Constructing primate phylogenies from ancient retrovirus sequences

August 31, 1999
96 (18) 10254-10260

Abstract

The genomes of modern humans are riddled with thousands of endogenous retroviruses (HERVs), the proviral remnants of ancient viral infections of the primate lineage. Most HERVs are nonfunctional, selectively neutral loci. This fact, coupled with their sheer abundance in primate genomes, makes HERVs ideal for exploitation as phylogenetic markers. Endogenous retroviruses (ERVs) provide phylogenetic information in two ways: (i) by comparison of integration site polymorphism and (ii) by orthologous comparison of evolving, proviral, nucleotide sequence. In this study, trees are constructed with the noncoding long terminal repeats (LTRs) of several ERV loci. Because the two LTRs of an ERV are identical at the time of integration but evolve independently, each ERV locus can provide two estimates of species phylogeny based on molecular evolution of the same ancestral sequence. Moreover, tree topology is highly sensitive to conversion events, allowing for easy detection of sequences involved in recombination as well as correction for such events. Although other animal species are rich in ERV sequences, the specific use of HERVs in this study allows comparison of trees to a well established phylogenetic standard, that of the Old World primates. HERVs, and by extension the ERVs of other species, constitute a unique and plentiful resource for studying the evolutionary history of the Retroviridae and their animal hosts.

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Data Availability

Data deposition: The sequences reported in this paper have been deposited in the GenBank database (accession nos. 172454–172500).

Acknowledgments

We dedicate this paper to the memory of Igor Slobodkin, Ph.D. We thank Steve O’Brien for helpful comments and discussion. J.M.C. was supported by National Cancer Institute Grant R35CA44385 and is a Research Professor of the American Cancer Society. W.E.J. was supported by National Institutes of Health Training Grants T32GM07310 and T32AI07422.

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Information & Authors

Information

Published in

The cover image for PNAS Vol.96; No.18
Proceedings of the National Academy of Sciences
Vol. 96 | No. 18
August 31, 1999
PubMed: 10468595

Classifications

Data Availability

Data deposition: The sequences reported in this paper have been deposited in the GenBank database (accession nos. 172454–172500).

Submission history

Accepted: July 6, 1999
Published online: August 31, 1999
Published in issue: August 31, 1999

Acknowledgments

We dedicate this paper to the memory of Igor Slobodkin, Ph.D. We thank Steve O’Brien for helpful comments and discussion. J.M.C. was supported by National Cancer Institute Grant R35CA44385 and is a Research Professor of the American Cancer Society. W.E.J. was supported by National Institutes of Health Training Grants T32GM07310 and T32AI07422.

Authors

Affiliations

Welkin E. Johnson
Department of Molecular Microbiology, Tufts University School of Medicine, Boston, MA 02111
John M. Coffin
Department of Molecular Microbiology, Tufts University School of Medicine, Boston, MA 02111

Notes

Present address: Division of Microbiology, New England Regional Primate Research Center, Harvard Medical School, Southborough, MA 01772-9102.
To whom reprint requests should be addressed at: Tufts University School of Medicine, Department of Molecular Biology and Microbiology, 136 Harrison Ave., Boston, MA 02111. E-mail: [email protected].
This contribution is part of the special series of Inaugural Articles by members of the National Academy of Sciences elected on April 27, 1999.
Contributed by John M. Coffin

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    Constructing primate phylogenies from ancient retrovirus sequences
    Proceedings of the National Academy of Sciences
    • Vol. 96
    • No. 18
    • pp. 9967-10548

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