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RESEARCH PRODUCT

A Revised Timescale for Human Evolution Based on Ancient Mitochondrial Genomes

David ReichDavid ReichMartina LariAnnamaria RonchitelliSergi CastellanoRalf SchmitzRuth BollonginoKirsten I. BosKirsten I. BosLiane GiemschAlissa MittnikPeter BauerRenata Grifoni CremonesiSvante PääboFabio MartiniJiří SvobodaJiří SvobodaDavid CaramelliQiaomei FuQiaomei FuJoachim BurgerPhilip L. F. JohnsonJohannes KrauseChengkai Sun

subject

Mitochondrial DNATime Factorsancient modern humansMolecular Sequence DataPopulationancient modern humans; mitochondrial genome; mitochondrial clockBiologyGenomeArticleGeneral Biochemistry Genetics and Molecular BiologyEvolution Molecular03 medical and health sciences0302 clinical medicineHumanseducationancient DNA Human EvolutionPhylogenyDemography030304 developmental biologyGeneticsHuman mitochondrial molecular clock0303 health scienceseducation.field_of_studyBase SequenceModels GeneticAgricultural and Biological Sciences(all)FossilsGenome HumanBiochemistry Genetics and Molecular Biology(all)HaplotypeHigh-Throughput Nucleotide SequencingBayes TheoremHaplogroup L3mitochondrial clockHaplotypesHuman evolutionmitochondrial genomeGenome MitochondrialLinear ModelsHuman genomeGeneral Agricultural and Biological Sciences030217 neurology & neurosurgery

description

Summary Background Recent analyses of de novo DNA mutations in modern humans have suggested a nuclear substitution rate that is approximately half that of previous estimates based on fossil calibration. This result has led to suggestions that major events in human evolution occurred far earlier than previously thought. Results Here, we use mitochondrial genome sequences from ten securely dated ancient modern humans spanning 40,000 years as calibration points for the mitochondrial clock, thus yielding a direct estimate of the mitochondrial substitution rate. Our clock yields mitochondrial divergence times that are in agreement with earlier estimates based on calibration points derived from either fossils or archaeological material. In particular, our results imply a separation of non-Africans from the most closely related sub-Saharan African mitochondrial DNAs (haplogroup L3) that occurred less than 62–95 kya. Conclusions Though single loci like mitochondrial DNA (mtDNA) can only provide biased estimates of population divergence times, they can provide valid upper bounds. Our results exclude most of the older dates for African and non-African population divergences recently suggested by de novo mutation rate estimates in the nuclear genome.

10.1016/j.cub.2013.02.044http://dx.doi.org/10.1016/j.cub.2013.02.044