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通过将应激信号重定向为生长因子反应来鉴定丝裂原活化蛋白激酶结构域。

Identification of MAP kinase domains by redirecting stress signals into growth factor responses.

作者信息

Brunet A, Pouysségur J

机构信息

Centre de Biochemie-CNRS, UMR134, Parc Valrose, Faculté des Sciences, Nice, France.

出版信息

Science. 1996 Jun 14;272(5268):1652-5. doi: 10.1126/science.272.5268.1652.

Abstract

Mitogen-activated protein kinase (MAPK) cascades, termed MAPK modules, channel extracellular signals into specific cellular responses. Chimeric molecules were constructed between p38 and p44 MAPKs, which transduce stress and growth factor signals, respectively. A discrete region of 40 residues located in the amono-terminal p38MAPK lobe directed the specificity of response to extracellular signals, whereas the p44MAPK chimera, expressed in vivo, redirected stress signals into early mitogenic responses, demonstrating the functional independence of these domains.

摘要

有丝分裂原激活蛋白激酶(MAPK)级联反应,也称为MAPK模块,可将细胞外信号传导至特定的细胞反应。分别转导应激和生长因子信号的p38和p44 MAPK之间构建了嵌合分子。位于p38 MAPK氨基末端叶的一个40个残基的离散区域决定了对细胞外信号反应的特异性,而在体内表达的p44 MAPK嵌合体则将应激信号重定向为早期促有丝分裂反应,证明了这些结构域的功能独立性。

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