One of the first Mendelian traits identified in humans was a dominant condition known as brachydactyly. This gene causes an abnormal shortening of the fingers or toes (or both). At the time, some researchers thought that the dominant trait would spread until 75 percent of the population would be affected (because the phenotypic ratio of dominant to recessive is 3 : 1). Show that the reasoning was incorrect.
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
21. Population Genetics
Allelic Frequency Changes
Problem 17
Textbook Question
A recent study examining the mutation rates of 5669 mammalian genes (17,208 sequences) indicates that, contrary to popular belief, mutation rates among lineages with vastly different generation lengths and physiological attributes are remarkably constant [Kumar, S., and Subramanian, S. (2002). Proc. Natl. Acad. Sci. USA 99:803–808]. The average rate is estimated at 12.2×10⁻⁹ per bp per year. What is the significance of this finding in terms of mammalian evolution?
Verified step by step guidance1
Understand the context: The study reports a nearly constant mutation rate across diverse mammalian lineages, despite differences in generation length and physiology. Mutation rate here refers to the frequency at which changes in the DNA sequence occur per base pair (bp) per year.
Recall the molecular clock hypothesis: This hypothesis suggests that genetic mutations accumulate at a relatively constant rate over time, allowing us to estimate divergence times between species based on genetic differences.
Interpret the significance: A constant mutation rate across mammals implies that the molecular clock can be reliably used to estimate evolutionary timelines, even when species have different life histories or generation times.
Consider evolutionary implications: This finding suggests that mutation rates are more influenced by time rather than by factors like generation length or metabolic rate, which challenges previous assumptions about mutation rate variability.
Summarize the impact: The constancy of mutation rates supports the use of molecular data to reconstruct mammalian evolutionary history and provides a more robust framework for comparing genetic divergence across species.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Molecular Clock Hypothesis
The molecular clock hypothesis proposes that genetic mutations accumulate at a relatively constant rate over time, allowing estimation of divergence times between species. This study supports the idea by showing consistent mutation rates across diverse mammals, suggesting a reliable molecular clock for evolutionary timelines.
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Translation:Wobble Hypothesis
Mutation Rate and Generation Time
Mutation rate is often thought to vary with generation length, as species with shorter generations might accumulate mutations faster. However, this finding challenges that assumption by demonstrating similar mutation rates regardless of generation time, implying other factors stabilize mutation rates across mammals.
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Point Mutations
Implications for Mammalian Evolution
A constant mutation rate across mammals means evolutionary changes can be more accurately timed, improving phylogenetic analyses and understanding of species divergence. It also suggests evolutionary pressures or molecular mechanisms maintain mutation rates, influencing how genetic diversity and adaptation occur.
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