Scaffolding Protein INAD Regulates Deactivation of Vision by Promoting Phosphorylation of Transient Receptor Potential by Eye Protein Kinase C in Drosophila

Drosophila visual signaling is one of the fastest G-protein-coupled transduction cascades, because effector and modulatory proteins are organized into a macromolecular complex (“transducisome”). Assembly of the complex is orchestrated by inactivation no afterpotential D(INAD),whichcolocalizesthetransientreceptorpotential(TRP)Ca 2 (cid:1) channel,phospholipaseC (cid:1) ,andeyeproteinkinaseC(eye-PKC), formoreefficientsignaltransduction.Eye-PKCiscriticalfordeactivationofvision.Moreover,deactivationisregulatedbytheinteractionbetweenINADandTRP,becauseabrogationofthisinteractionin InaD p215 resultsinslowdeactivationsimilartothatof inaC p209 lacking eye-PKC. To elucidate the mechanisms whereby eye-PKC modulates deactivation, here we demonstrate that eye-PKC, via tethering to INAD,phosphorylatesTRP invitro .WerevealthatSer 982 ofTRPisphosphorylatedbyeye-PKC invitro and,importantly,intheflyeye,as shownbymassspectrometry.Furthermore,transgenicexpressionofmodifiedTRPbearinganAlasubstitutionleadstoslowdeactivationofthevisualresponsesimilartothatof InaD p215 . These results suggest that the INAD macromolecular complex plays an essential role in termination of the light response by promoting efficient phosphorylation at Ser 982 of TRP for fast deactivation of the visual signaling. Here, we report the identification and functional characterization of an eye-PKC phosphorylation site in We show that by and this By differential mass spectrometry we confirm eye-PKC. Moreover, we demonstrate that transgenic slow for positioning eye-PKCincloseproximitytoTRP,tofacilitateitsphosphorylationatSer


Introduction
Drosophila visual transduction is a G-protein-coupled signaling pathway that provides a model system for understanding the molecular basis of signal transduction in the vertebrate nervous systems. Drosophila visual signaling is initiated with the activation of rhodopsin by light. Activated rhodopsin, via a Gq heterotrimeric protein, stimulates phospholipase C␤ (PLC␤) named noreceptor potential A (NORPA) (Bloomquist et al., 1988). NORPA hydrolyzes PIP 2 (phosphatidylinositol 4,5bisphosphate) to inositol 1,4,5-trisphosphate (IP 3 ) and 1,2diacylglycerol (DAG), which leads to opening of the transient receptor potential (TRP) Ca 2ϩ and TRP-like channels, and depolarization of photoreceptors (Niemeyer et al., 1996;Reuss et al., 1997). The key second messenger that activates the TRP Ca 2ϩ channel is thought to be either DAG or its lipid metabolites (Chyb et al., 1999;Raghu et al., 2000a), whereas IP 3 does not appear to play a role (Montell, 1999;Raghu et al., 2000b). DAG may have a dual function, because it also activates the eye-specific protein kinase C (eye-PKC) essential for deactivation of the light response Smith et al., 1991).
To gain a better understanding of how the INAD complex modulates the kinetics of vision, we and others have shown that the INAD-TRP interaction is required for normal deactivation of the light response, because a loss of the interaction leads to slow deactivation in InaD p215 flies (Shieh and Niemeyer, 1995;Henderson et al., 2000). In addition, the INAD-eye-PKC interaction is essential for the in vivo activity of eye-PKC, because expression of modified eye-PKC that does not interact with INAD, fails to rescue inaC p209 flies lacking eye-PKC (Adamski et al., 1998). Indeed, two proteins in the complex, INAD and TRP, were found to be phosphorylated in vitro by eye-PKC (Huber et al., 1996a(Huber et al., , 1998Liu et al., 2000).
Here, we report the identification and functional characterization of an eye-PKC phosphorylation site in TRP. We show that TRP is phosphorylated at Ser 982 by eye-PKC and this phosphorylation depends on INAD in vitro. By differential mass spectrometry (MS), we confirm that Ser 982 of TRP is phosphorylated in vivo by eye-PKC. Moreover, we demonstrate that transgenic flies lacking this phosphorylation site display a slow deactivation phenotype similar to that of InaD p215 . Our results indicate that INAD is critical for deactivation of visual signaling by positioning eye-PKC in close proximity to TRP, to facilitate its phosphorylation at Ser 982 .

Materials and Methods
Preparation of fly head extracts. Approximately 100 l of young wild-type, inaD 1 , or InaD p215 fly heads were homogenized with 1 ml of extraction buffer or EB (50 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1% Triton X-100, and a mixture of protease inhibitors). Head homogenates were incubated at 4°C with constant agitation for 1 h. The mixture was then centrifuged for 10 min (12,000 ϫ g), and the supernatant was used for the in vitro complex-dependent kinase assay. Protein concentrations were determined by BCA (Pierce, Rockford, IL).
Liquid chromatography-MS analysis. Liquid chromatography (LC)-MS was performed by the Proteomics Laboratory in the Vanderbilt Mass Spectrometry Research Center. Approximately 14 pmol of TRP was excised from SDS-PAGE gels for in-gel digestion with either trypsin or chymotrypsin (Ham, 2005). The resulting peptides were separated by reverse-phase HPLC that is coupled directly with automatic tandem MS (LC-MS) using a ThermoFinnigan LTQ ion trap mass spectrometer equipped with a Thermo MicroAS autosampler and Thermo Surveyor HPLC pump, Nanospray source, and Xcalibur 1.4 instrument control. MS/MS scans were acquired using an isolation width of 2 m/z, an activation time of 30 ms, and activation Q of 0.250 and 30% normalized collision energy using 1 microscan and ion time of 100 for each scan. The mass spectrometer was tuned before analysis using the synthetic peptide TpepK (AVAGKAGAR). Typical tune parameters were as follows: spray voltage of 1.8 kV, a capillary temperature of 150°C, a capillary voltage of 50 V, and tube lens of 100 V. Initial analysis was performed using datadependent scanning in which one full MS spectra, using a full mass range of 400 -2000 amu, were followed by three MS/MS spectra. Incorporated into the method was a data-dependent scan for the neutral loss of phosphoric acid or phosphate (Ϫ98, Ϫ80), such that if these masses were found, an MS/MS/MS of the neutral loss ion was performed. Peptides were identified using a cluster compatible version SEQUEST algorithm (Yates et al., 1995), using a Drosophila subset of proteins from the nonredundant database from the National Center for Biotechnology Information (NCBI). Sequest searches are done on a high speed, multiprocessor Linux cluster in the Advanced Computing Center for Research. In addition to using the SEQUEST algorithm to search for phosphorylation on serines or threonines, the data were also analyzed using the Pmod algorithm (Hansen et al., 2005). All possible modified peptides were verified by manual inspection of the spectra.
P-element-mediated germline transformation. Wild-type and modified trp cDNA were subcloned into a modified pCaSpeR 4 vector (Thummel and Pirrotta, 1992) that contains Drosophila hsp70 promoter without the hsp70 3Ј trailer region. The P-element construct and a transposase plasmid ("wings-clipped") were injected into y[1] w[67c23] embryos (CBRC Transgenic Drosophila Core, Massachusetts General Hospital/Harvard Medical School, Charlestown, MA). Flies with the transgene integrated into the second or third chromosome were selected and made homozygotes in the trp p301 background for additional analysis.
Electroretinogram recordings. Electroretinogram (ERG) recordings were performed using red-eye young flies (1-3 d of age) that were reared in a 12 h light/dark cycle. The flies were anesthetized by carbon dioxide and immobilized using nondrying modeling clay. Glass electrodes were filled with physiological saline (0.7% NaCl). White light stimulation (light intensity, 4.45 mW) was delivered by a fiber optic light source (Oriel, Stratford, CT) and attenuated using absorptive nd filters (Newport, Irvine, CA). Signals were amplified by means of a WPI Dam 50 differential amplifier (World Precision Instruments, Sarasota, FL), displayed on an oscilloscope. Data were digitalized and analyzed using Ax-onScope 9.0 software (Molecular Devices, Sunnyvale, CA).
Statistical analysis. All bar graph data were analyzed with GraphPad (San Diego, CA) Prism 4.0 software one-way ANOVA. Data represent the means Ϯ SEM, unless otherwise noted, from several independent experiments.

The C-terminal tail of TRP contains PKC phosphorylation sites
To investigate the regulation of TRP by eye-PKC, we first identified potential eye-PKC phosphorylation sites in TRP. TRP consists of six transmembrane domains with both N and C termini localized intracellularly. By NetPhos 2.0 (http://www.cbs.dtu.dk/ services/NetPhos/) and Prosite (http://www.expasy.ch/prosite/) software using the PKC consensus sequence motif (S/T)-X-(R/ K), we found 16 putative phosphorylation sites in TRP with 14 present within the C-terminal sequence ( Fig. 1 A). Because the C-terminal tail of TRP has been implicated in gating and regulation of the channel, phosphorylation of this region may serve to switch on/off the channel activity. To investigate whether any of the putative PKC sites are bona fide PKC phosphorylation sites, we generated GST fusion proteins containing different intracellular regions of TRP and subjected them to in vitro kinase assays. As positive and negative controls, we used a fusion protein containing full-length INAD and GST alone, respectively. We first determined whether a recombinant PKC␣ could phosphorylate these fusion proteins because both PKC␣ and eye-PKC belong to the conventional PKC family. Indeed, we found that TRP 906 -1275 containing the last 370 residues of TRP including the six putative PKC sites became phosphorylated by PKC␣ ( Fig. 1 B), whereas TRP 1-367 , which contains two PKC sites did not (data not shown). Sequences spanning TRP 657-905 failed to produce stable fusion proteins in Escherichia coli and therefore were not tested. The stoichiometry of TRP 906 -1275 phosphorylation by PKC␣ was ϳ0.55 mol phosphate/moles fusion protein. These findings indicated that TRP 906 -1275 contains one PKC phosphorylation site.

Phosphorylation of TRP 906 -1275 by eye-PKC is dependent on INAD in vitro
Next we investigated whether TRP 906 -1275 can be phosphorylated by eye-PKC. In Drosophila photoreceptors, eye-PKC and TRP form a macromolecular complex by tethering to INAD. To obtain eye-PKC, immobilized GST fusion proteins containing TRP 906 -1275 were incubated with wild-type fly head extracts to compete with endogenous TRP for retrieval of the INAD complex, including eye-PKC. The resulting complex was recovered by centrifugation and used for in vitro kinase assays. We found that TRP 906 -1275 pulled down INAD and eye-PKC, and became phosphorylated after the addition of a PKC activator, PMA, by this complexdependent kinase assay ( Fig. 2 A, lane 2). To demonstrate that the observed phosphorylation of TRP 906 -1275 is dependent on INAD, we used fly extracts prepared from inaD 1 and InaD p215 . inaD 1 is a loss-of-function allele of inaD (Tsunoda et al., 1997), whereas InaD p215 expresses a modified protein resulting in a loss of the TRP-INAD association (Shieh and Zhu, 1996). As shown in Figure 2 A (lanes 3-6), both extracts failed to support TRP 906 -1275 phosphorylation by the complex-dependent kinase assay. In both cases, phosphorylation was diminished because TRP 906 -1275 was unable to isolate INAD and consequently, eye-PKC, from these two extracts ( Fig. 2 A, middle and bottom).
To further support the role of INAD in directing eye-PKC to TRP, we investigated phosphorylation of a modified TRP 906 -1275 containing an Asp substitution at Val 1266 , which has been previously shown to disrupt the interaction between TRP and INAD (Shieh and Zhu, 1996;Li and Montell, 2000). We found that phosphorylation of TRP 906 -1275, V1266D was greatly reduced (Fig.  2 B, C), because this modified TRP failed to recruit INAD and, consequently, eye-PKC (Fig. 2 B, bottom). Importantly, this modified TRP remained an excellent substrate for recombinant human PKC␣ (Fig. 2 D). Together, these results indicate that the phosphorylation of TRP 906 -1275 by endogenous eye-PKC in vitro is dependent on the interaction between TRP and INAD.
To demonstrate that eye-PKC is involved in phosphorylation of TRP 906 -1275 , we show that this phosphorylation is abolished in the presence of a specific conventional PKC inhibitor Go6976 (5 M) (Fig. 3A). To further confirm that eye-PKC is responsible for the observed phosphorylation of TRP 906 -1275 , we performed the complex-dependent kinase assay using extracts from inaC p209 (Pak, 1979), which lacks endogenous eye-PKC (Smith et al., 1991). As expected, phosphorylation of TRP 906 -1275 and fulllength INAD was greatly reduced, by 82 and 86%, respectively ( Fig. 3B) (mean Ϯ SEM; TRP 906 -1275 , 17.77 Ϯ 2.5%; INAD, 13.81 Ϯ 4.13%; n ϭ 3). The absence of phosphorylation is attributable to a lack of eye-PKC recovery when inaC p209 extracts were used (Fig. 3B, middle). These findings indicate that eye-PKC is indeed responsible for phosphorylation of TRP 906 -1275 .

TRP is phosphorylated at Ser 982 in vitro
To investigate which of the six putative PKC sites in TRP 906 -1275 is phosphorylated by eye-PKC, we examined phosphorylation of two shorter TRP fusion proteins that contain one (TRP 1157(TRP -1275 or four (TRP 1030 -1275 ) predicted PKC sites. We found that TRP 1030 -1275 and TRP 1157-1275 displayed a drastic reduction of phosphorylation by 78 and 91%, respectively ( Fig. 4 A) (Fig. 4 B). Interestingly, these two fusion proteins were also not phosphorylated by recombinant PKC␣ ( Fig. 4C). These data indicate that Ser 958 or Ser 982 , the two sites present in TRP 906 -1275 but not in TRP 1030 -1275 , are the potential phosphorylation sites for both eye-PKC and recombinant PKC␣.
To further confirm that Ser 982 of TRP is a PKC phosphorylation site, we obtained a synthetic peptide, ALRAS 982 VKNVD, spanning Ser 982 of TRP, and used it for in vitro kinase assays. This oligopeptide was a substrate of recombinant human PKC␣ with a K m of 263.1 M and a V max of 17.35 pmol/min. Together, these data indicate that Ser 982 represents a major in vitro PKC phosphorylation site in TRP 906 -1275 .

TRP is phosphorylated in vivo at Ser 982 by eye-PKC
Once we established that Ser 982 of TRP was phosphorylated in vitro by eye-PKC, we investigated whether Ser 982 is phosphorylated in vivo by eye-PKC using LC-MS analysis. First, we isolated the INAD complexes from light-adapted wild-type flies via immunoprecipitation, using anti-INAD antibodies. The proteins in the INAD complexes were separated by SDS-PAGE and visualized by staining with Colloidal Blue. The 145 kDa protein band corresponding to TRP was excised (Fig. 5A), digested "in-gel" with trypsin or chymotrypsin, and the resulting peptide mixture was subjected to LC-MS analysis. Peptide fragments were analyzed and identified by a cluster compatible version SEQUEST algorithm (Yates et al., 1995), using a subset of Drosophila proteins from the NCBI database. We obtained ϳ70% amino acid coverage of TRP (Fig. 5B) including sequences spanning Ser 982 . We also used collision induced dissociation (CID), which fragments peptides such that the fragmentation pattern can be used to discern the amino acid sequence and the exact site(s) of phosphorylation. By CID analysis, we identified and confirmed the amino acid sequence of the peptide RAS 982 VKNVDEKS-GADGKPGTM and revealed the presence of a phosphate group at Ser 982 . Moreover, we also found the spectra of the unmodified peptide as well as both the doubly and triply charged phosphopeptides (Fig. 5C,D). Importantly, only the unphosphorylated peptide RAS 982 VKNVDEKSGADGKPGTM was detected in TRP isolated from inaC p209 flies. Based on these data, we conclude that TRP is phosphorylated in vivo at Ser 982 by eye-PKC.

trp S982A displays slow deactivation of the visual response
To gain insight into the functional significance of TRP phosphorylation at Ser 982 , we generated and characterized transgenic flies expressing a modified trp, trp S982A , in which the phosphorylation site is eliminated. As a control, we also generated transgenic flies expressing a wild-type trp (trp wt ). The expression of wild-type or modified trp was under the control of the hsp70 promoter, and the function of TRP was analyzed in a null genetic background (trp p301 ) (Montell and Rubin, 1989;Shieh and Zhu, 1996). We first determined whether the modified TRP is stably expressed by Western blotting. Indeed, we observed that the TRP protein in trp S982A flies reaches a steady-state concentration similar to that of wild-type flies [Oregon-R (OR)] or transgenic flies expressing a wild-type trp, trp wt (Fig. 6 A). It appears that basal transcription driven by the hsp70 promoter is sufficient for transcription of trp leading to wild-type level of TRP in trp wt and trp S982A flies.
Next, we characterized the visual electrophysiology by ERG for gaining insight into the in vivo activity of the modified TRP. ERG is an extracellular recording of the compound eye. Briefly, red-eye flies were dark-adapted for 2 min, and then given a 2 s  white light stimulation. Using this stimulation paradigm, wild-type flies displayed the characteristic ERG waveform consisting of fast depolarization, maintained depolarization, and fast repolarization components (Fig. 6 B). In contrast, trp p301 flies displayed the initial fast depolarization but lacked the maintained component, and therefore the membrane potential returned gradually to baseline. This abnormal phenotype of trp p301 was completely rescued by transgenic expression of wildtype trp (Fig. 6 B). Remarkably, transgenic expression of trp S982A rescued the trp p301 phenotype but with delayed deactivation kinetics (Fig. 6 B). Close inspection of the deactivation kinetics in ERG revealed two subcomponents: a fast and a slow component. The fast subcomponent occurs immediately after light termination and achieves over 50% repolarization. The fast subcomponent is followed by the slow subcomponent, which eventually returns the potential to baseline. It appears that trp S982A flies exhibit defects in the fast subcomponent.
To further characterize trp S982A flies, we examined their visual response to various intensities of light over 4 log units. We show that the prolonged deactivation kinetics is more prominent during the brightest light stimulation (log I/I 0 ϭ 0): the half-repolarization time of trp S982A is approximately twofold longer than that of wild-type flies (Fig. 6C) (mean Ϯ SEM; wild type, 0.801 Ϯ 0.119 s; trp wt , 0.842 Ϯ 0.064 s; trp S982A , 1.668 Ϯ 0.253 s; n ϭ 5). In contrast, the amplitude of the ERG responses in trp S982A was comparable with that of trp wt flies (mean Ϯ SEM; trp wt , 18.008 Ϯ 0.95 mV; trp S982A , 20.71 Ϯ 2.73 mV; n ϭ 5), indicating that activation of visual signaling is not affected in trp S982A . These results demonstrate that expression of trp S982A leads to slow deactivation of visual response, which is likely attributable to a loss of eye-PKC phosphorylation of the modified TRP.
We compared the deactivation kinetics of trp S982A with that of inaC p209 flies that lack eye-PKC. Interestingly, inaC p209 exhibited prolonged deactivation kinetics similar to trp S982A , in response to bright light stimuli. However, inaC p209 also shows defects in deactivation at lower light intensities: the half-repolarization time was at least twofold longer than that of wild type, regardless of the light intensity used (mean Ϯ SEM; log I/I 0 ϭ 0, inaC p209 , inaC p209 , 1.219 Ϯ 0.1 s; n ϭ 5). These results indicate that the deactivation defect in inaC p209 is more complex than that of trp S982A and suggest that phosphorylation of addi-  A, Western blotting (WB). The expression of TRP in the fly head or body was analyzed. B, ERG analysis. Shown are representative ERG recordings of wild-type (OR), trp p301 , trp wt , trp S982A , inaC p209 , and InaD p215 flies after stimulation of a 2 s pulse of the brightest light stimulus (log I/I 0 ϭ 0). C, A histogram that compares half-repolarization times (n ϭ 5; mean Ϯ SEM) at different light stimuli. The stimuli were 2 s white lights without any attenuation (log I/I 0 ϭ 0, where I represents stimulus intensity used and I 0 represents maximum stimulus intensity available) or attenuated by 1 (log I/I 0 ϭ Ϫ1), 2 (log I/I 0 ϭ Ϫ2), or 3 (log I/I 0 ϭ Ϫ3) log units. The half-repolarization time is the time required to reach 50% of repolarization, as diagrammatically depicted for trp S982A flies in B. Two independent transgenic lines for both trp wt and trp S982A were used for quantification. ***p ϭ 0.001. tional PKC sites in TRP or other substrates may be responsible for the fast deactivation of the visual response.
We also investigated the deactivation kinetics of trp S982A in comparison with that of InaD p215 (Pak, 1979). InaD p215 contains a modified INAD, INAD M442K , which fails to associate with TRP (Shieh and Zhu, 1996). The lack of the TRP-INAD interaction leads to a slow recovery of the visual response (Shieh and Zhu, 1996). We found that InaD p215 displayed an ERG phenotype similar to that of trp S982A with deactivation defects that manifested at bright light stimulation. Moreover, as for trp S982A , the deactivation kinetics of InaD p215 at low light intensities were indistinguishable from wild type (Fig. 6C) (mean Ϯ SEM; halfrepolarization time for InaD p215 , log I/I 0 ϭ 0, 1.432 Ϯ 0.064 s; log I/I 0 ϭ Ϫ1, 0.815 Ϯ 0.045 s; log I/I 0 ϭ Ϫ2, 0.374 Ϯ 0.052 s; log I/I 0 ϭ Ϫ3, 0.398 Ϯ 0.041 s; n ϭ 5). These results indicate that the slow recovery of InaD p215 may be attributable to a loss of eye-PKC phosphorylation in TRP.
Together, our biochemical and electrophysiological analyses demonstrate that phosphorylation of TRP at Ser 982 by eye-PKC is important for the rapid deactivation of visual signaling in Drosophila.

Discussion
Reversible phosphorylation modulates the dynamics of signal transduction by transiently altering activities of signaling proteins. Members of the conventional PKC family (Newton, 1995), which are activated by Ca 2ϩ and DAG, are capable of phosphorylating a wide variety of protein substrates for temporal and spatial regulation of signaling processes (Violin and Newton, 2003). In Drosophila, eye-PKC is involved in the negative regulation of visual signaling, because inaC p209 flies lacking eye-PKC display abnormal desensitization, slow deactivation, and defects in light adaptation (Smith et al., 1991;Hardie et al., 1993). Eye-PKC is anchored to a macromolecular complex by tethering to INAD (Tsunoda et al., 1997;Adamski et al., 1998). Interaction with INAD enhances the stability of eye-PKC as well as targets eye-PKC to the rhabdomeres of photoreceptors (Tsunoda et al., 2001), in which visual signaling occurs. Importantly, the in vivo function of eye-PKC is regulated by interaction with INAD. Previously, it was shown that eye-PKC phosphorylates TRP in vitro (Huber et al., 1998;Liu et al., 2000). In the present study, we investigated the molecular basis of TRP phosphorylation by eye-PKC.
To mimic eye-PKC phosphorylation of TRP in vitro, we designed a complex-dependent kinase assay. We demonstrated that the in vitro complex-specific phosphorylation of TRP is regulated by the presence of the INAD-interacting domain in TRP, as well as the existence of INAD in the fly extracts. We showed that extracts lacking either eye-PKC or INAD fail to support TRP phosphorylation. Similarly, extracts prepared from InaD p215 that expresses a modified INAD devoid of the TRP binding (Shieh and Zhu, 1996), are not able to promote TRP phosphorylation. Together, these findings indicate that INAD targets eye-PKC to its substrates, similar to RACK (receptor for activated C kinase) (Liu et al., 2000). By the complex-dependent kinase assay, we identified Ser 982 of TRP as an eye-PKC phosphorylation site. Moreover, we analyzed TRP isolated from flies by LC-MS and found that Ser 982 of TRP is indeed phosphorylated in vivo by eye-PKC, because phosphorylated peptides encompassing Ser 982 of TRP were present in wild-type, but absent in inaC p209 flies.
Next, we investigated the in vivo functional contribution of phosphorylation by characterizing transgenic flies expressing a modified TRP bearing an Ala substitution at Ser 982 (trp S982A ).
Remarkably, these transgenic flies displayed prolonged deactivation kinetics in response to bright light stimuli, indicating that phosphorylation of TRP at Ser 982 by eye-PKC is involved in inactivation of TRP, leading to fast deactivation. A model of the TRP regulation by eye-PKC is proposed (Fig. 7). TRP is an integral part of the INAD complex and is opened by light. After light termination, the visual response is rapidly deactivated. Although molecular mechanisms underlying deactivation remain elusive, Ca 2ϩ is known to play a vital role in response termination (Hardie, 1991;Ranganathan et al., 1991Ranganathan et al., , 1994Peretz et al., 1994). The increased intracellular Ca 2ϩ (primarily mediated by TRP) and DAG activate eye-PKC, which, in turn, phosphorylates TRP at Ser 982 . Phosphorylation of TRP leads to a rapid inactivation of the channel on cessation of the light stimulation (Fig. 7B), without affecting the interaction between TRP and INAD (data not shown). How does phosphorylation influence the TRP channel activity? Ser 982 is located within the Lys-Pro-rich region of TRP (Fig. 5B), which may function in TRP gating (Sinkins et al., 1996). We speculate that phosphorylation at Ser 982 may induce a conformational change in the pore domain, which in turn leads to a rapid closure and inactivation of TRP. Phosphorylation has been linked directly to conformational changes that play key roles in the regulation of ion channels (Dulhanty and Riordan, 1994). It is also possible that phosphorylation of TRP at Ser 982 affects the interaction with some yet-unidentified proteins that may be important for the modulation of the TRP channel activity.
In the absence of eye-PKC-mediated phosphorylation of TRP, deactivation of visual signaling is slower as observed in inaC p209 or trp S982A . We found that inaC p209 displays a more complex deactivation defect, whereas trp S982A exhibits prolonged deactivation only in response to bright light. These findings suggest that, in addition to TRP, eye-PKC phosphorylates other substrates for efficient termination of the light response. Indeed, eye-PKC has been shown to phosphorylate INAD (Huber et al., 1996a;Liu et al., 2000), but the functional relevance of this phosphorylation is not known. Furthermore, Gu et al. (2005) reported that eye-PKC is required for the Ca 2ϩ -dependent inhibition of Meanwhile, increases in the concentrations of intracellular Ca 2ϩ and DAG activate eye-PKC, which, in turn, phosphorylates TRP (III). When light stimulation is off, phosphorylated TRP rapidly becomes inactivated (IV). It is likely that eye-PKC-mediated phosphorylation at Ser 982 of TRP facilitates the conformational changes associated with the closure of the channel. To return the TRP channels to the resting state, dephosphorylation with the participation of protein phosphatases may occur. Shown at the bottom is a representative ERG of a wild-type fly.
NORPA. NORPA is part of the INAD complex; however, it is not known to be phosphorylated by eye-PKC. Gu et al. (2005) also showed that the Ca 2ϩ -dependent inactivation of the lightinduced current was unaltered in inaC p209 . This finding suggests the existence of a parallel Ca 2ϩ -dependent mechanism in inaC p209 by which TRP is inactivated or of an upregulation of a Ca 2ϩ -dependent mechanism that activates other kinases (Matsumoto et al., 1994) to compensate for the loss of eye-PKC in inaC p209 .
Importantly, trp S982A displays slow deactivation kinetics similar to that of InaD p215 . InaD p215 was isolated by Pak (1979) based on the ina (inactivation no afterpotential) phenotype elicited by ERG. By whole-cell recordings, Shieh and Niemeyer (1995) showed that InaD p215 exhibits slow deactivation kinetics. However, Tsunoda et al. (1997) reported a delay in latency of the quantum bump and proposed that activation was affected in the InaD p215 mutant. To resolve this discrepancy, Henderson et al. (2000) reexamined the mutant and concluded that the primary defect in InaD p215 is prolonged deactivation and not slow activation. InaD p215 expresses INAD M442K , which fails to associate with TRP (Shieh and Niemeyer, 1995). How does a loss of INAD-TRP interaction lead to abnormal deactivation of visual signaling? It is likely that the lack of the INAD-TRP interaction prevents the recruitment of TRP to the INAD complex and, consequently, eye-PKC-mediated regulation. Indeed, both trp S982A and In-aD p215 exhibit similar deactivation defects, indicating that the molecular basis underlying the slow deactivation defect in In-aD p215 is attributable to a lack of negative regulation of the TRP channel by eye-PKC. Together, these findings suggest that formation of the INAD complex is essential for fast deactivation of the visual response by promoting phosphorylation of TRP by eye-PKC. Moreover, Ser 982 may be the sole eye-PKC phosphorylation site in TRP, because trp S982A and InaD p215 display similar deactivation defects. A loss of INAD-TRP interaction was previously investigated in transgenic flies expressing modified TRP in which the INAD-interacting domain was deleted (trp ⌬1272 ). Li and Montell (2000) reported a reduced light response with normal deactivation kinetics in trp ⌬1272 . These authors proposed that the suppression of the delayed termination, which is attributable to a reduced eye-PKC level in trp ⌬1272 is probably masked by a concomitant decrease in TRP and INAD levels (Li and Montell, 2000).
To date, many proteins related to Drosophila TRP have been discovered in both invertebrates and vertebrates. These TRP ion channels are subdivided into seven subfamilies (TRPC, TRPV, TRPM, TRPN, TRPA, TRPP, and TRPML) (Ramsey et al., 2006). Drosophila TRP belongs to the TRPC subfamily. Members of the TRPC subfamily are also activated by receptor-induced activation of phospholipase C (Montell et al., 2002) and therefore may be regulated by PKC. Indeed, phosphorylation of the TRPC channels by PKC appears important for modulating the channel activity. For example, the PKC-mediated phosphorylation of TRPC1 was shown to contribute to its SOC (store operated channel) activation, triggering Ca 2ϩ entry into endothelial cells (Ahmmed et al., 2004). In contrast, PKC-mediated phosphorylation was demonstrated to inhibit the activity of TRPC3 in HEK 293 cells (Trebak et al., 2005) and of TRPC6 in PC12D neuronal cells (Kim and Saffen, 2005). In both cases, TRPC3 and TRPC6 are activated by DAG, whereas DAG also turns on PKC. The authors proposed that timing is important because the channels are activated by DAG more rapidly than they are inhibited by DAG-activated PKC (Kim and Saffen, 2005). Heterologously expressed TRPC7 was also shown to be regulated by PKC: inhibi-tion of PKC prolonged inactivation of the channel (Shi et al., 2004). Moreover, PKC phosphorylation of heterologously expressed TRPC5 resulted in desensitization of this channel, a process that was dependent on both extracellular and intracellular Ca 2ϩ concentrations (Zhu et al., 2005).
In conclusion, here we uncover the molecular mechanism underlying the complex-dependent phosphorylation of TRP by eye-PKC and its role in fast deactivation of vision. Specifically, we show that eye-PKC phosphorylates TRP at Ser 982 in vitro and in vivo. Importantly, phosphorylation of TRP facilitates rapid inactivation of the channel because transgenic flies bearing an Ala substitution at Ser 982 display prolonged deactivation kinetics of the light response. Significantly, this slow deactivation defect is similar to that observed in InaD p215 in which TRP fails to associate with INAD. Our findings provide insights into the mechanistic basis of slow deactivation in InaD p215 , suggesting that INAD plays a critical role in targeting eye-PKC to TRP for rapid deactivation of the visual signaling. Together, these data indicate that the INAD macromolecular complex is important for deactivation of the visual response by directing eye-PKC to TRP. Furthermore, PKC-mediated phosphorylation of TRP at Ser 982 leads to fast deactivation of vision by promoting inactivation of the TRP channel.