Normal p21N-ras couples bombesin and other growth factor receptors to inositol phosphate production

• DOI: 10.1038/323173a0
• Publication Date: 2004-11-18T05:39:18Z
• Authors: Michael J. O. Wak...; Shireen A. Davies; Miles D. Houslay; Ian McKay; Christopher J. Ma...; Alan Hall
• Keywords: 0303 health sciences; Dose-Response Relationship, Drug; Inositol Phosphates; Receptors, Cell Surface; Dexamethasone; Cell Line; ErbB Receptors; Mice; 03 medical and health sciences; GTP-Binding Proteins; Proto-Oncogenes; Animals; Bombesin; Sugar Phosphates; Growth Substances; Cell Division

Many receptors, in response to ligand activation, trigger inositol phospholipid breakdown, which leads to rapid intracellular responses. The sustained activation of this pathway is believed to be at least one of the factors involved in the stimulation of cell growth and there has been much speculation that certain oncogenes use this pathway to effect uncontrolled cellular proliferation. It has been suggested, by analogy with the receptor-mediated control of adenylate cyclase, that the receptor stimulation of inositol phospholipid metabolism is mediated through a guanine nucleotide regulatory protein (G-protein) called Gp (or Np). Although such a species has not been identified, there is now strong experimental evidence that this process is mediated by a G-protein distinct from the stimulatory and inhibitory G-proteins (Gs and Gi, respectively). The ras genes code for a plasma membrane protein, p21, whose only known biochemical property is a high-affinity GTPase activity. We show here that the expression of normal p21N-ras in NIH 3T3 fibroblasts leads to the coupling of certain growth factor receptors to stimulated inositol phosphate production. We propose that the N-ras proto-oncogene encodes a protein which couples the receptors for certain growth factors to the stimulation of phospholipase C. Thus, N-ras p21 may be the putative Gp or a functionally related protein.