The extracellular signal-regulated kinase pathway regulates the phosphorylation of 4E-BP1 at multiple sites

Herbert, Terence and Tee, A.R. and Proud, C.G. (2002) The extracellular signal-regulated kinase pathway regulates the phosphorylation of 4E-BP1 at multiple sites. Journal of Biological Chemistry, 277 (13). pp. 11591-11596. ISSN 0021-9258

Full content URL: http://www.jbc.org/content/277/13/11591.short

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The extracellular signal-regulated kinase pathway regulates the phosphorylation of 4E-BP1 at multiple sites
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Abstract

The phorbol ester, 12-O-tetradecanoylphorbol 13-acetate (TPA), a potent stimulator of Erk, leads to the phosphorylation of 4E-BP1 and its dissociation from eIF4E. In contrast to agonists such as insulin, this occurs independently of PKB activation. In this report, we investigate the mechanism by which TPA regulates 4E-BP1 phosphorylation. Treatment of HEK293 cells with TPA was found to result in the phosphorylation of 4E-BP1 at Ser64, Thr69, and Thr36/45. The TPA-stimulated phosphorylation of all these sites is sensitive to inhibitors of MEK and to the inhibitor of mTOR, rapamycin, indicating that inputs from both mTOR and MEK are required for the regulation of 4E-BP1 phosphorylation by TPA. Indeed, evidence is presented that mTOR may initially be required for the phosphorylation of Thr45 in a priming step, which is necessary for the subsequent phosphorylation of Ser64 and Thr69 through an Erk-dependent pathway. Overexpression of constitutively active MEK in HEK293 cells resulted both in the phosphorylation of 4E-BP1 at Ser64 and Thr36/45 and its release from eIF4E. In this case, the phosphorylation of these sites was also blocked by inhibitors of MEK or by rapamycin. In conclusion, the Erk pathway, via mechanisms also requiring mTOR, regulates the phosphorylation of multiple sites in 4E-BP1 in vivo and this is sufficient for the release of 4E-BP1 from eIF4E.

Additional Information:cited By 140
Keywords:extracellular, phosphorylation
Subjects:B Subjects allied to Medicine > B200 Pharmacology, Toxicology and Pharmacy
Divisions:College of Science > School of Pharmacy
ID Code:28235
Deposited On:13 Sep 2018 13:17

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