The C-elegans ric-3 gene is required for maturation of nicotinic acetylcholine receptors

被引:196
作者
Halevi, S
McKay, J
Palfreyman, M
Yassin, L
Eshel, M
Jorgensen, E
Treinin, M [1 ]
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Sch, Dept Physiol, IL-91120 Jerusalem, Israel
[2] Univ Texas, SW Med Ctr, Dept Mol Biol, Dallas, TX 75235 USA
[3] Univ Utah, Dept Biol, Salt Lake City, UT 84112 USA
关键词
biogenesis; Caenorhabditis elegans; ion channel; nicotinic acetylcholine receptor;
D O I
10.1093/emboj/21.5.1012
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
Mutations in ric-3 ((r) under bar esistant to (i) under bar nhibitors of (c) under bar holinesterase) suppress the neuronal degenerations caused by a gain of function mutation in the Caenorhabditis elegans DEG-3 acetylcholine receptor. RIC-3 is a novel protein with two transmembrane domains and extensive coiled-coil domains. It is expressed in both muscles and neurons, and the protein is concentrated within the cell bodies. We demonstrate that RIC-3 is required for the function of at least four nicotinic acetylcholine receptors. However, GABA and glutamate receptors expressed in the same cells are unaffected. In ric-3 mutants, the DEG-3 receptor accumulates in the cell body instead of in the cell processes. Moreover, co-expression of ric-3 in Xenopus laevis oocytes enhances the activity of the C.elegans DEG-3/DES-2 and of the rat alpha-7 acetylcholine receptors. Together, these data suggest that RIC-3 is specifically required for the maturation of acetylcholine receptors.
引用
收藏
页码:1012 / 1020
页数:9
相关论文
共 51 条
[1]   The genome sequence of Drosophila melanogaster [J].
Adams, MD ;
Celniker, SE ;
Holt, RA ;
Evans, CA ;
Gocayne, JD ;
Amanatides, PG ;
Scherer, SE ;
Li, PW ;
Hoskins, RA ;
Galle, RF ;
George, RA ;
Lewis, SE ;
Richards, S ;
Ashburner, M ;
Henderson, SN ;
Sutton, GG ;
Wortman, JR ;
Yandell, MD ;
Zhang, Q ;
Chen, LX ;
Brandon, RC ;
Rogers, YHC ;
Blazej, RG ;
Champe, M ;
Pfeiffer, BD ;
Wan, KH ;
Doyle, C ;
Baxter, EG ;
Helt, G ;
Nelson, CR ;
Miklos, GLG ;
Abril, JF ;
Agbayani, A ;
An, HJ ;
Andrews-Pfannkoch, C ;
Baldwin, D ;
Ballew, RM ;
Basu, A ;
Baxendale, J ;
Bayraktaroglu, L ;
Beasley, EM ;
Beeson, KY ;
Benos, PV ;
Berman, BP ;
Bhandari, D ;
Bolshakov, S ;
Borkova, D ;
Botchan, MR ;
Bouck, J ;
Brokstein, P .
SCIENCE, 2000, 287 (5461) :2185-2195
[2]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[3]  
[Anonymous], 1988, NEMATODE CAENORHABDI
[4]   THE CYCLOPHILIN HOMOLOG NINAA FUNCTIONS AS A CHAPERONE, FORMING A STABLE COMPLEX IN-VIVO WITH ITS PROTEIN TARGET RHODOPSIN [J].
BAKER, EK ;
COLLEY, NJ ;
ZUKER, CS .
EMBO JOURNAL, 1994, 13 (20) :4886-4895
[5]   Neurobiology of the Caenorhabditis elegans genome [J].
Bargmann, CI .
SCIENCE, 1998, 282 (5396) :2028-2033
[6]   PREDICTING COILED COILS BY USE SF PAIRWISE RESIDUE CORRELATIONS [J].
BERGER, B ;
WILSON, DB ;
WOLF, E ;
TONCHEV, T ;
MILLA, M ;
KIM, PS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (18) :8259-8263
[7]   BIP ASSOCIATES WITH NEWLY SYNTHESIZED SUBUNITS OF THE MOUSE MUSCLE NICOTINIC RECEPTOR [J].
BLOUNT, P ;
MERLIE, JP .
JOURNAL OF CELL BIOLOGY, 1991, 113 (05) :1125-1132
[8]  
BLUMENTHAL T, 1997, C ELEGANS, V2, P117
[9]   Calnexin-dependent enhancement of nicotinic acetylcholine receptor assembly and surface expression [J].
Chang, W ;
Gelman, MS ;
Prives, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (46) :28925-28932
[10]   DEFECTIVE INTRACELLULAR-TRANSPORT IS THE MOLECULAR-BASIS OF RHODOPSIN-DEPENDENT DOMINANT RETINAL DEGENERATION [J].
COLLEY, NJ ;
CASSILL, JA ;
BAKER, EK ;
ZUKER, CS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (07) :3070-3074