TY - JOUR
T1 - Vezatin, a potential target for ADP-ribosylation factor 6, regulates the dendritic formation of hippocampal neurons
AU - Sanda, Masashi
AU - Ohara, Naoki
AU - Kamata, Akifumi
AU - Hara, Yoshinobu
AU - Tamaki, Hideaki
AU - Sukegawa, Jun
AU - Yanagisawa, Teruyuki
AU - Fukunaga, Kohji
AU - Kondo, Hisatake
AU - Sakagami, Hiroyuki
N1 - Funding Information:
We thank Dr. Kazuhisa Nakayama (Kyoto University Graduate School of Pharmaceutical Sciences) for donating the expression vectors for the ARFs and GGA1-GAT-GST fusion protein, Dr. Atsushi Miyawaki (RIKEN) for donating the Venus/pCS2+ vector, Dr. David L. Turner (University of Michigan) for donating the mU6pro vector. This work was supported by Grants-in-Aid for Scientific Research to H.S. (# 19300119 and 21659049 ) and the Private Universities Grant for Promotion of Fundamental Strategic Research from the Ministry of Education, Science, Sports, Culture, and Technology of Japan .
PY - 2010/6
Y1 - 2010/6
N2 - ADP-ribosylation factor 6 (ARF6) is a small GTPase that regulates neuronal morphogenesis processes such as axonal, dendritic, and spine formation possibly through the actin cytoskeleton and membrane trafficking. In an attempt to define the molecular mechanisms that regulate neuronal morphogenesis by ARF6, we identified vezatin as a novel binding partner of active GTP-bound ARF6 using yeast two-hybrid screening. Vezatin was able to bind specifically to GTP-ARF6 among the ARF family. In the adult mouse brain, vezatin exhibited widespread gene expression with high levels in the hippocampus and medial habenular nucleus. In hippocampal neurons, vezatin was localized at dendrites as well as cell bodies. Knockdown of endogenous vezatin significantly reduced total dendritic length and arborization of cultured hippocampal neurons, while overexpression of vezatin increased dendritic length. Our present study suggests that vezatin may regulate dendritic formation as a downstream effector of ARF6.
AB - ADP-ribosylation factor 6 (ARF6) is a small GTPase that regulates neuronal morphogenesis processes such as axonal, dendritic, and spine formation possibly through the actin cytoskeleton and membrane trafficking. In an attempt to define the molecular mechanisms that regulate neuronal morphogenesis by ARF6, we identified vezatin as a novel binding partner of active GTP-bound ARF6 using yeast two-hybrid screening. Vezatin was able to bind specifically to GTP-ARF6 among the ARF family. In the adult mouse brain, vezatin exhibited widespread gene expression with high levels in the hippocampus and medial habenular nucleus. In hippocampal neurons, vezatin was localized at dendrites as well as cell bodies. Knockdown of endogenous vezatin significantly reduced total dendritic length and arborization of cultured hippocampal neurons, while overexpression of vezatin increased dendritic length. Our present study suggests that vezatin may regulate dendritic formation as a downstream effector of ARF6.
KW - ADP-ribosylation factor
KW - Cadherin
KW - Dendrite
KW - Small GTPase
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U2 - 10.1016/j.neures.2010.02.008
DO - 10.1016/j.neures.2010.02.008
M3 - Article
C2 - 20188128
AN - SCOPUS:77952852535
SN - 0168-0102
VL - 67
SP - 126
EP - 136
JO - Neuroscience Research
JF - Neuroscience Research
IS - 2
ER -