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牛鸟嘌呤核苷酸结合蛋白 Gs 亚基α(Gsα)编码(GNAS)基因组印记域内的 DNA 序列多态性与性能性状相关。

DNA sequence polymorphisms within the bovine guanine nucleotide-binding protein Gs subunit alpha (Gsα)-encoding (GNAS) genomic imprinting domain are associated with performance traits.

机构信息

Genetics and Biotechnology Laboratory, Department of Biochemistry, University College Cork, Cork, Ireland.

出版信息

BMC Genet. 2011 Jan 7;12:4. doi: 10.1186/1471-2156-12-4.

Abstract

BACKGROUND

Genes which are epigenetically regulated via genomic imprinting can be potential targets for artificial selection during animal breeding. Indeed, imprinted loci have been shown to underlie some important quantitative traits in domestic mammals, most notably muscle mass and fat deposition. In this candidate gene study, we have identified novel associations between six validated single nucleotide polymorphisms (SNPs) spanning a 97.6 kb region within the bovine guanine nucleotide-binding protein Gs subunit alpha gene (GNAS) domain on bovine chromosome 13 and genetic merit for a range of performance traits in 848 progeny-tested Holstein-Friesian sires. The mammalian GNAS domain consists of a number of reciprocally-imprinted, alternatively-spliced genes which can play a major role in growth, development and disease in mice and humans. Based on the current annotation of the bovine GNAS domain, four of the SNPs analysed (rs43101491, rs43101493, rs43101485 and rs43101486) were located upstream of the GNAS gene, while one SNP (rs41694646) was located in the second intron of the GNAS gene. The final SNP (rs41694656) was located in the first exon of transcripts encoding the putative bovine neuroendocrine-specific protein NESP55, resulting in an aspartic acid-to-asparagine amino acid substitution at amino acid position 192.

RESULTS

SNP genotype-phenotype association analyses indicate that the single intronic GNAS SNP (rs41694646) is associated (P ≤ 0.05) with a range of performance traits including milk yield, milk protein yield, the content of fat and protein in milk, culled cow carcass weight and progeny carcass conformation, measures of animal body size, direct calving difficulty (i.e. difficulty in calving due to the size of the calf) and gestation length. Association (P ≤ 0.01) with direct calving difficulty (i.e. due to calf size) and maternal calving difficulty (i.e. due to the maternal pelvic width size) was also observed at the rs43101491 SNP. Following adjustment for multiple-testing, significant association (q ≤ 0.05) remained between the rs41694646 SNP and four traits (animal stature, body depth, direct calving difficulty and milk yield) only. Notably, the single SNP in the bovine NESP55 gene (rs41694656) was associated (P ≤ 0.01) with somatic cell count--an often-cited indicator of resistance to mastitis and overall health status of the mammary system--and previous studies have demonstrated that the chromosomal region to where the GNAS domain maps underlies an important quantitative trait locus for this trait. This association, however, was not significant after adjustment for multiple testing. The three remaining SNPs assayed were not associated with any of the performance traits analysed in this study. Analysis of all pairwise linkage disequilibrium (r2) values suggests that most allele substitution effects for the assayed SNPs observed are independent. Finally, the polymorphic coding SNP in the putative bovine NESP55 gene was used to test the imprinting status of this gene across a range of foetal bovine tissues.

CONCLUSIONS

Previous studies in other mammalian species have shown that DNA sequence variation within the imprinted GNAS gene cluster contributes to several physiological and metabolic disorders, including obesity in humans and mice. Similarly, the results presented here indicate an important role for the imprinted GNAS cluster in underlying complex performance traits in cattle such as animal growth, calving, fertility and health. These findings suggest that GNAS domain-associated polymorphisms may serve as important genetic markers for future livestock breeding programs and support previous studies that candidate imprinted loci may act as molecular targets for the genetic improvement of agricultural populations. In addition, we present new evidence that the bovine NESP55 gene is epigenetically regulated as a maternally expressed imprinted gene in placental and intestinal tissues from 8-10 week old bovine foetuses.

摘要

背景

通过基因组印迹进行表观遗传调控的基因可能成为动物育种过程中人工选择的潜在目标。事实上,印迹基因已被证明是一些重要的数量性状的基础,这些数量性状在家畜中表现为肌肉质量和脂肪沉积。在这项候选基因研究中,我们在牛 13 号染色体上的鸟嘌呤核苷酸结合蛋白 Gs 亚单位α基因(GNAS)结构域内跨越 97.6kb 区域确定了六个已验证的单核苷酸多态性(SNP)与一系列性能性状之间的新关联,这些性能性状在 848 头经后裔测试的荷斯坦-弗里森公牛中得到遗传。哺乳动物 GNAS 结构域由许多相互印迹、交替剪接的基因组成,这些基因在老鼠和人类的生长、发育和疾病中起着重要作用。基于当前对牛 GNAS 结构域的注释,分析的四个 SNP(rs43101491、rs43101493、rs43101485 和 rs43101486)位于 GNAS 基因的上游,而一个 SNP(rs41694646)位于 GNAS 基因的第二个内含子中。最后一个 SNP(rs41694656)位于编码假定的牛神经内分泌特异性蛋白 NESP55 的转录本的第一个外显子中,导致第 192 位氨基酸天冬氨酸-天冬酰胺氨基酸取代。

结果

SNP 基因型-表型关联分析表明,单个内含子 GNAS SNP(rs41694646)与一系列性能性状相关(P ≤ 0.05),包括产奶量、乳蛋白产量、乳脂肪和蛋白质含量、淘汰牛胴体重和后代胴体结构、动物体型、直接分娩困难(即由于小牛大小引起的分娩困难)和妊娠长度。rs43101491 SNP 也与直接分娩困难(即由于小牛大小引起的分娩困难)和母体分娩困难(即由于母体骨盆宽度大小引起的分娩困难)相关(P ≤ 0.01)。经过多次测试调整后,rs41694646 SNP 与四个性状(动物体型、体深、直接分娩困难和产奶量)之间仅存在显著关联(q ≤ 0.05)。值得注意的是,牛 NESP55 基因中的单个 SNP(rs41694656)与体细胞计数相关(体细胞计数通常是衡量对乳腺炎抵抗力和乳腺系统整体健康状况的指标),先前的研究表明,GNAS 结构域所在的染色体区域是该性状的一个重要数量性状位点。然而,这种关联在经过多次测试调整后并不显著。所检测的其余三个 SNP 与本研究分析的任何性能性状均无关。所有成对连锁不平衡(r2)值的分析表明,观察到的大多数 SNP 等位基因替代效应是独立的。最后,在一系列牛胎儿组织中测试了假定的牛 NESP55 基因中的多态性编码 SNP,以检验该基因的印迹状态。

结论

在其他哺乳动物物种中的先前研究表明,印迹 GNAS 基因簇内的 DNA 序列变异导致了几种生理和代谢紊乱,包括人类和老鼠的肥胖症。同样,这里呈现的结果表明,印迹 GNAS 簇在牛的一些复杂性能性状中起着重要作用,例如动物生长、分娩、繁殖和健康。这些发现表明,GNAS 结构域相关的多态性可能成为未来家畜繁殖计划的重要遗传标记,并支持先前的研究,即候选印迹基因可能作为农业种群遗传改良的分子靶点。此外,我们提供了新的证据,证明牛 NESP55 基因作为胎盘和 8-10 周龄牛胎儿肠组织中的母系表达印迹基因受到表观遗传调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8287/3025900/4751f496b597/1471-2156-12-4-1.jpg

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