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EML5的WD-40结构域重复序列中的一个非同义点突变导致牛精子质量和生育力下降。

A Non-Synonymous Point Mutation in a WD-40 Domain Repeat of EML5 Leads to Decreased Bovine Sperm Quality and Fertility.

作者信息

Nogueira Eriklis, Tirpák Filip, Hamilton Lauren E, Zigo Michal, Kerns Karl, Sutovsky Miriam, Kim JaeWoo, Volkmann Dietrich, Jovine Luca, Taylor Jeremy F, Schnabel Robert D, Sutovsky Peter

机构信息

Division of Animal Sciences, University of Missouri, Columbia, MO, United States.

Embrapa Pantanal, Corumbá, Brazil.

出版信息

Front Cell Dev Biol. 2022 Apr 5;10:872740. doi: 10.3389/fcell.2022.872740. eCollection 2022.

Abstract

This study is part of a concerted effort to identify and phenotype rare, deleterious mutations that adversely affect sperm quality, or convey high developmental and fertility potential to embryos and ensuing progeny. A rare, homozygous mutation in ( ), which encodes a microtubule-associated protein with high expression in testis and brain was identified in an Angus bull used extensively in artificial insemination (AI) for its outstanding progeny production traits. The bull's fertility was low in cross-breeding timed AI (TAI) (Pregnancy/TAI = 25.2%; = 222) and, in general, AI breeding to Nellore cows (41%; = 822). A search of the 1,000 Bull Genomes Run9 database revealed an additional 74 heterozygous animals and 8 homozygous animals harboring this exact mutation across several different breeds (0.7% frequency within the 6,191 sequenced animals). Phenotypically, spermatozoa from the homozygous Angus bull displayed prominent piriform and tapered heads, and outwardly protruding knobbed acrosomes. Additionally, an increased retention of EML5 was also observed in the sperm head of both homozygous and heterozygous Angus bulls compared to wild-type animals. This non-synonymous point mutation is located within a WD40 signaling domain repeat of and is predicted to be detrimental to overall protein function by genomic single nucleotide polymorphism (SNP) analysis and protein modeling. Future work will examine how this rare mutation affects field AI fertility and will characterize the role of EML5 in spermatogenesis.

摘要

本研究是一项协同努力的一部分,旨在识别和表型分析罕见的有害突变,这些突变会对精子质量产生不利影响,或者赋予胚胎及后续后代高发育和生育潜力。在一头因出色的后代生产性状而广泛用于人工授精(AI)的安格斯公牛中,发现了一个罕见的纯合突变( ),该突变编码一种在睾丸和大脑中高表达的微管相关蛋白。这头公牛在杂交定时人工授精(TAI)中的生育力较低(妊娠率/TAI = 25.2%; = 222),总体而言,与内洛尔牛进行人工授精时的妊娠率为41%( = 822)。对1000头公牛基因组Run9数据库的搜索显示,在几个不同品种中还有74头杂合动物和8头纯合动物携带此确切突变(在6191头测序动物中的频率为0.7%)。从表型上看,来自纯合安格斯公牛的精子显示出明显的梨形和锥形头部,以及向外突出的带瘤顶体。此外,与野生型动物相比,在纯合和杂合安格斯公牛的精子头部还观察到EML5的保留增加。这种非同义点突变位于 的WD40信号域重复序列内,通过基因组单核苷酸多态性(SNP)分析和蛋白质建模预测对整体蛋白质功能有害。未来的工作将研究这种罕见突变如何影响现场人工授精的生育力,并将表征EML5在精子发生中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a8/9037033/5ae59bb7d28a/fcell-10-872740-g001.jpg

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