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
Types of Mutations
1:41 minutes
Problem 9a
Textbook Question
Textbook QuestionDescribe the purpose of the Ames test. How are his⁻ bacteria used in the Ames test? What mutational event is identified using his⁻ bacteria?
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Ames Test Purpose
The Ames test is a widely used assay that evaluates the mutagenic potential of chemical compounds. It assesses whether a substance can cause mutations in the DNA of a test organism, typically a strain of bacteria. By identifying mutagens, the Ames test helps in assessing the potential carcinogenic risk of chemicals to humans.
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his⁻ Bacteria
His⁻ bacteria are mutant strains of bacteria that lack the ability to synthesize histidine, an essential amino acid. In the Ames test, these bacteria are exposed to the test substance, and if mutations occur that restore their ability to produce histidine, it indicates that the substance is mutagenic. This restoration is a key indicator of genetic change due to the test compound.
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Mutational Events
The mutational event identified using his⁻ bacteria in the Ames test is the reversion mutation, where a mutation in the bacterial DNA restores the original function lost in the his⁻ strain. This event signifies that the test substance has induced a genetic change, allowing the bacteria to regain the ability to synthesize histidine, thus providing evidence of mutagenicity.
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