Genome-wide approaches in the study of microRNA biology

被引:18
|
作者
Wilbert, Melissa L. [1 ]
Yeo, Gene W. [1 ]
机构
[1] Univ Calif San Diego, Inst Genom Med, Stem Cell Program, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
EMBRYONIC STEM-CELLS; MESSENGER-RNA TARGETS; C-ELEGANS; BINDING-SITES; RIBONUCLEOPROTEIN COMPLEXES; SYSTEMATIC IDENTIFICATION; REGULATED MICRORNAS; MAMMALIAN MICRORNAS; AMINO-ACIDS; PROTEIN;
D O I
10.1002/wsbm.128
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
MicroRNAs (miRNAs), a class of similar to 21-23 nucleotide long non-coding RNAs (ncRNAs), have critical roles in diverse biological processes that encompass development, proliferation, apoptosis, stress response, and fat metabolism. miRNAs recognize their target mRNA transcripts by partial sequence complementarity and collectively have been estimated to regulate the majority of human genes. Consequently, misregulation of miRNAs or disruption of their target sites in genes has been implicated in a variety of human diseases ranging from cancer metastasis to neurological disorders. With the development and availability of genomic technologies and computational approaches, the field of miRNA biology has advanced tremendously over the last decade. Here we review the genome-wide approaches that have allowed for the discovery of new miRNAs, the characterization of their targets, and a systems-level view of their impact. (C) 2010 John Wiley & Sons, Inc. WIREs Syst Biol Med 2011 3 491-512 DOI: 10.1002/wsbm.128
引用
收藏
页码:491 / 512
页数:22
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