Centrins in retinal photoreceptor cells:: Regulators in the connecting cilium

被引:69
作者
Trojan, Philipp [1 ]
Krauss, Norbert [2 ]
Choe, Hui-Woog [3 ,4 ]
Giessl, Andreas [1 ]
Pulvermueller, Alexander [3 ]
Wolfrum, Uwe [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Inst Zool, D-55099 Mainz, Germany
[2] Univ London, Sch Biol & Chem Sci, London E1 4NS, England
[3] Humboldt Univ, Inst Med Phys & Biophys, Univ Klinikum Charite, D-10098 Berlin, Germany
[4] Chonbuk Natl Univ, Dept Chem, Coll Nat Sci, Chonju 561756, South Korea
关键词
Ca(2+)-binding proteins; centrins; retina; photoreceptor cells; transducin; light-dependent translocation;
D O I
10.1016/j.preteyeres.2008.01.003
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Changes in the intracellular Ca(2+) concentration regulate the visual signal transduction cascade directly or more often indirectly through Ca(2+)-binding proteins. Here we focus on centrins, which are members of a highly conserved subgroup of the EF-hand superfamily of Ca(2+)-binding proteins in photoreceptor cells of the vertebrate retina. Centrins are commonly associated with centrosome-related structures. In mammalian retinal photoreceptor cells, four centrin isoforms are expressed as prominent components in the connecting cilium linking the light-sensitive outer segment compartment with the metabolically active inner segment compartment. Our data indicate that Ca(2+)-activated centrin isoforms assemble into protein complexes with the visual heterotrimeric G-protein transducin. This interaction of centrins with transducin is mediated by binding to the beta gamma-dimer of the heterotrimeric G-protein. More recent findings show that these interactions of centrins with transducin are reciprocally regulated via site-specific phosphorylations mediated by the protein kinase CK2. The assembly of centrin/G-protein complexes is a novel aspect of translocation regulation of signalling proteins in sensory cells, and represents a potential link between molecular trafficking and signal transduction in general. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:237 / 259
页数:23
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