Experiments by Charles Yanofsky in the 1950s and 1960s helped characterize the nature of tryptophan synthesis in E. coli. In one of Yanofsky's experiments, he identified glycine (Gly) as the wild-type amino acid in position 211 of tryptophan synthetase, the product of the trpA gene. He identified two independent missense mutants with defective tryptophan synthetase at these positions that resulted from base-pair substitutions. One mutant encoded arginine (Arg) and another encoded glutamic acid (Glu). At position 235, wild-type tryptophan synthetase contains serine (Ser) but a base-pair substitution mutant encodes leucine (Leu). At position 243, the wild-type polypeptide contains glutamine and a base-pair substitution mutant encodes a stop codon. Identify the most likely wild-type codons for positions 211, 235, and 243. Justify your answer in each case.
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
Induced Mutations
Problem 34d
Textbook Question
Using your knowledge of DNA repair pathways, choose the pathway that would be used to repair the following types of DNA damage. Explain your reasoning.
A double-strand break that occurs just after replication in an actively dividing cell

1
Identify the type of DNA damage described in the problem. A double-strand break (DSB) is a severe form of DNA damage where both strands of the DNA helix are broken. This type of damage can lead to genomic instability if not repaired properly.
Consider the context of the damage. The problem specifies that the double-strand break occurs just after replication in an actively dividing cell. This is important because the cell has recently duplicated its DNA, meaning sister chromatids are available.
Recall the DNA repair pathways available for double-strand breaks. The two primary pathways are non-homologous end joining (NHEJ) and homologous recombination (HR). NHEJ directly joins the broken ends but is error-prone, while HR uses a homologous sequence (such as a sister chromatid) as a template for accurate repair.
Determine which pathway is most likely to be used in this scenario. Since the damage occurs just after replication, sister chromatids are present and can serve as templates for homologous recombination. HR is preferred in this case because it ensures high-fidelity repair by using the sister chromatid.
Explain the reasoning. Homologous recombination is the most suitable pathway for repairing double-strand breaks in actively dividing cells with sister chromatids available. This ensures accurate repair and prevents mutations or chromosomal rearrangements that could arise from error-prone repair mechanisms like NHEJ.

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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Double-Strand Breaks (DSBs)
Double-strand breaks are severe forms of DNA damage where both strands of the DNA helix are broken. These breaks can lead to genomic instability if not repaired properly. DSBs can occur due to various factors, including ionizing radiation, chemical agents, or during DNA replication. Understanding the nature of DSBs is crucial for identifying the appropriate repair mechanisms.
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Homologous Recombination (HR)
Homologous recombination is a DNA repair pathway that accurately repairs double-strand breaks using a homologous sequence as a template. This process is particularly active in dividing cells, especially after DNA replication when sister chromatids are available. HR is essential for maintaining genomic integrity and preventing mutations, making it the preferred method for repairing DSBs that occur shortly after replication.
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Recombination after Single Strand Breaks
Non-Homologous End Joining (NHEJ)
Non-homologous end joining is a DNA repair mechanism that directly ligates the broken ends of DNA without the need for a homologous template. This pathway is faster and often used in non-dividing cells or when homologous sequences are not available. While NHEJ is crucial for quick repairs, it can lead to insertions or deletions, making it less accurate than homologous recombination, especially in actively dividing cells.
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Double Strand Breaks
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