Palmitoylation regulates plasma membrane-nuclear shuttling of R7BP, a novel membrane anchor for the RGS7 family

被引:116
作者
Drenan, RM
Doupnik, CA
Boyle, MP
Muglia, LJ
Huettner, JE
Linder, ME
Blumer, KJ [1 ]
机构
[1] Washington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[3] Univ S Florida, Coll Med, Dept Physiol & Biophys, Tampa, FL 33612 USA
关键词
D O I
10.1083/jcb.200502007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The RGS7 (R7) family of RGS proteins bound to the divergent G beta subunit G beta 5 is a crucial regulator of G protein - coupled receptor ( GPCR) signaling in the visual and nervous systems. Here, we identify R7BP, a novel neuronally expressed protein that binds R7-G beta 5 complexes and shuttles them between the plasma membrane and nucleus. Regional expression of R7BP, G beta 5, and R7 isoforms in brain is highly coincident. R7BP is palmitoylated near its COOH terminus, which targets the protein to the plasma membrane. Depalmitoylation of R7BP translocates R7BP-R7-G beta 5 complexes from the plasma membrane to the nucleus. Compared with non-palmitoylated R7BP, palmitoylated R7BP greatly augments the ability of RGS7 to attenuate GPCR-mediated G protein regulated inward rectifying potassium channel activation. Thus, by controlling plasma membrane nuclear - shuttling of R7BP-R7-G beta 5 complexes, reversible palmitoylation of R7BP provides a novel mechanism that regulates GPCR signaling and potentially transduces signals directly from the plasma membrane to the nucleus.
引用
收藏
页码:623 / 633
页数:11
相关论文
共 60 条
[1]   Regulators of G-protein signaling form a quaternary complex with the agonist, receptor, and G-protein - A novel explanation for the acceleration of signaling activation kinetics [J].
Benians, A ;
Nobles, M ;
Hosny, S ;
Tinker, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (14) :13383-13394
[2]   GAIP and RGS4 are GTPase-activating proteins for the G(i) subfamily of G protein alpha subunits [J].
Berman, DM ;
Wilkie, TM ;
Gilman, AG .
CELL, 1996, 86 (03) :445-452
[3]   Brain-specific RGS9-2 is localized to the nucleus via its unique proline-rich domain [J].
Bouhamdan, M ;
Michelhaugh, SK ;
Calin-Jageman, I ;
Ahern-Djamali, S ;
Bannon, MJ .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2004, 1691 (2-3) :141-150
[4]   RGS9-2 modulates D2 dopamine receptor-mediated Ca2+ channel inhibition in rat striatal cholinergic interneurons [J].
Cabrera-Vera, TM ;
Hernandez, S ;
Earls, LR ;
Medkova, M ;
Sundgren-Andersson, AK ;
Surmeier, DJ ;
Hamm, HE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (46) :16339-16344
[5]   Molecular neurobiology of drug addiction [J].
Chao, J ;
Nestler, EJ .
ANNUAL REVIEW OF MEDICINE, 2004, 55 :113-132
[6]   Human RGS6 gene structure, complex alternative splicing, and role of N terminus and G protein γ-subunit-like (GGL) domain in subcellular localization of RGS6 splice variants [J].
Chatterjee, TK ;
Liu, ZY ;
Fisher, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (32) :30261-30271
[7]   Slowed recovery of rod photoresponse in mice lacking the GTPase accelerating protein RGS9-1 [J].
Chen, CK ;
Burns, ME ;
He, W ;
Wensel, TG ;
Baylor, DA ;
Simon, MI .
NATURE, 2000, 403 (6769) :557-560
[8]   Instability of GGL domain-containing RGS proteins in mice lacking the G protein β-subunit Gβ5 [J].
Chen, CK ;
Eversole-Cire, P ;
Zhang, HK ;
Mancino, V ;
Chen, YJ ;
He, W ;
Wensel, TG ;
Simon, MI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (11) :6604-6609
[9]   Evidence that the nucleotide exchange and hydrolysis cycle of G proteins causes acute desensitization of G-protein gated inward rectifier K+ channels [J].
Chuang, HH ;
Yu, M ;
Jan, YN ;
Jan, LY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (20) :11727-11732
[10]  
Cowan CW, 2001, PROG NUCLEIC ACID RE, V65, P341