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PHAS-I作为丝裂原活化蛋白激酶与翻译起始之间的连接物。

PHAS-I as a link between mitogen-activated protein kinase and translation initiation.

作者信息

Lin T A, Kong X, Haystead T A, Pause A, Belsham G, Sonenberg N, Lawrence J C

机构信息

Department of Molecular Biology and Pharmacology, Washington University School of Medicine, St. Louis, MO 63110.

出版信息

Science. 1994 Oct 28;266(5185):653-6. doi: 10.1126/science.7939721.

Abstract

PHAS-I is a heat-stable protein (relative molecular mass approximately 12,400) found in many tissues. It is rapidly phosphorylated in rat adipocytes incubated with insulin or growth factors. Nonphosphorylated PHAS-I bound to initiation factor 4E (eIF-4E) and inhibited protein synthesis. Serine-64 in PHAS-I was rapidly phosphorylated by mitogen-activated (MAP) kinase, the major insulin-stimulated PHAS-I kinase in adipocyte extracts. Results obtained with antibodies, immobilized PHAS-I, and a messenger RNA cap affinity resin indicated that PHAS-I did not bind eIF-4E when serine-64 was phosphorylated. Thus, PHAS-I may be a key mediator of the stimulation of protein synthesis by the diverse group of agents and stimuli that activate MAP kinase.

摘要

PHAS-I是一种在许多组织中发现的热稳定蛋白(相对分子质量约为12400)。在与胰岛素或生长因子一起孵育的大鼠脂肪细胞中,它会迅速被磷酸化。未磷酸化的PHAS-I与起始因子4E(eIF-4E)结合并抑制蛋白质合成。PHAS-I中的丝氨酸-64被丝裂原活化(MAP)激酶迅速磷酸化,MAP激酶是脂肪细胞提取物中主要的胰岛素刺激的PHAS-I激酶。用抗体、固定化的PHAS-I和信使核糖核酸帽亲和树脂获得的结果表明,当丝氨酸-64被磷酸化时,PHAS-I不与eIF-4E结合。因此,PHAS-I可能是激活MAP激酶的多种因子和刺激物刺激蛋白质合成的关键介质。

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