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The evolution of two transmissible cancers in Tasmanian devils
Tasmanian devils have spawned two transmissible cancer lineages, named devil facial tumour 1 (DFT1) and devil facial tumour 2 (DFT2). We investigated the genetic diversity and evolution of these clones by analysing 78 DFT1 and 41 DFT2 genomes relative to a newly assembled chromosome-level reference....
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614631/ https://www.ncbi.nlm.nih.gov/pubmed/37079675 http://dx.doi.org/10.1126/science.abq6453 |
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author | Stammnitz, Maximilian R. Gori, Kevin Kwon, Young Mi Harry, Ed Martin, Fergal J. Billis, Konstantinos Cheng, Yuanyuan Baez-Ortega, Adrian Chow, William Comte, Sebastien Eggertsson, Hannes Fox, Samantha Hamede, Rodrigo Jones, Menna Lazenby, Billie Peck, Sarah Pye, Ruth Quail, Michael A. Swift, Kate Wang, Jinhong Wood, Jonathan Howe, Kerstin Stratton, Michael R. Ning, Zemin Murchison, Elizabeth P. |
author_facet | Stammnitz, Maximilian R. Gori, Kevin Kwon, Young Mi Harry, Ed Martin, Fergal J. Billis, Konstantinos Cheng, Yuanyuan Baez-Ortega, Adrian Chow, William Comte, Sebastien Eggertsson, Hannes Fox, Samantha Hamede, Rodrigo Jones, Menna Lazenby, Billie Peck, Sarah Pye, Ruth Quail, Michael A. Swift, Kate Wang, Jinhong Wood, Jonathan Howe, Kerstin Stratton, Michael R. Ning, Zemin Murchison, Elizabeth P. |
author_sort | Stammnitz, Maximilian R. |
collection | PubMed |
description | Tasmanian devils have spawned two transmissible cancer lineages, named devil facial tumour 1 (DFT1) and devil facial tumour 2 (DFT2). We investigated the genetic diversity and evolution of these clones by analysing 78 DFT1 and 41 DFT2 genomes relative to a newly assembled chromosome-level reference. Time-resolved phylogenetic trees reveal that DFT1 first emerged in 1986 (1982-1989), and DFT2 in 2011 (2009-2012). Subclone analysis documents transmission of heterogeneous cell populations. DFT2 has faster mutation rates than DFT1 across all variant classes, including substitutions, indels, rearrangements, transposable element insertions and copy number alterations, and we identify a hypermutated DFT1 lineage with defective DNA mismatch repair. Several loci show plausible evidence of positive selection in DFT1 or DFT2, including loss of chromosome Y and inactivation of MGA, but none are common to both cancers. This study reveals the parallel long-term evolution of two transmissible cancers inhabiting a common niche in Tasmanian devils. |
format | Online Article Text |
id | pubmed-7614631 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-76146312023-06-08 The evolution of two transmissible cancers in Tasmanian devils Stammnitz, Maximilian R. Gori, Kevin Kwon, Young Mi Harry, Ed Martin, Fergal J. Billis, Konstantinos Cheng, Yuanyuan Baez-Ortega, Adrian Chow, William Comte, Sebastien Eggertsson, Hannes Fox, Samantha Hamede, Rodrigo Jones, Menna Lazenby, Billie Peck, Sarah Pye, Ruth Quail, Michael A. Swift, Kate Wang, Jinhong Wood, Jonathan Howe, Kerstin Stratton, Michael R. Ning, Zemin Murchison, Elizabeth P. Science Article Tasmanian devils have spawned two transmissible cancer lineages, named devil facial tumour 1 (DFT1) and devil facial tumour 2 (DFT2). We investigated the genetic diversity and evolution of these clones by analysing 78 DFT1 and 41 DFT2 genomes relative to a newly assembled chromosome-level reference. Time-resolved phylogenetic trees reveal that DFT1 first emerged in 1986 (1982-1989), and DFT2 in 2011 (2009-2012). Subclone analysis documents transmission of heterogeneous cell populations. DFT2 has faster mutation rates than DFT1 across all variant classes, including substitutions, indels, rearrangements, transposable element insertions and copy number alterations, and we identify a hypermutated DFT1 lineage with defective DNA mismatch repair. Several loci show plausible evidence of positive selection in DFT1 or DFT2, including loss of chromosome Y and inactivation of MGA, but none are common to both cancers. This study reveals the parallel long-term evolution of two transmissible cancers inhabiting a common niche in Tasmanian devils. 2023-04-21 2023-04-20 /pmc/articles/PMC7614631/ /pubmed/37079675 http://dx.doi.org/10.1126/science.abq6453 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/) International license. |
spellingShingle | Article Stammnitz, Maximilian R. Gori, Kevin Kwon, Young Mi Harry, Ed Martin, Fergal J. Billis, Konstantinos Cheng, Yuanyuan Baez-Ortega, Adrian Chow, William Comte, Sebastien Eggertsson, Hannes Fox, Samantha Hamede, Rodrigo Jones, Menna Lazenby, Billie Peck, Sarah Pye, Ruth Quail, Michael A. Swift, Kate Wang, Jinhong Wood, Jonathan Howe, Kerstin Stratton, Michael R. Ning, Zemin Murchison, Elizabeth P. The evolution of two transmissible cancers in Tasmanian devils |
title | The evolution of two transmissible cancers in Tasmanian devils |
title_full | The evolution of two transmissible cancers in Tasmanian devils |
title_fullStr | The evolution of two transmissible cancers in Tasmanian devils |
title_full_unstemmed | The evolution of two transmissible cancers in Tasmanian devils |
title_short | The evolution of two transmissible cancers in Tasmanian devils |
title_sort | evolution of two transmissible cancers in tasmanian devils |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614631/ https://www.ncbi.nlm.nih.gov/pubmed/37079675 http://dx.doi.org/10.1126/science.abq6453 |
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