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Sequence variants in the bovine gonadotrophin releasing hormone receptor gene and their associations with fertility
Author(s) -
Derecka K.,
Ahmad S.,
Hodgman T. C.,
Hastings N.,
Royal M. D.,
Woolliams J. A.,
Flint A. P. F.
Publication year - 2010
Publication title -
animal genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 81
eISSN - 1365-2052
pISSN - 0268-9146
DOI - 10.1111/j.1365-2052.2009.01996.x
Subject(s) - biology , gene , sequence (biology) , fertility , genetics , hormone , hormone receptor , endocrinology , medicine , population , demography , cancer , sociology , breast cancer
Summary Seven sequence variants (SVs) have been identified in exon 1 and in the promoter region upstream of the bovine gonadotrophin releasing hormone (GnRH) receptor gene, at nucleotides g.−331A>G, g.−108T>C, g.+206G>A, g.+260C>T, g.+341C>T, g.+383C>T and g.+410C>T relative to the translation start site. The SVs at nucleotides g.−108, g.260, g.341 and g.410 and those at g.206 and g.383 formed two groups with complete linkage disequilibrium within groups, but incomplete linkage disequilibrium between groups, and none of the SVs altered receptor amino acid sequence. The g.−108T>C allelic variants were associated with an approximately 0.4 day reduction in predicted transmitting ability for days to first service. None of the allelic variants affected the pattern of circulating LH following administration of GnRH. The g.260C>T alteration introduced a new transcription factor binding site in a region of DNA with relatively low nucleosome formation potential. The data suggest that selection for animals carrying the g.‐108T>C group of alterations will improve fertility in the dairy cow.