Akt phosphorylates the Yes-associated protein, YAP, to induce interaction with 14-3-3 and attenuation of p73-mediated apoptosis

被引:897
作者
Basu, S
Totty, NF
Irwin, MS
Sudol, M
Downward, J
机构
[1] Canc Res UK, London Res Inst, Signal Transduct Lab, London WC2A 3PX, England
[2] Canc Res UK, London Res Inst, Prot Sequencing Lab, London WC2A 3PX, England
[3] Hosp Sick Children, Div Hematol Oncol, Toronto, ON M5G 1X8, Canada
[4] CUNY Mt Sinai Sch Med, Dept Biochem & Mol Biol, New York, NY 10029 USA
关键词
D O I
10.1016/S1097-2765(02)00776-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
We have used an affinity purification method to identify substrates of protein kinase B/Akt. One protein that associates with 14-3-3 in an Akt-dependent manner is shown here to be the Yes-associated protein (YAP), which is phosphorylated by Akt at serine 127, leading to binding to 14-3-3. Akt promotes YAP localization to the cytoplasm, resulting in loss from the nucleus where it functions as a coactivator of transcription factors including p73. p73-mediated induction of Bax expression following DNA damage requires YAP function and is attenuated by Akt phosphorylation of YAP. YAP overexpression increases, while YAP depletion decreases, p73-mediated apoptosis following DNA damage, in an Akt inhibitable manner. Akt phosphorylation of YAP may thus suppress the induction of the proapoptotic gene expression response following cellular damage.
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页码:11 / 23
页数:13
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