回顾马舟骨放射学改变的遗传方面。

U Diesterbeck, O Distl
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引用次数: 0

摘要

长期以来,人们都知道舟状病或足癣会导致马的前肢跛行。有人提出足癣的发展与人类骨关节炎(OA)复合体有相似之处。舟骨的改变只能在早期的x线片上发现。关于舟骨疾病患病率的报告表明,不同温血人群中舟骨的影像学改变发生率在14.9%至87.6%之间。遗传因素在放射学征象的发展中起重要作用。使用动物阈值模型估计的遗传率范围从h2 = 0.09到h2 = 0.40。据估计,舟骨放射学变化与其他骨科健康特征之间的加性遗传相关性表明,它们在遗传上大多是相互独立的。舟骨的放射学变化与参赛次数和名次之间存在负的遗传相关性。研究还表明,如果选择同时基于这些性状的育种值,则可以减少舟骨的放射学变化并提高骑马性能的育种值。建立了一个优化的标记集,用于检测汉诺威温血马舟骨病理变化的数量性状位点(QTL)。利用214个高多态性微卫星对马基因组进行扫描,发现显著QTL位于马染色体(ECA) 2、3、4、10和26上。ECA2和ECA10上存在全基因组显著QTL。揭示与舟骨病相关的QTL将促进马健康肢体结构的选择进程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Review of genetic aspects of radiological alterations in the navicular bone of the horse.

Navicular disease or podotrochlosis has long been known to cause forelimb lameness in horses. It had been proposed that the development of podotrochlosis has similarities to the human osteoarthritis (OA) complex. Alterations of the navicular bone can be made visible early in life only on the basis of radiographs. Reports on the prevalences of navicular disease indicate that radiological alterations in the navicular bone are present in different warmblood populations at frequencies of between 14.9% and 87.6%. Genetic factors play an important role in the development of the radiological signs. Estimates of heritability using animal threshold models range from h2 = 0.09 to h2 = 0.40. Estimated additive genetic correlations between radiological changes in the navicular bone and other orthopaedic health traits indicated that they mostly develop genetically independently of each other. There was a negative genetic correlation between radiological changes in the navicular bone and the number of tournament entries and placings. It has also been shown that reduction of radiological changes of navicular bones and improvement of breeding values for performance of riding horses can be achieved if selection is based on breeding values for these traits simultaneously. An optimised markerset was developed to detect quantitative trait loci (QTL) for pathologic changes in the navicular bone of Hanoverian warmblood horses. The horse genome was scanned using 214 highly polymorphic microsatellites chromosome-wide significant QTL were located on equine chromosomes (ECA) 2, 3, 4, 10, and 26. Genome-wide significant QTL were on ECA2 and on ECA10. Unravelling QTL associated with navicular disease will enhance selection progress for a healthy limb constitution in horses.

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