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Evolution and lineage dynamics of a transmissible cancer in Tasmanian devils

Devil facial tumour 1 (DFT1) is a transmissible cancer clone endangering the Tasmanian devil. The expansion of DFT1 across Tasmania has been documented, but little is known of its evolutionary history. We analysed genomes of 648 DFT1 tumours collected throughout the disease range between 2003 and 20...

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Autores principales: Kwon, Young Mi, Gori, Kevin, Park, Naomi, Potts, Nicole, Swift, Kate, Wang, Jinhong, Stammnitz, Maximilian R., Cannell, Naomi, Baez-Ortega, Adrian, Comte, Sebastien, Fox, Samantha, Harmsen, Colette, Huxtable, Stewart, Jones, Menna, Kreiss, Alexandre, Lawrence, Clare, Lazenby, Billie, Peck, Sarah, Pye, Ruth, Woods, Gregory, Zimmermann, Mona, Wedge, David C., Pemberton, David, Stratton, Michael R., Hamede, Rodrigo, Murchison, Elizabeth P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685465/
https://www.ncbi.nlm.nih.gov/pubmed/33232318
http://dx.doi.org/10.1371/journal.pbio.3000926
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author Kwon, Young Mi
Gori, Kevin
Park, Naomi
Potts, Nicole
Swift, Kate
Wang, Jinhong
Stammnitz, Maximilian R.
Cannell, Naomi
Baez-Ortega, Adrian
Comte, Sebastien
Fox, Samantha
Harmsen, Colette
Huxtable, Stewart
Jones, Menna
Kreiss, Alexandre
Lawrence, Clare
Lazenby, Billie
Peck, Sarah
Pye, Ruth
Woods, Gregory
Zimmermann, Mona
Wedge, David C.
Pemberton, David
Stratton, Michael R.
Hamede, Rodrigo
Murchison, Elizabeth P.
author_facet Kwon, Young Mi
Gori, Kevin
Park, Naomi
Potts, Nicole
Swift, Kate
Wang, Jinhong
Stammnitz, Maximilian R.
Cannell, Naomi
Baez-Ortega, Adrian
Comte, Sebastien
Fox, Samantha
Harmsen, Colette
Huxtable, Stewart
Jones, Menna
Kreiss, Alexandre
Lawrence, Clare
Lazenby, Billie
Peck, Sarah
Pye, Ruth
Woods, Gregory
Zimmermann, Mona
Wedge, David C.
Pemberton, David
Stratton, Michael R.
Hamede, Rodrigo
Murchison, Elizabeth P.
author_sort Kwon, Young Mi
collection PubMed
description Devil facial tumour 1 (DFT1) is a transmissible cancer clone endangering the Tasmanian devil. The expansion of DFT1 across Tasmania has been documented, but little is known of its evolutionary history. We analysed genomes of 648 DFT1 tumours collected throughout the disease range between 2003 and 2018. DFT1 diverged early into five clades, three spreading widely and two failing to persist. One clade has replaced others at several sites, and rates of DFT1 coinfection are high. DFT1 gradually accumulates copy number variants (CNVs), and its telomere lengths are short but constant. Recurrent CNVs reveal genes under positive selection, sites of genome instability, and repeated loss of a small derived chromosome. Cultured DFT1 cell lines have increased CNV frequency and undergo highly reproducible convergent evolution. Overall, DFT1 is a remarkably stable lineage whose genome illustrates how cancer cells adapt to diverse environments and persist in a parasitic niche.
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spelling pubmed-76854652020-12-02 Evolution and lineage dynamics of a transmissible cancer in Tasmanian devils Kwon, Young Mi Gori, Kevin Park, Naomi Potts, Nicole Swift, Kate Wang, Jinhong Stammnitz, Maximilian R. Cannell, Naomi Baez-Ortega, Adrian Comte, Sebastien Fox, Samantha Harmsen, Colette Huxtable, Stewart Jones, Menna Kreiss, Alexandre Lawrence, Clare Lazenby, Billie Peck, Sarah Pye, Ruth Woods, Gregory Zimmermann, Mona Wedge, David C. Pemberton, David Stratton, Michael R. Hamede, Rodrigo Murchison, Elizabeth P. PLoS Biol Research Article Devil facial tumour 1 (DFT1) is a transmissible cancer clone endangering the Tasmanian devil. The expansion of DFT1 across Tasmania has been documented, but little is known of its evolutionary history. We analysed genomes of 648 DFT1 tumours collected throughout the disease range between 2003 and 2018. DFT1 diverged early into five clades, three spreading widely and two failing to persist. One clade has replaced others at several sites, and rates of DFT1 coinfection are high. DFT1 gradually accumulates copy number variants (CNVs), and its telomere lengths are short but constant. Recurrent CNVs reveal genes under positive selection, sites of genome instability, and repeated loss of a small derived chromosome. Cultured DFT1 cell lines have increased CNV frequency and undergo highly reproducible convergent evolution. Overall, DFT1 is a remarkably stable lineage whose genome illustrates how cancer cells adapt to diverse environments and persist in a parasitic niche. Public Library of Science 2020-11-24 /pmc/articles/PMC7685465/ /pubmed/33232318 http://dx.doi.org/10.1371/journal.pbio.3000926 Text en © 2020 Kwon et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kwon, Young Mi
Gori, Kevin
Park, Naomi
Potts, Nicole
Swift, Kate
Wang, Jinhong
Stammnitz, Maximilian R.
Cannell, Naomi
Baez-Ortega, Adrian
Comte, Sebastien
Fox, Samantha
Harmsen, Colette
Huxtable, Stewart
Jones, Menna
Kreiss, Alexandre
Lawrence, Clare
Lazenby, Billie
Peck, Sarah
Pye, Ruth
Woods, Gregory
Zimmermann, Mona
Wedge, David C.
Pemberton, David
Stratton, Michael R.
Hamede, Rodrigo
Murchison, Elizabeth P.
Evolution and lineage dynamics of a transmissible cancer in Tasmanian devils
title Evolution and lineage dynamics of a transmissible cancer in Tasmanian devils
title_full Evolution and lineage dynamics of a transmissible cancer in Tasmanian devils
title_fullStr Evolution and lineage dynamics of a transmissible cancer in Tasmanian devils
title_full_unstemmed Evolution and lineage dynamics of a transmissible cancer in Tasmanian devils
title_short Evolution and lineage dynamics of a transmissible cancer in Tasmanian devils
title_sort evolution and lineage dynamics of a transmissible cancer in tasmanian devils
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685465/
https://www.ncbi.nlm.nih.gov/pubmed/33232318
http://dx.doi.org/10.1371/journal.pbio.3000926
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