4.7 Review

The complexity of miRNA-mediated repression

期刊

CELL DEATH AND DIFFERENTIATION
卷 22, 期 1, 页码 22-33

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/cdd.2014.112

关键词

-

资金

  1. BBSRC [BB/F011806/1, BB/F011806/2] Funding Source: UKRI
  2. MRC [MC_EX_G0902052, MC_UP_A600_1024] Funding Source: UKRI
  3. Biotechnology and Biological Sciences Research Council [BB/F011806/2] Funding Source: researchfish
  4. Biotechnology and Biological Sciences Research Council [BB/F011806/1] Funding Source: Medline
  5. Medical Research Council [MC_EX_G0902052, MC_UP_A600_1024] Funding Source: Medline

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据