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
4. Genetic Mapping and Linkage
Mapping Genes
2:16 minutes
Problem 29b
Textbook Question
Textbook QuestionA 2006 genetic study of a large American family (Ikeda et al., 2006) identified genetic linkage between DNA markers on chromosome 11 and the gene producing the autosomal dominant neuromuscular disorder spinocerebellar ataxia type 5 (SCA5). The following lod score data are taken from the 2006 study: Theta (θ) Value 0.01 0.05 0.10 0.20 0.30 0.40SCA5 11.02 12.26 11.94 10.04 7.26 3.77 and DNA marker A SCA5 0.35. 0.94. 1.07 0.99 0.75 0.43 and DNA marker B What is the maximum value for each set of lod scores?
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Lod Score
A lod score (logarithm of the odds) is a statistical measure used in genetics to evaluate the likelihood of a particular genetic linkage. It compares the probability of observing the data if two loci are linked versus if they are unlinked. A lod score of 3 or higher is typically considered significant evidence for linkage, indicating that the loci are likely inherited together.
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Theta (θ) Value
Theta (θ) represents the recombination fraction between two genetic markers, indicating the probability that a crossover will occur between them during meiosis. Values range from 0 (no recombination, markers are linked) to 0.5 (independent assortment). Understanding θ is crucial for interpreting lod scores, as it directly influences the likelihood of linkage between genes.
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Step 3
Autosomal Dominant Inheritance
Autosomal dominant inheritance is a pattern where only one copy of a mutated gene from an affected parent can cause the disorder in offspring. This means that the trait can be passed down through generations, and each child of an affected parent has a 50% chance of inheriting the condition. Spinocerebellar ataxia type 5 (SCA5) is an example of a disorder that follows this inheritance pattern.
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