Abstract
This brief article will focus on the possible role of p21ras in signal transduction. There is a plethora of conflicting information as to its function in cell signaling. Earlier studies suggested that p21ras acted to couple certain membrane receptors to phospholipase C (PLC), which when activated, caused an elevation in inositol phosphates and a subsequent increase in intracellular free calcium ([Ca2+]i). However, more recent studies do not support this notion,1 and suggest that the role of p21ras maybe to alter transcription of transforming genes, thereby coupling hormone receptors to the activity of PLC. Evidence supporting this new concept will be presented.
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References
I.G. Macara, Oncogenes and cellular signal transduction, Physiological Revs 69:797–820 (1989).
M.J. Berridge and R.F. Irvine, Nature 345:142–52 (1985).
I.H. Exton and P.F. Blackmore, Calcium-mediated hormonal responses in: “Endocrinology”, L.J. DeGroot (ed.), W.B. Saunders Co., pp. 58–74 (1989).
T. Furuichi, S. Yoshikawa, A. Miyawaki, K. Wada, N. Maeda, and K. Mikoshiba, Primary structure and functional expression of the inositol 1,4,5-triphophate-binding protein PLLOO, Nature 342:32–8 (1989).
Y. Nishizuka, Studies and perspectives of protein kinase C, Science 233:305–12 (1986).
I.H. Exton, Signalling through phosphatidylcholine breakdown, J Biol Chem 265:1–4 (1990).
S.G. Rhee, Inositol phospholipid-specific phospholipase C: interaction of the γ1 isoform with tyrosine kinase, Trends Biochem Sci 16:297–301 (1991).
W J. Wasilenko, D.M. Payne, D.L. Fitzgerald, and M.J. Weber, Phosphorylation and activation of epidermal growth factor receptors in cells transformed by the src oncogene, Mol Cell Biol 11:309–21, 1991.
A.G. Gilman, G proteins: transducers of receptor-generated signals, Annu Rev Biochem 56:615–49 (1987).
W.T. Tang and A.G. Gilman, Type-specific regulation of adenylyl cyclase by G protein βγ subunits, Science 254:1500–03 (1991).
M. Strathmann and M.I. Simon, G protein diversity: A distinct class of α subunits is present in vertebrates and inverterates, Proc Natl Acad Sci USA 87:9113–17 (1990).
S.J. Taylor and I.H. Exton, Two alpha subunits of the Gq class of G proteins stimulate phosphoinositide phospholipase c-bl activity, FEBS Lett 286:214–6 (1991).
S.B. Bocckino, P.F. Blackmore, P.B. Wilson, and I.H. Exton, Phosphatidate accumulation in hormonetreated hepatocytes via a phospholipase D mechanism J. Biol Chem., 262:15309–15 (1987).
M.J. Berridge, The molecular basis of communication within the cell, Scientific American. 253:142–52 (1985).
R.J.A. Grand and D. Owen, The biochemistry of rasp21, Biochem J 279:609–31 (1991).
C.J. Marshall, The ras oncogenes, J Cell Sci Suppl. 10:157–69 (1988).
A. Hall, Ras and GAP-Who’s controlling whom?, Cell. 61:921–23 (1990).
L.C. Cantley, K.R. Auger, C. Carpenter, B. Duckworth, A. Graziani, Kapeller, and S. Soltoff, Oncogenes and signal transduction, Cell 64:281–302 (1991).
A. Yatani, K. Okabe, P. Polakis, R. Halenbeck, F. McCormick, and A.M. Brown, Ras p21 and GAP inhibit coupling of muscarinic receptors to alrial K+ channels, Cell 61:709–76 (1990).
A. Hall, The cellular functions of small GTP-binding proteins, Science 249:635–40 (1990).
H.F. Paterson, A.J. Self, M.D. Garrett, I. Just, K. Aktories, and A. Hall, Microinjection of recombinant p21rho induces rapid changes in cell morphology, J Cell Biol 111:1001–07 (1990).
G. Parries, R. Hoebel, and E. Racker, Opposing effects of a ras oncogene on growth factor stimulated phosphoinositide hydrolysis-Desansitisation to platelet-derived growth factor and enhanced sensitivity to bradykinin, Proc Natl Acad Sci USA 84:2648–52 (1987).
S.G. Oakes, P.F. Blackmore, and K.D. Somers, K-ras transformed BALB-3T3 cells express HI receptors coupled to increases in intracellular (Ca2+ not found in normal or H-ras transformed cells, FASEB J 4:A499 (1990).
S.G. Oakes, K.D. Somers, and P.F. Blackmore, Kirsten-ras transformed normal mt kidney (NRK) cells lose vasopressin receptors, FASEB J 4:A2987 (1991).
C. Wasylyk, J.C. Imler, J. Perez-Mutul and B. Wasylyk, The c-Ha-ras oncogene and a tumor promoter activates the polyoma vimus enhancer, Cell 48:525–34 (1987).
C. Wasylyk, J.C. Imler, and B. Wasylyk, Transforming but not immortalizing oncogenes activate the transcription factor PEA-1, EMBO J 7:2475–83 (1988).
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Blackmore, P.F. (1992). Role of p21ras in Hormone Signalling and Cell Growth/Transformation. In: Vinik, A.I., Sirman, D.J. (eds) Pancreatic Islet Cell Regeneration and Growth. Advances in Experimental Medicine and Biology, vol 321. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-3448-8_15
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DOI: https://doi.org/10.1007/978-1-4615-3448-8_15
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