Guanylate cyclase-activating proteins: structure, function, and diversity

被引:74
作者
Palczewski, K [1 ]
Sokal, I
Baehr, W
机构
[1] Univ Washington, Dept Ophthalmol, Seattle, WA 98195 USA
[2] Univ Washington, Dept Pharmacol, Seattle, WA 98195 USA
[3] Univ Washington, Dept Chem, Seattle, WA 98195 USA
[4] Univ Utah, Dept Biol, Salt Lake City, UT 84112 USA
[5] Univ Utah, Dept Ophthalmol, Salt Lake City, UT 84112 USA
[6] Univ Utah, Dept Neurobiol & Anat, Salt Lake City, UT 84112 USA
关键词
guanylate cyclase; guanylate cyclase-activating proteins; phototransduction; Ca2+-binding proteins; rod and cone photoreceptors;
D O I
10.1016/j.bbrc.2004.07.122
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
The guanylate cyclase-activating proteins (GCAPs), Ca2+-binding proteins of the calmodulin gene superfamily, function as regulators of photoreceptor guanylate cyclases. In contrast to calmodulin, which is active in the Ca2+-bound form, GCAPs stimulate GCs in the [Ca2+]-free form and inhibit GCs upon Ca2+ binding. In vertebrate retinas, at least two GCAP1 and two GCs are present, a third GCAP3 is expressed in humans and fish, and at least five additional GCAP4-8 genes have been identified or are predicted in zebrafish and pufferfish. Missense mutations in GCAP1 (Y99C, I143NT, E155G, and P50L) have been associated with autosomal dominant cone dystrophy. Absence of GCAP1/2 in mice delays recovery of the photoresponse, a phenotype consistent with delay in cGMP synthesis. In the absence of GCAP2, GCAP1 supports the generation of wild-type flash responses in both rod and cone cells. Recent progress revealed an unexpected complexity of the GC-GCAP system, pointing, out a number of unsolved questions. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1123 / 1130
页数:8
相关论文
共 64 条
[1]   SECONDARY STRUCTURE OF MYRISTOYLATED RECOVERIN DETERMINED BY 3-DIMENSIONAL HETERONUCLEAR NMR - IMPLICATIONS FOR THE CALCIUM MYRISTOYL SWITCH [J].
AMES, JB ;
TANAKA, T ;
STRYER, L ;
IKURA, M .
BIOCHEMISTRY, 1994, 33 (35) :10743-10753
[2]   AMINO-TERMINAL MYRISTOYLATION INDUCES COOPERATIVE CALCIUM-BINDING TO RECOVERIN [J].
AMES, JB ;
PORUMB, T ;
TANAKA, T ;
IKURA, M ;
STRYER, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (09) :4526-4533
[3]   Three-dimensional structure of guanylyl cyclase activating protein-2, a calcium-sensitive modulator of photoreceptor guanylyl cyclases [J].
Ames, JB ;
Dizhoor, AM ;
Ikura, M ;
Palczewski, K ;
Stryer, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (27) :19329-19337
[4]   Molecular mechanics of calcium-myristoyl switches [J].
Ames, JB ;
Ishima, R ;
Tanaka, T ;
Gordon, JI ;
Stryer, L ;
Ikura, M .
NATURE, 1997, 389 (6647) :198-202
[5]   CALMODULIN STRUCTURE REFINED AT 1.7 ANGSTROM RESOLUTION [J].
CHATTOPADHYAYA, R ;
MEADOR, WE ;
MEANS, AR ;
QUIOCHO, FA .
JOURNAL OF MOLECULAR BIOLOGY, 1992, 228 (04) :1177-1192
[6]  
Dizhoor A, 2002, ADV EXP MED BIOL, V514, P291
[7]   Constitutive activation of photoreceptor guanylate cyclase by Y99C mutant of GCAP-1 - Possible role in causing human autosomal dominant cone degeneration [J].
Dizhoor, AM ;
Boikov, SG ;
Olshevskaya, EV .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (28) :17311-17314
[8]   CLONING, SEQUENCING, AND EXPRESSION OF A 24-KDA CA2+-BINDING PROTEIN ACTIVATING PHOTORECEPTOR GUANYLYL CYCLASE [J].
DIZHOOR, AM ;
OLSHEVSKAYA, EV ;
HENZEL, WJ ;
WONG, SC ;
STULTS, JT ;
ANKOUDINOVA, I ;
HURLEY, JB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (42) :25200-25206
[9]   Regulation of cGMP synthesis in photoreceptors: role in signal transduction and congenital diseases of the retina [J].
Dizhoor, AM .
CELLULAR SIGNALLING, 2000, 12 (11-12) :711-719
[10]   THE HUMAN PHOTORECEPTOR MEMBRANE GUANYLYL CYCLASE, RETGC, IS PRESENT IN OUTER SEGMENTS AND IS REGULATED BY CALCIUM AND A SOLUBLE ACTIVATOR [J].
DIZHOOR, AM ;
LOWE, DG ;
OLSHEVSKAYA, EV ;
LAURA, RP ;
HURLEY, JB .
NEURON, 1994, 12 (06) :1345-1352