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本文引用的文献

1
Novel ncRNAs transcribed by Pol III and elucidation of their functional relevance by biophysical approaches.由 Pol III 转录的新型 ncRNAs 及其通过生物物理方法阐明其功能相关性。
Front Cell Neurosci. 2013 Nov 7;7:203. doi: 10.3389/fncel.2013.00203.
2
Studying microRNAs in the brain: technical lessons learned from the first ten years.大脑中微小RNA的研究:前十载的技术经验
Exp Neurol. 2012 Jun;235(2):397-401. doi: 10.1016/j.expneurol.2011.12.004. Epub 2011 Dec 8.
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TarBase 6.0: capturing the exponential growth of miRNA targets with experimental support.TarBase 6.0:捕捉具有实验支持的 miRNA 靶标指数级增长。
Nucleic Acids Res. 2012 Jan;40(Database issue):D222-9. doi: 10.1093/nar/gkr1161. Epub 2011 Dec 1.
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Experimental strategies for microRNA target identification.miRNA 靶基因识别的实验策略
Nucleic Acids Res. 2011 Sep 1;39(16):6845-53. doi: 10.1093/nar/gkr330. Epub 2011 Jun 7.
5
Circulating plasma MiR-141 is a novel biomarker for metastatic colon cancer and predicts poor prognosis.循环血浆 miR-141 是转移性结直肠癌的新型生物标志物,可预测不良预后。
PLoS One. 2011 Mar 17;6(3):e17745. doi: 10.1371/journal.pone.0017745.
6
Clinical impact of down-regulated plasma miR-92a levels in non-Hodgkin's lymphoma.非霍奇金淋巴瘤患者血浆 miR-92a 水平下调的临床影响。
PLoS One. 2011 Feb 24;6(2):e16408. doi: 10.1371/journal.pone.0016408.
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A viral microRNA cluster strongly potentiates the transforming properties of a human herpesvirus.一种病毒 microRNA 簇强烈增强了一种人类疱疹病毒的转化特性。
PLoS Pathog. 2011 Feb;7(2):e1001294. doi: 10.1371/journal.ppat.1001294. Epub 2011 Feb 17.
8
miRTarBase: a database curates experimentally validated microRNA-target interactions.miRTarBase:一个整理经实验验证的微小RNA-靶标相互作用的数据库。
Nucleic Acids Res. 2011 Jan;39(Database issue):D163-9. doi: 10.1093/nar/gkq1107. Epub 2010 Nov 10.
9
In situ detection of microRNAs in paraffin embedded, formalin fixed tissues and the co-localization of their putative targets.原位检测石蜡包埋、福尔马林固定组织中的 microRNAs 及其潜在靶标的共定位。
Methods. 2010 Dec;52(4):307-15. doi: 10.1016/j.ymeth.2010.08.009. Epub 2010 Aug 17.
10
Circulating microRNAs: novel biomarkers for esophageal cancer.循环 microRNAs:食管癌的新型生物标志物。
World J Gastroenterol. 2010 May 21;16(19):2348-54. doi: 10.3748/wjg.v16.i19.2348.

RNA 的新世界。

The new world of RNAs.

机构信息

Departamento de Genética Médica, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brazil .

Faculdade de Ciências Básicas, Universidade Federal Fluminense, Nova Friburgo, RJ, Brazil .

出版信息

Genet Mol Biol. 2014 Mar;37(1 Suppl):285-93. doi: 10.1590/s1415-47572014000200014.

DOI:10.1590/s1415-47572014000200014
PMID:24764762
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3983583/
Abstract

One of the major developments that resulted from the human genome sequencing projects was a better understanding of the role of non-coding RNAs (ncRNAs). NcRNAs are divided into several different categories according to size and function; however, one shared feature is that they are not translated into proteins. In this review, we will discuss relevant aspects of ncRNAs, focusing on two main types: i) microRNAs, which negatively regulate gene expression either by translational repression or target mRNA degradation, and ii) small interfering RNAs (siRNAs), which are involved in the biological process of RNA interference (RNAi). Our knowledge regarding these two types of ncRNAs has increased dramatically over the past decade, and they have a great potential to become therapeutic alternatives for a variety of human conditions.

摘要

人类基因组测序项目的主要成果之一是更好地理解了非编码 RNA(ncRNA)的作用。ncRNA 根据大小和功能分为几个不同的类别;然而,它们有一个共同的特征,即它们不被翻译成蛋白质。在这篇综述中,我们将讨论 ncRNA 的相关方面,重点讨论两种主要类型:i)microRNAs,通过翻译抑制或靶 mRNA 降解来负调控基因表达,以及 ii)小干扰 RNA(siRNA),其参与 RNA 干扰(RNAi)的生物学过程。在过去的十年中,我们对这两种类型的 ncRNA 的认识有了显著提高,它们有可能成为多种人类疾病的治疗替代方法。