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日本鹿儿岛县日本黑牛的亮氨酰-tRNA 合成酶(IARS)基因 c.235G>C 突变的携带率,以及杂合牛代谢谱和繁殖性能的分析。

Carrier rate of the c.235G>C mutation in the bovine isoleucyl-tRNA synthetase (IARS) gene of Japanese Black cows at Kagoshima prefecture, Japan, and analysis of the metabolic profiling and reproductive performance of heterozygous cows.

机构信息

Laboratory of Clinical Pathology, Joint Faculty of Veterinary Medicine, Kagoshima University, 1-21-24 Korimoto, Kagoshima 890-0065, Japan.

Faculty of Veterinary Medicine, Chattogram Veterinary and Animal Sciences University, Khulshi, Chattogram 4225, Bangladesh.

出版信息

J Vet Med Sci. 2021 Mar 5;83(2):254-259. doi: 10.1292/jvms.20-0356. Epub 2020 Dec 8.

Abstract

Bovine isoleucyl-tRNA synthetase (IARS) disorder, a major cause of weak calf syndrome, is caused by a homozygous missense (c.235G>C) mutation in the bovine IARS gene of Japanese Black (JB) cattle, which was identified in 2013. However, the extent to which the carrier rate has changed at Kagoshima prefecture, Japan, and whether the carrier status is associated with any clinical or reproductive problems, have yet to be ascertained. In this study, using a real-time polymerase chain reaction-based genotyping assay, we determined the carrier rate in a regional JB cow population at Kagoshima prefecture. Comparative analyses were performed on the metabolic profile test (MPT) results and reproductive performance data obtained for heterozygous carrier and homozygous wild-type cows. In 2009 and 2018, DNA samples were collected from 130 and 462 clinically healthy JB cows, respectively, in Kagoshima prefecture. MPT results and reproductive performance data were evaluated for 62 cows, comprising four heterozygous carriers and 58 wild-type cows. Genotyping revealed that the carrier rate was 6.9% in 2009 and 1.5% in 2018, the difference of which was statistically significant (P<0.005). There were no statistically significant differences between the carrier and wild-type cows with respect to either MPT results or reproductive performance, indicating that the carrier cows have necessary IARS activity to maintain minimal health and reproductive potential.

摘要

牛亮氨酰-tRNA 合成酶(IARS)缺乏症是弱犊综合征的主要病因,是由日本黑牛(JB)牛 IARS 基因中的纯合错义突变(c.235G>C)引起的,该突变于 2013 年被发现。然而,在日本鹿儿岛县,这种突变的携带者频率是否发生了变化,以及携带者状态是否与任何临床或生殖问题有关,尚未确定。在这项研究中,我们使用实时聚合酶链反应(PCR)的基因分型检测方法,确定了鹿儿岛县地区 JB 牛的携带者频率。对代谢轮廓测试(MPT)结果和杂合子携带者与纯合野生型牛的繁殖性能数据进行了比较分析。2009 年和 2018 年,分别从鹿儿岛县的 130 头和 462 头临床健康的 JB 牛中采集了 DNA 样本。对 62 头牛(包括 4 头杂合子携带者和 58 头野生型牛)的 MPT 结果和繁殖性能数据进行了评估。基因分型显示,2009 年的携带者频率为 6.9%,2018 年为 1.5%,差异具有统计学意义(P<0.005)。在 MPT 结果或繁殖性能方面,携带者和野生型牛之间没有统计学上的显著差异,表明携带者牛具有维持最小健康和生殖潜力所需的 IARS 活性。

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本文引用的文献

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Aminoacyl-tRNA synthetase deficiencies in search of common themes.氨酰-tRNA 合成酶缺陷寻找共同主题。
Genet Med. 2019 Feb;21(2):319-330. doi: 10.1038/s41436-018-0048-y. Epub 2018 Jun 6.
2
Mapping of Calf Death in Japanese Black Cattle.日本黑牛犊死亡的定位。
Anim Biotechnol. 2017 Oct 2;28(4):242-247. doi: 10.1080/10495398.2016.1267643. Epub 2017 Jan 19.
3
IARS mutation causes prenatal death in Japanese Black cattle.IARS突变导致日本黑牛产前死亡。
Anim Sci J. 2016 Sep;87(9):1178-81. doi: 10.1111/asj.12639. Epub 2016 May 27.
7
Aminoacyl-tRNA synthetases in medicine and disease.氨基酸酰-tRNA 合成酶在医学和疾病中的作用。
EMBO Mol Med. 2013 Mar;5(3):332-43. doi: 10.1002/emmm.201100626. Epub 2013 Feb 21.

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