Adaptation of pineal expressed teleost exo-rod opsin to non-image forming photoreception through enhanced Meta II decay
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Photoreception by vertebrates enables both image-forming vision and non-image-forming responses such as circadian photoentrainment. Over the recent years, distinct non-rod non-cone photopigments have been found to support circadian photoreception in diverse species. By allowing specialization to this sensory task a selective advantage is implied, but the nature of that specialization remains elusive. We have used the presence of distinct rod opsin genes specialized to either image-forming (retinal rod opsin) or non-image-forming (pineal exo-rod opsin) photoreception in ray-finned fish (Actinopterygii) to gain a unique insight into this problem. A comparison of biochemical features for these paralogous opsins in two model teleosts, Fugu pufferfish (Takifugu rubripes) and zebrafish (Danio rerio), reveals striking differences. While spectral sensitivity is largely unaltered by specialization to the pineal environment, in other aspects exo-rod opsins exhibit a behavior that is quite distinct from the cardinal features of the rod opsin family. While they display a similar thermal stability, they show a greater than tenfold reduction in the lifetime of the signaling active Meta II photoproduct. We show that these features reflect structural changes in retinal association domains of helices 3 and 5 but, interestingly, not at either of the two residues known to define these characteristics in cone opsins. Our findings suggest that the requirements of non-image-forming photoreception have lead exo-rod opsin to adopt a characteristic that seemingly favors efficient bleach recovery but not at the expense of absolute sensitivity.
KeywordsRod opsin Exo-rod Rhodopsin GPCR Teleost Circadian
The first step in vertebrate vision is the absorption of light by rod and cone photoreceptors. This is achieved by photopigments comprising either a rod or cone opsin protein binding a vitamin A-derived retinaldehyde-based chromophore. Opsins are members of the G-protein coupled receptor superfamily of proteins. In the dark, they bind the A1 chromophore 11-cis retinaldehyde in their ligand-binding pocket covalently via a protonated Schiff base. This chromophore acts as an inverse agonist suppressing G-protein activation, but can be isomerized to the agonist (all-trans conformation) by light . As a result, opsins show light-dependent interaction with their G-protein signaling cascade. The opsin expressed in rods (rod opsin) was the first G-protein coupled receptor to have its structure solved at high resolution and remains one the best-understood members of this family .
Uniquely among vertebrates, the Actinopterygii (ray-finned fish) have not one but two quite distinct rod opsin genes. In this class, the true orthologue of the rod opsin gene found in other vertebrates (including mammals), is not actually expressed in the retina, but rather in the photosensitive pineal gland. The rod opsin found in retinal photoreceptors of ray-finned fish is instead encoded by an intronless gene  thought to have arisen by retrotransposition . Because the retinally expressed rod opsin was the first to be described in Actinopterygii, it was termed ‘rod opsin’ while the subsequently described pineal-specific version was called exo-rhodopsin (exo-rh) or extra-retinal rod-like opsin (hereafter termed exo-rod opsin) [5, 6]. The two rod-like opsins share ~75% amino acid identity.
Duplication of the Actinopterygian rod opsin gene appears to have been an evolutionarily ancient event. The intronless retinal rod opsin gene appears in basal representatives of this order including bowfin, gar, and sturgeon  as well as in the advanced Teleostei , but is absent in an extant sarcopterygian fish, the coelacanth Latimeria chalumnae . This places the first appearance of separate rod and exo-rod opsin genes somewhere between the separation of Sarcopterygii and Actinopterygii, ~416 million years ago (MYA) , and divergence of the neopterygian crown-group (bowfin, gar, and teleosts) at least 284 MYA .
Thus, the ray-finned fish have had two separate rod opsin genes for hundreds of millions of years. Assuming that through much of this time one was expressed in the retina and the other in the pineal, significant specialization to the differing demands of photoreception in these two organs might be expected. On this basis, we set out here to undertake the first comprehensive comparative biochemical analysis of rod and exo-rod photopigments. We find that, despite their evolutionary heritage, in at least one important respect (life-time of the principal signaling photoproduct Meta II), exo-rod opsin pigments from zebrafish (Danio rerio) and Fugu pufferfish (Takifugu rubripes) have a functional characteristic more typical of cone opsins. As the amino acid residues responsible for this characteristic in cone opsins are ‘rod-like’ in exo-rod opsins, these data indicate that exo-rod opsins have attained a cone-like characteristic by a quite different structural mechanism in a novel example of convergent evolution.
Materials and methods
1D4-tagging of opsins
PCR primers were designed to amplify the coding sequences of the Danio and Fugu rod opsin and exo-rod opsin such that the 5′ end contained a standardized Kozak consensus—GCCACCATG  and the stop-codon was substituted with an in-frame NheI site (GCTAGC). The Fugu rod and exo-rod opsin coding sequences were amplified from clones 27l6 (GenBank: AF201471) and 16h22 (GenBank: AF201472) previously described , using the following primer pairs: Fugu Rod 5′ Xho I F1, 5′-CCGCTCGAGGCCACCATGAACGGCACGGAGGGACC-3′ and Fugu Rod 3′ Nhe I R1, 5′-CCGCTAGCCGCAGGAGACACAGAACTGGAGGAGAC-3′; Fugu Exo-Rod 5′ Xho I F1, 5′-CCGCTCGAGGCCACCATGAACGGCACGGAAGGACC-3′ and Fugu Exo-Rod 3′ Nhe I R1, 5′-CCGCTAGCGGCGGGGGCCACCTGGCTGGAGGAGAC-3′. The Danio rod and exo-rod opsin coding sequences were amplified from the retinal and pineal cDNA using the following primer pairs: dRod BamHI Kozak F1, 5′-CGGATCCGCCACCATGAACGGTACAGAGGGACCGGCATTC-3′ and dRod NheI NoStop R1, 5′-CGCTAGCCGCCGGAGACACGGAGCTGGAAGAC-3′; dExo-Rod BamHI Kozak F1, 5′-CGGATCCGCCACCATGAACGGGACGGAGGGACCCAACTTC-3′ and dExo-Rod NheI NoStop R1, 5′-CGCTAGCGGCTGGAGACACCTGAGCGGAGGAC-3′. The amplified Danio exo-rod and rod opsin sequences are consistent with previous reports, respectively  (GenBank: AB025312) and  (GenBank: AB187811). A vector (pBluescript II) containing a bovine rod opsin 1D4-tag in the following context, NheI-TETSQVAPA-stop (kindly provided by T. Warne, MRC Laboratory of Molecular Biology, Cambridge) allowed in-frame 1D4-tagging of sequence verified opsin coding sequences.
Opsin protein expression
The Flp-In™ system (Invitrogen) has been used previously for inducible rod opsin expression . The Fugu and Danio 1D4-tagged rod and exo-rod opsins were cloned into pcDNA5/FRT/TO and then co-transfected with a pOG44 into Flp-In™-293 cells. Isogenic stable cell lines were selected with hygromycin at 100 μg/ml. Flp-In™-opsin-1D4 cell lines were maintained at 37°C in Dulbecco’s modified Eagle's medium, 4,500 mg/l d-Glucose, sodium pyruvate and l-glutamine (Sigma) with 10% fetal bovine serum (Sigma), 10 μg/ml blasticidin and 100 μg/ml hygromycin in a 5% CO2 atmosphere. Cells were grown in HYPERflasks (Corning) prior to opsin protein expression induction by the presence of 1 μg/ml tetracycline and 5 mM sodium butyrate (B5887, Sigma). Cells were harvested between 20 and 25 h after induction of expression.
Cell pellets were re-suspended in PBS, pH 7.0 in the presence of Complete Protease Inhibitors (Roche) and incubated with 50 μM 11-cis retinal for 2 h at 4°C. The cells were subsequently solubilized with 1% β-d-dodecylmaltoside (DDM) for 1 h at 4°C. Nuclei were pelleted by centrifugation at 21,500 × g and the supernatant was then incubated with 1D4 antibody coupled to CnBr-activated Sepharose (GE Healthcare). After 3 h rotating at 4°C, the 1D4 resin was washed with PBS (pH 6), 0.1% DDM followed by 2 mM sodium phosphate (pH 6), 0.02% DDM. The purified protein was eluted with the 1D4 peptide TETSQVAPA (160 μM in 2 mM sodium phosphate (pH 6), 0.02% DDM). All procedures after reconstitution were performed under dim red light.
Absorption spectra of the purified pigment samples were recorded on a Shimadzu UV-2450 dual-beam spectrophotometer. All spectra were recorded in the 250–750 nm range. For photo-bleaching experiments, the samples were illuminated with +515 nm light for 5 min and spectra were then recorded. Difference spectra were subsequently calculated. The λmax of each pigment was determined by fitting a standard A1 visual pigment template  to the difference spectra using the Solver add-in in Microsoft Excel to generate best-fit curves. This template was kindly provided by D.M. Hunt (Institute of Ophthalmology, University College London).
Chromophore stability of opsins in the dark
The thermal bleaching of the Fugu rod and exo-rod pigments were measured at selected temperatures by the decrease in absorption at 500 nm . Samples were incubated in the dark for 30 min at temperatures between 20 and 60°C on a gradient thermocycler. After 30 min, the spectra of the samples were re-measured. The amount of remaining pigment with bound chromophore was determined by measurement of the absorption at 500 nm, normalized to the protein absorption at 280 nm. Prism 4.0 (http://www.graphpad.com) was used to fit sigmoidal curves to the data.
Fluorescent thermal stability assay
A fluorescent dye, the thiol-specific fluorochrome N-[4-(7-diethylamino-4-methyl-3-coumarinyl)phenyl]maleimide (CPM) which fluoresces when bound to cysteine residues, was used to assay the thermal stability of the Fugu rod and exo-rod photopigments . Pre-cooled cuvettes were prepared, containing 10 μg of opsin protein in a total volume of 110 μl sample buffer with detergent (10 mM HEPES (pH 7.5), 100 mM NaCl, 0.1 mM MgCl2, and 0.03% DDM). Them, 10 μl of freshly prepared CPM buffer (sample buffer with 0.1 mg/ml CPM) was added and re-suspended by pipetting. A Varian Eclipse spectrofluorometer was used for the assay, with excitation wavelength set at 387 nm (±5 nm) and the emission wavelength at 463 nm (±10 nm). Dark state assays (in triplicate) were performed between 10 and 90°C and a simple mean calculated before normalization.
G-protein purification from bovine retina
Wild-type G-protein was obtained from 50 bovine retinae. On ice, following exposure to light, the retinae were resuspended in 150 ml of 47% (w/w) sucrose in 20 mM Tris (pH 7.4), 1 mM CaCl2, 2 mM DTT and 100 mM PMSF (buffer A) and broken apart against the edge of a beaker until separation was complete. Following centrifugation at 42,000 × g for 15 min the rod outer-segment (ROS) membranes were aspirated from the supernatant fraction. The ROS membranes were diluted 2× with approximately 200 ml of buffer A and centrifuged for 20 min at 19,600 × g. The pellets were resuspended in 60 ml of buffer A, placed on top of a discontinuous 25–30% sucrose gradient and centrifuged at 131,000 × g for 20 min. Piercing an injection needle at the orange ROS interface in the tube allowed collection of the membrane layer, which was then diluted in 80 ml buffer A and spun at 42,000 × g for 15 min. The resulting orange ROS pellet was resuspended and centrifuged once at 42,000 × g for 10 min in 10 mM Tris (pH 7.4), 100 mM NaCl, 5 mM MgCl2, 2 mM DTT, and 1 mM PMSF. This was then washed and centrifuged twice at 42,000 × g for 15 and 20 min using a low-magnesium buffer 10 mM Tris (pH 7.4), 0.1 mM EDTA, 2 mM DTT and 1 mM PMSF (buffer B). G-protein bound to the light-exposed rod opsin was eluted for 30 min from resuspended ROS membranes in 25 ml buffer B supplemented with 40 μM GTP. ROS membranes were separated from eluted G-protein by centrifugation at 257,000 × g for 15 min. Supernatant was allowed to dialyze in 10 mM Tris (pH7.4), 2 mM MgCl2, 2 mM DTT in 50% glycerol with three changes in 36 h. Extracted proteins were stored in aliquots at −20°C.
G-protein fluorescence GTPγS binding assay
Opsin interaction with the G-protein transducin (Gt) was analyzed by fluorescence spectroscopy, based on an intrinsic increase in tryptophan fluorescence of Gt . The assay makes use of the increase in tryptophan fluorescence after uptake of a non-hydrolysable GTPγS nucleotide by the Gα subunit upon activation. The increase in fluorescence quantum yield of the Gα(GTPγS) complex is 2.3 times higher than the Gα(GDP) complex . A total of 10 nM of each of the Fugu and Danio rod and exo-rod pigments were photobleached after continuous illumination at 515-nm wavelength of light for 20 s. This was then added to a cuvette containing 250 nM bovine rod transducin (Gt) in 10 mM Tris–HCl, pH 7.4, 100 mM NaCl, 2 mM MgCl2, 0.008% DDM in a total volume of 1.2 ml, and allowed to stir slowly for 100 s. A stock solution of 10 mM GTPγS was added to a 5 μM final concentration after 10 s. The increase in tryptophan fluorescence at an emission wavelength of 340 nm was then recorded for an additional 2,500 s in a Beckman LS55 spectrofluorometer. G-protein activation assays were carried out at 14°C. Bovine rod opsin was used as a comparable positive control in these experiments, and Fugu rod opsin in the absence of GTPγS provided a negative control.
FTIR spectroscopy was performed with Fugu rod and exo-rod pigments reconstituted into phosphatidyl choline lipids (from egg yolk). Lipid reconstitution was achieved at 4°C by combining the DDM-purified pigments with DDM-solubilized lipid at a molar ratio of 1:200. After incubation for 2 h, DDM was removed by three rounds of extraction using small washed polystyrene beads (with a detergent binding capacity 5× higher than the initially present DDM; Bio-Beads SM-2, Bio-Rad, Hercules, CA, USA) for 4 h. After careful removal of the Bio-Beads, proteoliposomes were collected by centrifugation for 4 h at 100,000 × g. Spectra were recorded at 4 cm−1 with a scanning time of 30 s using a Bruker Vertex 70 FTIR spectrometer equipped with an MCT detector using 100 pmol reconstituted pigment in sandwich samples  and 200 mM BTP (at pH 6.0) or MES buffer (at pH 5.0). Meta II spectra of Fugu exo-rod opsin were recorded with a time resolution of 6 s at 10°C to compensate for its faster decay rate. Photoactivation was achieved by a 1 s photolysis using an array of 6 LEDs at 530 nm . Meta II decay was monitored by following the decrease of intensity of bands in the range between 1,800 and 1,600 cm−1 and at 1,570 cm−1.
Spectral sensitivity of the Fugu and Danio opsins
We next turned to the thermal stability of the opsin protein itself using CPM, a thiol-specific fluorochrome . This fluorochrome fluoresces when covalently bound to cysteines, but not when free in solution. As such an attachment requires (partial) unfolding of the protein, its fluorescence can be used to analyze the thermal integrity of detergent solubilized membrane proteins. Thermal denaturation scans generated curves whose shape mirrored those of chromophore release (Fig. 2b), enabling thermal ‘half-melting’ temperatures (Tm 50) of 60.4°C for Fugu rod opsin and 56.3°C for Fugu exo-rod opsin to be calculated.
FTIR difference spectroscopy of Fugu pigment photoproducts
The difference spectra of both Fugu pigments revealed a positive band at 1,712 cm−1 similar to that of bovine rod opsin, reflecting protonation of Glu113 by proton transfer from the PSB  and of Glu134 by proton uptake from the solvent in Meta II . This indicates a similar triggering of these two protonation switches of the activation process as in rod opsin . In Fugu rod Meta II, this band was superimposed upon an additional band at 1,702 cm−1 that is not assigned.
The difference band at 1,728 cm−1 (−)/1,747 cm−1 (+) in rod opsin is attributed to changes of hydrogen bonding of Glu122 close to the ring of retinal, which participates in an interhelical network between H3 and H5 involving His211 and Trp126 and which is a key residue in the decay of the signaling state of rod and cone pigments . Similar to bovine rod opsin, both Fugu pigments reveal a downshift of this band, corresponding to a decrease of the hydrogen bonding of this residue. In addition, the intensity of its positive lobe at 1,747 cm−1 is reduced in Fugu exo-rod opsin Meta II, indicating an altered environment of Glu122 as compared with bovine rod opsin Meta II or Fugu rod Meta II.
Finally, the environment of Asp83 of a conserved water-mediated network between H1, H2, and H7 can be monitored using its difference band at 1,768 cm−1 (−)/1,747 cm−1 (+) (its positive lobe overlapping with that of Glu122). Both in Fugu rod and (to a slightly lesser extent) in Fugu exo-rod opsin the dark absorption of Asp83 is downshifted from its position at 1,768 cm−1 in bovine rod opsin, leading to an overall reduction of the difference band. This alteration of the interhelical network in the dark state is possibly induced by substitutions of neighboring Ser298Ala299 to Ser298Ser299 in Fugu rod and Ala298Ala299 in Fugu exo-rod opsin, of which residue 299 is a known ±2 nm spectral tuning site .
The thermal decay of the Meta II state to opsin and free all-trans retinal was followed by time-resolved spectroscopy at 20°C, pH 6.0, using the conformationally sensitive bands in the range between 1,600 and 1,800 cm−1 and bands of retinal at around 1,570 cm−1 (Fig. 4b) . Under these conditions, no significant decay to Meta III  nor structural instability of the pigment  were observed. While Fugu rod and bovine rod Meta II decayed with a similar time constant (τ = ~8 min), Fugu exo-rod opsin Meta II decay was accelerated by more than an order of magnitude (τ = 0.6 min). The identity of the decay product with opsin was confirmed by comparison with opsin generated by illumination in the presence of hydroxylamine (Supplementary Material Fig. 1). The Meta II decay of Danio exo-rod opsin exhibits a similar time constant (τ = ~0.5 min) to that of Fugu exo-rod opsin.
To our knowledge, these data represent the first biochemical characterization of exo-rod opsin pigments. We show that while Danio and Fugu exo-rod opsins have spectral sensitivities within the range expected for rod opsins (λmax around 500 nm), in other respects their behavior is quite atypical for the rod opsin family.
Of all the differences that we have observed in this study between the rod and exo-rod pigments, the least distinct is that in spectral sensitivity. The native habitat for Danio is freshwater pools and streams , while that of Fugu is of coastal marine waters to a maximal depth of 150 m . Vertebrates residing in such environments typically possess a rod with λmax ~500 nm , and our description of the A1 spectral sensitivities of rod opsins from these two species matches this prediction. In both of these species, we find that the exo-rod pigment is blue shifted by ~3.5 nm, with the ~498 nm λmax that we have determined for A1 Danio exo-rod being consistent with a prediction based on its primary structure , and with the spectral sensitivity of the major peak for light induced pineal melatonin suppression in this species at ~500 nm . Recently, one of the likely signaling consequences of exo-rod opsin in the zebrafish pineal has been shown to be the regulation of expression of aanat2 , which encodes the pineal specific version of arylalkylamine N-acetyltransferase , the penultimate enzyme in the synthetic pathway for melatonin.
Even though the λmax of the A1 rod and exo-rod pigments in this study are very similar, this observation appears not to hold for all teleost species since microspectrophotometric evidence from both marine and freshwater teleosts indicates that opsin moiety spectral differences exist between the λmax of retinal rod and presumed exo-rod pineal photoreceptors [21, 42]. In addition freshwater fish can exhibit substitution or co-utilization of the A1 and porphyropsin-forming A2 chromophore, 11-cis 3-dehydroretinal , which will red-shift the λmax of both the rod and exo-rod pigment . Thus, both opsin tuning and chromophore usage could provide scope for significant differences in the in vivo spectral sensitivity of the rod and pineal photoreceptors.
Among the cardinal biochemical features of retinal rod photopigments is their low rate of spontaneous (thermal) activation in the dark , e.g., salamander rods have an estimated spontaneous activation of ~0.03 s−1  whereas L cones experience a rate of ~600 s−1 , which when corrected for pigment density suggests that the cone pigment is 6 × 105 times less stable than the rod pigment . Correspondingly, expression of cone opsins in rod photoreceptors results in low-level activation of phototransduction in the dark, precluding full dark adaptation and reducing sensitivity [30, 46]. This low level of spontaneous rod opsin activation is thought to be critical for the extremely high sensitivity of rod photoreceptors , and can be attributed to the ability of the opsin moiety to retain the 11-cis-retinal chromophore that acts as an inverse agonist suppressing activation of the receptor . We show here that at physiological temperatures both Fugu rod and exo-rod pigments show roughly similar levels of thermal stability and it is only at higher temperatures do differences in stability manifest themselves. This physiological stability is consistent with that previously observed for rod opsin , and contrasts markedly with the stability of cone opsins . The relative stability of the pineal photopigment is consistent with the observation that the estimated absolute sensitivity of pineal photoreceptors is comparable to those of retinal rods . This is perhaps not unexpected given the anatomical position of the pineal and the associated filtering effects of the skull and associated tissues, light intensities experienced by the pineal in situ are typically between 1/10th and 1/100th that of ambient and enriched for longer wavelengths [52, 53, 54, 55]. Note, however, the rate at which photoreceptors experience spontaneous activation of the phototransduction cascade in the dark would depend not only on the rate of thermal bleach but also on the total quantity of pigment. Although rod and pineal photopigment density does seem to be comparable with similar optical densities reported by microspectrophotometry on rod and pineal photoreceptors in trout , the pineal photoreceptors lack the extensive pigment-dense outer segment discs found in retinal rods (typically in excess of 1,000) and have 20–70 lamellae , with correspondingly low levels of chromophore—concentrations being 1/300–1/1,000 that of retinal photoreceptors .
Another important difference between rod and cone pigments is the lifetime of their light-activated state. Following light absorption both opsin classes progress through a series of meta-stable photoproduct states, including the Meta II signaling state capable of activating the G protein . However, rod signal transduction is characterized by a much longer lifetime of the Meta II product than in cone pigments , with Meta II time constants of ~480 s (~8 min) for rods and ~5 s (~0.12 min) for cones . In vitro assays indicate that this difference between the Meta II lifetime of rod and cone pigments results in significantly reduced G-protein activation by cone opsins compared to rod opsin . Here, we found an equivalent discrepancy in G-protein activation between rod and exo-rod opsin pigments. In theory, the reduced activity of exo-rod opsin could reflect lower affinity for the G-protein provided (bovine transducin). However, this seems unlikely given the high sequence similarity between exo-rod opsin and bovine rod opsin in G-protein interaction domains (predicted intracellular loops 2 and 3 show 91 and 67% identity; for reference these figures are 82 and 62% for Fugu rod opsin), and the fact that the Fugu genome has only a single rod transducin alpha-subunit (GNAT1) , which is presumably used by both rod opsin and exo-rod opsin pigments. However, given that both rod and cone transducins are expressed in the teleost pineal , we cannot exclude the possibility that exo-rod opsin interacts with the cone transducin alpha-subunit (GNAT2). Recent evidence from transgenic mice indicates that Gnat2 will interact with rod opsin leading to rods that exhibit responses with a decreased sensitivity and rate of activation half that of Gnat1 . The equivalent sensitivity of the pineal and rod photoreceptors would suggest that exo-rod opsin is interacting with a GNAT1 rather than a GNAT2 subunit. The alternative explanation, that it reflects lower lifetime of signaling photoproducts, is supported by our FTIR analysis. Thus, time-resolved FTIR spectroscopy reveals that the Meta II lifetime of Fugu exo-rod opsin is reduced by about one order of magnitude compared with Fugu or bovine rod opsins. In vivo, the reduction in Meta II lifetime for cone opsins may facilitate bleach recovery, allowing cones to function under continuous bright illumination. The reduction in Meta II lifetime of exo-rod opsin could perform a similar function for teleost pineal photoreceptors, with a fast bleach recovery allowing them to maintain a high absolute sensitivity while having a low level of photopigment. Thus, the reduced Meta II lifetime of exo-rod opsin could contribute to the observation that pineal photoreceptors are active over a greater range of light intensities than retinal photoreceptors , e.g., from physiological recordings it has been estimated that the dynamic range of pineal photoreceptors can be 2–3 times larger than their retinal counterparts .
Relative Meta II decay rates of photopigments in relation to the amino acid content of positions 122 and 189
Relative Meta II decay rate
Chicken rod (wild-type)
Chicken rod (double mutant)
Chicken green cone (wild-type)
Chicken green cone (double mutant)
What then is the structural basis for this cone-like characteristic of exo-rod opsin? Ala132 and Tyr223 are conserved residues and so can be excluded . The FTIR results show a considerably changed environment of Glu122 in exo-rod opsin Meta II when compared to Meta II of the bovine and Fugu rod opsins. The cone-like rapid decay of exo-rod opsin Meta II may therefore not reflect a ‘cone-type’ residue at position 122, but rather other alterations in the H3/H5 interhelical network around Glu122 and His211. Possible origins for such an effect could be residue 166 (on H4 facing His211), which is Ala166 in the bovine and Fugu rod opsins, but Thr166 in the exo-rod opsin pigment. This exchange might alter the helix packing in Meta II and be responsible for faster retinal release and the observed spectral alteration of Glu122 in exo-rod opsin Meta II.
The finding that the pineal exo-rod opsins have attained an enhanced Meta II decay rate seemingly without the decreased thermal stability exhibited by cone opsins , and have done so without replicating cone-like residues at positions 122 and 189 has implications for the evolution of these photopigments. Current evidence suggests that rod opsin evolved from a cone opsin [68, 69]. Thus, one potential explanation for the cone-like characteristic of the exo-rod opsin pigments is that they simply reflect those of the ancestral pigment. In this view, it would be the retinal rod opsin whose characteristics had evolved to match its sensory function. In fact, the structural basis for accelerated Meta II decay appears quite different between the cone and exo-rod opsin pigments (see above). Thus it seems that the ancestor of both Actinopterygian rod proteins had classical rod-like functional characteristics, and it has been the exo-rod opsin that has diverged to attain a cone-like characteristic by convergent evolution.
This work was supported by funding from The Wellcome Trust to RJL, JB, GFXS, and MWH (grant numbers 078808/A/05/Z, 078808/B/05/Z); Deutsche Forschungsgemeinschaft to RV (grant number VO 811/4-1); and additional support from the National Institute for Health Research Manchester Biomedical Research Centre and the Manchester Academic Health Science Centre was provided to JB.
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