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Oriented Cell Division in the C. Elegans Embryo Is Coordinated by G-Protein Signaling Dependent on the Adhesion GPCR LAT-1

Overview
Journal PLoS Genet
Specialty Genetics
Date 2015 Oct 28
PMID 26505631
Citations 55
Authors
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Abstract

Orientation of spindles and cell division planes during development of many species ensures that correct cell-cell contacts are established, which is vital for proper tissue formation. This is a tightly regulated process involving a complex interplay of various signals. The molecular mechanisms underlying several of these pathways are still incompletely understood. Here, we identify the signaling cascade of the C. elegans latrophilin homolog LAT-1, an essential player in the coordination of anterior-posterior spindle orientation during the fourth round of embryonic cell division. We show that the receptor mediates a G protein-signaling pathway revealing that G-protein signaling in oriented cell division is not solely GPCR-independent. Genetic analyses showed that through the interaction with a Gs protein LAT-1 elevates intracellular cyclic AMP (cAMP) levels in the C. elegans embryo. Stimulation of this G-protein cascade in lat-1 null mutant nematodes is sufficient to orient spindles and cell division planes in the embryo in the correct direction. Finally, we demonstrate that LAT-1 is activated by an intramolecular agonist to trigger this cascade. Our data support a model in which a novel, GPCR-dependent G protein-signaling cascade mediated by LAT-1 controls alignment of cell division planes in an anterior-posterior direction via a metabotropic Gs-protein/adenylyl cyclase pathway by regulating intracellular cAMP levels.

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References
1.
Gillies T, Cabernard C . Cell division orientation in animals. Curr Biol. 2011; 21(15):R599-609. DOI: 10.1016/j.cub.2011.06.055. View

2.
Brenner S . The genetics of Caenorhabditis elegans. Genetics. 1974; 77(1):71-94. PMC: 1213120. DOI: 10.1093/genetics/77.1.71. View

3.
Kamath R, Martinez-Campos M, Zipperlen P, Fraser A, Ahringer J . Effectiveness of specific RNA-mediated interference through ingested double-stranded RNA in Caenorhabditis elegans. Genome Biol. 2001; 2(1):RESEARCH0002. PMC: 17598. DOI: 10.1186/gb-2000-2-1-research0002. View

4.
Gotta M, Ahringer J . Distinct roles for Galpha and Gbetagamma in regulating spindle position and orientation in Caenorhabditis elegans embryos. Nat Cell Biol. 2001; 3(3):297-300. DOI: 10.1038/35060092. View

5.
Promel S, Langenhan T, Arac D . Matching structure with function: the GAIN domain of adhesion-GPCR and PKD1-like proteins. Trends Pharmacol Sci. 2013; 34(8):470-8. DOI: 10.1016/j.tips.2013.06.002. View