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
5. Genetics of Bacteria and Viruses
Bacterial Transformation
3:12 minutes
Problem 25a
Textbook Question
Define the term genetic complementation.
Does the term genetic complementation have the same meaning in both cases? Explain.
Verified step by step guidance
1
<Genetic complementation refers to a phenomenon where two different mutations in the genome of an organism result in a wild-type or non-mutant phenotype when present together.>
<This occurs when the mutations are in different genes, allowing each gene to provide the function that the other lacks.>
<In a genetic complementation test, two organisms with different recessive mutations that produce the same phenotype are crossed.>
<If the offspring display the wild-type phenotype, it indicates that the mutations complement each other, meaning they are in different genes.>
<The term genetic complementation can have different implications depending on the context, such as in diploid organisms versus haploid organisms, but the core concept remains the same: the restoration of a function through the combination of different mutations.>
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