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Evolution and lineage dynamics of a transmissible cancer in Tasmanian devils.

Published version
Peer-reviewed

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Authors

Kwon, Young Mi 
Gori, Kevin 
Park, Naomi 
Potts, Nicole 

Abstract

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.

Description

Keywords

Animal Diseases, Animals, DNA Copy Number Variations, Evolution, Molecular, Facial Neoplasms, Female, Genomic Instability, Male, Marsupialia, Phylogeny, Tasmania, Telomere Shortening, Tumor Cells, Cultured

Journal Title

PLoS Biol

Conference Name

Journal ISSN

1544-9173
1545-7885

Volume Title

18

Publisher

Public Library of Science (PLoS)
Sponsorship
Wellcome Trust (102942/Z/13/Z)
National Science Foundation (NSF) (via Washington State University (WSU)) (G003286)
Leverhulme Trust (PLP-2014-131)
University of Tasmania Foundation
University of Tasmania Foundation (unknown)
University of Tasmania Foundation (Unknown)
This work was supported by grants from Wellcome (102942/Z/13/A), the National Science Foundation (DEB-1316549), the University of Tasmania Foundation (Eric Guiler Tasmanian Devil Research Grants), the Australian Research Council (DE 170101116) and a Philip Leverhulme Prize from the Leverhulme Trust. YMK was supported by a Herchel Smith Postgraduate Fellowship.