| Literature DB >> 24458646 |
Elizabeth P Murchison1,2, David C Wedge1, Ludmil B Alexandrov1, Beiyuan Fu1, Inigo Martincorena1, Zemin Ning1, Jose M C Tubio1, Emma I Werner1, Jan Allen3, Andrigo Barboza De Nardi4, Edward M Donelan3, Gabriele Marino5, Ariberto Fassati6, Peter J Campbell1, Fengtang Yang1, Austin Burt7, Robin A Weiss6, Michael R Stratton1.
Abstract
Canine transmissible venereal tumor (CTVT) is the oldest known somatic cell lineage. It is a transmissible cancer that propagates naturally in dogs. We sequenced the genomes of two CTVT tumors and found that CTVT has acquired 1.9 million somatic substitution mutations and bears evidence of exposure to ultraviolet light. CTVT is remarkably stable and lacks subclonal heterogeneity despite thousands of rearrangements, copy-number changes, and retrotransposon insertions. More than 10,000 genes carry nonsynonymous variants, and 646 genes have been lost. CTVT first arose in a dog with low genomic heterozygosity that may have lived about 11,000 years ago. The cancer spawned by this individual dispersed across continents about 500 years ago. Our results provide a genetic identikit of an ancient dog and demonstrate the robustness of mammalian somatic cells to survive for millennia despite a massive mutation burden.Entities:
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Year: 2014 PMID: 24458646 PMCID: PMC3918581 DOI: 10.1126/science.1247167
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728