C3G localizes to mother centriole dependent on cenexin, and regulates centrosome duplication and primary cilia length

Author:

Nayak Sanjeev Chavan1ORCID,Radha Vegesna1ORCID

Affiliation:

1. CSIR-Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad – 500 007, India

Abstract

C3G (RapGEF1) plays a role in cell differentiation and is essential for early embryonic development in mice. In this study, we identify C3G as a centrosomal protein colocalizing with cenexin at the mother centriole in interphase cells. C3G interacts through its catalytic domain with cenexin, and they show interdependence for localization to the centrosome. C3G depletion caused a decrease in cellular cenexin levels. Centrosomal localization is lost as myocytes differentiate to form myotubes. Stable clone of cells depleted of C3G by CRISPR/Cas9 showed the presence of supernumerary centrioles. Overexpression of C3G, or a catalytically active deletion construct inhibited centrosome duplication. Cilia length is longer in C3G knockout cells, and the phenotype could be reverted upon reintroduction of C3G or its catalytic domain. Association of C3G with the basal body is dynamic, decreasing upon serum starvation, and increasing upon reentry into the cell cycle. C3G inhibits cilia formation and length dependent on its catalytic activity. We conclude that C3G inhibits centrosome duplication and maintains ciliary homeostasis, properties that may be important for its role in embryonic development.

Funder

Council of Scientific and Industrial Research, India

Department of Biotechnology , Ministry of Science and Technology

Publisher

The Company of Biologists

Subject

Cell Biology

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