Many human endogenous retrovirus K (HERV-K) proviruses are unique to humans

Madalina Barbulescu, Geoffrey Turner, Michael I. Seaman, Amos S Deinard, Kenneth K. Kidd, Jack Lenz

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188 Scopus citations


Background: Endogenous retroviruses contribute to the evolution of the host genome and can be associated with disease. Human endogenous retrovirus K (HERV-K) is related to the mouse mammary tumor virus and is present in the genomes of humans, apes and cercopithecoids (Old World monkeys). It is unknown how long ago in primate evolution the full-length HERV-K proviruses that are in the human genome today were formed. Results: Ten full-length HERV-K proviruses were cloned from the human genome. Using provirus-specific probes, eight of the ten were found to be present in a genetically diverse set of humans but not in other extant hominoids. Intact preintegration sites for each of these eight proviruses were present in the apes. A ninth provirus was detected in the human, chimpanzee, bonobo and gorilla genomes, but not in the orang-utan genome. The tenth was found only in humans, chimpanzees and bonobos. Complete sequencing of six of the human-specific proviruses showed that full-length open reading frames for the retroviral protein precursors Gag-Pro-Pol or Env were each present in multiple proviruses. Conclusions: At least eight full-length HERV-K genomes that are in the human germline today integrated after humans diverged from chimpanzees. All of the viral open reading frames and cis-acting sequences necessary for HERV-K replication must have been intact during the recent time when these proviruses formed. Multiple full-length open reading frames for all HERV-K proteins are present in the human genome today.

Original languageEnglish (US)
Pages (from-to)861-868
Number of pages8
JournalCurrent Biology
Issue number16
StatePublished - Aug 26 1999
Externally publishedYes

Bibliographical note

Funding Information:
We thank A. Trubetskoy, R. Kim, B. Morrow, L. Edelmann, P. Etkind and R. Kucherlapati for advice and assistance, and S. Masseling and M. Su for participation in initial experiments. Ape tissue samples were kindly provided by Stanford University, the Yerkes Regional Primate Center, the Henry Doorly Zoo and the Milwaukee County Zoo. This work was supported by grant CA44822 from the NIH.


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