Human Endogenous Retroviral Elements as Indicators of Ectopic Recombination Events in the Primate Genome
Abstract
HERV elements make up a significant fraction of the human genome and, as interspersed repetitive elements, have the capacity to provide substrates for ectopic recombination and gene conversion events. To understand the extent to which these events occur and gain further insight into the complex evolutionary history of these elements in our genome, we undertook a phylogenetic study of the long terminal repeat sequences of 15 HERV-K(HML-2) elements in various primate species. This family of human endogenous retroviruses first entered the primate genome between 35 and 45 million years ago. Throughout primate evolution, these elements have undergone bursts of amplification. From this analysis, which is the largest-scale study of HERV sequence dynamics during primate evolution to date, we were able to detect intraelement gene conversion and recombination at five HERV-K loci. We also found evidence for replacement of an ancient element by another HERV-K provirus, apparently reflecting an occurrence of retroviral integration by homologous recombination. The high frequency of these events casts doubt on the accuracy of integration time estimates based only on divergence between retroelement LTRs.
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The chimpanzee-specific CERV 3 (HERVS71) insertion on the Y chromosome most likely inserted after the chimpanzee-human divergence (about 6 MYA), and its exceptionally high LTR-LTR sequence divergence is due to an inter-element recombination or conversion event.
“However, the clear absence of this insert, both in the sequenced human genome (pre-integration site in tact) and in the genomes of several randomly sampled ethnically and geographically diverse humans (data not shown), indicates that this element most likely inserted after the chimpanzee-human divergence (about 6 MYA) and that the exceptionally high level of LTR-LTR sequence divergence is due to a”
From Identification, characterization and comparative genomics of chimpanzee endogenous retroviruses (2006) · cites this paper as [23]
HERV-K (HML2) proviruses can naturally recombine.
“HERV-K (HML2) proviruses can also naturally recombine 12,86”
From Are human endogenous retroviruses pathogenic? An approach to testing the hypothesis (2013) · cites this paper as [86]
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References 30 · Cited by 104
- Authors
- Hughes, J. F., & Coffin, J. M.
- Affiliations
- Tufts University (US)
- Corresponding author
- Coffin, John M
- Venue
- Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 2005-11-01
- Volume
- 171
- Issue
- 3
- Pages
- 1183-1194
- ISSN
- 0016-6731 (ISSN-L)
- 1943-2631
- OpenAlex
- W2125040797
- Cited by
- 104
- References
- 30
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 8 · 2023: 3 · 2022: 13 · 2021: 4 · 2019: 5 · 2018: 4 · 2017: 1 · 2016: 4 · 2015: 10 · 2014: 3 · 2013: 7 · 2012: 3
- FWCI
- 8.02
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- Genetics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (R01CA89441, R01CA089441, CA 5441)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Chromosomal and Genetic Variations
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomic variations and chromosomal abnormalities
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genome Rearrangement Algorithms
- Keywords
- human endogenous retroviruses, HERV-K(HML-2), long terminal repeat, ectopic recombination, gene conversion, homologous recombination, retroviral integration, primate genome evolution
- MeSH terms
- Animals, Gene Conversion, Genetic Markers, Humans, Molecular Sequence Data, Phylogeny, Primates, Recombination, Genetic, Genome, Evolution, Molecular, Endogenous Retroviruses, Terminal Repeat Sequences
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