Post-transcriptional gene regulation by MAP kinases via AU-rich elements

被引:52
|
作者
Clark, Andrew [1 ]
Dean, Jonathan [1 ]
Tudor, Corina [1 ]
Saklatvala, Jeremy [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Kennedy Inst Rheumatol Div, London W6 8LH, England
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2009年 / 14卷
基金
英国医学研究理事会;
关键词
Adenylate/Uridylate-Rich Element; Auf; ERK; HuR; JNK; KSRP; mitogen-activated protein kinase; mRNA stability; mRNA translation; p38; MAPK; Posttranscriptional regulation; processing body; Protein Phosphorylation; Tristetraprolin; Cytokine Production; Inflammation; Review; ACTIVATED PROTEIN-KINASE; TUMOR-NECROSIS-FACTOR; MESSENGER-RNA STABILITY; 3' UNTRANSLATED REGION; ZINC-FINGER PROTEINS; MACROPHAGE INFLAMMATORY PROTEIN-2; INTESTINAL EPITHELIAL-CELLS; OXIDE SYNTHASE EXPRESSION; TNF-ALPHA EXPRESSION; INITIATION-FACTOR; 4E;
D O I
10.2741/3282
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
Eukaryotic cells must continuously sense their environments, for example their attachment to extracellular matrix and proximity to other cells, differences in temperature or redox conditions, the presence of nutrients, growth factors, hormones, cytokines or pathogens. The information must then be integrated and an appropriate response initiated by modulating the cellular programme of gene expression. The mitogen-activated protein kinase (MAPK) signaling pathways play a critical role in this process. Decades of research have illuminated the many ways in which MAPKs regulate the synthesis of mRNA (transcription) via phosphorylation of transcription factors, cofactors, and other proteins. In recent years it has become increasingly clear that the control of mRNA destruction is equally important for cellular responses to extracellular cues, and is equally subject to regulation by MAPKs. This review will summarize our current understanding of post-transcriptional regulation of gene expression by the MAPKs and the proteins that are involved in this process.
引用
收藏
页码:847 / 871
页数:25
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