Immediate-early gene activation by the MAPK pathways: what do and don't we know?

被引:82
作者
O'Donnell, Amanda [1 ]
Odrowaz, Zaneta [1 ]
Sharrocks, Andrew D. [1 ]
机构
[1] Univ Manchester, Fac Life Sci, Manchester M13 9PT, Lancs, England
基金
英国惠康基金;
关键词
E26-like kinase 1 (ELK1); FOS; immediate-early gene; mitogen-activated protein kinase (MAPK); ternary complex factor (TCF); C-FOS GENE; SERUM RESPONSE FACTOR; KINASE SIGNALING CASCADES; TERNARY COMPLEX FACTORS; TRANSCRIPTION FACTORS; GROWTH-FACTOR; INDUCED PHOSPHORYLATION; FUNCTIONAL VERSATILITY; HISTONE ACETYLATION; H3; PHOSPHORYLATION;
D O I
10.1042/BST20110636
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
The study of IE (immediate-early) gene activation mechanisms has provided numerous paradigms for how transcription is controlled in response to extracellular signalling. Many of the findings have been derived from investigating one of the IE genes, FOS, and the models extrapolated to regulatory mechanisms for other IE genes. However, whereas the overall principles of activation appear similar, recent evidence suggests that the underlying mechanistic details may differ depending on cell type, cellular stimulus and IE gene under investigation. In the present paper, we review recent advances in our understanding of IE gene transcription, chiefly focusing on FOS and its activation by ERK (extracellular-signal-regulated kinase) MAPK (mitogen-activated protein kinase) pathway signalling. We highlight important fundamental regulatory principles, but also illustrate the gaps in our current knowledge and the potential danger in making assumptions based on extrapolation from disparate studies.
引用
收藏
页码:58 / 66
页数:9
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