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对汉诺威温血马舟状骨病放射学特征的10号马染色体数量性状基因座的优化

Refinement of quantitative trait loci on equine chromosome 10 for radiological signs of navicular disease in Hanoverian warmblood horses.

作者信息

Lopes M S, Diesterbeck U, Machado A Da Câmara, Distl O

机构信息

Institute for Animal Breeding and Genetics, University of Veterinary Medicine Hannover, Bünteweg 17p, 30559 Hannover, Germany.

出版信息

Anim Genet. 2010 Dec;41 Suppl 2:36-40. doi: 10.1111/j.1365-2052.2010.02096.x.

Abstract

Navicular disease is characterized by a progressive degenerative alteration of the equine podotrochlea. In this study, we refined a previously identified quantitative trait locus (QTL) on horse chromosome 10 for the abnormal development of canales sesamoidales (DCS) of the navicular bone in Hanoverian warmblood horses. Genotyping was done in 192 Hanoverian warmblood horses from 17 paternal half-sib groups. The whole marker set comprised 45 markers including seven newly developed microsatellites and 13 single nucleotide polymorphisms (SNPs) within positional candidate genes. Chromosome-wide significant QTL were confirmed and refined for DCS on horse chromosome (ECA) 10 at 0.16-2.70 Mb and at 14.45-36.37 Mb. Nine microsatellites and three SNP markers reached the highest multipoint Zmeans and LOD scores at 19.34-20.38 Mb and at 23.17-30.73 Mb with genome-wide error probabilities of P<0.05. In addition, a significant association of a SNP within VSTM1 and a significant haplotype-trait association within IRF3 could be shown. These results support a possible role of the candidate genes VSTM1 and IRF3 within the QTL on ECA10 for DCS. This study is a further step towards the identification of the genes responsible for navicular disease in Hanoverian warmblood horses.

摘要

舟状骨病的特征是马舟状骨的渐进性退行性改变。在本研究中,我们对先前在10号马染色体上鉴定出的一个数量性状基因座(QTL)进行了优化,该基因座与汉诺威温血马舟状骨籽骨管(DCS)的异常发育有关。对来自17个父系半同胞组的192匹汉诺威温血马进行了基因分型。整个标记集包括45个标记,其中包括7个新开发的微卫星和定位候选基因内的13个单核苷酸多态性(SNP)。在马染色体(ECA)10上0.16 - 2.70 Mb和14.45 - 36.37 Mb处,对DCS的全染色体显著QTL进行了确认和优化。9个微卫星和3个SNP标记在19.34 - 20.38 Mb和23.17 - 30.73 Mb处达到了最高的多点Z均值和LOD分数,全基因组错误概率为P<0.05。此外,还发现VSTM1内的一个SNP与IRF3内的一个显著单倍型-性状关联。这些结果支持了候选基因VSTM1和IRF3在ECA10上DCS的QTL中可能发挥的作用。这项研究朝着鉴定汉诺威温血马舟状骨病相关基因又迈进了一步。

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