Studies of Rh1 Metarhodopsin Stabilization in Wild-Type Drosophila and in Mutants Lacking One or Both Arrestins
- 1 February 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Biochemistry
- Vol. 36 (8) , 2188-2196
- https://doi.org/10.1021/bi9621268
Abstract
We have used Drosophila mutants which are deficient in one or both of the arrestins present in photoreceptor cells to critically test the requirements for arrestin in the stabilization of Rh1 metarhodopsin under in vitro and in vivo conditions. Heads from flies illuminated with blue light were homogenized to obtain membranes or micellar extracts, and the amount of metarhodopsin present was quantitated by spectroscopic methods. Compared to wild-type, approximately 64% Rh1 metarhodopsin was recovered in flies deficient in arrestin-1 (arr1(1) mutant), approximately 38% in flies deficient in arrestin-2 (arr2(3) mutant), and approximately 6% in flies deficient in both arrestin-1 and arrestin-2 (arr1(1), arr2(3) double mutant). In contrast, no decrease was observed in the amounts of Rh1 metarhodopsin recovered from illuminated flies which were deficient either in the eye-specific phosphatase (rdgC mutant) or in the eye-specific phospholipase C (norpA(H24) and norpA(H52) mutants). Further, reconstitution experiments in total head homogenates showed that metarhodopsin produced in the arr1(1), arr2(3) double mutant could be stabilized upon the addition of exogenous arrestin-2. These studies provide definitive evidence that arrestin binding stabilizes Rh1 metarhodopsin under in vitro conditions. To test whether arrestin was also required to stabilize metarhodopsin in intact photoreceptor cells, metarhodopsin was generated in arr1(1), arr2(3) double mutant flies by in vivo illumination, and after a wait period of 20 min, converted back into rhodopsin by further illumination with red light. Quantitation of the regenerated rhodopsin in extracts from Drosophila heads showed no significant change in the level of rhodopsin recovered by this illumination protocol. Together, these experiments demonstrate that in disrupted photoreceptor cells, metarhodopsin is not stabilized unless arrestin is present, but in intact photoreceptor cells, significant metarhodopsin stabilization occurs even in the absence of bound arrestin.Keywords
This publication has 10 references indexed in Scilit:
- Rhodopsin and phototransduction: a model system for G protein‐linked receptorsThe FASEB Journal, 1992
- Isolation of a novel visual-system-specific arrestin: an in vivo substrate for light-dependent phosphorylationMechanisms of Development, 1990
- Deactivation of Photoactivated Rhodopsin by Rhodopsin-Kinase and ArrestinJournal of Receptor Research, 1987
- Light‐modulated ADP‐ribosylation, protein phosphorylation and protein binding in isolated fly photoreceptor membranesEuropean Journal of Biochemistry, 1986
- Transduction in invertebrate photoreceptors: role of pigment bistability.Physiological Reviews, 1983
- Light-Induced Interaction between Rhodopsin and the GTP-Binding Protein. Metarhodopsin II Is the Major Photoproduct InvolvedEuropean Journal of Biochemistry, 1982
- Complex formation between metarhodopsin II and GTP‐binding protein in bovine protoreceptor membranes leads to a shift of the photoproduct equilibriumFEBS Letters, 1982
- Characteristics of Drosophila rhodopsin in wild-type and norpA vision transduction mutants.The Journal of general physiology, 1978
- Formation, structure, and spectrophotometry of air-water interface films containing rhodopsinThe Journal of Membrane Biology, 1977
- Kinetics of slow thermal reactions during the bleaching of rhodopsin in the perfused frog retinaThe Journal of Physiology, 1972