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Interaction of Rab3B with microtubule-binding protein Gas8 in NIH 3T3 cells.

作者信息

Nishimura Noriyuki, Araki Kunihiko, Shinahara Wakako, Nakano Yumiko, Nishimura Kaho, Higashio Hironori, Sasaki Takuya

机构信息

Department of Biochemistry, Institute of Health Biosciences, The University of Tokushima Graduate School, 3-18-15 Kuramoto-cho, Tokushima 770-8503, Japan.

出版信息

Arch Biochem Biophys. 2008 Jun 1;474(1):136-42. doi: 10.1016/j.abb.2008.03.032. Epub 2008 Mar 31.

DOI:10.1016/j.abb.2008.03.032
PMID:18396146
Abstract

Rab3 subfamily small G proteins (Rab3A, Rab3B, Rab3C, and Rab3D) control the regulated exocytosis in neuronal/secretory cells. Rab3B is also detected and upregulated in non-neuronal/non-secretory cells, whereas its function remains elusive. In the present study, we identified growth-arrest-specific gene 8 (Gas8), an evolutionally conserved microtubule-binding protein that is upregulated in growth-arrested NIH 3T3 cells and involved in the dynein motor regulation in flagellar/ciliary axoneme, as a novel Rab3B-binding protein using a yeast two-hybrid system. Rab3B as well as Gas8 was upregulated in growth-arrested NIH 3T3 cells and enriched in testis and lung with well-developed flagella/cilia. Gas8 was specifically interacted with the GTP-bound form of Rab3B and co-localized with Rab3B at the Golgi in NIH 3T3 cells. Furthermore, Rab3B was relocated upon expression of the Rab3B-binding domain of Gas8. These results suggest that Gas8 links Rab3B to microtubules in NIH 3T3 cells.

摘要

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