Light stimulates rhodopsin in a retinal rod to activate the G protein transducin, which binds to phosphodiesterase (PDE), relieving PDE inhibition and decreasing guanosine 3′,5′-cyclic monophosphate (cGMP) concentration. The decrease in cGMP closes outer segment channels, producing the rod electrical response. Prolonged exposure to light decreases sensitivity and accelerates response kinetics in a process known as light adaptation, mediated at least in part by a decrease in outer segment Ca2+. Recent evidence indicates that one of the mechanisms of adaptation in mammalian rods is down-regulation of PDE. To investigate the effect of light and a possible role of rhodopsin kinase (G protein–coupled receptor kinase 1 [GRK1]) and the GRK1-regulating protein recoverin on PDE modulation, we used transgenic mice with decreased expression of GTPase-accelerating proteins (GAPs) and, consequently, a less rapid decay of the light response. This slowed decay made the effects of genetic manipulation of GRK1 and recoverin easier to observe and interpret. We monitored the decay of the light response and of light-activated PDE by measuring the exponential response decay time (τREC) and the limiting time constant (τD), the latter of which directly reflects light-activated PDE decay under the conditions of our experiments. We found that, in GAP-underexpressing rods, steady background light decreased both τREC and τD, and the decrease in τD was nearly linear with the decrease in amplitude of the outer segment current. Background light had little effect on τREC or τD if the gene for recoverin was deleted. Moreover, in GAP-underexpressing rods, increased GRK1 expression or deletion of recoverin produced large and highly significant accelerations of τREC and τD. The simplest explanation of our results is that Ca2+-dependent regulation of GRK1 by recoverin modulates the decay of light-activated PDE, and that this modulation is responsible for acceleration of response decay and the increase in temporal resolution of rods in background light.

## INTRODUCTION

Light-stimulated rhodopsin (Rh*) activates the rod heterotrimeric G protein transducin by facilitating exchange of GTP for GDP on the transducin guanine–nucleotide-binding site (see Fain, 2014). Transducin-GTP then binds to an inhibitory γ subunit of phosphodiesterase (PDE), releasing inhibition and activating PDE to hydrolyze cGMP, the second messenger controlling the photoreceptor light-dependent channels. Transducin turns itself off by hydrolyzing bound GTP to GDP with a rate that is greatly accelerated by a GTPase-accelerating protein (GAP) complex consisting of three components: RGS9-1, Gβ5-L, and R9AP (see Arshavsky and Wensel, 2013). Transducin-GDP is then released from the PDE γ subunit, extinguishing PDE activation.

Sensory receptors adapt in the presence of maintained stimulation, but the mechanism of adaptation remains unresolved. In mammalian rods, adaptation seems to be produced by modulation of the synthesis and hydrolysis of cGMP. Considerable evidence indicates a role for Ca2+-binding guanylyl cyclase–activating proteins (GCAPs; see Arshavsky and Burns, 2012; Morshedian and Fain, 2014), in the following way. Light activates PDE, which decreases cGMP, reduces channel conductance, and decreases outer segment Ca2+. The decrease in Ca2+ reduces Ca2+ binding to the GCAPs, stimulating guanylyl cyclase to increase cGMP synthesis and oppose the decrease in cGMP produced by light.

Although the GCAPs clearly contribute, rods still show considerable adaptation in constant light or after bleaches in rods for which the GCAPs have been deleted (Mendez et al., 2001; Burns et al., 2002; J. Chen et al., 2010; Nymark et al., 2012). We (Woodruff et al., 2008; J. Chen et al., 2010) and others (Soo et al., 2008) have proposed that the decrease in cGMP produced by light is also countered by negative regulation of PDE activity, producing an important additional component of adaptation (see Fain, 2011; Morshedian and Fain, 2014). Background light can decrease the limiting time constant (τD) of response decay (Woodruff et al., 2008), which under the conditions of our experiments directly reflects light-dependent acceleration of the decay of PDE (Krispel et al., 2006; Tsang et al., 2006; C.K. Chen et al., 2010). Rods lacking GCAP proteins show large current overshoots after steady light exposure (Burns et al., 2002; J. Chen et al., 2010), which are most likely caused by a transient increase in cGMP concentration. We believe that this increase in cGMP is produced by a decrease in the rate of spontaneous and light-activated PDE, either through direct modulation of PDE itself or one of the other proteins controlling PDE activity such as transducin or the GAP proteins. A detailed model of adaptation including both cyclase and PDE regulation can account for all of the changes in sensitivity and waveform of rods in background light (J. Chen et al., 2010).

How is PDE activity controlled? Our experiments suggest that rhodopsin kinase (G protein receptor kinase 1 [GRK1]) and the Ca2+-binding protein recoverin, in addition to their well-known roles in phosphorylating and turning off light-activated rhodopsin, may also alter the rate of PDE decay by phosphorylating some component of the PDE–transducin–GAP complex. Overexpression of GRK1 or deletion of recoverin can shorten τD, and recoverin deletion eliminates the acceleration of response decay by background light (Chen et al., 2012). Our results differ from those of Krispel et al. (2006), Sakurai et al. (2011), and Gross et al. (2012), who also recorded from mouse rods with varying degrees of increased GRK1 expression but did not observe a significant effect on the limiting time constant and decay of light-activated PDE. To resolve this discrepancy, we reasoned that effects on response kinetics might be easier to observe if the decay of the rod response was further slowed by underexpressing the GAPs.

In this paper, we show in GAP-underexpressing rods that background light produces a systematic decrease in τD that is linear with the decrease in circulating current, but there is little change in τD if recoverin has been deleted. Moreover, in GAP-underexpressing rods, overexpression of GRK1 and recoverin deletion both produce large and highly significant reductions of the limiting time constant τD. Because under the conditions of our experiments the limiting time constant is a direct reflection of the decay of PDE (Krispel et al., 2006; Tsang et al., 2006; C.K. Chen et al., 2010) and is not affected by the decay of Rh*, which is much too rapid to limit the decay of the rod light response (Burns and Pugh, 2010), our results strongly suggest that GRK1 may also act at targets in addition to Rh*, and that Ca2+-dependent regulation of rhodopsin kinase by recoverin is largely responsible for acceleration of the decay of the rod light response in background light.

## MATERIALS AND METHODS

### Transgenic mice

WT mice were C57BL/6 from The Jackson Laboratory. Homozygous R9AP knockout mice (Keresztes et al., 2004) were provided by V. Arshavsky (Duke University, Durham, NC). They were mated with WT C57BL/6J mice to produce heterozygous R9AP+/− mice with about half the transducin-GAP level in the retina (see Results). To reduce the transducin-GAP level further to below 50%, we generated compound heterozygous mice that were R9AP+/− and RGS9-1+/− by mating individual heterozygous knockouts, genotyping, and comparing GAP expression levels in resulting offspring. In compound R9AP+/− and RGS9+/− heterozygous knockouts, the GAP level could be reliably reduced to ∼34% (see Fig. 1). Genotypes of these various lines were determined by PCR before electrical recoding with procedures described previously (see, for example, Krispel et al., 2006). All experiments were performed on pigmented mice of either sex in accordance with the rules and regulations of the National Institutes of Health guidelines for research animals, as approved by the institutional animal care and use committees of the Virginia Commonwealth University and the University of California, Los Angeles. Animals were kept in cyclic 12/12 h on/off lighting in approved cages and supplied with ample food and water. Animals in all experiments were killed before tissue extraction by approved procedures, usually CO2 inhalation or decerebration.

### Antibodies

Rabbit anti-Gβ5 (CT-215), anti–RGS9-1 (CT318), and anti-Gβ1 (BN-1) antibodies were provided by M. Simon (California Institute of Technology, Pasadena, CA). Rabbit anti-GAPDH antibody was obtained from Cell Signaling Technologies. Mouse anti-PDE6B antibody and horseradish peroxidase–conjugated secondary antibodies were from Santa Cruz Biotechnology, Inc.

### Immunoblotting

Retinal extracts (10 µg) were resolved by 12% SDS-PAGE and transferred onto nitrocellulose membranes. The membranes were blocked with 10% dry milk in TBST buffer containing 25 mM Tris, pH 7.5, 137 mM NaCl, and 0.05% Tween-20. For the detection of both forms of Gβ5, CT215 was used at a 1:4,000 dilution. To detect RGS9-1, CT318 was used at a 1:4,000 dilution. For Gβ1, BN-1 was used at a 1:50,000 dilution. Anti-R9AP antibody was used at a 1:500 dilution. For PDE6β, the mouse antibody was used at a 1:500 dilution. Anti-GAPDH antibody was used at a 1:100,000 dilution, and the GAPDH signal was used as a loading control. Species-specific secondary antibodies were used at a 1:25,000 dilution. The signal was detected by enhanced chemiluminescence with the SuperSignal West Dura substrate kit (Thermo Fisher Scientific). Gel images were captured and quantified in an imaging station (IS440; Kodak) with an accompanying 1-D image analysis program (Kodak).

### Electrophysiology

Methods for making suction-electrode recordings from mouse rods have been given previously (C.K. Chen et al., 2010; Chen et al., 2012). Rods were perfused at 37°C with Dulbecco’s modified Eagle’s medium (D-2902; Sigma-Aldrich), supplemented with 15 mM NaHCO3, 2 mM Na succinate, 0.5 mM Na glutamate, 2 mM Na gluconate, and 5 mM NaCl, bubbled with 95% O2/5% CO2, pH 7.4. Unless otherwise indicated, data were filtered at 35 Hz (eight-pole Bessel) and sampled at 100 Hz. Flashes of 500-nm light at 20 ms in duration were attenuated to different light levels by absorptive neutral density filters. A 500-nm light was also used for background illumination. Other information about the details of response presentation are given in the figure legends. The values of τD were measured as in Woodruff et al. (2008) by giving a series of five flashes at each of between four to seven intensities chosen for each rod to fall within one and a half log units above the flash intensity that just produced saturation of that rod’s response amplitude. The time in saturation (Tsat) was measured as the time from the beginning of the flash to the time at which the mean circulating current recovered to 25% of its dark-adapted value. Single-photon responses were calculated from the squared mean and variance as described previously (Chen et al., 2000; Tsang et al., 2006). Unless otherwise stated, errors are given as SEM, and significance was tested either with ANOVA or Student’s t. Curve fitting, statistical tests, and plotting of data were done with the program Origin (OriginLab).

## RESULTS

To produce rod responses with prolonged PDE activation and slowed decay, we used two lines of mice with reduced GAP expression (Fig. 1). The first was an R9AP heterozygous knockout mouse (R9AP+/−), with reduced expression of the RGS9-1 protein and also of Gβ5-L to a mean value of 51%. The second line of mice was doubly heterozygous for both R9AP and RGS9, which for convenience we call “GAPux” or simply “ux.” Expression levels for RGS9-1 and Gβ5-L in GAPux rods were reduced to a mean value of 34%. The levels of other similar proteins not part of the rod GAP complex such as Gβ5-S and Gβ1 were unaffected in both mouse lines (Fig. 1 A). Moreover, the expression level of PDE6β was unaffected by underexpressing the GAP proteins (Fig. 1, B and D). Keresztes et al. (2004) showed previously that underexpression of GAP proteins is also without effect on the level of transducin.

### R9AP+/− rods

In Fig. 2, we show that reduction of GAP expression in R9AP+/− rods resulted in responses to brief stimuli that decayed more slowly than those of WT rods for the same flash intensities (Fig. 2, A and B). To simplify comparison of waveforms, we show in red the responses to flashes of 23 photons µm−2. The limiting time constant was greater in R9AP+/− rods than in WT rods (see Table 1), and this difference was highly significant (t test, P = 0.0026).

To test the effects of overexpression of rhodopsin kinase, we mated R9AP−/− mice with RKS561L mice, which our previous experiments have shown to express ∼12 times more kinase than WT rods and which show more rapid phosphorylation of bleached rhodopsin (Chen et al., 2012). Responses of R9AP+/−;RKS561L rods decayed more rapidly than R9AP+/− rods (Fig. 2 C). Response decay was also accelerated when we deleted recoverin in the R9AP+/− background (Fig. 2 D). Deletion of recoverin should release rhodopsin kinase from inhibition by recoverin binding (Kawamura, 1993; Chen et al., 1995), effectively increasing the amount of rhodopsin kinase available to phosphorylate target proteins. Table 1 shows that the values of τD for R9AP+/−;RKS561L (182 ± 10 ms) and R9AP+/−;Rv−/− rods (187 ± 16 ms) were smaller than for R9AP+/− rods (254 ± 18 ms). A one-way ANOVA reported that the mean values for τD were significantly different among these three groups of animals, at least at the 0.001 level. Pairwise t tests revealed that the difference in the values of τD for R9AP+/− and R9AP+/−;RKS561L rods was highly significant (P = 0.0006), and the difference in the value of τD between R9AP+/− rods and R9AP+/−;Rv−/− rods was also statistically significant (P = 0.045).

### GAPux rods

Because GAPux mice express the GAP-complex proteins at an even lower level than R9AP+/− mice, we subjected GAPux rods to more extensive analysis. GAPux responses (Fig. 3 A) again decayed more slowly than WT rods. The mean integration time increased from 262 ms in WT rods to 418 ms in GAPux rods (t test, P = 0.00016). Overexpression of GRK1 (Fig. 3 B) or deletion of recoverin (Fig. 3 C) both accelerated the decay of the response and reduced the integration time (see Table 1). The decreases in integration time were again highly significant (GAPux vs. GAPux;RKS561L, P = 0.00001; GAPux vs. GAPux;Rv−/−, P = 0.00011) and brought them nearly to the value of the integration time in WT animals. There were no significant differences in integration times between WT and GAPux;RKS561L (P = 0.21) or WT and GAPux;Rv−/− (P = 0.61), indicating that overexpression of rhodopsin kinase or the deletion of the recoverin gene can effectively compensate for the slowing of response kinetics produced by underexpressing the GAP proteins.

In Fig. 4, we examine the time course of response decay in more detail. In Fig. 4 A, we show mean responses to single photons calculated as in previous experiments from the squared mean and variance of a series of responses to dim-intensity flashes (see, for example, Chen et al., 2000; Tsang et al., 2006). Overexpression of rhodopsin kinase (red trace) produced about a twofold decrease in response amplitude and a marked acceleration of the single-exponential time constant of response decay. Deletion of recoverin (blue trace) had little effect on response amplitude but greatly quickened the rate of response decay. The decay time was quantitated by fitting a single-exponential decay function to the declining phases of the responses (smooth curves in Fig. 4 A). The value of the decay time constant (τREC) was considerably smaller for GAPux;RKS561L rods (193 ms) and GAPux;Rv−/− rods (174 ms) than for GAPux rods (331 ms). We also show for comparison the single-photon response of WT rods. The initial time courses of all of the responses are not detectably different, indicating that none of the genetic manipulations we have made had a significant effect on the time course of activation.

In Fig. 4 B, we show the effects of GRK1 overexpression and recoverin deletion on response decay in a different way. We fitted the waveform of responses rod by rod to exponential decay functions in the linear range of response amplitude to derive the mean value of the time constant τREC as a function of flash intensity. Fits were done from threshold to just-saturating flash intensities and did not include responses to flashes above saturation, which evoked slowly decaying “tails” (as in the responses to the brightest flashes in Fig. 3). The exponential fit was constrained only to the part of the current <0.5 of the peak current amplitude to avoid the nonlinearity produced by response saturation. No other constraints were placed on the fits. There was some variability in the value of τREC at different intensities for all three mouse lines, as well as a tendency for τREC to increase with increasing flash brightness. These results nevertheless document the systematic decrease in τREC and acceleration of flash decay for both the GAPux;RKS561L and GAPux;Rv−/− rods compared with the GAPux rods.

### Limiting time constant τD

We also characterized rod response decay by estimating the value of the limiting time constant τD from measurements of the time in saturation (Tsat) as a function of flash intensity (Pepperberg et al., 1992). Values of Tsat for GAPux, GAPux;RKS561L, and GAPux;Rv−/− rods were determined as the duration between the beginning of the flash and the time at which responses decayed to 25% of the dark circulating current, as indicated by the horizontal lines in Fig. 3. We plotted Tsat as a function of the natural log of the flash intensity and took best-fitting straight lines as estimates of τD (Pepperberg et al., 1992).

In Fig. 5, we have plotted mean values (with SEMs) of Tsat for the three GAPux mouse lines. The mean values of the first three flash intensities in the figure were well fit by straight lines with slopes of 249 ms (GAPux), 176 ms (GAPux;RKS561L), and 209 ms (GAPux;Rv−/−). Because the GAPux;RKS561L rods were less sensitive than the other two (Table 1), we used a different range of intensities to ensure that the flash intensities for the measurements were uniformly a factor of ∼30 (1.5 log10 units) above those just causing response saturation (see Materials and methods). We used only three data points in these fits, because the fourth brightest intensity for each of the mouse strains was slightly above the resulting straight line, indicating that by this fourth intensity Tsat was already beginning to depart from linearity (see Martemyanov et al., 2008). If four data points were included in our fits, the best-fitting values of τD uniformly increased to 276 ms (GAPux), 195 ms (GAPux;RKS561L), and 230 ms (GAPux;Rv−/−), but there was very little change in the difference between the value for GAPux rods on the one hand and GAPux;RKS561L rods or GAPux;Rv−/− rods on the other.

In Table 1, we show mean values of τD estimated as in Fig. 5 from Tsat values determined rod by rod from fits for each photoreceptor. The mean values of the fits in the table are in close agreement with the fit to the means in Fig. 5. The values of τD of both the GAPux;RKS561L rods (179 ± 10 ms) and the GAPux;Rv−/− rods (204 ± 14 ms) were smaller than GAPux rods (248 ± 12 ms). A one-way ANOVA reported differences in the mean values for τD at least at the 0.001 level. Pairwise t tests showed that the difference between GAPux and GAPux;RKS561L was highly significant (P = 0.00005), and the difference between GAPux and GAPux;Rv−/− was also significant (P = 0.022).

### The effect of background light and circulating current on τD

We have shown previously that the limiting time constant in WT rods can be decreased by steady background light (Woodruff et al., 2008). Because the value of τD in darkness is larger for R9AP+/− rods and GAPux rods than for WT rods (Table 1), it seemed to us possible that rods underexpressing the GAP proteins would provide a larger range over which to investigate the effects of background light intensity on τD. We therefore measured τD by stimulating GAPux rods with bright, saturating flashes to measure Tsat as in the experiments of Fig. 5, but in the presence of a range of steady background intensities.

The results of these experiments are given in Fig. 6 A. The open symbols show the mean value of τD for GAPux rods, plotted as a function of the background light intensity IB (in photons µm−2 s−1). The solid curve fitted to the data is the equation τD = τD0 + A[exp(−IB/k)], with τD0, A, and k constants whose best-fitting values were τD0 = 69 ms, A = 160 ms, and k = 538 photons µm−2 s−1. These data show that the value of the limiting time constant was systematically reduced as the intensity of the background light was increased and declined asymptotically for GAPux rods to a value of ∼70 ms in bright light, in approximate agreement with our previous measurement of τD in bright background light for WT rods of 75 ± 5 ms (Woodruff et al., 2008). The closed symbols give the data for GAPux;Rv−/− rods and indicate that there is a much smaller change (if any) in the value of τD with background light in rods lacking recoverin. The value of τD was smaller for GAPux;Rv−/− rods than for GAPux rods in darkness and was little changed by dim or even bright background light. The dashed curve was determined by linear regression with the slope constrained to be zero; the best-fitting value of τD was 191 ms.

Because photoreceptor response amplitude as a function of light intensity can be adequately fitted in some cases with exponential saturation functions (Lamb et al., 1981), we thought it possible that the exponential decrease in τD in Fig. 6 A might result from a linear dependence of τD on circulating current. We therefore estimated circulating current in background light for each of the rods in Fig. 6 A from the peak amplitude of saturating responses in the presence of each of the background intensities. The relationship of τD to circulating current is given in Fig. 6 B. For GAPux rods, the mean values of τD can be adequately fitted with a straight line, particularly at the dimmer background intensities. For the two brightest backgrounds, the means showed some departure from the best-fitting straight line; but for these bright backgrounds, the measurements of τD and of circulating current were more difficult to make accurately because responses were small. Even with all of the data points in Fig. 6 B used for the linear fit, the coefficient of determination r2 had a value of 0.76. For GAPux;Rv−/− rods, there was again little change in τD. Collectively, the data in Fig. 6 (A and B) indicate that background light produces a decrease in τD nearly in proportion to the decrease in circulating current, and that this modulation of τD is dependent on the Ca2+-binding protein recoverin.

### Light adaptation in GAPux and GAPux;Rv−/− rods

Because background light reduces τD in GAPux rods but not in GAPux;Rv−/− rods, we were curious to know whether other aspects of light adaptation would also be affected if recoverin were deleted. Fig. 7 shows measurements of sensitivity (SF) divided by sensitivity in darkness ($SFD$) as a function of background light intensity. Sensitivity was calculated as the peak response amplitude for small-amplitude responses divided by the flash intensity in photons µm−2. Means have been fitted with the Weber–Fechner equation, SF/$SFD$ = I0/(I0 + IB), where I0 is a constant and IB is the intensity of the background light. Both GAPux and GAPux;Rv−/− rods show decreases in sensitivity in approximate agreement with this equation, as has been shown previously for WT rods and Rv−/− rods on a WT background (Makino et al., 2004; J. Chen et al., 2010). The best-fitting value of I0 is somewhat smaller for GAPux rods (20 photons µm−2 s−1) than for WT rods (77 photons µm−2 s−1), and I0 is somewhat larger for GAPux;Rv−/− rods (154 photons µm−2 s−1). Thus, GAPux rods are somewhat more sensitive and GAPux;Rv−/− rods somewhat less sensitive to background light than WT rods. The increase in sensitivity for GAPux rods may reflect in part the greater integration time of these photoreceptors (Table 1).

In the inset to Fig. 7, we show normalized responses to brief flashes of the same intensity in the presence of background light in GAPux rods (top) and GAPux;Rv−/− rods (bottom). The decay time of the GAPux rod response was progressively accelerated with increasing background light intensity, as we have shown previously for WT rods (Woodruff et al., 2008) and GCAPs−/− rods (J. Chen et al., 2010). There was, however, much less acceleration of the time course of decay in rods lacking recoverin (Chen et al., 2012). The results of Figs. 6 and 7 together show that background light produces a progressive decrease in τREC as well as in τD, and that both effects are largely ablated when recoverin is deleted from the genome. They also show that there is little effect produced by recoverin deletion on the decrease of sensitivity in background light, indicating that the control of sensitivity and response waveform during light adaptation may be produced by different mechanisms.

## DISCUSSION

Our work has two principal conclusions. First, overexpression of GRK1 or deletion of recoverin can produce not only an acceleration in the time course of decay of the photoreceptor light response but also a significant decrease in the limiting time constant τD. This result is important, because Nikonov et al. (1998) showed that the limiting decay of light-activated PDE activity is given by a difference of exponential decay functions for Rh* and the Gα–PDE complex (PDE*), with the time constant of the slowest decay always dominating; previous experiments have shown that the decay of PDE* in WT mouse rods (∼200 ms) is much slower than the decay of Rh* (∼50 ms) and is directly responsible for the limiting time constant of response decay (Krispel et al., 2006; Tsang et al., 2006; Burns and Pugh, 2010; C.K. Chen et al., 2010). Although our experiments indicate that overexpression of GRK1 and recoverin deletion would be expected to accelerate the decay of both Rh* and of PDE*, we have shown previously for rods in a WT background that the decay of PDE* is slower than Rh* decay and continues to determine the time course of response decay even when GRK1 is overexpressed or recoverin deleted (Chen et al., 2012). Rods with decreased GAP expression have an even slower PDE* decay, and the difference in the decay time constants for Rh* and PDE* should be even greater. We are therefore confident that the value of τD in our experiments reflects the decay of light-activated PDE in all of the rods we have examined.

We have now looked at GRK1 overexpression in three different backgrounds: WT mice (Chen et al., 2012) and, in this study, R9AP+/− and GAPux mice. The differences in the values of τD with and without GRK1 overexpression were highly significant for all three: P = 0.001 (WT), P = 0.0006 (R9AP+/−), and P = 0.00005 (GAPux). Moreover, the relative reduction in τD produced by GRK1 overexpression was approximately the same in all three mouse background strains, in WT and after reducing GAP expression. This is not the result we would expect if GRK1 were acting only on Rh* decay. Our results now firmly establish an effect of GRK1 on the rate of decay of light-activated PDE, and because deletion of recoverin also produces a significant reduction in τD (see also Makino et al., 2004; Bush and Makino, 2007), modulation of PDE decay by GRK1 seems to be produced at least in part through the action of the GRK1-binding protein recoverin. We conclude that, contrary to current thinking, GRK1 together with recoverin—in addition to phosphorylating rhodopsin—may alter the activities of one or more phototransduction proteins, either by directly phosphorylating them or indirectly through some unknown mechanism.

The second major conclusion of our work is that background light produces a progressive decrease in the value of the rod-limiting time constant (Fig. 6 A) in addition to a systematic acceleration of the rate of decay of the light response (Fig. 7 and Woodruff et al., 2008; Chen et al., 2012). The decrease in τD is nearly linear with the reduction in circulating current (Fig. 6 B). Little or no change was observed in either τD (Fig. 6 A) or τREC (Fig. 7 and Chen et al., 2012) after deletion of recoverin. Because a reduction in circulating current should produce a proportionate decrease in the rod outer segment Ca2+ concentration by decreasing the rate of Ca2+ influx, and because the k1/2 for the binding of Ca2+ to recoverin is several micromolar (Chen et al., 1995) and much higher than the resting free-Ca2+ concentration in a mouse rod outer segment (Woodruff et al., 2002), the simplest explanation of our observations is that background light decreases Ca2+ and relieves inhibition of GRK1 by recoverin, which then increases the phosphorylation of some protein that accelerates the rate of light-activated PDE decay. This mechanism is apparently responsible for the acceleration of rod response decay in background light and the increase in the scotopic flicker-fusion frequency with increasing ambient light intensity. We discuss these two principal conclusions in more detail below.

### GAP underexpression, GRK1 overexpression, and recoverin deletion

To record from rods with prolonged time constants of decay, we used animals heterozygous for the R9AP gene. Overexpression and underexpression of R9AP has been shown previously to produce commensurate changes in expression of the GAP proteins (Keresztes et al., 2004; Krispel et al., 2006), whereas inactivation of one copy of either RGS9-1 (Chen et al., 2000) or Gβ5 (Chen et al., 2003) has by itself little effect on GAP expression. The results in Fig. 1 show that R9AP+/− rods contain about half the normal amount of both R9AP and Gβ5-L; expression levels of other similar proteins and of PDE are unaffected. Our measurement of the level of GAP expression in R9AP+/− is similar to that of Keresztes et al. (2004) but considerably higher than the value of 20% of WT reported by Burns and Pugh (2009). The responses we recorded from R9AP+/− rods decayed more slowly than those of WT rods, but the difference in decay time was not as pronounced as that reported previously (see Fig. 1S in Supporting Material of Burns and Pugh, 2009). We are unable at present to offer an explanation for these differences, as the R9AP−/− animals used in both sets of experiments were taken from the same source (Keresztes et al., 2004).

We also reduced GAP expression further by breeding animals to be heterozygous for both the R9AP and RGS9-1 genes. Our results show that a reduction in the copy number of the RGS9-1 gene can influence expression of GAP proteins in animals that are also R9AP+/−, because in GAPux animals we succeeded in reducing the expression of both RGS9-1 and Gβ5-L to about one third of WT levels. The response integration time was even greater in GAPux rods than in R9AP+/− rods (t test, P = 0.017), but we were surprised that we could not detect a significant difference in the limiting time constant between these two groups of animals. The difference might have been greater and more easily detected had we also deleted the GCAP proteins and prevented acceleration of response decay by the guanylyl cyclase (Gross et al., 2012).

We tested the effect of GRK1 expression on R9AP+/− and GAPux rods by interbreeding them with RKS561L mice, which our previous experiments have shown to overexpress GRK1 by a factor of ∼12 and to speed the rate of rhodopsin phosphorylation (Chen et al., 2012; see also Gross et al., 2012). Overexpression of GRK1 in both R9AP+/− and GAPux rods produced a reduction of integration time (Table 1), a decrease in the single-exponential decay time constant τREC (Fig. 4), and an acceleration of the limiting time constant τD (Table 1 and Fig. 5). The acceleration of τD in R9AP+/− and GAPux rods are in contrast to previous attempts to detect an effect of GRK1 overexpression on τD (Krispel et al., 2006; Sakurai et al., 2011; Gross et al., 2012), which all failed to show a statistically significant effect. We believe that these previous attempts were unsuccessful either because the amount of GRK1 expression was lower than in our experiments (Krispel et al., 2006; Sakurai et al., 2011) or because measurements were made on a WT background, in which a small decrease in τD could not be shown to be significant (Gross et al., 2012).

Decreases in integration time and τD were also produced in both R9AP+/− and GAPux rods by deleting the recoverin gene (Table 1). Similar effects of recoverin deletion have been observed previously on a WT background (Makino et al., 2004; Bush and Makino, 2007; Chen et al., 2012). Deleting recoverin would increase the effective activity of GRK1 by preventing recoverin-dependent inhibition. For GAPux rods, the effects of recoverin deletion were smaller than 12 times GRK1 overexpression, both on the limiting time constant (Table 1) and on the amplitude of the single-photon response (Fig. 4 A). One possible explanation for this difference is that the effective increase in GRK1 activity was smaller in Rv−/− mice than in RKS561L animals, but deletion of recoverin might also have other effects on rod responses, perhaps as the result of a change in outer segment Ca2+ buffering (Makino et al., 2004). These additional effects may explain why τD is smaller in the brightest background intensities than after recoverin deletion (Fig. 6 A).

### Mechanism of modulation of light-activated PDE

Our experiments on R9AP+/− and GAPux rods, together with previous work on rods with normal GAP expression (Chen et al., 2012), indicate that the decay of light-activated PDE can be modulated by GRK1 in concert with recoverin. GRK1 overexpression and recoverin deletion accelerate τD, whose value under the conditions of our experiments reflects the rate of decay of light-activated PDE (Krispel et al., 2006; Tsang et al., 2006; C.K. Chen et al., 2010). These effects are unlikely to be caused by nonspecific protein interactions between GRK1 and the PDE, because modulation of the rod decay rate requires the GAP proteins; GRK1 overexpression has no effect on rod response decay if RGS9-1 and the other GAP proteins are completely deleted (Chen et al., 2012).

Because GRK1 overexpression and recoverin deletion have similar effects on light-activated PDE decay, we suggest that the two proteins act in concert. Recoverin may inhibit GRK1 at high levels of outer segment Ca2+ in darkness. During steady light exposure, the decrease in Ca2+ produced by the reduction in the probability of opening of the cGMP-gated channels would cause recoverin to be released from GRK1, freeing the kinase to phosphorylate target proteins. This mechanism would explain why τD decreases in proportion to the decrease in circulating current during background light exposure (Fig. 6 B) and would also clarify why deletion of recoverin largely prevents modulation of τREC (Fig. 7) and τD (Fig. 6). The linear relationship in Fig. 6 B could be the result of a linear dependence of outer segment free-Ca2+ concentration on circulating current (see, for example, Woodruff et al., 2007), together with the elevated k1/2 for the binding of Ca2+ to recoverin (Chen et al., 1995). Our experiments do not indicate the nature of the phosphorylated protein, which we speculate to be PDE itself (see, for example, Tsang et al., 2007), one of the GAP proteins (Balasubramanian et al., 2001; Hu et al., 2001), or transducin. One possibility is that phosphorylation accelerates the binding of transducin to the GAP proteins so that transducin is shut off more rapidly. Rapid binding of transducin to the GAPs could cause transducin to be shut off even before it activates PDE, perhaps explaining why rods with six times overexpressed GAP proteins (C.K. Chen et al., 2010) or 12 times overexpressed GRK1 (Table 1 and Chen et al., 2012; Gross et al., 2012) show a two- to threefold decrease in sensitivity. Moreover, the value of the limiting time constant in rods with six times overexpressed GAP proteins is not further accelerated when GRK1 is also overexpressed (Chen et al., 2012), perhaps because the rate of binding is already so rapid that it cannot be made faster.

We propose that GRK1 and recoverin are together primarily responsible for the progressive acceleration of rod response decay (Fig. 7, inset) and the limiting time constant (Fig. 6) during adaptation to steady background light. Because the rate of photoreceptor response decay determines the sensitivity of the visual system to change and motion, the modulation of light-activated PDE provides an essential Ca2+-dependent mechanism that permits the rods to respond more rapidly to changes in light intensity in the presence of brighter ambient illumination. We suggest that this mechanism is also responsible at least in part for the acceleration of the scotopic flicker-fusion frequency during light adaptation (Brindley, 1970).

Our experiments show, however, that the change in sensitivity in background light is nearly unaffected by recoverin deletion (Fig. 7). Although the fit of increment sensitivity to the Weber function for the GAPux;Rv−/− rods is not terribly good, the fit of these data to the exponential saturation function is even worse: the sensitivity of the GAPux;Rv−/− rods at a background intensity of 1,000 photons µm−2 s−1 is two orders of magnitude greater than the exponential saturation function would predict (Mendez et al., 2001). Moreover, both J. Chen et al. (2010) and Makino et al. (2004) have shown that deletion of the recoverin gene on a WT background has no effect on the change in increment sensitivity in steady light. These results indicate that other mechanisms must also be present in the rod outer segment in addition to GCAP modulation of cyclase and GRK1 regulation of PDE decay, which can also regulate the transduction cascade to produce adaptation during background illumination.

## Acknowledgments

We thank Joung Jang, Xin Guan, Viet Chau, and Frank Chen for excellent technical assistance, and an anonymous reviewer for helpful comments.

This work was supported by National Institutes of Health grants EY01844 (to G.L. Fain) and EY013811 (to C.-K. Chen). C.-K. Chen is the Alice R. McPherson Retina Research Foundation Endowed Professor.

The authors declare no competing financial interests.

Angus C. Nairn served as editor.

## References

Arshavsky
,
V.Y.
, and
M.E.
Burns
.
2012
.
Photoreceptor signaling: Supporting vision across a wide range of light intensities
.
J. Biol. Chem.
287
:
1620
1626
.
Arshavsky
,
V.Y.
, and
T.G.
Wensel
.
2013
.
Timing is everything: GTPase regulation in phototransduction
.
Invest. Ophthalmol. Vis. Sci.
54
:
7725
7733
.
Balasubramanian
,
N.
,
K.
Levay
,
T.
Keren-Raifman
,
E.
Faurobert
, and
V.Z.
Slepak
.
2001
.
Phosphorylation of the regulator of G protein signaling RGS9-1 by protein kinase A is a potential mechanism of light- and Ca2+-mediated regulation of G protein function in photoreceptors
.
Biochemistry.
40
:
12619
12627
.
Brindley
,
G.S.
1970
.
Physiology of the retina and visual pathway
.
Williams and Wilkins
,
Baltimore, MD
.
315 pp
.
Burns
,
M.E.
, and
E.N.
Pugh
Jr
.
2009
.
RGS9 concentration matters in rod phototransduction
.
Biophys. J.
97
:
1538
1547
.
Burns
,
M.E.
, and
E.N.
Pugh
Jr
.
2010
.
Lessons from photoreceptors: Turning off G-protein signaling in living cells
.
Physiology (Bethesda).
25
:
72
84
.
Burns
,
M.E.
,
A.
Mendez
,
J.
Chen
, and
D.A.
Baylor
.
2002
.
Dynamics of cyclic GMP synthesis in retinal rods
.
Neuron.
36
:
81
91
.
Bush
,
R.A.
, and
C.
Makino
.
2007
.
Recoverin shapes the photoresponse of retinal rods
.
In
Neuronal Calcium Sensor Proteins.
P.
Philippov
and
K.W.
Koch
,
editors
.
Nova Science Publishers
,
Hauppauge, NY
.
153
180
.
Chen
,
C.K.
,
J.
Inglese
,
R.J.
Lefkowitz
, and
J.B.
Hurley
.
1995
.
Ca2+-dependent interaction of recoverin with rhodopsin kinase
.
J. Biol. Chem.
270
:
18060
18066
.
Chen
,
C.K.
,
M.E.
Burns
,
W.
He
,
T.G.
Wensel
,
D.A.
Baylor
, and
M.I.
Simon
.
2000
.
Slowed recovery of rod photoresponse in mice lacking the GTPase accelerating protein RGS9-1
.
Nature.
403
:
557
560
.
Chen
,
C.K.
,
P.
Eversole-Cire
,
H.
Zhang
,
V.
Mancino
,
Y.J.
Chen
,
W.
He
,
T.G.
Wensel
, and
M.I.
Simon
.
2003
.
Instability of GGL domain-containing RGS proteins in mice lacking the G protein β-subunit Gβ5
.
100
:
6604
6609
.
Chen
,
C.K.
,
M.L.
Woodruff
,
F.S.
Chen
,
D.
Chen
, and
G.L.
Fain
.
2010
.
Background light produces a recoverin-dependent modulation of activated-rhodopsin lifetime in mouse rods
.
J. Neurosci.
30
:
1213
1220
.
Chen
,
C.K.
,
M.L.
Woodruff
,
F.S.
Chen
,
Y.
Chen
,
M.C.
Cilluffo
,
D.
Tranchina
, and
G.L.
Fain
.
2012
.
Modulation of mouse rod response decay by rhodopsin kinase and recoverin
.
J. Neurosci.
32
:
15998
16006
.
Chen
,
J.
,
M.L.
Woodruff
,
T.
Wang
,
F.A.
Concepcion
,
D.
Tranchina
, and
G.L.
Fain
.
2010
.
Channel modulation and the mechanism of light adaptation in mouse rods
.
J. Neurosci.
30
:
16232
16240
.
Fain
,
G.L.
2011
.
Adaptation of mammalian photoreceptors to background light: Putative role for direct modulation of phosphodiesterase
.
Mol. Neurobiol.
44
:
374
382
.
Fain
,
G.L.
2014
.
Molecular and Cellular Physiology of Neurons
. Second edition.
Harvard University Press
,
Cambridge, MA
.
752 pp
.
Gross
,
O.P.
,
E.N.
Pugh
Jr
, and
M.E.
Burns
.
2012
.
Calcium feedback to cGMP synthesis strongly attenuates single-photon responses driven by long rhodopsin lifetimes
.
Neuron.
76
:
370
382
.
Hu
,
G.
,
G.F.
Jang
,
C.W.
Cowan
,
T.G.
Wensel
, and
K.
Palczewski
.
2001
.
Phosphorylation of RGS9-1 by an endogenous protein kinase in rod outer segments
.
J. Biol. Chem.
276
:
22287
22295
.
Kawamura
,
S.
1993
.
Molecular aspects of photoreceptor adaptation in vertebrate retina
.
Int. Rev. Neurobiol.
35
:
43
86
.
Keresztes
,
G.
,
K.A.
Martemyanov
,
C.M.
Krispel
,
H.
Mutai
,
P.J.
Yoo
,
S.F.
Maison
,
M.E.
Burns
,
V.Y.
Arshavsky
, and
S.
Heller
.
2004
.
Absence of the RGS9·Gβ5 GTPase-activating complex in photoreceptors of the R9AP knockout mouse
.
J. Biol. Chem.
279
:
1581
1584
.
Krispel
,
C.M.
,
D.
Chen
,
N.
Melling
,
Y.J.
Chen
,
K.A.
Martemyanov
,
N.
Quillinan
,
V.Y.
Arshavsky
,
T.G.
Wensel
,
C.K.
Chen
, and
M.E.
Burns
.
2006
.
RGS expression rate-limits recovery of rod photoresponses
.
Neuron.
51
:
409
416
.
Lamb
,
T.D.
,
P.A.
McNaughton
, and
K.W.
Yau
.
1981
.
Spatial spread of activation and background desensitization in toad rod outer segments
.
J. Physiol.
319
:
463
496
.
Makino
,
C.L.
,
R.L.
Dodd
,
J.
Chen
,
M.E.
Burns
,
A.
Roca
,
M.I.
Simon
, and
D.A.
Baylor
.
2004
.
Recoverin regulates light-dependent phosphodiesterase activity in retinal rods
.
J. Gen. Physiol.
123
:
729
741
.
Martemyanov
,
K.A.
,
C.M.
Krispel
,
P.V.
Lishko
,
M.E.
Burns
, and
V.Y.
Arshavsky
.
2008
.
Functional comparison of RGS9 splice isoforms in a living cell
.
105
:
20988
20993
.
Mendez
,
A.
,
M.E.
Burns
,
I.
Sokal
,
A.M.
Dizhoor
,
W.
Baehr
,
K.
Palczewski
,
D.A.
Baylor
, and
J.
Chen
.
2001
.
Role of guanylate cyclase-activating proteins (GCAPs) in setting the flash sensitivity of rod photoreceptors
.
98
:
9948
9953
.
Morshedian
,
A.
, and
G.L.
Fain
.
2014
.
Molecular Mechanism of Adaptation in Vertebrate Rods
.
In
Vertebrate Photoreceptors: Functional Molecular Bases.
T.
Furukawa
,
J.B.
Hurley
, and
S.
Kawamura
,
editors
.
Springer
,
Berlin
.
73
90
.
Nikonov
,
S.
,
N.
Engheta
, and
E.N.
Pugh
Jr
.
1998
.
Kinetics of recovery of the dark-adapted salamander rod photoresponse
.
J. Gen. Physiol.
111
:
7
37
.
Nymark
,
S.
,
R.
Frederiksen
,
M.L.
Woodruff
,
M.C.
Cornwall
, and
G.L.
Fain
.
2012
.
Bleaching of mouse rods: microspectrophotometry and suction-electrode recording
.
J. Physiol.
590
:
2353
2364
.
Pepperberg
,
D.R.
,
M.C.
Cornwall
,
M.
Kahlert
,
K.P.
Hofmann
,
J.
Jin
,
G.J.
Jones
, and
H.
Ripps
.
1992
.
Light-dependent delay in the falling phase of the retinal rod photoresponse
.
Vis. Neurosci.
8
:
9
18
.
Sakurai
,
K.
,
J.E.
Young
,
V.J.
Kefalov
, and
S.C.
Khani
.
2011
.
Variation in rhodopsin kinase expression alters the dim flash response shut off and the light adaptation in rod photoreceptors
.
Invest. Ophthalmol. Vis. Sci.
52
:
6793
6800
.
Soo
,
F.S.
,
P.B.
Detwiler
, and
F.
Rieke
.
2008
.
Light adaptation in salamander L-cone photoreceptors
.
J. Neurosci.
28
:
1331
1342
.
Tsang
,
S.H.
,
M.L.
Woodruff
,
C.K.
Chen
,
C.Y.
Yamashita
,
M.C.
Cilluffo
,
A.L.
Rao
,
D.B.
Farber
, and
G.L.
Fain
.
2006
.
GAP-independent termination of photoreceptor light response by excess gamma subunit of the cGMP-phosphodiesterase
.
J. Neurosci.
26
:
4472
4480
.
Tsang
,
S.H.
,
M.L.
Woodruff
,
K.M.
Janisch
,
M.C.
Cilluffo
,
D.B.
Farber
, and
G.L.
Fain
.
2007
.
Removal of phosphorylation sites of gamma subunit of phosphodiesterase 6 alters rod light response
.
J. Physiol.
579
:
303
312
.
Woodruff
,
M.L.
,
A.P.
Sampath
,
H.R.
Matthews
,
N.V.
Krasnoperova
,
J.
Lem
, and
G.L.
Fain
.
2002
.
Measurement of cytoplasmic calcium concentration in the rods of wild-type and transducin knock-out mice
.
J. Physiol.
542
:
843
854
.
Woodruff
,
M.L.
,
E.V.
Olshevskaya
,
A.B.
Savchenko
,
I.V.
Peshenko
,
R.
Barrett
,
R.A.
Bush
,
P.A.
Sieving
,
G.L.
Fain
, and
A.M.
Dizhoor
.
2007
.
Constitutive excitation by Gly90Asp rhodopsin rescues rods from degeneration caused by elevated production of cGMP in the dark
.
J. Neurosci.
27
:
8805
8815
.
Woodruff
,
M.L.
,
K.M.
Janisch
,
I.V.
Peshenko
,
A.M.
Dizhoor
,
S.H.
Tsang
, and
G.L.
Fain
.
2008
.
Modulation of phosphodiesterase6 turnoff during background illumination in mouse rod photoreceptors
.
J. Neurosci.
28
:
2064
2074
.

Abbreviations used in this paper:

• GAP

GTPase-accelerating protein

•
• GCAP

guanylyl cyclase–activating protein

•
• GRK1

G protein–coupled receptor kinase 1

•
• PDE

phosphodiesterase

•
• Rh*

light-stimulated rhodopsin