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首页> 外文期刊>BMC Genomics >Analysis of DNA methylation profiles during sheep skeletal muscle development using whole-genome bisulfite sequencing
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Analysis of DNA methylation profiles during sheep skeletal muscle development using whole-genome bisulfite sequencing

机译:用全基因组亚硫酸氢盐测序分析绵羊骨骼肌发育中的DNA甲基化谱

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BACKGROUND:DNA methylation is an epigenetic regulatory form that plays an important role in regulating the gene expression and the tissues development.. However, DNA methylation regulators involved in sheep muscle development remain unclear. To explore the functional importance of genome-scale DNA methylation during sheep muscle growth, this study systematically investigated the genome-wide DNA methylation profiles at key stages of Hu sheep developmental (fetus and adult) using deep whole-genome bisulfite sequencing (WGBS).RESULTS:Our study found that the expression levels of DNA methyltransferase (DNMT)-related genes were lower in fetal muscle than in the muscle of adults. The methylation levels in the CG context were higher than those in the CHG and CHH contexts, and methylation levels were highest in introns, followed by exons and downstream regions. Subsequently, we identified 48,491, 17, and 135 differentially methylated regions (DMRs) in the CG, CHG, and CHH sequence contexts and 11,522 differentially methylated genes (DMGs). The results of bisulfite sequencing PCR (BSP) correlated well with the WGBS-Seq data. Moreover, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) functional annotation analysis revealed that some DMGs were involved in regulating skeletal muscle development and fatty acid metabolism. By combining the WGBS-Seq and previous RNA-Seq data, a total of 159 overlap genes were obtained between differentially expressed genes (DEGs) and DMGs (FPKM ?10 and fold change ?4). Finally, we found that 9 DMGs were likely to be involved in muscle growth and metabolism of Hu sheep.CONCLUSIONS:We systemically studied the global DNA methylation patterns of fetal and adult muscle development in Hu sheep, which provided new insights into a better understanding of the epigenetic regulation of sheep muscle development.
机译:背景:DNA甲基化是一种表观遗传调节形式,在调节基因表达和组织发育方面发挥着重要作用。但是,参与绵羊肌肉发育的DNA甲基化调节剂仍然尚不清楚。为了探讨绵羊肌肉生长过程中基因组DNA甲基化的功能重要性,本研究使用深全基因组亚硫酸氢盐测序(WGBS)系统地研究了Hu绵羊发育(胎儿和成人)的关键阶段的基因组DNA甲基化谱。结果:我们的研究发现,胎儿肌肉中DNA甲基转移酶(DNMT)的表达水平比成人肌肉低于胎儿肌肉。 CG上下文中的甲基化水平高于CHG和CHH的上下文中的水平,内含子的甲基化水平最高,其次是外显子和下游区域。随后,在CG,CHG和CHH序列上下文中鉴定48,491,17和135个差异甲基化区域(DMRS)和11,522个差异甲基化基因(DMG)。亚硫酸氢盐测序PCR(BSP)的结果与WGBS-SEQ数据良好相关。此外,基因本体(GO)和基因组(KEGG)功能注释分析的基因本体论(GO)和京都百科全书显示,一些DMG参与调节骨骼肌发育和脂肪酸代谢。通过组合WGBS-SEQ和先前的RNA-SEQ数据,在差异表达基因(DEGS)和DMG(FPKM> 10和折叠变化> 4)之间获得总共159个重叠基因。最后,我们发现9个DMG可能参与Hu羊的肌肉生长和代谢。结论:我们在Hu羊来系统地研究了胎儿和成人肌肉发育的全球DNA甲基化模式,为更好的理解提供了新的见解绵羊肌肉发育的表观遗传调控。

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