Saltar al contenido
Merck

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

The EMBO journal (2007-05-12)
Pallavi Sachdev, Santosh Menon, David B Kastner, Jen-Zen Chuang, Ting-Yu Yeh, Cecilia Conde, Alfredo Caceres, Ching-Hwa Sung, Thomas P Sakmar
RESUMEN

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.

MATERIALES
Product Number
Marca
Descripción del producto

Sigma-Aldrich
Monoclonal Anti-Tubulin, Tyrosine antibody produced in mouse, clone TUB-1A2, ascites fluid
Sigma-Aldrich
Anti-Dynein Antibody, 74 kDa Intermediate chains, cytoplasmic, clone 74.1, clone 74.1, Chemicon®, from mouse