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1000 Titel
  • Degradation and remobilization of endogenous retroviruses by recombination during the earliest stages of a germ-line invasion
1000 Autor/in
  1. Löber, Ulrike |
  2. Hobbs, Matthew |
  3. Dayaram, Anisha |
  4. Tsangaras, Kyriakos |
  5. Jones, Kiersten |
  6. Alquezar-Planas, David E. |
  7. Ishida, Yasuko |
  8. Meers, Joanne |
  9. Mayer, Jens |
  10. Quedenau, Claudia |
  11. Chen, Wei |
  12. Johnson, Rebecca N. |
  13. Timms, Peter |
  14. Young, Paul R. |
  15. Roca, Alfred L. |
  16. Greenwood, Alex |
1000 Erscheinungsjahr 2018
1000 LeibnizOpen
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2018-08-06
1000 Erschienen in
1000 Quellenangabe
  • 115(34):8609-8614
1000 FRL-Sammlung
1000 Copyrightjahr
  • 2018
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1073/pnas.1807598115 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6112702/ |
1000 Ergänzendes Material
  • https://www.pnas.org/content/115/34/8609/tab-figures-data |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • SIGNIFICANCE: Endogenous retroviruses (ERVs) are proviral sequences that result from host germ-line invasion by exogenous retroviruses. The majority of ERVs are degraded. Using the koala retrovirus (KoRV) as a model system, we demonstrate that recombination with an ancient koala retroelement disables KoRV, and that recombination occurs frequently and early in the invasion process. Recombinant KoRVs (recKoRVs) are then able to proliferate in the koala germ line. This may in part explain the generally degraded nature of ERVs in vertebrate genomes and suggests that degradation via recombination is one of the earliest processes shaping retroviral genomic invasions. ABSTRACT: Endogenous retroviruses (ERVs) are proviral sequences that result from colonization of the host germ line by exogenous retroviruses. The majority of ERVs represent defective retroviral copies. However, for most ERVs, endogenization occurred millions of years ago, obscuring the stages by which ERVs become defective and the changes in both virus and host important to the process. The koala retrovirus, KoRV, only recently began invading the germ line of the koala (Phascolarctos cinereus), permitting analysis of retroviral endogenization on a prospective basis. Here, we report that recombination with host genomic elements disrupts retroviruses during the earliest stages of germ-line invasion. One type of recombinant, designated recKoRV1, was formed by recombination of KoRV with an older degraded retroelement. Many genomic copies of recKoRV1 were detected across koalas. The prevalence of recKoRV1 was higher in northern than in southern Australian koalas, as is the case for KoRV, with differences in recKoRV1 prevalence, but not KoRV prevalence, between inland and coastal New South Wales. At least 15 additional different recombination events between KoRV and the older endogenous retroelement generated distinct recKoRVs with different geographic distributions. All of the identified recombinant viruses appear to have arisen independently and have highly disrupted ORFs, which suggests that recombination with existing degraded endogenous retroelements may be a means by which replication-competent ERVs that enter the germ line are degraded.
1000 Sacherschließung
lokal recombination
lokal koala retrovirus
lokal endogenous retrovirus
lokal retrovirus
lokal genome evolution
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/TMO2YmVyLCBVbHJpa2U=|https://frl.publisso.de/adhoc/uri/SG9iYnMsIE1hdHRoZXc=|https://frl.publisso.de/adhoc/uri/RGF5YXJhbSwgQW5pc2hh|https://frl.publisso.de/adhoc/uri/VHNhbmdhcmFzLCBLeXJpYWtvcw==|https://frl.publisso.de/adhoc/uri/Sm9uZXMsIEtpZXJzdGVu|https://frl.publisso.de/adhoc/uri/QWxxdWV6YXItUGxhbmFzLCBEYXZpZCBFLg==|https://frl.publisso.de/adhoc/uri/SXNoaWRhLCBZYXN1a28=|https://frl.publisso.de/adhoc/uri/TWVlcnMsIEpvYW5uZQ==|https://frl.publisso.de/adhoc/uri/TWF5ZXIsIEplbnM=|https://frl.publisso.de/adhoc/uri/UXVlZGVuYXUsIENsYXVkaWE=|https://frl.publisso.de/adhoc/uri/Q2hlbiwgV2Vp|https://frl.publisso.de/adhoc/uri/Sm9obnNvbiwgUmViZWNjYSBOLg==|https://frl.publisso.de/adhoc/uri/VGltbXMsIFBldGVy|https://frl.publisso.de/adhoc/uri/WW91bmcsIFBhdWwgUi4=|https://frl.publisso.de/adhoc/uri/Um9jYSwgQWxmcmVkIEwu|https://orcid.org/0000-0002-8249-1565
1000 (Academic) Editor
1000 Label
1000 Förderer
  1. Australian Museum Foundation |
  2. BioPlatforms Australia |
  3. NSW Environmental Trust |
  4. National Institute of General Medical Sciences |
  5. Morris Animal Foundation |
  6. Deutscher Akademischer Austauschdienst |
1000 Fördernummer
  1. -
  2. -
  3. R01GM092706
  4. D14ZO-94
  5. 2014 57129705
  6. -
1000 Förderprogramm
  1. -
  2. -
  3. -
  4. -
  5. -
  6. -
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Australian Museum Foundation |
    1000 Förderprogramm -
    1000 Fördernummer -
  2. 1000 joinedFunding-child
    1000 Förderer BioPlatforms Australia |
    1000 Förderprogramm -
    1000 Fördernummer -
  3. 1000 joinedFunding-child
    1000 Förderer NSW Environmental Trust |
    1000 Förderprogramm -
    1000 Fördernummer R01GM092706
  4. 1000 joinedFunding-child
    1000 Förderer National Institute of General Medical Sciences |
    1000 Förderprogramm -
    1000 Fördernummer D14ZO-94
  5. 1000 joinedFunding-child
    1000 Förderer Morris Animal Foundation |
    1000 Förderprogramm -
    1000 Fördernummer 2014 57129705
  6. 1000 joinedFunding-child
    1000 Förderer Deutscher Akademischer Austauschdienst |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 @id frl:6415201.rdf
1000 Erstellt am 2019-07-16T11:13:41.796+0200
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1000 Zuletzt bearbeitet 2021-04-14T14:43:45.050+0200
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1000 Vgl. frl:6415201
1000 Oai Id
  1. oai:frl.publisso.de:frl:6415201 |
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