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早期即刻基因产物对ERK信号持续时间的分子解读

Molecular interpretation of ERK signal duration by immediate early gene products.

作者信息

Murphy Leon O, Smith Sallie, Chen Rey-Huei, Fingar Diane C, Blenis John

机构信息

Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, MA 02115, USA.

出版信息

Nat Cell Biol. 2002 Aug;4(8):556-64. doi: 10.1038/ncb822.

Abstract

The duration of intracellular signalling is associated with distinct biological responses, but how cells interpret differences in signal duration are unknown. We show that the immediate early gene product c-Fos functions as a sensor for ERK1 (extracellular-signal-regulated kinase 1) and ERK2 signal duration. When ERK activation is transient, its activity declines before the c-Fos protein accumulates, and under these conditions c-Fos is unstable. However, when ERK signalling is sustained, c-Fos is phosphorylated by still-active ERK and RSK (90K-ribosomal S6 kinase). Carboxy-terminal phosphorylation stabilizes c-Fos and primes additional phosphorylation by exposing a docking site for ERK, termed the FXFP (DEF) domain. Mutating the DEF domain disrupts the c-Fos sensor and c-Fos-mediated signalling. Other immediate early gene products that control cell cycle progression, neuronal differentiation and circadium rhythms also contain putative DEF domains, indicating that multiple sensors exist for sustained ERK signalling. Together, our data identify a general mechanism by which cells can interpret differences in ERK activation kinetics.

摘要

细胞内信号传导的持续时间与不同的生物学反应相关,但细胞如何解读信号持续时间的差异尚不清楚。我们发现,即早基因产物c-Fos可作为细胞外信号调节激酶1(ERK1)和细胞外信号调节激酶2(ERK2)信号持续时间的传感器。当ERK激活是短暂的时,其活性在c-Fos蛋白积累之前就会下降,在这些条件下c-Fos是不稳定的。然而,当ERK信号持续存在时,c-Fos会被仍具有活性的ERK和90K核糖体S6激酶(RSK)磷酸化。羧基末端磷酸化使c-Fos稳定,并通过暴露一个ERK对接位点(称为FXFP(DEF)结构域)引发额外的磷酸化。突变DEF结构域会破坏c-Fos传感器和c-Fos介导的信号传导。其他控制细胞周期进程、神经元分化和昼夜节律的即早基因产物也含有推定的DEF结构域,这表明存在多种持续ERK信号的传感器。总之,我们的数据确定了一种细胞可以解读ERK激活动力学差异的通用机制。

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