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Revising the human mutation rate: implications for understanding human evolution
Nature Reviews Geneticsvolume 13, pages745–753 (2012)Cite this article
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AnErratum to this article was published on 19 September 2012
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Abstract
It is now possible to make direct measurements of the mutation rate in modern humans using next-generation sequencing. These measurements reveal a value that is approximately half of that previously derived from fossil calibration, and this has implications for our understanding of demographic events in human evolution and other aspects of population genetics. Here, we discuss the implications of a lower-than-expected mutation rate in relation to the timescale of human evolution.
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Change history
19 September 2012
In the second paragraph of the subsection entitled 'African and non-African split' in this article, both instances of the range '60,000–120,000 years ago' were incorrectly written as '120,000–160,000 years ago'. The editors apologize for this mistake.
References
Takahata, N. & Satta, Y. Evolution of the primate lineage leading to modern humans: phylogenetic and demographic inferences from DNA sequences.Proc. Natl Acad. Sci. USA94, 4811–4815 (1997).
Green, R. E. et al. A draft sequence of the Neandertal genome.Science328, 710–722 (2010).
Roach, J. C. et al. Analysis of genetic inheritance in a family quartet by whole-genome sequencing.Science328, 636–639 (2010).
Consortium, G. P. A map of human genome variation from population-scale sequencing.Nature467, 1061–1073 (2010).
Awadalla, P. et al. Direct measure of thede novo mutation rate in autism and schizophrenia cohorts.Am. J. Hum. Genet.87, 316–324 (2010).
Sanders, S. J. et al.De novo mutations revealed by whole-exome sequencing are strongly associated with autism.Nature485, 237–241 (2012).
O'Roak, B. J. et al. Sporadic autism exomes reveal a highly interconnected protein network ofde novo mutations.Nature485, 246–250 (2012).
Lynch, M. Rate, molecular spectrum, and consequences of human mutation.Proc. Natl Acad. Sci.107, 961–968 (2010).
Nelson, M. R. et al. An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people.Science337, 100–104 (2012).
Fenner, J. N. Cross-cultural estimation of the human generation interval for use in genetics-based population divergence studies.Am. J. Phys. Anthropol.128, 415–423 (2005).
Matsumura, S. & Forster, P. Generation time and effective population size in Polar Eskimos.Proc. R. Soc. B275, 1501–1508 (2008).
Teleki, G., Hunt, E. E. & Pfifferling, J. H. Demographic observations on the chimpanzees of Gombe National Park, Tanzania.J. Hum. Evol.5, 559–598 (1976).
Ho, S. Y. W., Lanfear, R., Bromham, L. & Phillips, M. J. Time-dependent rates of molecular evolution.Mol. Ecol.20, 3087–3101 (2011).
Haag-liautard, C. et al. Direct estimation of per nucleotide and genomic deleterious mutation rates inDrosophila.Nature445, 82–85 (2007).
Denver, D. R., Morris, K., Lynch, M. & Thomas, W. K. High mutation rate and predominance of insertions in theCaenorhabditis elegans nuclear genome.Nature430, 679–682 (2004).
Kim, S.-H., Elango, N., Warden, C., Vigoda, E. & Yi, S. V. Heterogeneous genomic molecular clocks in primates.PLoS Genet.2, e163 (2006).
Fleagle, J. G.Primate Adaptation and Evolution 2nd edn (Academic Press, 1998).
Hartwig, W. C.The Primate Fossil Record (Cambridge Univ. Press, 2002).
Scally, A. et al. Insights into hominid evolution from the gorilla genome sequence.Nature483, 169–175 (2012).
Toews, D. P. L. & Brelsford, A. The biogeography of mitochondrial and nuclear discordance in animals.Mol. Ecol.21, 3907–3930 (2012).
Soares, P. et al. Correcting for purifying selection: an improved human mitochondrial molecular clock.Am. J. Hum. Genet.84, 740–759 (2009).
Endicott, P. & Ho, S. Y. W. A Bayesian evaluation of human mitochondrial substitution rates.Am. J. Hum. Genet.82, 895–902 (2008).
Endicott, P., Ho, S. Y. W., Metspalu, M. & Stringer, C. Evaluating the mitochondrial timescale of human evolution.Trends Ecol. Evol.24, 515–521 (2009).
Behar, Doron, M. et al. A “copernican” reassessment of the human mitochondrial DNA tree from its root.Am. J. Hum. Genet.90, 675–684 (2012).
Reich, D. et al. Genetic history of an archaic hominin group from Denisova Cave in Siberia.Nature468, 1053–1060 (2010).
Endicott, P., Ho, S. Y. W. & Stringer, C. Using genetic evidence to evaluate four palaeoanthropological hypotheses for the timing of Neanderthal and modern human origins.J. Hum. Evol.59, 87–95 (2010).
Mounier, A., Marchal, F. & Condemi, S. IsHomo heidelbergensis a distinct species? New insight on the Mauer mandible.J. Hum. Evol.56, 219–246 (2009).
Stringer, C. What makes a modern human.Nature485, 4–6 (2012).
Behar, D. M. et al. The dawn of human matrilineal diversity.J. Hum. Genet.82, 1130–1140 (2008).
Li, H. & Durbin, R. Inference of human population history from individual whole-genome sequences.Nature475, 493–496 (2011).
Millard, A. R. A critique of the chronometric evidence for hominid fossils: I. Africa and the Near East 500–550 ka.J. Hum. Evol.54, 848–874 (2008).
Armitage, S., Jasim, S., Marks, A. & Parker, A. The southern route “out of Africa”: evidence for an early expansion of modern humans into Arabia.Science331, 453–456 (2011).
Rose, J. I. et al. The nubian complex of Dhofar, Oman: an African middle stone age industry in southern Arabia.PLoS ONE6, e28239 (2011).
Petraglia, M. et al. Middle Paleolithic assemblages from the Indian subcontinent before and after the Toba super-eruption.Science317, 114–116 (2007).
Lawler, A. Did modern humans travel out of Africa via Arabia?Science331, 387 (2011).
Gravel, S. et al. Demographic history and rare allele sharing among human populations.Proc. Natl Acad. Sci. USA108, 11983–11988 (2011).
Rosenberg, T. M. et al. Humid periods in southern Arabia: windows of opportunity for modern human dispersal.Geology39, 1115–1118 (2011).
Castañeda, I. S. et al. Wet phases in the Sahara/Sahel region and human migration patterns in North Africa.Proc. Natl Acad. Sci. USA106, 20159–20163 (2009).
Osborne, A. H. et al. A humid corridor across the Sahara for the migration of early modern humans out of Africa 120,000 years ago.Proc. Natl Acad. Sci. USA105, 16444–16447 (2008).
Pinhasi, R., Higham, T. F. G., Golovanova, L. V. & Doronichev, V. B. Revised age of late Neanderthal occupation and the end of the Middle Paleolithic in the northern Caucasus.108, 8611–8616 (2011).
Soares, P. et al. The Expansion of mtDNA Haplogroup L3 within and out of Africa.Molecular Biol. Evol. 16 Nov 2011 (doi:10.1093/molbev/msr245).
Gibbs, R., Belmont, J., Hardenbol, P. & Willis, T. The international HapMap project.Nature63 (Suppl. 1), 29–34 (2003).
Reed, F. & Tishkoff, S. A. African human diversity, origins and migrations.Curr. Opin. Genet. Dev.16, 597–605 (2006).
Gronau, I., Hubisz, M. J., Gulko, B., Danko, C. G. & Siepel, A. Bayesian inference of ancient human demography from individual genome sequences.Nature Genet.43, 1031–1034 (2011).
Carrión, J. S., Rose, J. & Stringer, C. Early human evolution in the western Palaearctic: ecological scenarios.Quat. Sci. Rev.30, 1281–1295 (2011).
Higham, T. et al. The earliest evidence for anatomically modern humans in northwestern Europe.Nature479, 31–34 (2011).
Hoffecker, J. F. et al. From the Bay of Naples to the River Don: the Campanian Ignimbrite eruption and the Middle to Upper Paleolithic transition in Eastern Europe.J. Hum. Evol.55, 858–870 (2008).
O'Connell, J. Dating the colonization of Sahul (Pleistocene Australia–New Guinea): a review of recent research.J. Archaeol. Sci.31, 835–853 (2004).
Shen, G., Wang, W., Cheng, H. & Edwards, R. L. Mass spectrometric U-series dating of Laibin hominid site in Guangxi, southern China.J. Archaeol. Sci.34, 2109–2114 (2007).
Shen, G., Wang, W., Wang, Q. & Zhao, J. U-Series dating of Liujiang hominid site in Guangxi, Southern China.J. Hum.43, 817–829 (2002).
Trinkaus, E. et al. An early modern human from the Pes¸tera cu Oase, Romania.Proc. Natl Acad. Sci. USA100, 11231–11236 (2003).
Reich, D. et al. Denisova admixture and the first modern human dispersals into Southeast Asia and Oceania.Am. J. Hum. Genet.89, 516–528 (2011).
Rasmussen, M. et al. An aboriginal Australian genome reveals separate human dispersals into Asia.Science334, 94–98 (2011).
Ho, S. Y. W. & Larson, G. Molecular clocks: when times are a-changin'.Trends Genet.22, 79–83 (2006).
Hammer, M. F., Woerner, A. E., Mendez, F. L., Watkins, J. C. & Wall, J. D. Genetic evidence for archaic admixture in Africa.Proc. Natl Acad. Sci. USA 6 Sep 2011 (doi:10.1073/pnas.1109300108).
Haldane, J. The rate of spontaneous mutation of a human gene.J. Genet.83, 235–244 (1935).
Kondrashov, A. S. Direct estimates of human per nucleotide mutation rates at 20 loci causing Mendelian diseases.Hum. Mut.21, 12–27 (2003).
Conrad, D. D. F. et al. Variation in genome-wide mutation rates within and between human families.Nature43, 712–714 (2011).
Steiper, M. E. & Young, N. M. Timing primate evolution: Lessons from the discordance between molecular and paleontological estimates.Evol. Anthropol.17, 179–188 (2008).
Tyekucheva, S. et al. Human-macaque comparisons illuminate variation in neutral substitution rates.Genome Biol.9, R76 (2008).
Lanfear, R., Welch, J. J. & Bromham, L. Watching the clock: studying variation in rates of molecular evolution between species.Trends Ecol. Evol.25, 495–503 (2010).
Locke, D. P. et al. Comparative and demographic analysis of orang-utan genomes.Nature469, 529–533 (2011).
Patterson, N., Richter, D. J., Gnerre, S., Lander, E. S. & Reich, D. Genetic evidence for complex speciation of humans and chimpanzees.Nature441, 1103–1108 (2006).
Wegmann, D. & Excoffier, L. Bayesian inference of the demographic history of chimpanzees.Mol. Biol. Evol.27, 1425–1435 (2010).
Zhu, T. & Yang, Z. Maximum likelihood implementation of an isolation-with-migration model with three species for testing speciation with gene flow.Mol. Biol. Evol. 13 Apr 2012 (doi:10.1093/molbev/mss118).
Becquet, C. & Przeworski, M. Learning about modes of speciation by computational approaches.Evolution63, 2547–2562 (2009).
Strasburg, J. L. & Rieseberg, L. H. How robust are “isolation with migration” analyses to violations of the IM model? A simulation study.Mol. Biol. Evol.27, 297–310 (2010).
Elango, N., Thomas, J. W., Program, N. C. S. & Yi, S. V. Variable molecular clocks in hominoids.Proc. Natl Acad. Sci. USA103, 1370–1375 (2006).
Benton, M. Paleontological evidence to date the tree of life.Mol. Biol. Evol.24, 26–53 (2007).
Green, R. E. et al. A complete Neandertal mitochondrial genome sequence determined by high-throughput sequencing.Cell134, 416–426 (2008).
Krause, J. et al. The complete mitochondrial DNA genome of an unknown hominin from southern Siberia.Nature464, 894–897 (2010).
Veeramah, K. R. et al. An early divergence of KhoeSan ancestors from those of other modern humans is supported by an ABC-based analysis of autosomal re-sequencing data.Mol. Biol. Evol.29, 617–630 (2012).
Acknowledgements
We would like to acknowledge discussions with attendees at the Workshop on Coancestry, Association and Population Genomics at the Institute for Pure and Applied Mathematics, University of California, Los Angeles, November 2011, where these ideas were initially presented. We also thank T. Kivisild for comments. The authors were supported by Wellcome Trust grant WT098051.
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Wellcome Trust Sanger Institute, Hinxton, UK
Aylwyn Scally & Richard Durbin
- Aylwyn Scally
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- Richard Durbin
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Correspondence toAylwyn Scally orRichard Durbin.
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Revising the human mutation rate: implications for understanding human evolution (PDF 152 kb)
Glossary
- Effective population sizes
(Ne). Indicate how many individuals actually contribute alleles to the next generation, as opposed to the total number of individuals in a population. The expected time to the most recent common ancestor of two individual copies of a locus is proportional toNe.
- Hominoid slowdown
The phenomenon in which shorter phylogenetic branch lengths are found within apes relative to other primate lineages.
- Haplogroups
Branches of the mitochondrial DNA phylogenetic tree that comprise a collection of related haplotypes. Each haplotype represents a unique pattern of DNA substitutions.
- Coalescence
When two genetic lineages find a common ancestor.
- Homo heidelbergensis
Fossil hominin predominantly found in Europe but also in Africa that typically dates to 400,000–600,000 years ago and a possible ancestor of both Neanderthals and modernHomo sapiens.
- Recent African origin model
(RAO model). A model of human origins in which the transition from archaic forms to modernHomo sapiens occurred solely within Africa, followed later by migration out of Africa and dispersal across Eurasia.
- Khoe–San
Indigenous people of the Kalahari desert in Southern Africa.
- Molecular clock
The idea that nucleotide substitutions accumulate at a constant rate over time and that this rate can therefore be used to estimate divergence times between sequences.
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Scally, A., Durbin, R. Revising the human mutation rate: implications for understanding human evolution.Nat Rev Genet13, 745–753 (2012). https://doi.org/10.1038/nrg3295
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