ORIGINS AND EVOLUTION OF A TRANSMISSIBLE CANCER |
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Authors: | Clare A Rebbeck Rachael Thomas Matthew Breen Armand M Leroi Austin Burt |
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Institution: | Department of Biology, Imperial College London, Silwood Park, Ascot, Berks., SL5 7PY, United Kingdom;Department of Molecular Biomedical Sciences, College of Veterinary Medicine, North Carolina State University, 4700 Hillsborough St., Raleigh North Carolina 27606;Center for Comparative Medicine and Translational Research, North Carolina State University, 4700 Hillsborough St., Raleigh North Carolina 27606;E-mail: |
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Abstract: | 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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Keywords: | Chromosomal evolution evolutionary genomics genetic variation molecular evolution population genetics sex |
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