A novel active endogenous retrovirus family contributes to genome variability in rat inbred strains
- Yongming Wang1,4,
- František Liška1,2,4,
- Claudia Gosele1,
- Lucie Šedová2,
- Vladimír Křen2,
- Drahomíra Křenová2,
- Zoltán Ivics1,3,
- Norbert Hubner1,5 and
- Zsuzsanna Izsvák1,3,5
- 1 Max-Delbrück-Center for Molecular Medicine (MDC), 13125 Berlin, Germany;
- 2 Institute of Biology and Medical Genetics, 1st Faculty of Medicine, Charles University in Prague, 128 00 Prague 2, Czech Republic;
- 3 University of Debrecen, 4032 Debrecen, Hungary
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↵4 These authors contributed equally to this work.
Abstract
Endogenous retroviruses (ERVs) contribute to a range of germline, as well as somatic mutations in mammals. However, autonomous retrotransposition of potentially active elements has not been demonstrated in the rat genome. We cloned an insertion that disrupted the normal splicing of the Cntrob gene that was subsequently identified as a nonautonomous, novel endogenous retrovirus of the RnERV-K8e family. The RnERV-K8e family is closely related to the recently reported MmERV-K10c elements, but differs from the autonomous mouse MusD or IAP families. In addition, we identified a novel, unexpectedly close relative of RnERV-K8e in the mouse, suggesting ERV-K cross-species transmission between mice and rats. We cloned a potentially autonomous RnERV-K8e element identified by in silico analysis and, using an in vitro retrotransposition assay, demonstrated that it is capable of retrotransposition. This particular element (named Rat-ρ, pronounced “retro”) encodes a retroviral envelope gene (env); however, env is not required for de novo retrotransposition events. Significant levels of RnERV-K8e-associated genetic polymorphisms were detected among inbred rat strains, suggesting ongoing retrotransposition in the rat genome. This study identifies an ERV-K-type family in rats that shows obvious signs of recent activity. Ongoing retrotranspositional activity may significantly add to genomic variability among inbred rat strains.
Footnotes
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↵5 Corresponding authors.
E-mail nhuebner{at}mdc-berlin.de; fax 49-30-9406-3147.
E-mail zizsvak{at}mdc-berlin.de; fax 49-30-9406-3382.
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[Supplemental material is available online at http://www.genome.org. The sequence data from this study have been submitted to GenBank (http://www.ncbi.nlm.nih.gov/Genbank/) under accession nos. EF532341–EF532350.]
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Article published online before print. Article and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.100073.109.
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- Received August 28, 2009.
- Accepted October 21, 2009.
- Copyright © 2010 by Cold Spring Harbor Laboratory Press











