G protein beta gamma subunit interaction with the dynein light-chain component Tctex-1 regulates neurite outgrowth.

TitleG protein beta gamma subunit interaction with the dynein light-chain component Tctex-1 regulates neurite outgrowth.
Publication TypeJournal Article
Year of Publication2007
AuthorsSachdev P, Menon S, Kastner DB, Chuang J-Z, Yeh T-Y, Conde C, Cáceres A, Sung C-H, Sakmar TP
JournalEMBO J
Volume26
Issue11
Pagination2621-32
Date Published2007 Jun 06
ISSN0261-4189
KeywordsAmino Acid Sequence, Animals, Brain, Cells, Cultured, Dyneins, Fluorescence Polarization, GTP-Binding Protein beta Subunits, GTP-Binding Protein gamma Subunits, Immunoprecipitation, Mice, Microscopy, Fluorescence, Microtubule-Associated Proteins, Models, Molecular, Molecular Sequence Data, Neurites, Nuclear Proteins, Protein Binding, Protein Structure, Tertiary, t-Complex Genome Region
Abstract

Tctex-1, a light-chain component of the cytoplasmic dynein motor complex, can function independently of dynein to regulate multiple steps in neuronal development. However, how dynein-associated and dynein-free pools of Tctex-1 are maintained in the cell is not known. Tctex-1 was recently identified as a Gbetagamma-binding protein and shown to be identical to the receptor-independent activator of G protein signaling AGS2. We propose a novel role for the interaction of Gbetagamma with Tctex-1 in neurite outgrowth. Ectopic expression of either Tctex-1 or Gbetagamma promotes neurite outgrowth whereas interfering with their function inhibits neuritogenesis. Using embryonic mouse brain extracts, we demonstrate an endogenous Gbetagamma-Tctex-1 complex and show that Gbetagamma co-segregates with dynein-free fractions of Tctex-1. Furthermore, Gbeta competes with the dynein intermediate chain for binding to Tctex-1, regulating assembly of Tctex-1 into the dynein motor complex. We propose that Tctex-1 is a novel effector of Gbetagamma, and that Gbetagamma-Tctex-1 complex plays a key role in the dynein-independent function of Tctex-1 in regulating neurite outgrowth in primary hippocampal neurons, most likely by modulating actin and microtubule dynamics.

DOI10.1038/sj.emboj.7601716
Alternate JournalEMBO J.
PubMed ID17491591
PubMed Central IDPMC1888676
Grant ListR01 EY011307 / EY / NEI NIH HHS / United States
T32 EY007138 / EY / NEI NIH HHS / United States
EY07138 / EY / NEI NIH HHS / United States
EY11307 / EY / NEI NIH HHS / United States