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使用序列水平基因型推断对荷斯坦牛双侧外斜视伴眼球突出的全基因组关联分析。

GWAS Hits for Bilateral Convergent Strabismus with Exophthalmos in Holstein Cattle Using Imputed Sequence Level Genotypes.

机构信息

Department of Animal Sciences, Georg-August-University Göttingen, Burckhardtweg 2, 37077 Göttingen, Germany.

Clinic for Ruminants, Vetsuisse Faculty, University of Bern, Bremgartenstr. 109a, 3012 Bern, Switzerland.

出版信息

Genes (Basel). 2021 Jul 4;12(7):1039. doi: 10.3390/genes12071039.

Abstract

Bilateral convergent strabismus with exophthalmos (BCSE) is a malformation of the eyes and is recognized as a mild but progressive disorder that affects cattle in the first two years of life. This most likely inherited disorder is rarely described in cattle resembling autosomal dominantly inherited forms of human progressive external ophthalmoplegia (PEO). In German Braunvieh cattle, two linked genome regions were found that could be responsible for the development and/or progression of BCSE. The goal of this study was to phenotypically characterize BCSE in Holstein cattle from Germany and Switzerland as well as to identify associated genome regions by GWAS. The clinicopathological phenotype of 52 BCSE-affected Holstein cattle was in accordance with the phenotype described in German Braunvieh cattle, but in addition, signs of degeneration and cellular infiltration in the eye muscles were found. By using imputed sequence level genotype data, three genome-wide significant GWAS hits were revealed on different chromosomes that were not detected by initial GWAS based on high density SNP array data highlighting the usefulness of this approach for mapping studies. The associated genome regions include the gene as well as markers adjacent to the and genes all illustrating possible functional candidate genes. Our results challenge a monogenic mode of inheritance and indicate a more complex inheritance of BCSE in Holstein cattle. Furthermore, in comparison to previous results from German Braunvieh cattle, it illustrates an obvious genetic heterogeneity causing BSCE in cattle. Subsequent whole genome sequencing (WGS)-based analyses might elucidate pathogenic variants in the future.

摘要

双侧会聚性斜视伴眼球突出(BCSE)是一种眼部畸形,被认为是一种轻度但进行性的疾病,影响生命头两年的牛。这种最有可能遗传的疾病在类似于人类进行性眼外肌麻痹(PEO)的常染色体显性遗传形式的牛中很少被描述。在德国红牛中,发现了两个连锁的基因组区域,它们可能负责 BCSE 的发展和/或进展。本研究的目的是对德国和瑞士的荷斯坦奶牛的 BCSE 进行表型特征分析,并通过 GWAS 鉴定相关的基因组区域。52 头 BCSE 受影响的荷斯坦奶牛的临床病理表型与德国红牛中描述的表型一致,但此外,还发现了眼外肌退化和细胞浸润的迹象。通过使用 imputed sequence level 基因型数据,在不同染色体上揭示了三个全基因组显著的 GWAS 命中,这些命中在最初基于高密度 SNP 阵列数据的 GWAS 中没有检测到,这突出了这种方法在图谱研究中的有用性。相关的基因组区域包括基因以及邻近的基因和基因的标记,所有这些都说明了可能的功能候选基因。我们的结果对单基因遗传模式提出了挑战,并表明 BCSE 在荷斯坦奶牛中的遗传更为复杂。此外,与德国红牛的先前结果相比,它说明了导致 BSCE 的明显遗传异质性。随后的全基因组测序(WGS)分析可能会在未来阐明致病变异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6bd/8303712/c4d346e65672/genes-12-01039-g001.jpg

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