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
1:47 minutes
Problem 19a
Textbook Question
Textbook QuestionUsing the adenine–thymine base pair in this DNA sequence ...GCTC... ...CGAG... Give the sequence after a transversion mutation.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Transversion Mutation
A transversion mutation is a type of point mutation where a purine base (adenine or guanine) is replaced by a pyrimidine base (cytosine or thymine), or vice versa. This contrasts with transitions, where a purine is replaced by another purine or a pyrimidine by another pyrimidine. Transversions can lead to significant changes in the protein sequence, potentially altering the function of the resulting protein.
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DNA Base Pairing
DNA base pairing refers to the specific pairing of nitrogenous bases in the DNA double helix, where adenine pairs with thymine (A-T) and guanine pairs with cytosine (G-C). This complementary base pairing is crucial for DNA replication and transcription, ensuring that genetic information is accurately copied and expressed. Understanding base pairing is essential for predicting the effects of mutations on DNA sequences.
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Effects of Mutations
Mutations can have various effects on an organism, ranging from benign to harmful. They can alter the amino acid sequence of proteins, potentially affecting their structure and function. Some mutations may lead to diseases or disorders, while others can provide beneficial traits that enhance survival. Analyzing the specific type of mutation, such as a transversion, helps in understanding its potential impact on gene expression and phenotype.
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