A new approach to estimate parameters of speciation models with application to apes

  1. Celine Becquet1 and
  2. Molly Przeworski1
  1. Department of Human Genetics, University of Chicago, Chicago, Illinois 60637, USA

Abstract

How populations diverge and give rise to distinct species remains a fundamental question in evolutionary biology, with important implications for a wide range of fields, from conservation genetics to human evolution. A promising approach is to estimate parameters of simple speciation models using polymorphism data from multiple loci. Existing methods, however, make a number of assumptions that severely limit their applicability, notably, no gene flow after the populations split and no intralocus recombination. To overcome these limitations, we developed a new Markov chain Monte Carlo method to estimate parameters of an isolation-migration model. The approach uses summaries of polymorphism data at multiple loci surveyed in a pair of diverging populations or closely related species and, importantly, allows for intralocus recombination. To illustrate its potential, we applied it to extensive polymorphism data from populations and species of apes, whose demographic histories are largely unknown. The isolation-migration model appears to provide a reasonable fit to the data. It suggests that the two chimpanzee species became reproductively isolated in allopatry ∼850 Kya, while Western and Central chimpanzee populations split ∼440 Kya but continued to exchange migrants. Similarly, Eastern and Western gorillas and Sumatran and Bornean orangutans appear to have experienced gene flow since their splits ∼90 and over 250 Kya, respectively.

Footnotes

  • 1 Corresponding authors.

    1 E-mail cbecquet{at}uchicago.edu; fax (773) 834-0505.

    1 E-mail mfp{at}uchicago.edu; fax (773) 834-0505.

  • [Supplemental material is available online at www.genome.org.]

  • Article published online before print. Article and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.6409707

    • Received February 16, 2007.
    • Accepted July 3, 2007.
  • Freely available online through the Genome Research Open Access option.

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