another on the \(\mathrm{X}\) chromosome and probably evolved from a common ancestral pigment gene. The two proteins demonstrate 76 percent homology in their amino acid sequences. A normal-visioned woman (with both genes present on each of her two \(x\) chromosomes) has a red-color-blind son who was shown to have one copy of the green- detecting gene and no copies of the red-detecting gene. Devise an explanation for these observations at the chromosomal level (involving meiosis).
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