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
2. Mendel's Laws of Inheritance
Sex-Linked Genes
3:13 minutes
Problem 12f
Textbook Question
Textbook QuestionA woman's father has ornithine transcarbamylase deficiency (OTD), an X-linked recessive disorder producing mental deterioration if not properly treated. The woman's mother is homozygous for the wild-type allele.
If the woman has a son with a man who does not have OTD, what is the chance the son will have OTD?
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
X-Linked Recessive Inheritance
X-linked recessive disorders are caused by mutations on the X chromosome. Males, having one X and one Y chromosome, are more likely to express these disorders if they inherit the affected X. Females, with two X chromosomes, can be carriers if they have one affected X and one normal X, but typically only express the disorder if both X chromosomes are affected.
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X-Inactivation
Genotype of the Parents
In this scenario, the woman is a carrier for ornithine transcarbamylase deficiency (OTD) because her father has the disorder and her mother is homozygous for the wild-type allele. This means the woman has one affected X chromosome (from her father) and one normal X chromosome (from her mother). The man does not have OTD, indicating he has a normal Y chromosome and a normal X chromosome.
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Punnett Square Analysis
A Punnett square is a tool used to predict the genetic outcomes of a cross between two individuals. In this case, it can be used to determine the probability of the son inheriting OTD. By analyzing the possible combinations of the mother's X chromosomes (one affected and one normal) with the father's normal X chromosome, we can calculate the likelihood of the son inheriting the disorder.
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Chi Square Analysis
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