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Pituitary Transcriptomic Study Reveals the Differential Regulation of lncRNAs and mRNAs Related to Prolificacy in Different FecB Genotyping Sheep

机译:垂体转录组学研究揭示了不同FecB基因分型绵羊的lncRNA和mRNA多能相关的差异调节

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Long non-coding RNA (LncRNA) have been identified as important regulators in the hypothalamic-pituitary-ovarian axis associated with sheep prolificacy. However, their expression pattern and potential roles in the pituitary are yet unclear. To explore the potential mRNAs and lncRNAs that regulate the expression of the genes involved in sheep prolificacy, we used stranded specific RNA-seq to profile the pituitary transcriptome (lncRNA and mRNA) in high prolificacy (genotype FecB BB, litter size = 3; H) and low prolificacy sheep (genotype FecB B+; litter size = 1; L). Our results showed that 57 differentially expressed (DE) lncRNAs and 298 DE mRNAs were found in the pituitary between the two groups. The qRT-PCR results correlated well with the RNA-seq results. Moreover, functional annotation analysis showed that the target genes of the DE lncRNAs were significantly enriched in pituitary function, hormone-related pathways as well as response to stimulus and some other terms related to reproduction. Furthermore, a co-expression network of lncRNAs and target genes was constructed and reproduction related genes such as SMAD2 , NMB and EFNB3 were included. Lastly, the interaction of candidate lncRNA MSTRG.259847.2 and its target gene SMAD2 were validated in vitro of sheep pituitary cells. These differential mRNA and lncRNA expression profiles provide a valuable resource for understanding the molecular mechanisms underlying Hu sheep prolificacy.
机译:长非编码RNA(LncRNA)已被确定为与绵羊多产相关的下丘脑-垂体-卵巢轴的重要调控因子。但是,它们的表达方式和在垂体中的潜在作用尚不清楚。为了探索潜在的mRNA和lncRNAs,调节参与绵羊多产的基因的表达,我们使用链状特异性RNA-seq对高多产的垂体转录组(lncRNA和mRNA)进行了分析(基因型FecB BB,窝数= 3; H) )和低产羊(基因型FecB B +;产仔数= 1; L)。我们的结果表明,在两组的垂体中发现了57个差异表达(DE)lncRNA和298个DE mRNA。 qRT-PCR结果与RNA-seq结果密切相关。此外,功能注释分析表明,DE lncRNA的靶基因在垂体功能,激素相关途径以及对刺激的反应和与生殖有关的其他术语方面显着丰富。此外,构建了lncRNA与靶基因的共表达网络,并包括了与繁殖相关的基因,如SMAD2,NMB和EFNB3。最后,在绵羊垂体细胞的体外验证了候选lncRNA MSTRG.259847.2与其靶基因SMAD2的相互作用。这些差异的mRNA和lncRNA表达谱为了解胡绵羊多产的分子机制提供了宝贵的资源。

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