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A cytoplasmic inhibitor of the JNK signal transduction pathway

机译:JNK信号转导途径的细胞质抑制剂

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The c-Jun amino-terminal kinase (JNK) is a member of the stress-activated group of mitogen-activated protein (MAP) kinases that are implicated in the control of cell growth. A murine cytoplasmic protein that binds specifically to JNK [the JNK interacting protein-1 (JIP-1)] was characterized and cloned. JIP-1 caused cytoplasmic retention of JNK and inhibition of JNK-regulated gene expression. In addition, JIP-1 suppressed the effects of the JNK signaling pathway on cellular proliferation, including transformation by the Bcr-Abl oncogene. This analysis identifies JIP-1 as a specific inhibitor of the JNK signal transduction pathway and establishes protein targeting as a mechanism that regulates signaling by stress-activated MAP kinases.
机译:c-Jun氨基末端激酶(JNK)是有丝分裂原激活蛋白(MAP)激酶的应力激活组的成员,与细胞生长的控制有关。表征并克隆了与JNK特异性结合的鼠细胞质蛋白[JNK相互作用蛋白1(JIP-1)]。 JIP-1引起JNK的胞质保留并抑制JNK调控的基因表达。此外,JIP-1抑制了JNK信号通路对细胞增殖的影响,包括Bcr-Abl癌基因的转化。这项分析确定JIP-1是JNK信号转导途径的特异性抑制剂,并将蛋白质靶向确定为通过应激激活的MAP激酶调节信号传导的机制。

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