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
Problem 4c
Textbook Question
Textbook QuestionWhat are the differences between a synonymous mutation, a missense mutation, and a nonsense mutation?
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Synonymous Mutation
A synonymous mutation is a change in the DNA sequence that does not alter the amino acid sequence of the resulting protein. This occurs because multiple codons can code for the same amino acid due to the redundancy in the genetic code. As a result, synonymous mutations are often considered neutral, as they do not affect the protein's function.
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Missense Mutation
A missense mutation is a type of point mutation where a single nucleotide change results in the substitution of one amino acid for another in the protein. This can potentially alter the protein's function, depending on the role of the affected amino acid in the protein's structure or activity. Missense mutations can be classified as benign, harmful, or beneficial based on their effects on the organism.
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Nonsense Mutation
A nonsense mutation is a mutation that converts a codon encoding an amino acid into a stop codon, leading to premature termination of protein synthesis. This results in a truncated protein that is often nonfunctional. Nonsense mutations can have severe consequences for cellular function and are typically associated with genetic disorders.
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