Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
3. Extensions to Mendelian Inheritance
Sex Chromosome
Problem 26
Textbook Question
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.

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 reversal in human males and females involving the SRY gene. (Hint: See Experimental Insight 3.1 for a clue about the mutational mechanism.)

1
Understand the role of the SRY gene: The SRY (Sex-determining Region Y) gene is located on the Y chromosome near the pseudoautosomal region (PAR). It is responsible for initiating male sex determination by triggering the development of testes.
Analyze the diagram: The image shows the SRY gene positioned close to the PAR region on the Y chromosome. The PAR region is homologous between the X and Y chromosomes, allowing them to pair and undergo crossover during meiosis.
Consider the mechanism of sex reversal: During meiosis in males, crossover events can occur between the X and Y chromosomes in the PAR region. If the crossover extends beyond the PAR region and includes the SRY gene, the SRY gene can be translocated to the X chromosome.
Explain the outcome of SRY translocation: If the SRY gene is translocated to the X chromosome, an individual with two X chromosomes (XX) may develop as a phenotypic male due to the presence of the SRY gene. Conversely, if the Y chromosome loses the SRY gene, an individual with an X and Y chromosome (XY) may develop as a phenotypic female.
Summarize the mutational mechanism: Sex reversal in humans can occur due to errors in meiotic crossover that result in the translocation of the SRY gene to the X chromosome or its deletion from the Y chromosome. This explains the origin of apparent males with XX chromosomes and apparent females with XY chromosomes.

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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
SRY Gene
The SRY (Sex-determining Region Y) gene is crucial for male sex determination in humans. Located on the Y chromosome, it encodes a protein that triggers the development of male characteristics by initiating the formation of testes, which produce male hormones. Mutations or deletions in the SRY gene can lead to sex reversal, where individuals may have a male phenotype despite having two X chromosomes.
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Mapping Genes
Pseudoautosomal Region (PAR)
The pseudoautosomal region (PAR) is a small region on the X and Y chromosomes that shares homology, allowing these chromosomes to pair during meiosis. This region is essential for proper segregation of sex chromosomes during gamete formation. The presence of PAR facilitates genetic recombination, which can influence the inheritance of sex-linked traits and contribute to variations in sex determination.
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Regions of X Chromosomes
Sex Reversal
Sex reversal refers to a condition where an individual’s phenotypic sex does not match their chromosomal sex. In humans, this can occur when individuals with XY chromosomes develop female characteristics or those with XX chromosomes develop male characteristics. Such discrepancies often arise from mutations in the SRY gene or other genes involved in sex determination, leading to atypical development of sexual characteristics.
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Sex Determination
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Textbook Question
Cat breeders are aware that kittens expressing the X-linked calico coat pattern and tortoiseshell pattern are almost invariably females. Why are they certain of this?
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