在 Manech Tête Rousse 奶羊中寻找同源单倍型缺陷,发现 MMUT 基因中的一个无义变体会影响新生羔羊的存活率。

IF 3.6 1区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE Genetics Selection Evolution Pub Date : 2024-02-29 DOI:10.1186/s12711-024-00886-7
Maxime Ben Braiek, Carole Moreno-Romieux, Céline André, Jean-Michel Astruc, Philippe Bardou, Arnaud Bordes, Frédéric Debat, Francis Fidelle, Itsasne Granado-Tajada, Chris Hozé, Florence Plisson-Petit, François Rivemale, Julien Sarry, Némuel Tadi, Florent Woloszyn, Stéphane Fabre
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引用次数: 0

摘要

背景:众所周知,同人类一样,家畜群体中也会出现隐性有害变异,其中一些变异在同基因状态下可能是致命的:我们利用分阶段 50 k 单核苷酸多态性(SNP)基因型和血统数据扫描了 6845 只 Manech Tête Rousse 奶羊的基因组,以寻找同源单倍型(DHH)的缺陷。结果发现了五个 Manech Tête Rousse 基因缺陷同源单倍型 (MTRDHH1 至 5),其同源基因缺陷率从 84% 到 100% 不等。这些单倍型位于羱羊染色体(OAR)1(MTRDHH2 和 3)、OAR10(MTRDHH4)、OAR13(MTRDHH5)和 OAR20(MTRDHH1)上,携带者频率为 7.8% 至 16.6%。将 DHH 携带者之间的高风险配对与非携带者之间的安全配对进行比较,发现两个 DHH(MTRDHH1 和 2)与受精成功率降低和/或死胎率增加有关。我们研究了MTRDHH1单倍型,该单倍型大大增加了死胎率,并通过全基因组测序方法在甲基丙二酰-CoA突变酶(MMUT)基因中发现了一个诱导过早终止密码子(p.Gln409*)的单核苷酸变异(SNV)。我们通过杂合子携带者之间的风险交配产生了MMUT突变的同源羔羊,其中大部分羔羊在出生后24小时内死亡,且无任何明显的临床症状。对死后肝脏和肾脏生物样本进行的逆转录酶-qPCR和Western印迹检测显示,突变同源羔羊肝脏中MMUT mRNA的表达量减少,且没有全长的MMUT蛋白:我们在绵羊中发现了五个同基因缺陷单倍型,这些单倍型可能含有五个独立的有害隐性变体。其中一个变体在 MMUT 基因中被检测到,该变体在同基因状态下与羔羊致死有关。在 MTR 奶羊选育计划中对这些单倍型/变体进行特定管理将有助于提高整体繁殖力和羔羊存活率。
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Searching for homozygous haplotype deficiency in Manech Tête Rousse dairy sheep revealed a nonsense variant in the MMUT gene affecting newborn lamb viability.

Background: Recessive deleterious variants are known to segregate in livestock populations, as in humans, and some may be lethal in the homozygous state.

Results: We used phased 50 k single nucleotide polymorphism (SNP) genotypes and pedigree data to scan the genome of 6845 Manech Tête Rousse dairy sheep to search for deficiency in homozygous haplotypes (DHH). Five Manech Tête Rousse deficient homozygous haplotypes (MTRDHH1 to 5) were identified, with a homozygous deficiency ranging from 84 to 100%. These haplotypes are located on Ovis aries chromosome (OAR)1 (MTRDHH2 and 3), OAR10 (MTRDHH4), OAR13 (MTRDHH5), and OAR20 (MTRDHH1), and have carrier frequencies ranging from 7.8 to 16.6%. When comparing at-risk matings between DHH carriers to safe matings between non-carriers, two DHH (MTRDHH1 and 2) were linked with decreased insemination success and/or increased stillbirth incidence. We investigated the MTRDHH1 haplotype, which substantially increased stillbirth rate, and identified a single nucleotide variant (SNV) inducing a premature stop codon (p.Gln409*) in the methylmalonyl-CoA mutase (MMUT) gene by using a whole-genome sequencing approach. We generated homozygous lambs for the MMUT mutation by at-risk mating between heterozygous carriers, and most of them died within the first 24 h after birth without any obvious clinical symptoms. Reverse transcriptase-qPCR and western blotting on post-mortem liver and kidney biological samples showed a decreased expression of MMUT mRNA in the liver and absence of a full-length MMUT protein in the mutant homozygous lambs.

Conclusions: We identified five homozygous deficient haplotypes that are likely to harbor five independent deleterious recessive variants in sheep. One of these was detected in the MMUT gene, which is associated with lamb lethality in the homozygous state. A specific management of these haplotypes/variants in the MTR dairy sheep selection program would help enhance the overall fertility and lamb survival.

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来源期刊
Genetics Selection Evolution
Genetics Selection Evolution 生物-奶制品与动物科学
CiteScore
6.50
自引率
9.80%
发文量
74
审稿时长
1 months
期刊介绍: Genetics Selection Evolution invites basic, applied and methodological content that will aid the current understanding and the utilization of genetic variability in domestic animal species. Although the focus is on domestic animal species, research on other species is invited if it contributes to the understanding of the use of genetic variability in domestic animals. Genetics Selection Evolution publishes results from all levels of study, from the gene to the quantitative trait, from the individual to the population, the breed or the species. Contributions concerning both the biological approach, from molecular genetics to quantitative genetics, as well as the mathematical approach, from population genetics to statistics, are welcome. Specific areas of interest include but are not limited to: gene and QTL identification, mapping and characterization, analysis of new phenotypes, high-throughput SNP data analysis, functional genomics, cytogenetics, genetic diversity of populations and breeds, genetic evaluation, applied and experimental selection, genomic selection, selection efficiency, and statistical methodology for the genetic analysis of phenotypes with quantitative and mixed inheritance.
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