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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....

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
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.
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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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