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
4:48 minutes
Problem 35c
Textbook Question
Textbook QuestionBased on previous family studies, an autosomal recessive disease with alleles A and a is suspected to be linked to an RFLP marker. The RFLP marker has four alleles, R₁, R₂, R₃, and R₄. The accompanying pedigree shows a three-generation family in which the disease is present. The gel shows the RFLP alleles for each family member directly below the pedigree symbol for that person. After determining the genotypes for the RFLP and disease gene for each family member, answer the following questions. What is the most likely arrangement of syntenic alleles for the RFLP and the disease gene in I-1 and I-2?
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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 two copies of a mutated gene (one from each parent) are necessary for an individual to express a trait or disease. In this case, alleles A (normal) and a (mutated) represent the gene responsible for the disease. Individuals with the genotype aa will exhibit the disease, while those with AA or Aa will be unaffected. Understanding this inheritance pattern is crucial for analyzing the pedigree and determining the likelihood of disease expression in family members.
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Restriction Fragment Length Polymorphism (RFLP)
RFLP is a molecular technique used to analyze the length of DNA fragments produced by restriction enzyme digestion. Variations in DNA sequences can lead to different fragment lengths, which can be visualized on a gel. In this scenario, the RFLP marker with alleles R₁, R₂, R₃, and R₄ serves as a genetic marker to track inheritance patterns and potential linkage to the disease gene. Understanding RFLP is essential for interpreting the gel results and determining the genotypes of family members.
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Syntenic Alleles
Syntenic alleles refer to genes or genetic markers that are located close to each other on the same chromosome and are inherited together. In this context, the arrangement of syntenic alleles for the RFLP and the disease gene in individuals I-1 and I-2 can provide insights into their genetic relationship and the likelihood of carrying the disease allele. Analyzing the syntenic arrangement helps in understanding the genetic linkage and potential co-inheritance of the RFLP marker with the disease gene.
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