Regulation of gene expression in vertebrate skeletal muscle

被引:46
作者
Carvajal, Jaime J. [1 ]
Rigby, Peter W. J. [1 ]
机构
[1] Inst Canc Res, Chester Beatty Labs, Sect Gene Funct & Regulat, London SW3 6JB, England
关键词
Myogenesis; Myogenic regulatory factors; Myf5; Mrf4; MyoD; Myogenin; TRABS; Transcriptional regulation; General transcription factors; miRNAs; MOUSE EMBRYO; MYOD TRANSCRIPTION; MYF5; EXPRESSION; MULTIPLE PHASES; CONTROL ELEMENT; MRF4; GENE; MYOGENESIS; CELLS; ENHANCER; LOCUS;
D O I
10.1016/j.yexcr.2010.07.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
During embryonic development the integration of numerous synergistic signalling pathways turns a single cell into a multicellular organism with specialized cell types and highly structured, organized tissues. To achieve this, cells must grow, proliferate, differentiate and die according to their spatiotemporal position. Unravelling the mechanisms by which a cell adopts the correct fate in response to its local environment remains one of the fundamental goals of biological research. In vertebrates skeletal myogenesis is coordinated by the activation of the myogenic regulatory factors (MRFs) in response to signals that are interpreted by their associated regulatory elements in different precursor cells during development. The MRFs trigger a cascade of transcription factors and downstream structural genes, ultimately resulting in the generation of one of the fundamental histotypes. In this review we discuss the regulation of the different MRFs in relation to their position in the myogenic cascade, the changes in the general transcriptional machinery during muscle differentiation and the emerging importance of miRNA regulation in skeletal myogenesis. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:3014 / 3018
页数:5
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