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
Pedigrees
1:02 minutes
Problem 34
Textbook Question
Textbook QuestionThe accompanying pedigree below shows a family in which an autosomal recessive disorder is present. Family members I-2 and II-2 are affected by the disorder and have the genotype dd. A pregnancy involving II-4 has just undergone genetic testing for a VNTR that is linked to the disease gene. The VNTR has a recombination frequency of r = 20 with the disease gene. The VNTR has two alleles, V₁ and V₂. The gel electrophoresis patterns for each family member are shown, including the VNTR genotype for II-4. Based on the information given, answer the following questions about the family. Excluding II-4, what is the genotype of each family member for the disease gene?
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Autosomal Recessive Inheritance
Autosomal recessive inheritance occurs when a trait or disorder is expressed only when an individual has two copies of the recessive allele (e.g., dd). Carriers, who possess one dominant and one recessive allele (Dd), do not exhibit the disorder but can pass the recessive allele to their offspring. In a pedigree, affected individuals typically have unaffected parents, highlighting the need for both parents to contribute a recessive allele for the disorder to manifest.
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VNTR (Variable Number Tandem Repeat)
VNTRs are repetitive sequences in the DNA that vary in length between individuals. They can be used as genetic markers in linkage analysis, helping to identify the inheritance patterns of genes associated with specific traits or disorders. In this context, the VNTR's recombination frequency indicates its proximity to the disease gene, which is crucial for determining the genotypes of family members based on their gel electrophoresis patterns.
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Gel Electrophoresis
Gel electrophoresis is a laboratory technique used to separate DNA fragments based on their size and charge. In the context of genetic testing, it allows visualization of different alleles present in individuals by producing distinct banding patterns. By comparing these patterns, one can infer the genotypes of family members for specific genetic markers, such as the VNTR linked to the autosomal recessive disorder in the pedigree.
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