Involvement of IQGAP family proteins in the regulation of mammalian cell cytokinesis

• Published in: Genes to cells : devoted to molecular & cellular mechanisms Vol. 19; no. 11; pp. 803 - 820
• Main Authors: Adachi, Makoto, Kawasaki, Asami, Nojima, Hisashi, Nishida, Eisuke, Tsukita, Sachiko
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.11.2014
• Subjects: Anaphase; Animals; Contractile Proteins - metabolism; Cytokines; Cytokinesis; GTPase-Activating Proteins - genetics; GTPase-Activating Proteins - metabolism; HEK293 Cells - cytology; HeLa Cells - cytology; Humans; Mammals; Proteins; Proto-Oncogene Proteins - metabolism; ras GTPase-Activating Proteins - genetics; ras GTPase-Activating Proteins - metabolism; rhoA GTP-Binding Protein - metabolism
• ISSN: 1356-9597; 1365-2443
• DOI: 10.1111/gtc.12179

IQGAP family proteins, comprising IQGAP1, ‐2, and ‐3 in mammals, are involved in diverse ranges of cellular processes such as adhesion and migration. IQGAP proteins in yeast also play important roles in cytokinesis. However, the involvement of IQGAP proteins in cytokinesis in mammals remains unaddressed. In this study, we showed that IQGAP3 specifically localized to the equatorial cortex at anaphase, whereas IQGAP1 localized to the cell cortex uniformly and IQGAP2 was unexpressed in HeLa cells. IQGAP3, but neither IQGAP1 nor ‐2, was able to interact with anillin, which was required for the localization of IQGAP3 to the contractile ring. The suppressed expression of IQGAP3 inhibited the completion of cleavage furrow ingression and led to the multinucleation of cells. The suppression of IQGAP1 also had similar inhibitory effects on cytokinesis, and the simultaneous suppression of IQGAP1 and ‐3 induced more severe effects. The localization of anillin and RhoA to the contractile ring was impaired by the suppression of IQGAP1 and ‐3, whereas their upstream regulators, the centralspindlin complex and Ect2, remained unaffected. These results suggested that mammalian IQGAP proteins may play a role in cytokinesis by regulating the localization of key cytokinesis regulatory proteins to the contractile apparatus during mitosis.