Non-coding RNAs: regulators of disease

被引:799
作者
Taft, Ryan J. [1 ]
Pang, Ken C. [2 ]
Mercer, Timothy R. [1 ]
Dinger, Marcel [1 ]
Mattick, John S. [1 ]
机构
[1] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[2] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
non-coding RNAs; small RNAs; microRNAs; RNA interference; genome-wide association study; SMALL INTERFERING RNAS; TRANSCRIPTION START SITES; GENOME-WIDE ANALYSIS; DOUBLE-STRANDED-RNA; LET-7; MICRORNA; CODING REGIONS; MESSENGER-RNA; ENDOGENOUS SIRNAS; GENE-EXPRESSION; STEM-CELLS;
D O I
10.1002/path.2638
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
For 50 years the term 'gene' has been synonymous with regions of the genome encoding mRNAs that are translated into protein. However, recent genome-wide studies have shown that the human genome is pervasively transcribed and produces many thousands of regulatory non-protein-coding RNAs (ncRNAs), including microRNAs, small interfering RNAs, PIWI-interacting RNAs and various classes of long ncRNAs. It is now clear that these RNAs fulfil critical roles as transcriptional and post-transcriptional regulators and as guides of chromatin-modifying complexes. Here we review the biology of ncRNAs, focusing on the fundamental mechanisms by which ncRNAs facilitate normal development and physiology and, when dysfunctional, underpin disease. We also discuss evidence that intergenic regions associated with complex diseases express ncRNAs, as well as the potential use of ncRNAs as diagnostic markers and therapeutic targets. Taken together, these observations emphasize the need to move beyond the confines of protein-coding genes and highlight the fact that continued investigation of ncRNA biogenesis and function will be necessary for a comprehensive understanding of human disease. Copyright (C) 2009 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:126 / 139
页数:14
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