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MicroRNAs in disease and potential therapeutic applications.

机译:MicroRNA在疾病和潜在的治疗应用中。

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摘要

MicroRNAs (miRNAs) are 21-24 nucleotide (nt) duplex RNAs that are created from precursor transcripts by subsequent processing steps mediated by members of the RNAseIII family, Drosha and Dicer. One of the two strands is incorporated into the active sites of the Argonaute family of proteins, where it serves as a guide for Watson-Crick base pairing with complementary sequences in target messenger RNAs (mRNAs). In mammals, the majority of miRNAs guide the RNA-induced silencing complex (RISC) to the 3' untranslated regions (UTRs) of mRNA targets, with the consequence that translation of the target mRNAs is inhibited. The importance of miRNAs in normal cellular development and metabolism is only now being realized. miRNA deficiencies or excesses have been correlated with a number of clinically important diseases ranging from myocardial infarction to cancers. The loss or gain of miRNA function can be caused by a single point mutation in either the miRNA or its target or by epigenetic silencing of primary miRNA transcription units. This review summarizes miRNA biogenesis and biology, explores the potential roles miRNAs can play in a variety of diseases, and suggests some therapeutic applications for restoring or inhibiting miRNA function.
机译:MicroRNA(miRNA)是21-24个核苷酸(nt)的双链体RNA,由前体转录物通过RNAseIII家族成员Drosha和Dicer介导的后续加工步骤产生。两条链中的一条被整合到Argonaute蛋白质家族的活性位点中,在此充当与目标信使RNA(mRNA)中互补序列进行Watson-Crick碱基配对的指南。在哺乳动物中,大多数miRNA会将RNA诱导的沉默复合体(RISC)引导至mRNA靶标的3'非翻译区(UTR),从而抑制了靶标mRNA的翻译。直到现在,人们才意识到miRNA在正常细胞发育和代谢中的重要性。 miRNA缺乏或过量与许多临床上重要的疾病相关,从心肌梗塞到癌症。 miRNA功能的丧失或获得可能是由于miRNA或其靶标中的单点突变或主要miRNA转录单位的表观遗传沉默所致。这篇综述总结了miRNA的生物发生和生物学特性,探讨了miRNA在多种疾病中可能发挥的潜在作用,并提出了一些恢复或抑制miRNA功能的治疗方法。

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