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Publication — IRIC

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

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.

Publication date
October 8, 2007
Principal Investigators
Couwenbergs C, Labbé J, Goulding M, Marty T, Bowerman B, Gotta M
PubMed reference
J. Cell Biol. 2007;179(1):15-22
PubMed ID
17908918
Affiliation
ETH Zurich, Institute of Biochemistry, 8093 Zurich, Switzerland.