| Literature DB >> 18344998 |
Carole Charlier1, Wouter Coppieters, Frédéric Rollin, Daniel Desmecht, Jorgen S Agerholm, Nadine Cambisano, Eloisa Carta, Sabrina Dardano, Marc Dive, Corinne Fasquelle, Jean-Claude Frennet, Roger Hanset, Xavier Hubin, Claus Jorgensen, Latifa Karim, Matthew Kent, Kirsten Harvey, Brian R Pearce, Patricia Simon, Nico Tama, Haisheng Nie, Sébastien Vandeputte, Sigbjorn Lien, Maria Longeri, Merete Fredholm, Robert J Harvey, Michel Georges.
Abstract
The widespread use of elite sires by means of artificial insemination in livestock breeding leads to the frequent emergence of recessive genetic defects, which cause significant economic and animal welfare concerns. Here we show that the availability of genome-wide, high-density SNP panels, combined with the typical structure of livestock populations, markedly accelerates the positional identification of genes and mutations that cause inherited defects. We report the fine-scale mapping of five recessive disorders in cattle and the molecular basis for three of these: congenital muscular dystony (CMD) types 1 and 2 in Belgian Blue cattle and ichthyosis fetalis in Italian Chianina cattle. Identification of these causative mutations has an immediate translation into breeding practice, allowing marker assisted selection against the defects through avoidance of at-risk matings.Entities:
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Year: 2008 PMID: 18344998 DOI: 10.1038/ng.96
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330