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
6. Chromosomal Variation
Chromosomal Rearrangements: Deletions
1:36 minutes
Problem 5
Textbook Question
Textbook QuestionHuman late prophase karyotypes have about 2000 visible G bands. The human genome contains approximately 22,000 genes. Consider the region 5p1.5 through the end of the short arm of chromosome 5, which is identified on the late prophase chromosome in Figure 10.5, and assume the entire region is deleted. Approximately how many genes will be lost as a result of the deletion?
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Karyotype and G-banding
A karyotype is a visual representation of an individual's chromosomes, organized by size and shape. G-banding is a technique used to stain chromosomes, producing a pattern of light and dark bands that helps identify specific chromosomes and their structural features. In humans, there are about 2000 visible G bands, which correspond to regions of DNA that can be analyzed for genetic abnormalities.
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DNA Structure
Human Genome and Gene Count
The human genome is the complete set of genetic information for humans, consisting of approximately 22,000 genes. These genes are segments of DNA that encode instructions for building proteins, which perform various functions in the body. Understanding the distribution of genes across chromosomes is crucial for assessing the impact of genetic deletions or mutations.
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Human Genome Composition
Chromosomal Deletion
A chromosomal deletion is a type of genetic mutation where a segment of DNA is lost from a chromosome. This can lead to the loss of one or more genes, potentially resulting in various genetic disorders or phenotypic changes. In the context of the question, deleting the region 5p1.5 through the end of chromosome 5 would remove all genes located within that specific segment, affecting the overall gene count.
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Deletions
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