Regulation of light-dependent Gqα translocation and morphological changes in fly photoreceptors

被引:59
作者
Kosloff, M
Elia, N
Joel-Almagor, T
Timberg, R
Zars, TD
Hyde, DR
Minke, B
Selinger, Z [1 ]
机构
[1] Hebrew Univ Jerusalem, Inst Life Sci, Dept Biol Chem, IL-91904 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Inst Life Sci, Kuhne Minerva Ctr Studies Visual Transduct, IL-91904 Jerusalem, Israel
[3] Hebrew Univ Jerusalem, Dept Phys, IL-91120 Jerusalem, Israel
[4] Hebrew Univ Jerusalem, Kuhne Minerva Ctr Studies Visual Transduct, IL-91120 Jerusalem, Israel
[5] Univ Notre Dame, Dept Biol Sci, Notre Dame, IN 46556 USA
关键词
G-protein; localization; membrane attachment; rhabdomere; vision;
D O I
10.1093/emboj/cdg054
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
Heterotrimeric G-proteins relay signals between membrane-bound receptors and downstream effectors. Little is known, however, about the regulation of Galpha subunit localization within the natural endogenous environment of a specialized signaling cell. Here we show, using live Drosophila flies, that light causes massive and reversible translocation of the visual Gqalpha to the cytosol, associated with marked architectural changes in the signaling compartment. Molecular genetic dissection together with detailed kinetic analysis enabled us to characterize the translocation cycle and to unravel how signaling molecules that interact with Gqalpha affect these processes. Epistatic analysis showed that Gqalpha is necessary but not sufficient to bring about the morphological changes in the signaling organelle. Furthermore, mutant analysis indicated that Gqbeta is essential for targeting of Gqalpha to the membrane and suggested that Gqbeta is also needed for efficient activation of Gqalpha by rhodopsin. Our results support the 'two-signal model' hypothesis for membrane targeting in a living organism and characterize the regulation of both the activity-dependent Gq localization and the cellular architectural changes in Drosophila photoreceptors.
引用
收藏
页码:459 / 468
页数:10
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