Regulation of microRNA function in somatic stem cell proliferation and differentiation

被引:312
作者
Shenoy, Archana
Blelloch, Robert H. [1 ]
机构
[1] Univ Calif San Francisco, Ctr Reprod Sci, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
NUCLEAR RECEPTOR TLX; HEMATOPOIETIC STEM; SKELETAL-MUSCLE; SELF-RENEWAL; HUMAN FIBROBLASTS; NEURONAL DIFFERENTIATION; MEDIATED CONTROL; ENZYME DICER; EXPRESSION; MORPHOGENESIS;
D O I
10.1038/nrm3854
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
microRNAs (miRNAs) are important modulators of development. Owing to their ability to simultaneously silence hundreds of target genes, they have key roles in large-scale transcriptomic changes that occur during cell fate transitions. In somatic stem and progenitor cells - such as those involved in myogenesis, haematopoiesis, skin and neural development - miRNA function is carefully regulated to promote and stabilize cell fate choice. miRNAs are integrated within networks that form both positive and negative feedback loops. Their function is regulated at multiple levels, including transcription, biogenesis, stability, availability and/or number of target sites, as well as their cooperation with other miRNAs and RNA-binding proteins. Together, these regulatory mechanisms result in a refined molecular response that enables proper cellular differentiation and function.
引用
收藏
页码:565 / 576
页数:12
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