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蛋白激酶B对转录因子叉头家族成员FKHR的磷酸化作用。

Phosphorylation of the transcription factor forkhead family member FKHR by protein kinase B.

作者信息

Rena G, Guo S, Cichy S C, Unterman T G, Cohen P

机构信息

Department of Biochemistry, Medical Research Council Protein Phosphorylation Unit, University of Dundee, Dundee DD1 5EH, Scotland, United Kingdom.

出版信息

J Biol Chem. 1999 Jun 11;274(24):17179-83. doi: 10.1074/jbc.274.24.17179.

DOI:10.1074/jbc.274.24.17179
PMID:10358075
Abstract

Protein kinase B lies "downstream" of phosphatidylinositide (PtdIns) 3-kinase and is thought to mediate many of the intracellular actions of insulin and other growth factors. Here we show that FKHR, a human homologue of the DAF16 transcription factor in Caenorhabditis elegans, is rapidly phosphorylated by human protein kinase Balpha (PKBalpha) at Thr-24, Ser-256, and Ser-319 in vitro and at a much faster rate than BAD, which is thought to be a physiological substrate for PKB. The same three sites, which all lie in the canonical PKB consensus sequences (Arg-Xaa-Arg-Xaa-Xaa-(Ser/Thr)), became phosphorylated when FKHR was cotransfected with either PKB or PDK1 (an upstream activator of PKB). All three residues became phosphorylated when 293 cells were stimulated with insulin-like growth factor 1 (IGF-1). The IGF-1-induced phosphorylation was abolished by the PtdIns 3-kinase inhibitor wortmannin but not by PD 98059 (an inhibitor of the mitogen-activated protein kinase cascade) or by rapamycin. These results indicate that FKHR is a physiological substrate of PKB and that it may mediate some of the physiological effects of PKB on gene expression. DAF16 is known to be a component of a signaling pathway that has been partially dissected genetically and includes homologues of the insulin/IGF-1 receptor, PtdIns 3-kinase and PKB. The conservation of Thr-24, Ser-256, and Ser-319 and the sequences surrounding them in DAF16 therefore suggests that DAF16 is also a direct substrate for PKB in C. elegans.

摘要

蛋白激酶B位于磷脂酰肌醇-3激酶(PtdIns 3-激酶)的“下游”,被认为介导胰岛素及其他生长因子的许多细胞内作用。在此我们表明,FKHR是秀丽隐杆线虫中DAF16转录因子的人类同源物,在体外它能被人类蛋白激酶Bα(PKBα)迅速磷酸化,磷酸化位点为苏氨酸-24、丝氨酸-256和丝氨酸-319,且磷酸化速率比BAD快得多,BAD被认为是PKB的生理底物。当FKHR与PKB或PDK1(PKB的上游激活剂)共转染时,位于典型PKB共有序列(精氨酸-任意氨基酸-精氨酸-任意氨基酸-任意氨基酸-(丝氨酸/苏氨酸))中的相同三个位点会发生磷酸化。当用胰岛素样生长因子1(IGF-1)刺激293细胞时,所有这三个残基都会发生磷酸化。IGF-1诱导的磷酸化被磷脂酰肌醇-3激酶抑制剂渥曼青霉素消除,但不被PD 98059(丝裂原活化蛋白激酶级联反应的抑制剂)或雷帕霉素消除。这些结果表明FKHR是PKB的生理底物,并且它可能介导PKB对基因表达的一些生理作用。已知DAF16是一个信号通路的组成部分,该信号通路已通过遗传学方法进行了部分解析,包括胰岛素/IGF-1受体、磷脂酰肌醇-3激酶和蛋白激酶B的同源物。因此,DAF16中苏氨酸-24、丝氨酸-256和丝氨酸-319及其周围序列的保守性表明,DAF16在秀丽隐杆线虫中也是PKB的直接底物。

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