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ras effector loop mutations that dissociate p120GAP and neurofibromin interactions
Author(s) -
Stang Stacey,
Bottorff Drell,
Stone James C.
Publication year - 1996
Publication title -
molecular carcinogenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.254
H-Index - 97
eISSN - 1098-2744
pISSN - 0899-1987
DOI - 10.1002/(sici)1098-2744(199601)15:1<64::aid-mc9>3.0.co;2-s
Subject(s) - neurofibromin 1 , effector , biology , gene product , plasmid , gtpase activating protein , gtpase , microbiology and biotechnology , gtp' , mutation , gene , genetics , signal transduction , gene expression , biochemistry , g protein , enzyme
ras proteins are positively regulated by nucleotide exchange factors and negatively regulated by GTPase‐activating proteins (GAPs). Two GAPs have been found in mammalian cells, p120GAP and neurofibromin, the product of the type 1 neurofibromatosis ( NF1 ) gene. A library of substitutions in the effector loop region of ras in an Escherichia coli plasmid expression system was screened for c‐Ha‐ ras species with altered GAP interactions. Several substitutions preferentially disrupted the interaction of ras with p120GAP as compared with the interaction with the recombinant GAP‐related domain of neurofibromin (NF1‐GRD). The most extreme example, Tyr32His, encoded a ras species that was unaffected by p120GAP but was stimulated normally by NF1‐GRD. Tyr32His was weakly transforming in Rat2 cells. Tyr32His ras was primarily GDP‐bound in quiescent Rat2 cells, although it rapidly associated with GTP after treatment of cells with epidermal growth factor. These results show that the NF1 product has less stringent requirements than p120GAP for ras effector domain structure and that negative regulation of ras can be achieved in rat fibroblasts by the product of NF1 . © 1996 Wiley‐Liss, Inc.