Wang, Xuemin, Flynn, Andrea, Waskiewicz, Andrew J., Webb, Benjamin L. J., Vries, Robert G., Baines, Ian A., Cooper, Jonathan A., Proud, Christopher G. (1998) The phosphorylation of eukaryotic initiation factor eIF4E in response to phorbol esters, cell stresses, and cytokines is mediated by distinct MAP kinase pathways. Journal of Biological Chemistry, 273 (16). pp. 9373-9377. ISSN 0021-9258. (doi:10.1074/jbc.273.16.9373) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:17252)
The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided. | |
Official URL: https://doi.org/10.1074/jbc.273.16.9373 |
Abstract
Initiation factor eIF4E binds to the 5'-cap of eukaryotic mRNAs and plays a key role in the mechanism and regulation of translation. It may be regulated through its own phosphorylation and through inhibitory binding proteins (4E-BPs), which modulate its availability for initiation complex assembly. eIF4E phosphorylation is enhanced by phorbol esters. We show, using specific inhibitors, that this involves both the p38 mitogen-activated protein (MAP) kinase and Erk signaling pathways. Cell stresses such as arsenite and anisomycin and the cytokines tumor necrosis factor-alpha and interleukin-1 beta also cause increased phosphorylation of eIF4E, which is abolished by the specific p38 MAP kinase inhibitor, SB203580. These changes in eIF4E phosphorylation parallel the activity of the eIF4E kinase, Mnk1. However other stresses such as heat shock, sorbitol, and H2O2, which also stimulate p38 MAP kinase and increase Mnk1 activity, do not increase phosphorylation of eIF4E. The latter stresses increase the binding of eIF4E to 4E-BP1, and me show that this blocks the phosphorylation of eIF4E by Mnk1 in vitro, which may explain the absence of an increase in eIF4E phosphorylation under these conditions.
Item Type: | Article |
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DOI/Identification number: | 10.1074/jbc.273.16.9373 |
Subjects: |
Q Science Q Science > QP Physiology (Living systems) > QP517 Biochemistry Q Science > QP Physiology (Living systems) > QP506 Molecular biology |
Divisions: | Divisions > Division of Natural Sciences > Biosciences |
Depositing User: | Tara Puri |
Date Deposited: | 27 May 2009 10:33 UTC |
Last Modified: | 09 Mar 2023 11:31 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/17252 (The current URI for this page, for reference purposes) |
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