nRap GEP: A novel neural GDP/GTP exchange protein for Rap1 small G protein that interacts with synaptic scaffolding molecule (S-SCAM)

被引:90
作者
Ohtsuka, T
Hata, Y
Ide, N
Yasuda, T
Inoue, E
Inoue, T
Mizoguchi, A
Takai, Y
机构
[1] Osaka Univ, Fac Med, Grad Sch Med, Dept Mol Biol & Biochem, Suita, Osaka 5650871, Japan
[2] JCR Pharmaceut Co Ltd, ERATO, Takai Biotimer Project, Japan Sci & Technol Corp,Nishi Ku, Kobe, Hyogo 6512241, Japan
[3] Tokyo Med & Dent Univ, Dept Med Biochem, Bunkyo Ku, Tokyo 1138519, Japan
[4] Kyoto Univ, Grad Sch, Dept Anat & Neurobiol, Kyoto 6068315, Japan
关键词
D O I
10.1006/bbrc.1999.1619
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Synaptic scaffolding molecule (S-SCAM) has six PDZ domains through which it interacts with N-methyl-D-aspartate receptors and neuroligin at synaptic junctions. We isolated here a novel S-SCAM-binding protein. This protein has one PDZ, one Ras association, one Ras GDP/GTP exchange protein (Ras GEP) domain, and one C-terminal consensus motif for binding to PDZ domains. We named it nRap GEP (neural Rap GEP). nRap GEP moreover has an incomplete cyclic AMP (cAMP)-binding (CAB) domain. The domain organization of nRap GEP is similar to that of Epac/cAMP-guanine nucleotide exchange factor (GEF) I, except that Epac/cAMP-GEFI has complete CAB and Ras GEP domains but lacks the other two domains and the C-terminal motif. nRap GEP showed GEP activity for Rap1 but did not bind cAMP, nRap GEP was specifically expressed in rat brain. Immunohistochemical analysis revealed that nRap GEP and S-SCAM were localized at synaptic areas of the cerebellum. These results suggest that nRap GEP is a novel neural Rap1-specific GEP which is associated with S-SCAM. (C) 1999 Academic Press.
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页码:38 / 44
页数:7
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