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A more recent version of this article appeared on December 7, 2001
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Papers In Press, published online ahead of print October 10, 2001
J. Biol. Chem, 10.1074/jbc.M108865200
Submitted on September 13, 2001
Revised on October 9, 2001
Accepted on October 10, 2001

Trp56 of Rac1 specifies interaction with a subset of guanine nucleotide exchange factors

Yuan Gao, Jingchuan Xing, Michel Streuli, Thomas L. Leto, and Yi Zheng

Department of Biochemistry, University of Tennessee at Memphis, Memphis, TN 38163

Corresponding Author: yzheng{at}utmem.edu

Signaling specificity of Rho GTPase pathways is achieved in part by selective interaction between members of the Dbl family guanine nucleotide exchange factors (GEFs) and their Rho GTPase substrates. For example, Trio, GEF-H1, and Tiam1 are a subset of GEFs that specifically activate Rac1 but not the closely related Cdc42. The Rac1 specificity of these GEFs appears to be governed by Rac1-GEF binding interaction. To understand the detailed mechanism underlying the GEF specificity issue, we have analyzed a panel of chimeras made between Rac1 and Cdc42 and examined a series of point mutants of Rac1 made at the switch I, switch II, and b2/b3 regions for their ability to interact with and to be activated by the GEFs. The results reveal that Rac1 residues of both the switch I and switch II regions are involved in GEF docking and GEF-mediated nucleotide disruption, because mutation of Asp38, Asn39, Gln61, Tyr64, or Arg66/Leu67 into Ala results in the loss of GEF binding whereas mutation at Tyr32, Asp65, or Leu70/Ser71 position leads to the loss of GEF catalysis while retaining the binding capability. The region between amino acids 53-72 of Rac1 is required for specific recognition and activation by the GEFs, and Trp56 in b3 appears to be the critical determinant. Introduction of Trp56 to Cdc42 renders it fully responsive to the Rac-specific GEF in vitro and in cells. Further, a polypeptide derived from the b3 region of Rac1 including the Trp56 residue serves as a specific inhibitor for Rac1 interaction with the GEFs. Taken together, these results indicate that Trp56 is the necessary and sufficient determinant of Rac1 for discrimination by the subset of Rac1-specific GEFs, and suggest that compound mimicking Trp56 action could be explored as interfering reagent specifically targeting Rac1 activation.


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