Circular reasoning: microRNAs and cell-cycle control

被引:90
作者
Chivukula, Raghu R. [1 ,2 ]
Mendell, Joshua T. [1 ,3 ,4 ]
机构
[1] Johns Hopkins Univ, McKusick Nathans Inst Genet Med, Sch Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Program Human Genet & Mol Biol, Sch Med, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Dept Pediat, Sch Med, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Dept Mol Biol & Genet, Sch Med, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.tibs.2008.06.008
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
MicroRNAs (miRNAs) have attracted considerable attention because of their important roles in development, normal physiology, and disease states including cancer. Recent studies have identified specific miRNAs that regulate the cell cycle and have documented that the loss or gain of miRNA-mediated cell-cycle control contributes to malignancy. miRNAs regulate classic cell-cycle control pathways by directly targeting proteins such as E2F transcription factors, cyclin-dependent kinases (Cdks), cyclins and Cdk inhibitors. Moreover, from recent findings, it has been suggested that miRNAs themselves might be subject to cell-cycle dependent regulation. Together, these observations indicate that the reciprocal control of RNA silencing and the metazoan cell cycle impacts cellular behavior and disease.
引用
收藏
页码:474 / 481
页数:8
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