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牛 PRLR 的 SLICK1 等位基因的遗传。

Inheritance of the SLICK1 allele of PRLR in cattle.

机构信息

Department of Animal Sciences, University of Florida, Gainesville, FL, 32611-0910, USA.

Department of Animal Science, University of California, Davis, CA, 95616, USA.

出版信息

Anim Genet. 2021 Dec;52(6):887-890. doi: 10.1111/age.13145. Epub 2021 Oct 12.

Abstract

The slick-hair phenotype in cattle is due to one of a series of mutations in the prolactin receptor (PRLR) that cause truncation of the C-terminal region of the protein involved in JAK2/STAT5 activation during prolactin signaling. Here we evaluated whether the inheritance of the SLICK1 allele, the first slick mutation discovered, is inherited in a fashion consistent with Hardy-Weinberg equilibrium. It was hypothesized that any deleterious effect of inheriting the allele on embryonic or fetal function would result in reduced frequency of the allele in offspring. A total of 525 Holstein and Senepol cattle produced from matings involving one or both parents with the SLICK1 allele were genotyped. The observed frequency of the SLICK1 allele (0.247) was not significantly different than the expected frequency of 0.269. These results support the idea that inheritance of the SLICK1 allele does not act in the embryo or fetus to modify its competence to complete development to term.

摘要

牛的光滑毛发表型是由于一系列催乳素受体 (PRLR) 突变引起的,这些突变导致参与催乳素信号转导过程中 JAK2/STAT5 激活的蛋白质 C 末端区域截断。在这里,我们评估了首次发现的 SLICK1 等位基因的遗传是否符合哈迪-温伯格平衡。假设继承该等位基因对胚胎或胎儿功能的任何有害影响,将导致该等位基因在后代中的频率降低。对涉及一个或两个具有 SLICK1 等位基因的父母的交配所产生的 525 头荷斯坦和塞内波尔牛进行了基因分型。观察到的 SLICK1 等位基因的频率(0.247)与预期的 0.269 频率没有显著差异。这些结果支持这样一种观点,即 SLICK1 等位基因的遗传不会在胚胎或胎儿中发挥作用,以改变其完成发育的能力。

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