An insect species is discovered in which the heterogametic sex is unknown. An X-linked recessive mutation for reduced wing (rw) is discovered. Contrast the F1 and F2 generations from a cross between a female with reduced wings and a male with normal-sized wings when the female is the heterogametic sex.
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 14
Textbook Question
It has been suggested that any male-determining genes contained on the Y chromosome in humans cannot be located in the limited region that synapses with the X chromosome during meiosis. What might be the outcome if such genes were located in this region?
Verified step by step guidance1
Understand the structure of the human sex chromosomes: the X and Y chromosomes pair and synapse during meiosis only in a small region called the pseudoautosomal region (PAR). This region allows for proper segregation of the sex chromosomes.
Recognize that genes located within the PAR are present on both the X and Y chromosomes and undergo recombination during meiosis, which helps maintain genetic similarity in this region.
Consider that male-determining genes, such as SRY, are typically located outside the PAR in the non-recombining region of the Y chromosome to prevent them from being exchanged with the X chromosome during meiosis.
Analyze the consequence if male-determining genes were located within the PAR: because this region recombines with the X chromosome, these genes could be transferred to the X chromosome during meiosis, potentially disrupting the strict male-specific inheritance pattern.
Conclude that such recombination could lead to abnormal sex determination outcomes, such as males inheriting an X chromosome with male-determining genes or females inheriting Y-linked male-determining genes, which could cause disorders of sexual development.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Sex Chromosome Pairing and Synapsis
During meiosis, the X and Y chromosomes pair and synapse only in a small homologous region called the pseudoautosomal region. This limited synapsis allows for proper segregation of sex chromosomes. Genes located outside this region typically do not recombine between X and Y.
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Human Sex Chromosomes
Recombination and Gene Location on Sex Chromosomes
Recombination occurs in the pseudoautosomal region where X and Y chromosomes exchange genetic material. If male-determining genes were located within this region, they could be subject to recombination, potentially disrupting their male-specific function by mixing with X-linked alleles.
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Human Sex Chromosomes
Male-Determining Genes and Sex Determination
Male-determining genes, such as SRY, are typically located on the non-recombining region of the Y chromosome to ensure stable inheritance of male sex traits. If these genes recombined with the X chromosome, it could lead to sex reversal or loss of male-specific characteristics.
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Sex Determination
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