Comparative and demographic analysis of orang-utan genomes

Devin P. Locke(Washington University in St. Louis), LaDeana W. Hillier(Washington University in St. Louis), Wesley C. Warren(Washington University in St. Louis), Kim C. Worley(Baylor College of Medicine), Lynne V. Nazareth(Baylor Genetics), Donna M. Muzny(Baylor Genetics), Shiaw‐Pyng Yang(Washington University in St. Louis), Zhengyuan Wang(Washington University in St. Louis), Asif Chinwalla(Washington University in St. Louis), Pat Minx(Washington University in St. Louis), Makedonka Mitreva(Washington University in St. Louis), Lisa L. Cook(Washington University in St. Louis), Kim D. Delehaunty(Washington University in St. Louis), Catrina C. Fronick(Washington University in St. Louis), Heather K. Schmidt(Washington University in St. Louis), Lucinda A. Fulton(Washington University in St. Louis), Robert S. Fulton(Washington University in St. Louis), Joanne O. Nelson(Washington University in St. Louis), Vincent Magrini(Washington University in St. Louis), Craig Pohl(Washington University in St. Louis), Tina Graves(Washington University in St. Louis), Chris Markovic(Washington University in St. Louis), Andy Cree(Baylor College of Medicine), Huyen Dinh(Baylor College of Medicine), Jennifer Hume(Baylor Genetics), Christie Kovar(Baylor College of Medicine), Gerald Fowler(Baylor Genetics), Gerton Lunter(University of Oxford), Stephen Meader(Genomics (United Kingdom)), Andreas Heger(Genomics (United Kingdom)), Chris P. Ponting(Genomics (United Kingdom)), Tomàs Marquès‐Bonet(University of Washington), Can Alkan(University of Washington), Lin Chen(University of Washington), Ze Cheng(University of Washington), Jeffrey M. Kidd(University of Washington), Evan E. Eichler(Howard Hughes Medical Institute), Simon White(Wellcome Sanger Institute), Stephen M. J. Searle(Wellcome Sanger Institute), Albert J. Vilella(Wellcome Trust), Yuan Chen(European Bioinformatics Institute), Paul Flicek(Wellcome Trust), Jian Ma(University of California, Santa Cruz), Brian J. Raney(University of California, Santa Cruz), Bernard Suh(University of California, Santa Cruz), Richard Burhans(Pennsylvania State University), Javier Herrero(European Bioinformatics Institute), David Haussler(University of California, Santa Cruz), Rui Faria(Universidade do Porto), Olga Fernando(Universidade Nova de Lisboa), Fleur Darré(Institut de Biologia Evolutiva), Domènec Farré(Institut de Biologia Evolutiva), Élodie Gazave(Pompeu Fabra University), Meritxell Oliva(Pompeu Fabra University), Arcadi Navarro(Pompeu Fabra University), Roberta Roberto(University of Bari Aldo Moro), Oronzo Capozzi(University of Bari Aldo Moro), Nicoletta Archidiacono(University of Bari Aldo Moro), Giuliano Della Valle(University of Bologna), Stefania Purgato(University of Bologna), Mariano Rocchi(University of Bari Aldo Moro), Miriam K. Konkel(Louisiana State University), Jerilyn A. Walker(Louisiana State University), Brygg Ullmer(Louisiana State University), Mark A. Batzer(Louisiana State University), Arian F. A. Smit(Institute for Systems Biology), Robert Hubley(Institute for Systems Biology), Claudio Casola(Indiana University Bloomington), Daniel R. Schrider(Indiana University Bloomington), Matthew W. Hahn(Indiana University Bloomington), Vı́ctor Quesada(Universidad de Oviedo), Xosé S. Puente(Universidad de Oviedo), Gonzalo R. Ordóñez(Universidad de Oviedo), Carlos López-Otı́n(Universidad de Oviedo), Tomáš Vinař(Comenius University Bratislava), Broňa Brejová(Comenius University Bratislava), Aakrosh Ratan(Pennsylvania State University), Robert S. Harris(Pennsylvania State University), Webb Miller(Pennsylvania State University), Carolin Kosiol(University of Veterinary Medicine Vienna), Heather A. Lawson(Washington University in St. Louis), Vikas Taliwal(Cornell University), André L. Martins(Cornell University), Adam Siepel(Cornell University), Arindam RoyChoudhury(Columbia University), Xin Ma(Cornell University), Jeremiah D. Degenhardt(Cornell University), Carlos D. Bustamante(Stanford University), Ryan N. Gutenkunst(University of Arizona), Thomas Mailund(Aarhus University), Julien Y. Dutheil(Aarhus University), Asger Hobolth(Aarhus University), Mikkel Heide Schierup(Aarhus University), Oliver A. Ryder(San Diego Zoo Institute for Conservation Research), Yuko Yoshinaga, Pieter J. de Jong, George M. Weinstock(Washington University in St. Louis), Jeffrey Rogers(Baylor College of Medicine), Elaine R. Mardis(Washington University in St. Louis), Richard A. Gibbs(Baylor Genetics), Richard K. Wilson(Washington University in St. Louis)
Nature
January 25, 2011
Cited by 636Open Access
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Abstract

The genome of the Southeast Asian great ape or orang-utan has been sequenced — specifically a draft assembly of a Sumatran female individual and short-read sequence data from five further Sumatran and five Bornean orang-utan, Pongo abelii and Pongo pygmaeus, respectively. Orang-utan species appear to have split around 400,000 years ago, more recent than most previous estimates suggested, resulting in an average Bornean–Sumatran nucleotide identity of 99.68%. Structural evolution of the orang-utan genome seems to have proceeded much more slowly than that of other great apes, including chimpanzees and humans. With both orang-utan species on the endangered list, the authors hope that knowledge of the genome sequence and its variation between populations will provide a valuable resource for conservationists. The genome of the southeast Asian orang-utan has been sequenced. The draft assembly of a Sumatran individual alongside sequence data from five Sumatran and five Bornean orang-utan genomes is presented. The resources and analyses described offer new opportunities in evolutionary genomics, insights into hominid biology, and an extensive database of variation for conservation efforts. ‘Orang-utan’ is derived from a Malay term meaning ‘man of the forest’ and aptly describes the southeast Asian great apes native to Sumatra and Borneo. The orang-utan species, Pongo abelii (Sumatran) and Pongo pygmaeus (Bornean), are the most phylogenetically distant great apes from humans, thereby providing an informative perspective on hominid evolution. Here we present a Sumatran orang-utan draft genome assembly and short read sequence data from five Sumatran and five Bornean orang-utan genomes. Our analyses reveal that, compared to other primates, the orang-utan genome has many unique features. Structural evolution of the orang-utan genome has proceeded much more slowly than other great apes, evidenced by fewer rearrangements, less segmental duplication, a lower rate of gene family turnover and surprisingly quiescent Alu repeats, which have played a major role in restructuring other primate genomes. We also describe a primate polymorphic neocentromere, found in both Pongo species, emphasizing the gradual evolution of orang-utan genome structure. Orang-utans have extremely low energy usage for a eutherian mammal1, far lower than their hominid relatives. Adding their genome to the repertoire of sequenced primates illuminates new signals of positive selection in several pathways including glycolipid metabolism. From the population perspective, both Pongo species are deeply diverse; however, Sumatran individuals possess greater diversity than their Bornean counterparts, and more species-specific variation. Our estimate of Bornean/Sumatran speciation time, 400,000 years ago, is more recent than most previous studies and underscores the complexity of the orang-utan speciation process. Despite a smaller modern census population size, the Sumatran effective population size (Ne) expanded exponentially relative to the ancestral Ne after the split, while Bornean Ne declined over the same period. Overall, the resources and analyses presented here offer new opportunities in evolutionary genomics, insights into hominid biology, and an extensive database of variation for conservation efforts.


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