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Retroviral integrations contribute to elevated host cancer rates during germline invasion
Repeated retroviral infections of vertebrate germlines have made endogenous retroviruses ubiquitous features of mammalian genomes. However, millions of years of evolution obscure many of the immediate repercussions of retroviral endogenisation on host health. Here we examine retroviral endogenisatio...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910482/ https://www.ncbi.nlm.nih.gov/pubmed/33637755 http://dx.doi.org/10.1038/s41467-021-21612-7 |
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author | McEwen, Gayle K. Alquezar-Planas, David E. Dayaram, Anisha Gillett, Amber Tarlinton, Rachael Mongan, Nigel Chappell, Keith J. Henning, Joerg Tan, Milton Timms, Peter Young, Paul R. Roca, Alfred L. Greenwood, Alex D. |
author_facet | McEwen, Gayle K. Alquezar-Planas, David E. Dayaram, Anisha Gillett, Amber Tarlinton, Rachael Mongan, Nigel Chappell, Keith J. Henning, Joerg Tan, Milton Timms, Peter Young, Paul R. Roca, Alfred L. Greenwood, Alex D. |
author_sort | McEwen, Gayle K. |
collection | PubMed |
description | Repeated retroviral infections of vertebrate germlines have made endogenous retroviruses ubiquitous features of mammalian genomes. However, millions of years of evolution obscure many of the immediate repercussions of retroviral endogenisation on host health. Here we examine retroviral endogenisation during its earliest stages in the koala (Phascolarctos cinereus), a species undergoing germline invasion by koala retrovirus (KoRV) and affected by high cancer prevalence. We characterise KoRV integration sites (IS) in tumour and healthy tissues from 10 koalas, detecting 1002 unique IS, with hotspots of integration occurring in the vicinity of known cancer genes. We find that tumours accumulate novel IS, with proximate genes over-represented for cancer associations. We detect dysregulation of genes containing IS and identify a highly-expressed transduced oncogene. Our data provide insights into the tremendous mutational load suffered by the host during active retroviral germline invasion, a process repeatedly experienced and overcome during the evolution of vertebrate lineages. |
format | Online Article Text |
id | pubmed-7910482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79104822021-03-04 Retroviral integrations contribute to elevated host cancer rates during germline invasion McEwen, Gayle K. Alquezar-Planas, David E. Dayaram, Anisha Gillett, Amber Tarlinton, Rachael Mongan, Nigel Chappell, Keith J. Henning, Joerg Tan, Milton Timms, Peter Young, Paul R. Roca, Alfred L. Greenwood, Alex D. Nat Commun Article Repeated retroviral infections of vertebrate germlines have made endogenous retroviruses ubiquitous features of mammalian genomes. However, millions of years of evolution obscure many of the immediate repercussions of retroviral endogenisation on host health. Here we examine retroviral endogenisation during its earliest stages in the koala (Phascolarctos cinereus), a species undergoing germline invasion by koala retrovirus (KoRV) and affected by high cancer prevalence. We characterise KoRV integration sites (IS) in tumour and healthy tissues from 10 koalas, detecting 1002 unique IS, with hotspots of integration occurring in the vicinity of known cancer genes. We find that tumours accumulate novel IS, with proximate genes over-represented for cancer associations. We detect dysregulation of genes containing IS and identify a highly-expressed transduced oncogene. Our data provide insights into the tremendous mutational load suffered by the host during active retroviral germline invasion, a process repeatedly experienced and overcome during the evolution of vertebrate lineages. Nature Publishing Group UK 2021-02-26 /pmc/articles/PMC7910482/ /pubmed/33637755 http://dx.doi.org/10.1038/s41467-021-21612-7 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article McEwen, Gayle K. Alquezar-Planas, David E. Dayaram, Anisha Gillett, Amber Tarlinton, Rachael Mongan, Nigel Chappell, Keith J. Henning, Joerg Tan, Milton Timms, Peter Young, Paul R. Roca, Alfred L. Greenwood, Alex D. Retroviral integrations contribute to elevated host cancer rates during germline invasion |
title | Retroviral integrations contribute to elevated host cancer rates during germline invasion |
title_full | Retroviral integrations contribute to elevated host cancer rates during germline invasion |
title_fullStr | Retroviral integrations contribute to elevated host cancer rates during germline invasion |
title_full_unstemmed | Retroviral integrations contribute to elevated host cancer rates during germline invasion |
title_short | Retroviral integrations contribute to elevated host cancer rates during germline invasion |
title_sort | retroviral integrations contribute to elevated host cancer rates during germline invasion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910482/ https://www.ncbi.nlm.nih.gov/pubmed/33637755 http://dx.doi.org/10.1038/s41467-021-21612-7 |
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