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
17. Mutation, Repair, and Recombination
DNA Repair
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Join thousands of students who trust us to help them ace their exams!Watch the first videoMultiple Choice
Which of the following pathways is an error-free way to repair double-stranded breaks?
A
Homologous recombination
B
Non-homologous end joining
C
Translesion synthesis
D
Mismatch repair

1
Understand the context: Double-stranded breaks (DSBs) in DNA are severe types of damage that can lead to cell death or cancer if not repaired correctly.
Identify the repair mechanisms: There are several pathways to repair DSBs, including Homologous Recombination (HR), Non-Homologous End Joining (NHEJ), Translesion Synthesis, and Mismatch Repair.
Focus on Homologous Recombination: HR is a high-fidelity repair process that uses a homologous sequence as a template to accurately repair the break, ensuring error-free repair.
Contrast with other pathways: Non-Homologous End Joining (NHEJ) is quicker but can introduce errors as it directly ligates the broken ends without a template. Translesion Synthesis and Mismatch Repair are not primarily involved in DSB repair.
Conclude with the correct pathway: Given the need for accuracy in repairing DSBs, Homologous Recombination is the error-free pathway among the options provided.
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Open Question
Thinking back to the discussion of gain-of-function and loss-of-function mutations in Section 4.1, and putting those concepts together with the discussion of base substitution mutations in this chapter, explain why gain-of-function mutations are often dominant and why loss-of-function mutations are often recessive. Give an example of a type of gain-of-function mutation that is dominant and of a loss-of-function mutation that is recessive.