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复发性气道阻塞在欧洲温血马中的 QTL 复制和精细定位。

Replication and fine-mapping of a QTL for recurrent airway obstruction in European Warmblood horses.

机构信息

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bremgartenstrasse 109a, Berne, 3001, Switzerland.

出版信息

Anim Genet. 2012 Oct;43(5):627-31. doi: 10.1111/j.1365-2052.2011.02315.x. Epub 2012 Jan 26.

Abstract

Recurrent airway obstruction (RAO), or 'heaves', is a common performance-limiting allergic respiratory disease of mature horses. It is related to sensitization and exposure to mouldy hay and has a familial basis with a complex mode of inheritance. In a previous study, we detected a QTL for RAO on ECA 13 in a half-sib family of European Warmblood horses. In this study, we genotyped additional markers in the family and narrowed the QTL down to about 1.5 Mb (23.7-25.2 Mb). We detected the strongest association with SNP BIEC2-224511 (24,309,405 bp). We also obtained SNP genotypes in an independent cohort of 646 unrelated Warmblood horses. There was no genome-wide significant association with RAO in these unrelated horses. However, we performed a genotypic association study of the SNPs on ECA 13 in these unrelated horses, and the SNP BIEC2-224511 also showed the strongest association with RAO in the unrelated horses (p(raw) = 0.00037). The T allele at this SNP was associated with RAO both in the family and the unrelated horses. Thus, the association study in the unrelated animals provides independent support for the previously detected QTL. The association study allows further narrowing of the QTL interval to about 0.5 Mb (24.0-24.5 Mb). We sequenced the coding regions of the genes in the critical region but did not find any associated coding variants. Therefore, the causative variant underlying this QTL is likely to be a regulatory mutation.

摘要

复发性气道阻塞(RAO),又称“气喘”,是一种常见的限制成年马运动性能的过敏呼吸道疾病。它与对霉变干草的致敏和暴露有关,具有家族基础和复杂的遗传模式。在之前的一项研究中,我们在一个欧洲温血马半同胞家系中检测到 ECA13 上与 RAO 相关的 QTL。在这项研究中,我们在家系中对其他标记物进行了基因分型,并将 QTL 缩小到约 1.5Mb(23.7-25.2Mb)。我们检测到与 SNP BIEC2-224511(24,309,405bp)最强的关联。我们还在 646 匹无关的温血马的独立队列中获得了 SNP 基因型。在这些无关的马中,与 RAO 没有全基因组显著关联。然而,我们对这些无关马的 ECA13 上的 SNP 进行了基因型关联研究,SNP BIEC2-224511 也与 RAO 表现出最强的关联(p(raw)=0.00037)。该 SNP 的 T 等位基因与家系和无关马中的 RAO 均有关联。因此,无关动物的关联研究为之前检测到的 QTL 提供了独立的支持。关联研究进一步将 QTL 区间缩小到约 0.5Mb(24.0-24.5Mb)。我们对关键区域内的基因编码区进行了测序,但没有发现任何相关的编码变异。因此,该 QTL 下的致病变异很可能是调控突变。

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