A G protein-coupled receptor phosphatase required for rhodopsin function

被引:99
作者
Vinos, J
Jalink, K
Hardy, RW
Britt, SG
Zuker, CS
机构
[1] UNIV CALIF SAN DIEGO,HOWARD HUGHES MED INST,LA JOLLA,CA 92093
[2] UNIV CALIF SAN DIEGO,DEPT NEUROSCI,LA JOLLA,CA 92093
[3] UNIV CALIF SAN DIEGO,DEPT BIOL,LA JOLLA,CA 92093
关键词
D O I
10.1126/science.277.5326.687
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Heterotrimeric guanine nucleotide-binding protein (G protein)-coupled receptors are phosphorylated by kinases that mediate agonist-dependent receptor deactivation. Although many receptor kinases have been isolated, the corresponding phosphatases, necessary for restoring the ground state of the receptor, have not been identified. Drosophila RDGC (retinal degeneration C) is a phosphatase required for rhodopsin dephosphorylation in vivo. Loss of RDGC caused severe defects in the termination of the light response as well as extensive light-dependent retinal degeneration. These phenotypes resulted from the hyperphosphorylation of rhodopsin because expression of a truncated rhodopsin lacking the phosphorylation sites restored normal photoreceptor function. These results suggest the existence of a family of receptor phosphatases involved in the regulation of G protein-coupled signaling cascades.
引用
收藏
页码:687 / 690
页数:4
相关论文
共 54 条
[1]   STRUCTURE AND FUNCTION OF RECEPTORS COUPLED TO G-PROTEINS [J].
BALDWIN, JM .
CURRENT OPINION IN CELL BIOLOGY, 1994, 6 (02) :180-190
[2]   INACTIVATION OF PHOTOEXCITED RHODOPSIN IN RETINAL RODS - THE ROLES OF RHODOPSIN KINASE AND 48-KDA PROTEIN (ARRESTIN) [J].
BENNETT, N ;
SITARAMAYYA, A .
BIOCHEMISTRY, 1988, 27 (05) :1710-1715
[3]   FUNCTIONAL DESENSITIZATION OF THE ISOLATED BETA-ADRENERGIC-RECEPTOR BY THE BETA-ADRENERGIC-RECEPTOR KINASE - POTENTIAL ROLE OF AN ANALOG OF THE RETINAL PROTEIN ARRESTIN (48-KDA PROTEIN) [J].
BENOVIC, JL ;
KUHN, H ;
WEYAND, I ;
CODINA, J ;
CARON, MG ;
LEFKOWITZ, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (24) :8879-8882
[4]   PHOSPHORYLATION OF FROG PHOTORECEPTOR MEMBRANES INDUCED BY LIGHT [J].
BOWNDS, D ;
STAHLMAN, M ;
MILLER, J ;
DAWES, J .
NATURE-NEW BIOLOGY, 1972, 237 (73) :125-&
[5]   REGULATORY ARRESTIN CYCLE SECURES THE FIDELITY AND MAINTENANCE OF THE FLY PHOTORECEPTOR CELL [J].
BYK, T ;
BARYAACOV, M ;
DOZA, YN ;
MINKE, B ;
SELINGER, Z .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (05) :1907-1911
[6]   MECHANISMS OF RHODOPSIN INACTIVATION IN-VIVO AS REVEALED BY A COOH-TERMINAL TRUNCATION MUTANT [J].
CHEN, J ;
MAKINO, CL ;
PEACHEY, NS ;
BAYLOR, DA ;
SIMON, MI .
SCIENCE, 1995, 267 (5196) :374-377
[7]   ARRESTIN FUNCTION IN INACTIVATION OF G-PROTEIN COUPLED RECEPTOR RHODOPSIN INVIVO [J].
DOLPH, PJ ;
RANGANATHAN, R ;
COLLEY, NJ ;
HARDY, RW ;
SOCOLICH, M ;
ZUKER, CS .
SCIENCE, 1993, 260 (5116) :1910-1916
[8]  
Fong TM, 1996, CELL SIGNAL, V8, P217
[9]   INTERPLAY OF PHOSPHORYLATION AND DEPHOSPHORYLATION IN VISION - PROTEIN PHOSPHATASES OF BOVINE ROD OUTER SEGMENTS [J].
FOWLES, C ;
AKHTAR, M ;
COHEN, P .
BIOCHEMISTRY, 1989, 28 (24) :9385-9391
[10]  
GUREVICH VV, 1993, J BIOL CHEM, V268, P11628