| Literature DB >> 8756728 |
T Nakajima1, A Fukamizu, J Takahashi, F H Gage, T Fisher, J Blenis, M R Montminy.
Abstract
We have examined the mechanism by which growth factor-mediated induction of the Ras pathway interferes with signaling via the second messenger cAMP. Activation of cellular Ras with insulin or NGF stimulated recruitment of the S6 kinase pp90RSK to the signal-dependent coactivator CBP. Formation of the pp90RSK-CBP complex occurred with high stoichiometry and persisted for 6-8 hr following growth factor addition. pp90RSK specifically recognized the E1A-binding domain of the coactivator CBP. In addition, like E1A, binding of pp90RSK to CBP was sufficient to repress transcription of cAMP-responsive genes via the cAMP-inducible factor CREB. By contrast with its effects on the cAMP pathway, formation of the pp90RSK-CBP complex was required for induction of Ras-responsive genes. These results provide a demonstration of cross-coupling between two signaling pathways that occurs at the level of a signal-dependent coactivator.Entities:
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Year: 1996 PMID： 8756728 DOI： 10.1016/s0092-8674(00)80119-1
Source DB: PubMed Journal: Cell ISSN： 0092-8674 Impact factor: 41.582