Role of IQGAP1, a Target of the Small GTPases Cdc42 and Rac1, in Regulation of E-Cadherin- Mediated Cell-Cell Adhesion

Shinya Kuroda(Nara Institute of Science and Technology), Masaki Fukata(Nara Institute of Science and Technology), Masato Nakagawa(Nara Institute of Science and Technology), Katsuhiko Fujii(Nara Institute of Science and Technology), Tomoko Nakamura(Nara Institute of Science and Technology), T Ookubo(Nara Institute of Science and Technology), Ichiro Izawa(Nara Institute of Science and Technology), Takahiro Nagase(Nara Institute of Science and Technology), Nobuo Nomura(Nara Institute of Science and Technology), Hideki Tani(Nara Institute of Science and Technology), Ikuo Shoji(Nara Institute of Science and Technology), Yoshiharu Matsuura(Nara Institute of Science and Technology), Shin Yonehara(Nara Institute of Science and Technology), Kozo Kaibuchi(Nara Institute of Science and Technology)
Science
August 7, 1998
Cited by 501

Abstract

The small guanosine triphosphatases (GTPases) Cdc42 and Rac1 regulate E-cadherin-mediated cell-cell adhesion. IQGAP1, a target of Cdc42 and Rac1, was localized with E-cadherin and beta-catenin at sites of cell-cell contact in mouse L fibroblasts expressing E-cadherin (EL cells), and interacted with E-cadherin and beta-catenin both in vivo and in vitro. IQGAP1 induced the dissociation of alpha-catenin from a cadherin-catenin complex in vitro and in vivo. Overexpression of IQGAP1 in EL cells, but not in L cells expressing an E-cadherin-alpha-catenin chimeric protein, resulted in a decrease in E-cadherin-mediated cell-cell adhesive activity. Thus, IQGAP1, acting downstream of Cdc42 and Rac1, appears to regulate cell-cell adhesion through the cadherin-catenin pathway.


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