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
15. Genomes and Genomics
Comparative Genomics
2:11 minutes
Problem 21
Textbook Question
Textbook QuestionResearchers have compared candidate loci in humans and rats in search of loci in the human genome that are likely to contribute to the constellation of factors leading to hypertension [Stoll, M., et al. (2000). Genome Res. 10:473–482]. Through this research, they identified 26 chromosomal regions that they consider likely to contain hypertension genes. How can comparative genomics aid in the identification of genes responsible for such a complex human disease? The researchers state that comparisons of rat and human candidate loci to those in the mouse may help validate their studies. Why might this be so?
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Key Concepts
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Comparative Genomics
Comparative genomics is the field of study that involves comparing the genomic features of different organisms to identify similarities and differences. This approach helps researchers understand evolutionary relationships and functional elements within genomes. By analyzing conserved regions across species, scientists can pinpoint genes that may play critical roles in specific biological processes, such as disease susceptibility.
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Candidate Loci
Candidate loci refer to specific regions of the genome that are hypothesized to contain genes associated with particular traits or diseases. In the context of hypertension, researchers identify these loci based on previous studies or genetic markers linked to the condition. Investigating these regions can provide insights into the genetic basis of complex diseases by revealing potential gene candidates for further functional analysis.
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Gene Validation through Model Organisms
Using model organisms, such as rats and mice, allows researchers to validate findings from human studies by examining gene function and disease mechanisms in a controlled environment. These organisms often share significant genetic similarities with humans, making them valuable for testing hypotheses about gene involvement in diseases. By confirming the role of candidate genes in these models, researchers can strengthen the evidence for their relevance to human health.
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