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 with Markers
Problem 34b
Textbook Question
The 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.
![Pedigree chart illustrating inheritance patterns in a different family.](https://lightcat-files.s3.amazonaws.com/problem_images/a5b291b38029f828-1678987949391.jpg)
What are the syntenic disease gene and VNTR alleles in I-1 and I-2?
![Gel electrophoresis results displaying VNTR genotypes for family members.](https://lightcat-files.s3.amazonaws.com/problem_images/e3d5fd7275dfd812-1678912959868.jpg)
![Pedigree chart showing family members with an autosomal recessive disorder and VNTR genotypes.](https://lightcat-files.s3.amazonaws.com/problem_images/f816a95afdec0135-1678912970589.jpg)
![](/channels/images/assetPage/verifiedSolution.png)
1
Identify the genotypes of the affected individuals (I-2 and II-2) as 'dd' since they have the autosomal recessive disorder.
Observe the gel electrophoresis patterns to determine the VNTR alleles for each family member. I-2 and II-2 both show the same VNTR pattern, indicating they share the same VNTR alleles linked to the disease gene.
Note that the recombination frequency between the VNTR and the disease gene is 20%, which means there is a 20% chance of recombination occurring between these loci.
Determine the VNTR alleles for I-1 by analyzing the gel pattern. I-1 shows a different VNTR pattern compared to I-2, suggesting a different VNTR allele combination.
Conclude that the syntenic VNTR alleles for I-1 and I-2 are those that are consistently inherited with the 'd' allele in affected individuals, considering the recombination frequency.
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