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Mouse Endometrium Temporal and Spatial Expression mRNA and MicroRNA Associated With Embryo Implantation

机译:小鼠子宫内膜时空表达mRNA和microRNA与胚胎植入相关。

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Embryo implantation is a dynamic physiological process involving morphological and molecular changes in the endometrium during the pre-receptivity, receptivity, and implantation phases. A comprehensive analysis of messenger RNA (mRNA) and microRNA (miRNA) profiles during implantation will likely provide new clues to elucidate the underlying mechanisms governing embryo implantation. We characterized the mRNA and miRNA transcriptomes using next generation sequencing (NGS) of the endometrium 1 day postcoitum (dpc) and 4dpc and the implantation site (IMS) and inter-implantation (IIM) site of the endometrium on 5dpc. Real-time quantitative polymerase chain reaction was performed on selected miRNAs and their predicted target mRNAs to validate their negatively correlated expression. Statistical analysis of the data based on Gene Ontology (GO) group annotation and Kyoto Encyclopedia of Genes and Genomes pathway analysis demonstrated that the genes with significant expression at the IIM site were primarily involved in glucose, protein, and lipoprotein metabolism to provide energy for embryo implantation, while the genes identified at the IMS were involved in RNA functions to produce proteins in support of embryo development and trophoblast invasion. Extracellular matrix (ECM)-receptor interactions between cells and the ECM was the most remarkable event during implantation. The miRNA-mRNA interaction network unraveled the regulatory relationship between miRNAs and mRNAs. Hub miRNAs (mmu-miR-96 and mmu-miR-200b) were identified to target B-cell lymphoma 2 (Bcl-2), Kruppel-like factor 13 (Klf13), and Progesterone receptor (PGR), which are associated with the preparation of the receptive condition or the maintenance of early pregnancy.
机译:胚胎植入是一个动态的生理过程,涉及在接受前,接受和植入阶段子宫内膜的形态和分子变化。在植入过程中对信使RNA(mRNA)和微小RNA(miRNA)谱的全面分析可能会提供新的线索,以阐明控制胚胎植入的潜在机制。我们使用子宫内膜的下一代测序(NGS)的后天(dpc)和4dpc以及子宫内膜在5dpc上的植入位点(IMS)和植入间(IIM)部位来表征mRNA和miRNA转录组。对选定的miRNA及其预测的靶mRNA进行实时定量聚合酶链反应以验证其负相关表达。基于基因本体论(GO)组注释和《京都议定书》基因与基因组通路分析的数据的统计分析表明,在IIM位点表达显着的基因主要参与葡萄糖,蛋白质和脂蛋白的代谢,从而为胚胎提供能量植入时,在IMS处鉴定的基因参与RNA功能,以产生支持胚胎发育和滋养细胞入侵的蛋白质。细胞和ECM之间的细胞外基质(ECM)-受体相互作用是植入过程中最显着的事件。 miRNA-mRNA相互作用网络揭示了miRNA和mRNA之间的调节关系。集线器miRNA(mmu-miR-96和mmu-miR-200b)被鉴定为靶向B细胞淋巴瘤2(Bcl-2),Kruppel样因子13(Klf13)和孕激素受体(PGR),它们与准备接受状况或维持早孕。

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