| Literature DB >> 21709235 |
Webb Miller1, Vanessa M Hayes, Aakrosh Ratan, Desiree C Petersen, Nicola E Wittekindt, Jason Miller, Brian Walenz, James Knight, Ji Qi, Fangqing Zhao, Qingyu Wang, Oscar C Bedoya-Reina, Neerja Katiyar, Lynn P Tomsho, Lindsay McClellan Kasson, Rae-Anne Hardie, Paula Woodbridge, Elizabeth A Tindall, Mads Frost Bertelsen, Dale Dixon, Stephen Pyecroft, Kristofer M Helgen, Arthur M Lesk, Thomas H Pringle, Nick Patterson, Yu Zhang, Alexandre Kreiss, Gregory M Woods, Menna E Jones, Stephan C Schuster.
Abstract
The Tasmanian devil (Sarcophilus harrisii) is threatened with extinction because of a contagious cancer known as Devil Facial Tumor Disease. The inability to mount an immune response and to reject these tumors might be caused by a lack of genetic diversity within a dwindling population. Here we report a whole-genome analysis of two animals originating from extreme northwest and southeast Tasmania, the maximal geographic spread, together with the genome from a tumor taken from one of them. A 3.3-Gb de novo assembly of the sequence data from two complementary next-generation sequencing platforms was used to identify 1 million polymorphic genomic positions, roughly one-quarter of the number observed between two genetically distant human genomes. Analysis of 14 complete mitochondrial genomes from current and museum specimens, as well as mitochondrial and nuclear SNP markers in 175 animals, suggests that the observed low genetic diversity in today's population preceded the Devil Facial Tumor Disease disease outbreak by at least 100 y. Using a genetically characterized breeding stock based on the genome sequence will enable preservation of the extant genetic diversity in future Tasmanian devil populations.Entities:
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Year: 2011 PMID: 21709235 PMCID: PMC3145710 DOI: 10.1073/pnas.1102838108
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205