Dierks C, Komm K, Lampe V, Distl O
Institute for Animal Breeding and Genetics, University of Veterinary Medicine Hannover, 30559 Hannover, Germany.
Anim Genet. 2010 Dec;41 Suppl 2:87-90. doi: 10.1111/j.1365-2052.2010.02113.x.
In this study, we refine a quantitative trait locus for equine osteochondrosis (OC) on horse chromosome (ECA) 2 to a genome-wide significant interval at 20.08-30.94 Mb. The marker set contained 27 newly developed microsatellites equidistantly distributed over ECA2 and 44 nucleotide polymorphisms, located in 16 positional candidate genes for OC. Genotyping was performed in 211 Hanoverian horses from 14 paternal half-sib groups. A NCDN-associated SNP and haplotype were significantly associated with OC in fetlock and/or hock joints. This study is a further step towards the identification of genes responsible for OC in horses.
在本研究中,我们将马2号染色体(ECA)上的马骨软骨病(OC)数量性状基因座精细定位到20.08 - 30.94 Mb的全基因组显著区间。该标记集包含27个新开发的微卫星,它们在ECA2上均匀分布,还有44个核苷酸多态性,位于16个骨软骨病的位置候选基因中。对来自14个父系半同胞组的211匹汉诺威马进行了基因分型。一个与NCDN相关的单核苷酸多态性(SNP)和单倍型与跗关节和/或飞节的骨软骨病显著相关。这项研究朝着鉴定马骨软骨病相关基因又迈进了一步。