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MicroRNAs miR-1, -133 and -208: Same Faces, New Roles

机译:MicroRNA miR-1,-133和-208:相同的面孔,新的作用

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Micro-RNAs (miRNA) are noncoding RNAs that pair with specific mRNA targets and regulate their expression. The binding specificity of miRNAs depends on complementary base pairing at the 5' end of the miRNA with the 3' untranslated region of the corresponding mRNA. Binding of miRNAs to their cognate target mRNAs commonly leads to decreased expression of target genes through repression of translation or mRNA degradation. Increased expression of miRNAs can also result in paradoxical upregulation of previously suppressed target genes either directly, by decreasing the expression of inhibitory proteins and/or transcription factors, or indirectly, by inhibiting the expression levels of inhibitory miRNAs. Alternatively, decreased expression levels of inhibitory miRNAs can directly lead to increased target gene expression. Exponentially increasing research and understanding of the role played by miRNAs in post-transcriptional control and regulation of multifaceted processes, such as cardiac development, myocardial hypertrophy, arrhythmogenicity, heart failure and ventricular remodeling [reviewed in ref. 1], has perhaps been the single most novel advancement in molecular cardiology over the past decade.
机译:微小RNA(miRNA)是与特定的mRNA靶配对并调节其表达的非编码RNA。 miRNA的结合特异性取决于miRNA的5'端与相应mRNA的3'非翻译区的互补碱基配对。 miRNA与其同源靶mRNA的结合通常通过抑制翻译或mRNA降解而导致靶基因表达降低。通过减少抑制蛋白和/或转录因子的表达,或通过抑制抑制性miRNA的表达水平间接地,增加的miRNA的表达还可以导致先前抑制的靶基因的矛盾上调。或者,抑制性miRNA的表达水平降低可直接导致靶基因表达增加。对miRNA在转录后控制和多方面过程(例如心脏发育,心肌肥大,心律失常,心力衰竭和心室重塑)的转录后控制和调节中所起的作用的呈指数增长的研究和理解。 1],可能是过去十年中分子心脏病学中最新颖的发展。

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