Cdc42, Rac1, and their effector IQGAP1 as molecular switches for cadherin-mediated cell-cell adhesion

Citation
S. Kuroda et al., Cdc42, Rac1, and their effector IQGAP1 as molecular switches for cadherin-mediated cell-cell adhesion, BIOC BIOP R, 262(1), 1999, pp. 1-6
Citations number
62
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN journal
0006291X → ACNP
Volume
262
Issue
1
Year of publication
1999
Pages
1 - 6
Database
ISI
SICI code
0006-291X(19990819)262:1<1:CRATEI>2.0.ZU;2-Q
Abstract
Cell-cell adhesion is a dynamic process in various cellular and development al situations. Cadherins, well-known Ca2+-dependent adhesion molecules, are thought to play a major role in the regulation of cell-cell adhesion. Howe ver, the molecular mechanism underlying the rearrangement of cadherin-media ted cell-cell adhesion is largely unknown. Cdc42 and Rad, belonging to the Rho small GTPase family, have recently been shown to be involved in the reg ulation of cell-cell adhesion. In addition, IQGAP1, an effector for Cdc42 a nd Rad, has been shown to regulate the cadherin function through interactio n with beta-catenin, a molecule associated with cadherin. In this review, w e will summarize the mode of action of Cdc42 and Rad as well as IQGAP1 as m olecular switches for the cadherin function, and then discuss physiological processes in which the Cdc42/Rac1/IQGAP1 system may be involved. (C) 1999 Academic Press.