The complexity of miRNA-mediated repression

被引:366
作者
Wilczynska, A. [1 ]
Bushell, M. [1 ]
机构
[1] Univ Leicester, MRC, Toxicol Unit, Leicester LE1 7GD, Leics, England
基金
英国生物技术与生命科学研究理事会;
关键词
MESSENGER-RNA DEADENYLATION; LONG NONCODING RNA; TRANSLATIONAL REPRESSION; GW182; PROTEINS; BINDING-PROTEIN; POSTTRANSLATIONAL MODIFICATION; MAMMALIAN MICRORNAS; TARGET RECOGNITION; CCR4-NOT COMPLEX; UBIQUITIN LIGASE;
D O I
10.1038/cdd.2014.112
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Since their discovery 20 years ago, miRNAs have attracted much attention from all areas of biology. These short (similar to 22 nt) non-coding RNA molecules are highly conserved in evolution and are present in nearly all eukaryotes. They have critical roles in virtually every cellular process, particularly determination of cell fate in development and regulation of the cell cycle. Although it has long been known that miRNAs bind to mRNAs to trigger translational repression and degradation, there had been much debate regarding their precise mode of action. It is now believed that translational control is the primary event, only later followed by mRNA destabilisation. This review will discuss the most recent advances in our understanding of the molecular underpinnings of miRNA-mediated repression. Moreover, we highlight the multitude of regulatory mechanisms that modulate miRNA function.
引用
收藏
页码:22 / 33
页数:12
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