An expressed fgf4 retrogene is associated with breed-defining chondrodysplasia in domestic dogs.

نویسندگان

  • Heidi G Parker
  • Bridgett M VonHoldt
  • Pascale Quignon
  • Elliott H Margulies
  • Stephanie Shao
  • Dana S Mosher
  • Tyrone C Spady
  • Abdel Elkahloun
  • Michele Cargill
  • Paul G Jones
  • Cheryl L Maslen
  • Gregory M Acland
  • Nathan B Sutter
  • Keiichi Kuroki
  • Carlos D Bustamante
  • Robert K Wayne
  • Elaine A Ostrander
چکیده

Retrotransposition of processed mRNAs is a common source of novel sequence acquired during the evolution of genomes. Although the vast majority of retroposed gene copies, or retrogenes, rapidly accumulate debilitating mutations that disrupt the reading frame, a small percentage become new genes that encode functional proteins. By using a multibreed association analysis in the domestic dog, we demonstrate that expression of a recently acquired retrogene encoding fibroblast growth factor 4 (fgf4) is strongly associated with chondrodysplasia, a short-legged phenotype that defines at least 19 dog breeds including dachshund, corgi, and basset hound. These results illustrate the important role of a single evolutionary event in constraining and directing phenotypic diversity in the domestic dog.

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عنوان ژورنال:
  • Science

دوره 325 5943  شماره 

صفحات  -

تاریخ انتشار 2009