While elimination of either RGS7 or RGS11 alone does not substantially alter depolarizing activity of ON-BCs (Mojumder et al., 2009; Chen et al., 2010; Zhang et al., 2010), simultaneous loss of both proteins completely abolishes the responses of these cells to light flashes (Cao et al., 2012; Shim et al., 2012). In an effort to achieve an intermediate state of RGS expression we studied mice where elimination of one RGS is combined with the haploinsufficiency of the other (e.g., Rgs11−/−: Rgs7+/− or Rgs11+/−: Rgs7−/−). Evaluation of these mouse models by both electroretinography (ERG) and single cell recordings from rod ON-BCs revealed largely normal responses, that showed only minor delays in the onset time of the ERG b-wave (Figure 1; Table 1). Thus, normal depolarizing activity of ON-BCs is supported by a relatively low concentration of the RGS proteins.

Figure 1

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To achieve a greater reduction in RGS concentration we developed a model for inducible RGS7 elimination. A conditional Rgs7 allele (Rgs7flx/flx) was introduced in the Rgs11−/− background (cDKO) and the mice were further crossed with a ubiquitous driver line expressing inducible Cre-recombinase (cDKO:Cre+; Figure 2A). In the resulting model, RGS elimination can be induced postnatally by the oral administration of tamoxifen. We first characterized changes in RGS7 expression following tamoxifen administration in cDKO:Cre+ mice. Immunostaining of retinal cross-sections revealed a progressive loss of the RGS7-positive signal from the ON-BC synapses in the outer plexiform layer (Figure 2B). A reduction was evident in both the number of RGS7 puncta and staining intensity reaching minimal levels by day 35. During this timeframe, no changes in the postsynaptic concentration of mGluR6 were detected (Figure 2B). We further quantified the decline in RGS7 protein by quantitative Western blotting. Similar to the immunohistochemical analysis, we detected a progressive decrease in the RGS7-positive band (Figure 2C). Quantitative analysis found immunostaining and Western blotting data to be in good agreement, both showing monophasic decays in the RGS7 levels (Figure 2D). We further analyzed RGS7 concentration upon tamoxifen induction separately for synapses between rods and cones, and their respective ON-BCs (Figure 2B,D; Figure 2—figure supplement 1). Before tamoxifen administration (0 day), RGS7 levels in rod and cone ON-BC synapses were comparable, showing no more than a 5 ± 2% difference in staining intensity between the two. The time course of RGS7 loss induced by tamoxifen was also not different between rod and cone ON-BC synapses: half of RGS7 in rod ON-BC was found at 7.4 ± 1.5 days, vs 7.8 ± 1.3 days in cone ON-BCs. At day 35 following tamoxifen administration, RGS7 expression was reduced to 18 ± 3% in rod ON-BCs and to 17 ± 3% in cone ON-BC synapses. Importantly, the cytoarchitecture at the ON-BC dendritic tips of cDKO mice remained unaltered despite the RGS7 loss. Postsynaptic accumulations of both TRPM1 and mGluR6 and the alignment of pre- and post- synaptic compartments were both preserved (Figure 2E; Figure 2—figure supplement 2). Prior to tamoxifen administration both cDKO:Cre- and cDKO:Cre+ mice were indistinguishable from the previously characterized Rgs11−/− background strain in both RGS7 expression and localization (Figure 3A). Furthermore, no changes in RGS7 concentration or its postsynaptic accumulation were detected upon tamoxifen administration in cDKO littermates lacking Cre recombinase expression (Figure 3A). Consistent with these observations, ERG responses recorded in cDKO:Cre- and cDKO:Cre+ mice were indistinguishable from their Rgs11−/− controls and tamoxifen administration failed to alter ERG responses in cDKO:Cre- animals (Figure 3B). Thus, the observed effects are associated specifically with genomic editing of the Rgs7 locus.

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Figure 3

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To obtain a more quantitative picture, we determined the absolute expression levels of RGS7 and RGS11 referencing them to the levels of mGluR6. Using recombinant protein standards and quantitative Western blotting, we found that RGS7, RGS11, and mGluR6 are present at 20 ± 2, 23 ± 1, 31 ± 1 fmol per 10 mg of total protein, respectively (Figure 4). Based on immunohistochemical analysis, RGS11 (Cao et al., 2009), RGS7 (Cao et al., 2012; Figure 4—figure supplement 1) and mGluR6 (Masu et al., 1995) are found exclusively, in the outer plexiform layer of the retina, indicating that the values that we obtained reflect protein content specifically at the ON-BC synapses. Considering that mGluR6 receptors form obligate dimers that function as a single unit, there is about threefold molar excess of RGS proteins (∼43 fmol) relative to mGluR6 dimer (∼15 fmol) in ON-BCs. In summary, these data illustrate that RGS7 loss beyond its stoichiometry with mGluR6 can be induced postnatally in a graded manner without affecting synaptic morphology or retinal cytoarchitechture.

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To determine how progressive loss of RGS affects signal transmission in the rod pathway, we examined retinal responses to light in dark-adapted live anesthetized mice by ERG. In cDKO:Cre+ mice prior to tamoxifen administration, the delivery of very dim (scotopic) flashes, that activate rods but not cones, elicited a robust b-wave, whose generation requires the activity of rod ON-BCs (Figure 5A). These responses were indistinguishable from those observed in Rgs11−/− strain (Figure 3B). Administration of tamoxifen to cDKO:Cre+ mice dramatically changed these responses, progressively reducing their amplitude and slowing their time course (Figure 5A; Table 2). We next analyzed changes in response properties across a range of flash strengths. As flash strengths increase, the contribution of cones to the overall response becomes appreciable. However, rod- and cone- driven b-waves saturate at distinct light intensities leading to a characteristic biphasic shape of the intensity-response relationship (Figure 5B). Accordingly, the first phase of the curve is commonly considered to consist of relatively pure rod-driven component that can be extracted mathematically (Figure 5C; Equation 1). Analysis of this scotopic ERG b-wave showed marked time-dependent changes in both maximal response amplitude and sensitivity (Table 2). At 35 days following tamoxifen administration, the flash responses were barely distinguishable from the baseline seen upon constitutive elimination of both RGS7 and RGS11, with an approximately10-fold reduction in b-wave maximal amplitude and nearly a 100-fold decrease in its sensitivity. The responses further showed a time-dependent slowing in their onset, as evidenced by a progressive increase in b-waves time-to-peak and visible deceleration of the b-wave slopes (Figure 5D). Importantly, we observed no tamoxifen-induced changes in ERG b-wave characteristics in littermates lacking Cre recombinase (Figure 3B), indicating that these changes are caused specifically by the progressive loss in RGS7 expression.

Figure 5

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To determine how the en masse activity of ON-BCs seen in ERGs is set by the responses of single cells, we recorded the light-evoked activity of rod ON-BCs in dark-adapted retinal slices (Figure 6). Whole-cell patch clamp recordings revealed some variability in ON-BCs responses suggesting that efficiency of tamoxifen-induced recombination varied on a cell-by-cell basis (Table 3). For example, we noticed that some cells were very susceptible to tamoxifen treatment and completely lost responsiveness to light, perhaps due to stochastic hyperactivation of Cre-recombinase leading to rapid elimination of RGS proteins. Because the proportion of unresponsive cells remained relatively stable (∼31–46%) across different days following tamoxifen administration, and because elimination of RGS proteins result in complete abrogation of ON-BC responses to flashes (Cao et al., 2012), these cells were excluded from the analysis. Analysis of the remaining light-sensitive cells revealed a progressive increase in time-to-peak and concomitant decrease in maximal amplitudes following tamoxifen administration (Figure 6A; Table 3). We next compared the average half-maximal flash strengths across all rod ON-BCs recorded on days 17, 22, 28, and 35 and found their progressive increase, reflecting a reduction in sensitivity. No changes in noise variance were detected, suggesting that reduction in RGS concentration also effectively decreases the signal-to-noise ratio (Figure 6B; Table 3). Interestingly, the sensitivity reduction determined from patch clamp recordings matched well that obtained by ERG, which summates the responses of all cells across the retina (Figure 6C). In summary, we observed that gradual titration of RGS levels affects kinetics, sensitivity, and amplitude of rod ON-BC light responses.

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Because ON-BCs making synapses with cone photoreceptors utilize a similar mGluR6-TRPM1 signaling pathway for generating depolarizing responses, we examined how changes in RGS concentration affected the light-evoked responses in cone ON-BCs (Figure 7, Table 4). Given low abundance of cones in murine retinas and the functional heterogeneity of cone ON-BC that they connect to, we relied exclusively on ERG for these studies. Prior to tamoxifen administration, bright (photopic) flashes produced a characteristic two-component ERG waveform in cDKO mice. In contrast, after tamoxifen administration we observed a progressive reduction in the b-wave amplitudes and kinetics without detectable changes in the a-wave (Figure 7A). We performed dose-response studies analyzing the dependence of photopic b-wave amplitude on flash intensity across all treatment groups. As in the case of rods, the component of the response that reflects cone contribution (Figure 7B) was derived mathematically from the biphasic response profile (Figure 5C). The resulting traces revealed changes in cone-generated responses (Figure 7B) with a progressive decrease in maximal response amplitude and sensitivity. To verify that recorded responses reflected specifically changes in cone ON-BC signaling, we performed ERGs when rod function was suppressed by exposure to background light (Figure 7C; Figure 7—figure supplement 1). Light-evoked responses collected on this rod-suppressing background showed a progressive decline in b-wave amplitude and kinetics, just as for dark-adapted conditions. Quantification of the parameters derived from the analysis of intensity-response relationships indicated that maximal amplitude, sensitivity, and onset timing of the response similarly declined with time after tamoxifen administration (Figure 7D,E). Together, these results indicate that down-regulation of RGS proteins in the cone synapses lead to changes in cone ON-BC light-evoked responses, that are similar to changes observed in rod synapses.

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To assess how changing responses in rod ON-BCs affects dim light vision we developed a behavioral water maze assay. The assay measures the ability of mice to locate an escape platform under varying luminance levels. Under photopic conditions, trained wild-type mice reached the visible platform in ∼10 s (Figure 8A). Video rate analysis of tracks indicated that under these conditions mice swim directly to the visible platform taking the shortest path (Figure 8A). In contrast, when the platform was hidden mice randomly swam and appeared to encounter the platform by chance, increasing the time to escape by nearly fivefold. Thus, mouse vision in this test can be evaluated by measuring the time to escape on the platform.

Figure 8

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To validate the test, we evaluated the performance of the constitutive RGS7/11 double knockouts (DKO), which completely lack an ERG b-wave and thus are considered night blind. Under photopic conditions, the escape latency of DKO mice with the visible platform was no different from that of wild-type animals, indicating that they see the platform normally (Figure 8A). However, when the maze luminance was decreased to the scotopic range, the performance of DKO mice dropped sharply and their escape latencies became statistically equivalent to random encounters with the hidden platform, indicating a complete loss of scotopic vision (Figure 8A). Thus, RGS expression in rod ON-BCs is absolutely required for high sensitivity scotopic vision.

We next tested the performance of the cDKO mice under scotopic conditions. Before tamoxifen administration escape times of cDKO:Cre+ mice were substantially shorter than in DKO and no different from these of cDKO:Cre- littermates or WT mice, indicating that their scotopic vision remained intact (Figure 8B). This performance did not decline up to 22 days after the beginning of tamoxifen treatment. However, a marked increase in escape time was observed in cDKO:Cre+ mice at 28 days, and by 35 days they displayed similar difficulty in visually locating the platform as the constitutive DKO animals, indicating that they developed night blindness (Figure 8B). Administration of tamoxifen to RGS7 haploinsufficient or Rgs7−/− mice did not alter the performance compared to wild-type animals at any light levels (Figure 8C).

To understand better the relevance of RGS function in ON-BCs to behavior, we also assessed visual function of mice in a virtual environment using the optokinetic reflex (OKR). The optomotor response test is based on the ability of mice to respond reflexively to computer-generated rotating sine-wave gratings, which form a virtual cylinder around them (Prusky et al., 2004). Previous studies have established an essential contribution of ON-pathway to visual contrast sensitivity under both scotopic and photopic conditions reflecting the critical role of both rod and cone pathways to this behavior (Schiller et al., 1986; Iwakabe et al., 1997; Kolesnikov et al., 2011). To assess scotopic contrast sensitivity change in cDKO mice we used the optimal mouse scotopic temporal frequency of 0.75 Hz in combination with a moderate stimuli speed of 7.5 deg/s (Umino et al., 2008) at which the contrast sensitivity is close to maximal (Figure 9A). Before tamoxifen administration, both genotypes were indistinguishable in their ability to visualize rotating gratings at their contrast threshold. Tamoxifen treatment severely diminished the performance of cDKO:Cre+ mice without affecting their cDKO:Cre- littermates (Figure 9A). Interestingly, the deterioration of scotopic vision was somewhat resistant to tamoxifen treatment until day 22. These observations are in a good agreement with the data from the water maze task (Figure 9B). Thus, the loss of RGS affects mouse scotopic vision in a stereotyped manner that does not depend on the paradigm chosen to evaluate behavioral performance.

Figure 9

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Finally, we used the OKR approach to evaluate the effect of gradual RGS loss on photopic vision. The parallel processing of cone-generated signals by different classes of BCs makes signaling through ON-BC not entirely necessary for photopic vision (e.g., Figure 8). Therefore, we first determined the contribution of cone ON-BC to photopic (70 cd/m²) OKR performance using DKO mice lacking ON-BC responses and compared them to control Rgs11−/− littermates that show normal ON-BC function. We found that Rgs11−/− and DKO mice had virtually identical contrast sensitivity for slow stimuli (up to 12 deg/s), whereas at higher stimuli speeds (Sp) the DKOs displayed impaired discrimination of low-contrast gratings pattern compared to their Rgs11−/− counterparts (Figure 9C). In contrast, photopic visual acuity of DKO mice remained unaffected across most Sp and showed only a minor decline at the fastest speed of 50 deg/s (Figure 9D).

Having established the contribution of the cone ON-BC pathway to overall contrast discrimination, we evaluated the impact of declining RGS concentration on photopic vision. Tamoxifen administration in cDKO:Cre+ mice caused a 2.4-fold reduction in photopic contrast sensitivity observed at maximal stimuli speed of 50 deg/s in as early as 12 days (Figure 9E). The average photopic contrast sensitivity reached its lowest level by day 22, with a nearly a fivefold decline compared with either untreated littermates or a group of cDKO:Cre- controls that also received tamoxifen. This is in stark contrast to scotopic conditions (∼3 × 10⁻⁴ cd/m²) where contrast sensitivity did not start deteriorating until after day 22 following tamoxifen administration, and by day 35 it had reached a sevenfold decline as compared to cDKO:Cre- control mice (Figure 9F).

The availability of quantitative information regarding RGS levels at any time point in the analysis allowed us to determine how signal transmission to ON-BCs influences visually-guided behavior with the RGS concentration as a common denominator (Figures 10, 11). Thus, we compared how both ON-BC ERG response parameters (i.e., b-wave onset, amplitude, and sensitivity) and behavioral sensitivity varied as a function of the RGS7 concentration. These results reveal that the effect of RGS7 concentration on b-wave onset kinetics occurred with a half-saturating concentration of 37 ± 2% of available protein (Figure 10A). Similarly, a halving of the response amplitude in rod ERG b-wave occurred at RGS7 levels of 39 ± 3% of available protein (Figure 10B), and a twofold decline of scotopic response sensitivity occurred at RGS7 levels of 26 ± 2% (Figure 10C). A similarly sharp dependence on RGS7 levels was observed for the scotopic vision of mice (Figure 10D). Animals showed a precipitous drop in their visual contrast sensitivity once the levels of RGS7 declined below ∼35%, with 26 ± 2% reflecting the half-saturating level. To compare directly changes in rod ON-BC response characteristics to behavioral performance, we calculated RGS protein concentration that produced half-saturating responses across these different measures (Figure 10E). The data reveals that rod-driven ERG response amplitudes, onset and sensitivity are disproportionately affected by changes in RGS concentration. Although measured response parameters are interrelated by their underlying biochemical mechanism, they correlate differentially with the mouse behavioral performance. For example, a threefold reduction in response amplitude and a twofold deceleration of ERG b-wave onset did not appear to have an appreciable effect on scotopic visual performance. Instead, mouse scotopic behavior tightly correlated with the rod ON-BC response sensitivity, albeit compounded by pronounced changes in other response parameters.

Figure 10

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Figure 11

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A similar relationship was derived for the cone-driven photopic ERG responses and behavioral sensitivity (Figure 11). We found that a halving of the photopic ERG b-wave amplitude occurred at an RGS7 concentration of 43 ± 2% of available protein, a twofold effect on onset kinetics occurred at an RGS7 concentration of 38 ± 2% of available protein, and a twofold decline in sensitivity occurred at an RGS7 concentration of 25 ± 2% of available protein. Thus the photopic ERG b-wave amplitude was the response parameter most sensitive to the reduction in RGS7. However, in contrast to rod-mediated vision, we found that behavioral performance relying on the cone ON pathway was very sensitive to even small decline in RGS7, losing half of their photopic visual performance with 43 ± 2% of the RGS remaining (Figure 11D). To compare changes in cone ON-BC response characteristics to behavioral performance we plotted the absolute RGS protein concentration that produced half-saturating responses (Figure 11E). We found that photopic vision is more sensitive to changes in the amplitude and kinetics of the cone ON-BC light-evoked responses rather than their light sensitivity.

In this study, we used the well-defined rod and cone ON circuits of the retina to examine how changing key parameters of GPCR-mediated responses affected visually-guided behavior. Through genetic manipulations we observed graded alterations in the maximal response amplitudes, timing of response onset, and sensitivity of rod and cone ON-BCs, while testing the effect of these changes on mouse visual performance. We found stark differences between rod- and cone-driven ON circuits with respect to the influence of signal transfer parameters on visually-guided behavior. In the rod circuitry, changes in the timing or amplitude of signal transmission between photoreceptors and ON-BC neurons did not affect behavioral performance in visually-guided tasks that required intact dim vision. However, a change in the sensitivity of transmission at this synapse, albeit aggravated by kinetic deficits, was not tolerated behaviorally and loss of the response sensitivity strictly correlated with the decrease in behavioral performance of the animals. In contrast, cone-mediated vision was sensitive to minor changes in kinetic parameters of signal transmission, causing a pronounced decrease in behavioral performance even when light sensitivity was unaffected. The rod circuit is biased for high sensitivity to detect single photon absorptions close to absolute visual threshold (Pahlberg and Sampath, 2011), whereas cone pathways operate at higher light levels and require the capacity to extract temporal features from light stimuli (Rodieck, 1998). Thus, our observations suggest that differential specialization of rod and cone pathways involves adaptation at the first synapse in these respective circuits.

Here we find that the parameters of the GPCR-mediated response can be dissociated to provide a hierarchical influence on function. In ON-BCs, decreasing concentrations of two RGS proteins expressed in dendritic tips, RGS7 and RGS11, sequentially influence the onset timing, amplitude, and sensitivity of mGluR6-mediated responses (Figure 12). In this pathway, response kinetics and amplitude appeared to be the parameters most sensitive to changes in RGS concentration, whereas sensitivity required a much larger reduction in RGS concentration to produce an impact. There is a window in the RGS concentration range where profound effects on kinetics were not accompanied by appreciable changes in response sensitivity. These observations suggest a mechanism by which GPCRs can generate unique patterns of activity and differentially tune circuit properties based on varying levels of RGS proteins. Thus, regulatory nodes where information processing is mediated by GPCRs may be tuned to extract temporal features at one end of the RGS concentration range, whereas others may serve as sensitivity filters at the other end of the range. This possibility is supported by observations in photoreceptors where manipulation of RGS9 concentration affects temporal characteristics of the response without changes in sensitivity (Chen et al., 2000; Krispel et al., 2006) and in hippocampal pyramidal neurons where knockout of RGS proteins changes both response kinetics and sensitivity (Xie et al., 2010). Interestingly, levels of multiple RGS proteins have also been shown to fluctuate in response to extracellular cues (Hurst and Hooks, 2009; Traynor et al., 2009) suggesting that changes in RGS concentration may dynamically control GPCR response properties.

Figure 12

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Under native conditions, RGS proteins in ON-BCs appear to be present in substantial excess over the minimal amount needed for sustaining wild-type response properties. Rod ON-BCs tolerate an almost 75% reduction in RGS levels before any measurable effects on response properties could be observed. To understand the basis for this overexpression we compared levels of RGS7 and RGS11 to that of the mGluR6 receptors. We found that RGS proteins are present at approximately threefold stoichiometric excess over mGluR6 dimers. Several recent studies suggest that the signal transduction components of the ON-BC are organized in a macromolecular complex (Morgans et al., 2010; Dhingra and Vardi, 2012). Indeed, both RGS7 and RGS11 form physical complexes with mGluR6 (Cao et al., 2009) and a recently discovered orphan receptor GPR179 (Orlandi et al., 2012; Ray et al., 2014). These interactions are required for proper postsynaptic targeting of RGS7/11 (Cao et al., 2009; Orlandi et al., 2012). The expression of RGS proteins also depends on mGluR6, and its elimination in mice significantly decreases RGS7 and RGS11 levels (Cao et al., 2009). Additionally, mGluR6 and its effector channel TRPM1 are further integrated by a scaffolding protein, nyctalopin (Cao et al., 2011; Pearring et al., 2011). The relatively rapid (∼50–100 ms) response of ON-BCs to flashes of light is unlikely to be supported by the stochastic action of RGS proteins if they were deactivating Gα_o in the vicinity of TRPM1 simply by diffusion. Thus, these considerations suggest a model where functionally relevant RGS molecules must be physically integrated into the macromolecular signaling complex. Since RGS proteins are present in the molar excess over the mGluR6 complex, their depletion does not alter the signaling until the level reaches the stoichiometric threshold and RGS is reduced within the macromolecular assembly. Therefore, it seems reasonable to speculate that overexpression of RGS proteins over the stoichiometry with the mGluR6 signaling complex would minimize fluctuation in the kinetics and sensitivity of ON-BC responses, ensuring their reproducibility. In support of this hypothesis we find that titration of RGS proteins below a certain threshold point (∼1:1 stoichiometry with mGluR6 complex) detrimentally affects the signal-to-noise ratio of ON-BC responses and increases their variability.

These results additionally suggest that G protein deactivation normally is not a rate-limiting step in the cascade of events that lead to generation of a depolarizing response in ON-BCs. Previous studies in rod photoreceptors that utilize similar G protein cascade for light reception demonstrated that G protein deactivation limits the recovery of a photoresponse. In these neurons, increase in the concentration of RGS protein (RGS9) resulted in acceleration of the response termination kinetics (Krispel et al., 2006; Burns and Pugh, 2009). Since a reduction in mGluR6 activity underlies the light-evoked responses in ON-BCs (compared to an increase in rhodopsin's activity for phototransduction), G protein deactivation drives the activation phase of the response and RGS proteins influence its slope. By titrating the RGS concentration in the ON-BCs we found a critical threshold point, below which the onset of the ON-BC depolarization is sensitive to changes in G protein deactivation. The critical threshold point roughly corresponds to ∼25% of normal RGS levels (contributed by both RGS7 and RGS11) in wild-type synapses. Notably, a substantial excess in RGS concentration (threefold to fourfold), and hence G protein deactivation rates above this threshold, has no influence on ON-BC response properties. Thus, by setting the levels of RGS expression above this threshold, mGluR6 signaling in ON-BCs ensures that G protein deactivation is not a rate-limiting step in generation of a depolarizing response. Instead, this rate-limiting reaction could be associated with either TRPM1 channel opening or intrinsic deactivation of the mGluR6 receptor. Determining the identity of this rate limiting process that drives the onset of ON-BC depolarizing response will be an important area for future investigation.

Interestingly, we found that RGS proteins have similar impact on response properties of ON-BCs that form synapses with either rod or cone photoreceptors. Given monosynaptic connectivity between rods and rod ON-BCs, and the progressive night blindness associated with RGS loss, the implications of these changes for rod-mediated behavior are rather unequivocal. However, signaling of cones via parallel ON- and OFF- circuits, together with the heterogeneous nature of cone ON-BCs, complicates the interpretation of the dependence of photopic (cone) vision on cone-to-cone ON-BC signal transmission. The ability to discriminate changes in luminance across a broad range of stimulation frequencies is characteristic feature of photopic vision in many species, including mice (Umino et al., 2008). Previous studies have indicated that pharmacological or genetic blockade of the ON-pathway affects contrast sensitivity in mice and monkeys under photopic conditions (Schiller et al., 1986; Iwakabe et al., 1997). In line with these observations, we find that changes in amplitude and kinetics of the photopic ERG b-wave caused by the loss of RGS expression result in pronounced deficits in the temporal properties of contrast detection for cone vision. Ablation of RGS proteins severely impacted photopic contrast sensitivity for high-speed visual stimuli while leaving visual acuity relatively unaffected. This highlights an essential role that temporal regulation of mGluR6-TRPM1 signaling at the cone-to-cone ON-BC synapse plays for normal photopic vision. Although the details on how RGS proteins may contribute to the responses of individual cone ON-BCs remain to be established, it is possible that differential expression of RGS7 vs RGS11 at cone ON-BC synapses (Mojumder et al., 2009) may contribute to setting their unique profiles, thus increasing the temporal resolution of cone vision.

Generation of mice with the constitutive deletion in Rgs7 (Rgs7−/−) (Cao et al., 2012), Rgs11 (Rgs11−/−) (Cao et al., 2008), or both (DKO) (Cao et al., 2012) was previously described. Conditional targeting of RGS7 was achieved by flanking exon 4 with LoxP sites (Rgs7flx/flx) (Cao et al., 2012). The resulting mice were crossed with Rgs11−/− line to generate cDKO:Cre- strain (Rgs11−/−: Rgs7flx/flx), and further with a Cre driver line ubiquitously expressing tamoxifen-inducible Cre-ERT2 recombinase B6.Cg-Tg(CAG-cre/Esr1*)5Amc/J to produce cDKO:Cre+ mice (Rgs11−/−: Rgs7flx/flx: CAG-CreERT2). To induce Cre expression 20 mg/kg tamoxifen (Sigma, St. Louis, MO), dissolved in corn oil and 10% ethanol, was administered by oral gavage with an 18–24 gauge smooth tip needle. Tamoxifen was administered once daily for 5 consecutive days. All procedures were carried out in accordance with the National Institute of Health guidelines and were granted formal approval by the Institutional Animal Care and Use Committees of the Scripps Research Institute (IACUC protocol number 14-001), Washington University (IACUC protocol number 20140236), and the University of Southern California (IACUC protocol number 10890).

The generation of sheep anti-TRPM1 is described (Cao et al., 2011). Rabbit anti-RGS7 (7RC1), was a generous gifts from William Simonds (NINDDK/NIH) and the guinea pig anti-mGluR6 antibody was a gift from Dr Takahisa Furukawa (Osaka University). Mouse anti-PKCα (ab11723; Abcam, Cambridge, MA), rabbit anti-RGS7 antibodies (07-237; Upstate Biotechnology, Billerica, MA), mouse anti-CtBP2 (612044; BD Biosciences) and rabbit anti-cone arrestin (ab15282; Millipore, Billerica, MA) were purchased.

Recombinant His-tagged RGS7 and RGS11 were co-expressed in Sf9 insect cells together with Gβ5, via baculovirus-mediated delivery, then purified by Ni-NTA chromatography as described previously (Martemyanov et al., 2005). Glutathione S-transferase (GST)-tagged mouse mGluR6 C terminus protein (aa840-871) was expressed in Escherichia coli and affinity purified on GSTrap HP column (GE, Fairfield, CT). Protein concentration was determined by bicinchoninic acid (BCA) Protein Assay Kit (Pierce, Carlsbad, CA) and adjusted to reflect the protein purity determined by densitometry of Coomassie blue-stained gels.

Whole retinas were removed from mice and lysed by sonication in ice-cold PBS supplemented with 150 mM NaCl, 1% Triton X-100, and Complete protease inhibitor tablets (Roche, Basel, Switzerland). Lysates were cleared by centrifugation at 20,800×g for 15 min at 4°C. Total protein concentration in the supernatant was measured by using BCA Protein Assay Kit (Pierce, Carlsbad, CA). Supernatants were added with SDS sample buffer (pH 6.8) containing 8 M urea and were subjected to 12.5% SDS/PAGE. Protein bands were transferred onto PVDF membranes, subjected to Western blot analysis first with primary antibodies against RGS7, RGS11 or mGluR6 and then with HRP-conjugated secondary antibodies, and detected by using ECL West Pico system (Pierce, Carlsbad, CA). For the quantitative detection of RGS7 we used rabbit anti-RGS7 antibodies (07-237; Upstate Biotechnology, Billerica, MA). Signals were captured on film and scanned by densitometer, and band intensities were determined by using NIH ImageJ software.

Dissected eyecups were fixed for 15 min in 4% paraformaldehyde, cryoprotected with 30% sucrose in PBS for 2 hr at room temperature, and embedded in optimal cutting temperature medium. 12-micrometer frozen sections were obtained and blocked in PT1 (PBS with 0.1% Triton X-100 and 10% donkey serum) for 1 hr, then incubated with primary antibody in PT2 (PBS with 0.1% Triton X-100 and 2% donkey serum) for at least 1 hr. After four washes with PBS with 0.1% Triton, sections were incubated with fluorophore-conjugated secondary antibodies in PT2 for 1 hr. After four washes, sections were mounted in Fluoromount (Sigma, St. Louis, MO). Images were taken with a Leica SP800 confocal microscope. Quantitative analysis of immunofluorescence from confocal images was performed using Leica software. At each time point (day: 0, 12, 17, 22, 28, 35) immunohistochemical staining of cDKO:Cre+ was repeated twice and at least two sections obtained from two individual animals were used for analysis and averaging. Sections were double stained for RGS7 and marker protein mGluR6, which co-localizes with RGS7. Positive staining of mGluR6 was used as a reference for the normalization of the recorded fluorescence intensity in the channel containing RGS7 protein. Rod and cone synapses were differentiated by: (i) counter staining with PNA and/or b-arrestin that specifically label cone terminals, (ii) sublamina position in the outer plexiform layer, (iii) specific clustering pattern of synapses at cone terminals. The fluorescence intensity within synaptic puncta was analyzed using line-scan mode and a constant puncta-encircling area, which tightly surrounded the contours of each puncta. Mean intensity (measured in pixels) were averaged across ∼20 individual punctas per imaged section, taking three sections per retina, and two to three retinas used per time point. Imaging parameters were the same for all sections and retinas. Values for groups were normalized using pre-tamoxifen RGS7 values as a 100% percentage of protein remaining. RGS7 protein percentages were plotted vs the tamoxifen time course and fitted nicely with a simple decay function in GraphPad Prism 6.

Electroretinograms were recorded by using the UTAS system and a BigShot Ganzfeld (LKC Technologies, Gaithersburg, MD). Mice (4–8 wk old) were dark-adapted (≥6 hr) or light adapted (50 cd/m², 5 min) and prepared for recordings by using dim red light. Mice were anesthetized with an i.p. injection of ketamine and xylazine mixture containing 100 and 10 mg/kg, respectively. Recordings were obtained from the right eye only, and the pupil was dilated with 2.5% phenylephrine hydrochloride (Bausch & Lomb, Bridgewater, NJ), followed by the application of 0.5% methylcellulose. Recordings were performed with a gold loop electrode supplemented with contact lenses to keep the eyes immersed in solution. The reference electrode was a stainless steel needle electrode placed subcutaneously in the neck area. The mouse body temperature was maintained at 37°C by using a heating pad controlled by ATC 1000 temperature controller (World Precision Instruments, Sarasota, FL). ERG signals were sampled at 1 kHz and recorded with 0.3 Hz low-frequency and 300 Hz high-frequency cut-offs.

Full field white flashes were produced by a set of LEDs (duration < 5 ms) for flash strengths ≤2.5 cd·s/m² or by a Xenon light source for flashes > 2.5 cd·s/m² (flash duration < 5 ms). ERG responses were elicited by a series of flashes ranging from 2.5 × 10⁻⁴ to 2.5 × 10¹ cd·s/m² in increments of 10-fold. Ten trials were averaged for responses evoked by flashes up to 2.5 × 10⁻¹ cd·s/m², and three trials were averaged for responses evoked by 2.5 × 10⁰ cd·s/m² flashes. Single flash responses were recorded for brighter stimuli. To allow for recovery, interval times between single flashes were as follows: 5 s for 2.5 × 10⁻⁴ to 2.5 × 10⁻¹ cd·s/m² flashes, 30 s for 2.5 × 10⁰ cd·s/m² flashes, and 180 s for 2.5 × 10¹ cd·s/m² flashes.

ERG traces were analyzed using the EM LKC Technologies software, Sigma Plot and Microsoft Excel. The b-wave amplitude was calculated from the bottom of the a-wave response to the peak of the b-wave. To isolate the b-wave peak from sharp varying oscillatory potentials, a local regression smoothing algorithm using a bi-square weighting function was used in SigmaPlot (see Figure 7—figure supplement 1). Traces obtained from DKO, that completely lack the ON-BC triggered b-wave were subtracted from ERG traces recorded in cDKO:Cre+ mice following tamoxifen administration, each at corresponding light intensities. This was done to remove ambiquity of assigning diminishing b-wave due to interference with P1 component. The data points from the b-wave stimulus–response curves were fitted by Equation 1 using the least-square fitting method in GraphPad Prism6.

The first term of this equation describes rod-mediated responses (r), and the second term accounts primarily for responses that were cone mediated (usually at flash intensities ≥1 cd·s/m² for dark-adapted mice; index c). R_max,r and R_max,c are maximal response amplitudes, and I_0.5,r and I_0.5,c are the half-maximal flash intensities. Stimulus responses of retina cells increase in proportion to stimulus strength and then saturate, this is appropriately described by the hyperbolic curves of this function. The maximal amplitudes of rod and cone-driven b-wave stimulus–response curves in Tables 1, 2 are plotted against RGS7 protein concentration and fitted with a simple dose–response curve (variable slope) in GraphPad Prism6. Time to peak of the b-wave was measured as the time from the peak of a-wave to the peak of the b-wave.

Recordings of light-evoked currents in rod ON-BCs were performed as described previously (Okawa et al., 2010; Cao et al., 2012). Briefly, mice were dark-adapted overnight and euthanized according to protocols approved by the Institutional Animal Care and Use Committee of the University of Southern California (Protocol 10890). Retinas were isolated, embedded in a low-gelling temperature agar, and 200 µm slices were made on a vibrating microtome (Leica VT-1000S). Retinal slices were placed on the stage of an upright microscope and superfused with heated Ames Media (A-1420; 35-37°C) equilibrated with 5% CO₂/95% O₂. Whole-cell voltage clamp recordings (V_m = −60 mV) were made while delivering flashes of light that varied in strength from evoking a just-measurable response to those generating a maximal response. Noise variance was computed from the 0.2 s preceding the flash. Rod ON-BCs were identified in retinal slices based on the distinctive shape of the cell body and its position in the inner nuclear layer jammed up against the outer plexiform layer. The internal solution for whole-cell recordings consisted of (in mM): 125 K-Aspartate, 10 KCl, 10 HEPES, 5 NMG-HEDTA, 0.5 CaCl₂, 1 ATP-Mg, 0.2 GTP-Mg; pH was adjusted to 7.2 with NMG-OH. Membrane currents were filtered at 300 Hz by an 8-pole Bessel filter, and digitized at 1 KHz.

Mouse visual behavior was assessed using a water maze task with a visible escape platform. The method for assessing visual function in this experiment is principled on a Morris water maze (Morris, 1984) and previous reports describing evaluation of mouse vision by a swimming-based task (Prusky et al., 2000). Mice are natural swimmers and this task exploits their innate inclination to escape from water to a solid substrate. This task uses an ability of a mouse to see a visible platform with a timed escape from water, as an index of its visual ability. Before testing, mice readily learned to swim to the visible escape-platform and performance usually plateaued at around 10 s within 15 trials for all treated groups. Mice which did not learn the task, for example, performance did not improve or plateau for at least the last three or more consecutive trials or had any visible motor deficits were discarded from the experiment. Visual-guided behavior was tested at 100, 1, 0.1, 0.01, and 0.001 cd/m² and timed performances from 20 trials (four sessions of five trials each) for each mouse at each light-intensity were averaged. Uniform room luminance settings were stably achieved by an engineered adjustable light-source and constantly monitored with a luminance meter LS-100 (Konica Minolta, Tokyo, Japan). To be certain that we were measuring the mice's visual ability only and not memory, the platform was placed pseudo-randomly in the water tank and all external visual cues were eliminated.

Visual acuity and contrast sensitivity of mice was evaluated from optomotor responses using a two-alternative forced-choice protocol (Umino et al., 2008; Kolesnikov et al., 2011). Briefly, the animal was placed on a pedestal surrounded by four computer monitors and observed using infrared-sensitive television camera. For scotopic measurements, a round array of six infrared LEDs mounted above the platform was used to visualize the animal. Mice responded to visual stimuli (sine-wave vertical gratings presented by computer using staircase paradigm and invisible to the experimenter), by reflexively rotating their head in either clockwise or counterclockwise direction. The observer's task was to track the direction of optomotor responses and report it to the computer which determined the correctness of the choice (Prusky et al., 2004). Photopic visual acuity was determined as the threshold for spatial frequency (Fs) of the stimuli at 100% contrast. Contrast sensitivity was defined as the inverse of obtained contrast threshold values. Photopic responses of constitutive RGS7/11 DKO mice were measured at un-attenuated luminance of monitors (70 cd/m² at the mouse eye level), over a range of various Sp, from 3 to 50 deg/s. Fs of stimuli was kept constant at its optimal value of 0.128 cyc/deg for all speed regimes thus providing a range of corresponding temporal frequencies (Ft) from 0.38 to 6.4 Hz, according to following equation: Ft = Sp × Fs (Umino et al., 2008). Photopic contrast sensitivities of cDKO mice were determined at specified low (6 deg/s) or high (50 deg/s) Sp at 70 cd/m² luminance level. Scotopic contrast sensitivity of cDKO mice was evaluated at optimal values of Ft (0.75 Hz) and Sp (0.1 cyc/deg), and a corresponding stimuli speed of 7.5 deg/s. In this mode, the monitor luminance was attenuated to ∼3 × 10⁻⁴ cd/m² by several neutral density film filters that formed a cylinder around the animal. All data were analyzed using independent two-tailed Student t-test, with accepted significance level of p < 0.05.

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

We thank Mrs Martemyanova for help with animal breeding and genotyping and Dr Alicia Faruzzi Brantley for help with setting up behavioral experiments. This work was supported by NIH grants EY018139 (KAM), DA026405 (KAM), EY017606 (APS), EY019312 and EY021126 (VJK), EY002687 to the Department of Ophthalmology and Visual Sciences at Washington University, and EY000331 to the Jules Stein Eye Institute at UCLA.

Animal experimentation: All procedures were carried out in accordance with the National Institute of Health guidelines and were granted formal approval by the Institutional Animal Care and Use Committees of the Scripps Research Institute (IACUC protocol number 14-001), Washington University (IACUC protocol number 20140236), and the University of Southern California (IACUC protocol number 10890).

© 2015, Sarria et al.

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