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NF1 modulates the effects of ras oncogenes: Evidence of other NF1 function besides its GAP activity
Author(s) -
Corral Teresa,
Jiménez María,
HernándezMuñoz Inmaculada,
Castro Ignacio Pérez de,
Pellicer Angel
Publication year - 2003
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.10349
Subject(s) - function (biology) , anti apoptotic ras signalling cascade , microbiology and biotechnology , biology , chemistry , signal transduction , mapk/erk pathway
Neurofibromin (NF1) (the product of Nf1 gene) is a large cytosolic protein known as a negative regulator of Ras. A fragment of some 400 residues located at the center of the NF1 GAP‐Related Domain (NF1‐GRD) has strong identity with other molecules of the GAP family, which comprises, among others, the mammalian proteins NF1 and p120GAP, and the yeast proteins IRA1 and IRA2. GAP family members are known by their ability to promote the GTPase activity of Ras proteins, facilitating the transit of those proteins to their inactive state. Recent findings (Tong et al., 2002, Nat Neurosci 5:95–96) indicate that NF1 may be involved in the regulation of adenyl cyclase activity. Our results show that NF1‐GRD cooperates with Ras in the anchorage‐independent growth capacity of Ras‐expressing fibroblasts, without affecting: (i) their ability to grow in low serum, (ii) their cellular adhesion capability, or (iii) the expression of key proteins involved in cell–cell and cell–matrix interactions. On the other hand, NF1 overexpression induces an increase in the expression levels of the focal adhesion kinase (FAK), and specific changes in the activation status of the mitogen‐activated protein kinases (MAPKs). These results suggest the existence of a Ras‐independent NF1‐dependent pathway able to modify the levels of expression of FAK and the levels of activation of MAPKs. Because FAK and many proteins recently found to bind NF1 have a role in the cytoskeleton, this pathway may involve rearrangement of cytoskeletal components that facilitate anchorage independence. J. Cell. Physiol. 197: 214–224, 2003. © 2003 Wiley‐Liss, Inc.