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Intracellular mechanism by which genotoxic stress activates yeast SAPK Mpk1

机译:基因毒性应激激活酵母SAPK Mpk1的细胞内机制

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摘要

Stress-activated MAP kinases (SAPKs) respond to a wide variety of stressors. In most cases, the pathways through which specific stress signals are transmitted to the SAPKs are not known. The Saccharomyces cerevisiae SAPK Mpk1 (Slt2) is a well-characterized component of the cell-wall integrity (CWI) signaling pathway, which responds to physical and chemical challenges to the cell wall. However, Mpk1 is also activated in response to genotoxic stress through an unknown pathway. We show that, in contrast to cell-wall stress, the pathway for Mpk1 activation by genotoxic stress does not involve the stimulation of the MAP kinase kinases (MEKs) that function immediately upstream of Mpk1. Instead, DNA damage activates Mpk1 through induction of proteasomal degradation of Msg5, the dual-specificity protein phosphatase principally responsible for maintaining Mpk1 in a low-activity state in the absence of stress. Blocking Msg5 degradation in response to genotoxic stress prevented Mpk1 activation. This work raises the possibility that other Mpk1-activating stressors act intracellularly at different points along the canonical Mpk1 activation pathway.
机译:应激激活的MAP激酶(SAPK)对多种应激源都有反应。在大多数情况下,将特定应力信号传递到SAPK的途径尚不清楚。酿酒酵母SAPK Mpk1(Slt2)是细胞壁完整性(CWI)信号传导途径的一个特征鲜明的组成部分,可响应对细胞壁的物理和化学挑战。但是,Mpk1也通过未知途径响应遗传毒性应激而被激活。我们显示,与细胞壁应激相反,通过基因毒性应激激活Mpk1的途径不涉及对Mpk1上游功能起作用的MAP激酶激酶(MEKs)的刺激。相反,DNA损伤通过诱导蛋白酶体降解Msg5来激活Mpk1,Msg5是双重特异性蛋白磷酸酶,主要负责在没有压力的情况下将Mpk1维持在低活性状态。响应于遗传毒性胁迫而阻止Msg5降解可阻止Mpk1激活。这项工作提高了其他Mpk1激活应激源在细胞内沿经典Mpk1激活途径在不同点起作用的可能性。

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