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
6. Chromosomal Variation
Chromosomal Mutations: Aneuploidy
1:49 minutes
Problem 5
Textbook Question
Textbook QuestionWhat evidence suggests that Down syndrome is more often the result of nondisjunction during oogenesis rather than during spermatogenesis?
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Nondisjunction
Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate properly during cell division, leading to gametes with an abnormal number of chromosomes. In the context of Down syndrome, which is caused by an extra copy of chromosome 21 (trisomy 21), nondisjunction can occur during meiosis in either oogenesis or spermatogenesis, but the implications differ based on the parent of origin.
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Oogenesis vs. Spermatogenesis
Oogenesis is the process of egg (ovum) formation in females, which occurs in a finite number of oocytes that are arrested in development until ovulation. In contrast, spermatogenesis is the continuous production of sperm in males. Research indicates that maternal age significantly affects the risk of nondisjunction during oogenesis, suggesting that most cases of Down syndrome arise from errors in egg formation rather than sperm.
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Maternal Age Effect
The maternal age effect refers to the increased risk of chromosomal abnormalities, including Down syndrome, associated with advanced maternal age. As women age, the likelihood of nondisjunction during oogenesis rises, particularly after age 35. This phenomenon is less pronounced in males, where sperm production remains relatively constant, indicating that the majority of Down syndrome cases are linked to maternal rather than paternal nondisjunction.
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