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MITF基因5'区域的一个非编码调控变异与瑞士褐牛的白斑毛色相关。

A non-coding regulatory variant in the 5'-region of the MITF gene is associated with white-spotted coat in Brown Swiss cattle.

作者信息

Hofstetter S, Seefried F, Häfliger I M, Jagannathan V, Leeb T, Drögemüller C

机构信息

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland.

Qualitas AG, 6300, Zug, Switzerland.

出版信息

Anim Genet. 2019 Feb;50(1):27-32. doi: 10.1111/age.12751. Epub 2018 Dec 2.

Abstract

Recently, the Swiss breeding association reported an increasing number of white-spotted cattle in the Brown Swiss breed, which is normally solid brown coloured. A total of 60 Brown Swiss cattle with variably sized white abdominal spots, facial markings and depigmented claws were collected for this study. A genome-wide association study using 40k SNP genotypes of 20 cases and 1619 controls enabled us to identify an associated genome region on chromosome 22 containing the MITF gene, encoding the melanogenesis associated transcription factor. Variants at the MITF locus have been reported before to be associated with white or white-spotted phenotypes in other species such as horses, dogs and mice. Whole-genome sequencing of a single white-spotted cow and subsequent genotyping of 172 Brown Swiss cattle revealed two significantly associated completely linked single nucleotide variants (rs722765315 and rs719139527). Both variants are located in the 5'-regulatory region of the bovine MITF gene, and comparative sequence analysis showed that the variant rs722765315, located 139 kb upstream of the transcription start site of the bovine melanocyte-specific MITF transcript, is situated in a multi-species conserved sequence element which is supposed to be regulatory important. Therefore, we hypothesize that rs722765315 represents the most likely causative variant for the white-spotting phenotype observed in Brown Swiss cattle. Presence of the mutant allele in a heterozygous or homozygous state supports a dominant mode of inheritance with incomplete penetrance and results in a variable extent of coat colour depigmentation.

摘要

最近,瑞士育种协会报告称,在通常为纯棕色的瑞士褐牛品种中,出现白斑的牛的数量有所增加。本研究共收集了60头瑞士褐牛,这些牛腹部有大小不一的白色斑点、面部有斑纹且爪子色素脱失。利用20例病例和1619例对照的40k SNP基因型进行全基因组关联研究,使我们能够在22号染色体上鉴定出一个包含MITF基因的相关基因组区域,该基因编码与黑色素生成相关的转录因子。之前已有报道称,MITF基因座的变异与马、狗和小鼠等其他物种的白色或白斑表型有关。对一头白斑母牛进行全基因组测序,并随后对172头瑞士褐牛进行基因分型,发现了两个显著相关的完全连锁单核苷酸变异(rs722765315和rs719139527)。这两个变异均位于牛MITF基因的5'调控区,比较序列分析表明,位于牛黑素细胞特异性MITF转录本转录起始位点上游139 kb处的变异rs722765315,位于一个多物种保守序列元件中,该元件被认为具有重要的调控作用。因此,我们推测rs722765315是瑞士褐牛中观察到的白斑表型最可能的致病变异。突变等位基因以杂合或纯合状态存在支持显性遗传模式,具有不完全外显率,并导致毛色色素脱失程度不同。

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