Regulation of signalling by microRNAs

被引:48
|
作者
Avraham, Roi [1 ]
Yarden, Yosef [1 ]
机构
[1] Weizmann Inst Sci, Dept Regulat Biol, IL-76100 Rehovot, Israel
关键词
cancer; growth factor; microRNA (miRNA); network; tyrosine kinase; CANCER-CELLS; MESENCHYMAL TRANSITION; TRANSCRIPTION FACTORS; PROSTATE-CANCER; MIR-200; FAMILY; LET-7; EXPRESSION; GENES; RISC; SUPPRESSION;
D O I
10.1042/BST20110623
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
Stringent regulation of biochemical signalling pathways involves feedback and feedforward loops, which underlie robust cellular responses to external stimuli. Regulation occurs in all horizontal layers of signalling networks, primarily by proteins that mediate internalization of receptor-ligand complexes, dephosphorylation of kinases and their substrates, as well as transcriptional repression. Recent studies have unveiled the role of miRNAs (microRNAs), post-transcriptional regulators that control mRNA stability, as key modulators of signal propagation. By acting as genetic switches or fine-tuners, miRNAs can directly and multiply regulate cellular outcomes in response to diverse extracellular signals. Conversely, signalling networks temporally control stability, biogenesis and abundance of miRNAs, by regulating layers of the miRNA biogenesis pathway. In the present mini-review, we use a set of examples to illustrate the extensive interdependence between miRNAs and signalling networks.
引用
收藏
页码:26 / 30
页数:5
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