Genetic Analysis: An Integrated Approach (2nd Edition)
Genetic Analysis: An Integrated Approach (2nd Edition)
2nd Edition
ISBN: 9780321948908
Author: Mark F. Sanders, John L. Bowman
Publisher: PEARSON
bartleby

Concept explainers

bartleby

Videos

Textbook Question
Book Icon
Chapter 3, Problem 26P

In humans, SRY is located near a pseudoautosomal region (PAR) of the Y chromosome, a region of homology between the X and Y chromosomes that allows them to synapse during meiosis in males and is a region of crossover between the chromosomes. The diagram below shows SRY in relation to the pseudoautosomal region.

Chapter 3, Problem 26P, 26. In humans, SRY is located near a pseudoautosomal region (PAR) of the Y chromosome, a region of

About 1 in every 25,000 newborn infants is born with sex reversal; the infant is either an apparent male, but with two X chromosomes, or an apparent female, but with an X and a Y chromosome. Explain the origin of sex reversalin human males and females involving the SRY gene. (Hint: See Experimental Insight 3.1 for a clue about the mutational mechanism.)

Blurred answer
Students have asked these similar questions
Butterflies have an X-Y sex-determination system that is different from that of flies or humans. Female butterflies may be either XY or X0, while butterflies with two or more X chromosomes are males. This photograph shows a tiger swallowtail gynandromorph, which is half male (left side) and half female (right side). Given that the first division of the zygote divides the embryo into the future right and left halves of the butterfly, propose a hypothesis that explains how nondisjunction during the first mitosis might have produced this unusual-looking butterfly.   Question is also in the picture.
Consider a cell with 2 pairs of homologous chromosomes where Chromosome 1 with genes VWXYZ is the homolog of Chromosome 2 with genes vwxyz while Chromosome 3 with genes PQRST is the homolog of Chromosome 4 with genes parst. If a reciprocal translocation occurred between Chromosome 1 YZ genes and Chromosome 3 ST genes, give the following gamete types produced after meiosis: (Answer in Arabic numbers only) 1. Gamete/s with non-recombinant chromosomes 2. Gamete/s with 1 recombinant chromosome 3. Gamete/s with 2 recombinant chromosomes 4. Gamete/s with gene duplications 5. Gamete/s with gene deletions 6. Gamete/s with 2 normal chromosome sequences 7. Gamete/s with 1 normal chromosome sequence 8. Gamete/s with balanced translocation 9. Gametes/ with all dominant genes 10. Gamete/s with all recessive genes 11. Gamete/s with 10 different genes 12. Gamete/s with TSXWV genes 13. Gamete/s with vwxyz genes 14. Gamete/s with pqrst genes 15.Gamete/s with PORYZ
Kuliev and Verlinsky (2004) state that there was a relatively high number of separation errors at meiosis I. In these cases the centromere underwent a premature division, occurring at meiosis I rather than meiosis II. Regarding chromosome 21, what would you expect to be the chromosome 21 complement in the secondary oocyte in which you saw a single chromatid (monad) for chromosome 21 in the first polar body? If this secondary oocyte was involved in fertilization, what would be the expected consequences?

Chapter 3 Solutions

Genetic Analysis: An Integrated Approach (2nd Edition)

Knowledge Booster
Background pattern image
Biology
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Human Biology (MindTap Course List)
Biology
ISBN:9781305112100
Author:Cecie Starr, Beverly McMillan
Publisher:Cengage Learning
Text book image
Human Heredity: Principles and Issues (MindTap Co...
Biology
ISBN:9781305251052
Author:Michael Cummings
Publisher:Cengage Learning
Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY