Recent reconstructions of evolutionary history are often dependent on assigning divergence in terms of changes in amino acid or nucleotide sequences. For example, a comparison of cytochrome c shows 10 amino acid differences between humans and dogs, 24 differences between humans and moths, and 38 differences between humans and yeast. Such data provide no information as to the absolute times of divergence for humans, dogs, moths, and yeast. How might one calibrate the molecular clock to an absolute time clock? What problems might one encounter in such a calibration?
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
22. Evolutionary Genetics
Phylogenetic Trees
Problem D.2
Textbook Question
What insights have analyses of human mitochondrial DNA provided into our recent evolutionary past?

1
Understand that mitochondrial DNA (mtDNA) is inherited maternally and does not undergo recombination, making it a powerful tool for tracing maternal lineages over time.
Recognize that by comparing mtDNA sequences from diverse human populations, scientists can construct phylogenetic trees that reveal relationships and estimate the timing of common ancestors.
Learn that analyses of mtDNA have supported the 'Out of Africa' hypothesis, indicating that all modern humans share a recent common maternal ancestor who lived in Africa approximately 100,000 to 200,000 years ago.
Explore how mtDNA variation helps identify population bottlenecks, migrations, and expansions in human history, providing insights into how humans dispersed across the globe.
Note that mtDNA studies complement other genetic data and fossil evidence, together building a comprehensive picture of recent human evolutionary history.

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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Mitochondrial DNA (mtDNA) Characteristics
Mitochondrial DNA is a small, circular genome inherited maternally without recombination, making it a useful tool for tracing maternal lineages. Its high mutation rate allows for the detection of genetic differences over relatively short evolutionary timescales.
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Mitochondrial Eve and Human Evolution
Analyses of mtDNA have led to the concept of 'Mitochondrial Eve,' the most recent common maternal ancestor of all living humans, estimated to have lived in Africa about 150,000 to 200,000 years ago. This supports the 'Out of Africa' model of recent human evolution.
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Population Genetics and Human Migration
mtDNA variation patterns help reconstruct human migration routes and population expansions by revealing genetic diversity and lineage splits. These analyses provide insights into how modern humans dispersed globally and adapted to different environments.
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