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Dia1 and IQGAP1 interact in cell migration and phagocytic cup formation.

ABSTRACT: The Diaphanous-related formin Dia1 nucleates actin polymerization, thereby regulating cell shape and motility. Mechanisms that control the cellular location of Dia1 to spatially define actin polymerization are largely unknown. In this study, we identify the cytoskeletal scaffold protein IQGAP1 as a Dia1-binding protein that is necessary for its subcellular location. IQGAP1 interacts with Dia1 through a region within the Diaphanous inhibitory domain after the RhoA-mediated release of Dia1 autoinhibition. Both proteins colocalize at the front of migrating cells but also at the actin-rich phagocytic cup in macrophages. We show that IQGAP1 interaction with Dia1 is required for phagocytosis and phagocytic cup formation. Thus, we identify IQGAP1 as a novel component involved in the regulation of phagocytosis by mediating the localization of the actin filament nucleator Dia1.

SUBMITTER: Brandt DT

PROVIDER: S-EPMC2064439 | biostudies-literature | 2007 Jul

REPOSITORIES: biostudies-literature

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Dia1 and IQGAP1 interact in cell migration and phagocytic cup formation.

Brandt Dominique T DT Marion Sabrina S Griffiths Gareth G Watanabe Takashi T Kaibuchi Kozo K Grosse Robert R

The Journal of cell biology 20070709 2

The Diaphanous-related formin Dia1 nucleates actin polymerization, thereby regulating cell shape and motility. Mechanisms that control the cellular location of Dia1 to spatially define actin polymerization are largely unknown. In this study, we identify the cytoskeletal scaffold protein IQGAP1 as a Dia1-binding protein that is necessary for its subcellular location. IQGAP1 interacts with Dia1 through a region within the Diaphanous inhibitory domain after the RhoA-mediated release of Dia1 autoinh ...[more]

PMID: 17620407

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