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一项全基因组关联研究鉴定出德国温血马复发性眼色素层炎的风险位点。

A genome-wide association study identifies risk loci to equine recurrent uveitis in German warmblood horses.

机构信息

Institute for Animal Breeding and Genetics, University of Veterinary Medicine Hannover, Hannover, Germany ; Clinic for Horses, University of Veterinary Medicine Hannover, Hannover, Germany.

出版信息

PLoS One. 2013 Aug 14;8(8):e71619. doi: 10.1371/journal.pone.0071619. eCollection 2013.

Abstract

Equine recurrent uveitis (ERU) is a common eye disease affecting up to 3-15% of the horse population. A genome-wide association study (GWAS) using the Illumina equine SNP50 bead chip was performed to identify loci conferring risk to ERU. The sample included a total of 144 German warmblood horses. A GWAS showed a significant single nucleotide polymorphism (SNP) on horse chromosome (ECA) 20 at 49.3 Mb, with IL-17A and IL-17F being the closest genes. This locus explained a fraction of 23% of the phenotypic variance for ERU. A GWAS taking into account the severity of ERU, revealed a SNP on ECA18 nearby to the crystalline gene cluster CRYGA-CRYGF. For both genomic regions on ECA18 and 20, significantly associated haplotypes containing the genome-wide significant SNPs could be demonstrated. In conclusion, our results are indicative for a genetic component regulating the possible critical role of IL-17A and IL-17F in the pathogenesis of ERU. The associated SNP on ECA18 may be indicative for cataract formation in the course of ERU.

摘要

马属复发性葡萄膜炎(ERU)是一种常见的眼病,影响高达 3-15%的马群。使用 Illumina 马 SNP50 珠芯片进行了全基因组关联研究(GWAS),以确定赋予 ERU 风险的基因座。该样本包括总共 144 匹德国温血马。GWAS 显示马染色体(ECA)20 上的一个显著单核苷酸多态性(SNP)在 49.3Mb 处,IL-17A 和 IL-17F 是最接近的基因。该基因座解释了 ERU 表型变异的 23%。考虑到 ERU 严重程度的 GWAS 揭示了 ECA18 附近的一个 SNP 到晶体基因簇 CRYGA-CRYGF。对于 ECA18 和 20 上的这两个基因组区域,可以证明包含全基因组显著 SNP 的显著相关单倍型。总之,我们的结果表明,遗传成分可能调节 IL-17A 和 IL-17F 在 ERU 发病机制中的可能关键作用。ECA18 上的相关 SNP 可能提示 ERU 过程中白内障的形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69b8/3743750/68ce7d6e2c91/pone.0071619.g001.jpg

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