Heterotrimeric G protein signaling functions with dynein to promote spindle positioning in C. elegans

Author:

Couwenbergs Claudia1,Labbé Jean-Claude1,Goulding Morgan2,Marty Thomas1,Bowerman Bruce2,Gotta Monica13

Affiliation:

1. ETH Zurich, Institute of Biochemistry, 8093 Zurich, Switzerland

2. Institute of Molecular Biology, University of Oregon, Eugene, OR 97403

3. Department of Genetic Medicine and Development, University of Geneva School of Medicine, 1211 Geneva, Switzerland

Abstract

Proper orientation and positioning of the mitotic spindle is essential for the correct segregation of fate determinants during asymmetric cell division. Although heterotrimeric G proteins and their regulators are essential for spindle positioning in many cell types, their mechanism of action remains unclear. In this study, we show that dyrb-1, which encodes a dynein light chain, provides a functional link between heterotrimeric G protein signaling and dynein activity during spindle positioning in Caenorhabditis elegans. Embryos depleted of dyrb-1 display phenotypes similar to a weak loss of function of dynein activity, indicating that DYRB-1 is a positive regulator of dynein. We find that the depletion of dyrb-1 enhances the spindle positioning defect of weak loss of function alleles of two regulators of G protein signaling, LIN-5 and GPR-1/2, and that DYRB-1 physically associates with these two proteins. These results indicate that dynein activity functions with regulators of G protein signaling to regulate common downstream effectors during spindle positioning in the early C. elegans embryo.

Publisher

Rockefeller University Press

Subject

Cell Biology

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