CDC25(Mm)/Ras-GRF1 regulates both Ras and Rac signaling pathways.
The Ras-GRF1 exchange factor molecule contains in addition to the catalytic domain two pleckstrin homology (PH1 and PH2), one IQ and one Dbl homology (DH) domains. In this study we investigated the role of such additional domains. We found that a Ras-GRF1 mutant lacking PH1 and IQ domains is sufficient to activate c-fos promoter in response to lysophosphatidic acid (LPA). The same mutant did not increase external stimuli-regulated kinase ( ERK) activity, suggesting an additional mechanism for the induction of gene transcription. Isolated DH-PH2 module activates c-Jun NH(2)-terminal kinase and the c-fos promoter in response to LPA, providing the basis for an ERK-independent mechanism. These results provide evidence that Ras-GRF1 acts as a bifunctional molecule on both ERK-dependent and independent pathways.[1]References
- CDC25(Mm)/Ras-GRF1 regulates both Ras and Rac signaling pathways. Innocenti, M., Zippel, R., Brambilla, R., Sturani, E. FEBS Lett. (1999) [Pubmed]
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