Journal
EVOLUTION
Volume 63, Issue 9, Pages 2340-2349Publisher
WILEY
DOI: 10.1111/j.1558-5646.2009.00724.x
Keywords
Chromosomal evolution; evolutionary genomics; genetic variation; molecular evolution; population genetics; sex
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Funding
- National Environmental Research Council (NERC)
- Institute of Cancer Research (IRC)
- AKC Canine Health Foundation
- Morris Animal Foundation
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Canine transmissible venereal tumor (CTVT) is an infectious disease of dogs. Remarkably, the infectious agent is the cancerous cell itself. To investigate its origin and spread, we collected 37 tumor samples from four continents and determined their evolutionary relationships using microsatellite length differences and microarray-based comparative genomic hybridization (aCGH). The different tumors show very little microsatellite variation, and the pattern of variation that does exist is consistent with a purely asexual mode of transmission. Approximately one quarter of the loci scored by aCGH show copy number variation relative to normal dogs, again with little variation among different tumor samples. Sequence analysis of the RPPH1 gene indicates an origin from either dogs or wolves, and microsatellite analysis indicates that the tumor is more than 6000 years old, and perhaps originated when dogs were first domesticated. By contrast, the common ancestor of extant tumors lived within the last few hundred years, long after the first tumor. The genetic and genomic patterns we observe are typical of those expected of asexual pathogens, and the extended time since first origin may explain the many remarkable adaptations that have enabled this mammalian cell lineage to live as a unicellular pathogen.
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