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Link to original content: https://pubmed.ncbi.nlm.nih.gov/23667045
Expression dynamics and protein localization of rhabdomeric opsins in Platynereis larvae - PubMed Skip to main page content
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. 2013 Jul;53(1):7-16.
doi: 10.1093/icb/ict046. Epub 2013 May 10.

Expression dynamics and protein localization of rhabdomeric opsins in Platynereis larvae

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Expression dynamics and protein localization of rhabdomeric opsins in Platynereis larvae

Nadine Randel et al. Integr Comp Biol. 2013 Jul.

Abstract

The larval stages of polychaete annelids are often responsive to light and can possess one to six eyes. The early trochophore larvae of the errant annelid Platynereis dumerilii have a single pair of ventral eyespots, whereas older nectochaete larvae have an additional two pairs of dorsal eyes that will develop into the adult eyes. Early Platynereis trochophores show robust positive phototaxis starting on the first day of development. Even though the mechanism of phototaxis in Platynereis early trochophore larvae is well understood, no photopigment (opsin) expression has yet been described in this stage. In late trochophore larvae, a rhabdomeric-type opsin, r-opsin1, expressed in both the eyespots and the adult eyes has already been reported. Here, we identify another Platynereis rhabdomeric opsin, r-opsin3, that is expressed in a single photoreceptor in the eyespots in early trochophores, suggesting that it mediates early larval phototaxis. We also show that r-opsin1 and r-opsin3 are expressed in adjacent photoreceptor cells in the eyespots in later stages, indicating that a second eyespot-photoreceptor differentiates in late trochophore larvae. Using serial transmission electron microscopy (TEM), we identified and reconstructed both photoreceptors and a pigment cell in the late larval eyespot. We also characterized opsin expression in the adult eyes and found that the two opsins co-express there in several photoreceptor cells. Using antibodies recognizing r-opsin1 and r-opsin3 proteins, we demonstrate that both opsins localize to the rhabdomere in all six eyes. In addition, we found that r-opsin1 mRNA is localized to, and translated in, the projections of the adult eyes. The specific changes we describe in opsin transcription and translation and in the cellular complement suggest that the six larval eyes undergo spectral and functional maturation during the early planktonic phase of the Platynereis life cycle.

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Figures

Fig. 1
Fig. 1
Phylogenetic tree of protostome r-opsins. Bayesian phylogenetic tree inferred from a protein alignment of protostome r-opsins and c-opsins. The tree shows that r-opsin1 and r-opsin3 diverged early during the evolution of annelids. Posterior probabilities of a Bayesian phylogeny (Bayesian posterior probability/aLRT value) and bootstrap values of a maximum-likelihood tree are indicated at the main nodes.
Fig. 2
Fig. 2
Expression of r-opsin3 and r-opsin1 in Platynereis trochophore and nectochaete larvae. (A) Differential interference contrast (DIC) image of a 48-hpf larva with eyespots (red). (B) SEM image of a trochophore (48 hpf) larva. (C) DIC image of a 72-hpf larva with eyespots and adult eyes (red). (D, E) SEM images of nectochaete larvae (72 hpf) oriented dorsally (D) or anteriorly (E). (F–J) In situ hybridization in the indicated larval stages for r-opsin3 (red) counterstained for acetylated tubulin (white). (K–O) In situ hybridization in the indicated larval stages for r-opsin1 (red) counterstained for acetylated tubulin (white). (P) Double in situ hybridization for r-opsin3 (red) and FVRIamide precursor (cyan) counterstained for acetylated tubulin (white) in a 48-hpf larva reveals co-expression in the photoreceptor cell of the eyespot. (Q–T) Double in situ hybridization for r-opsin3 (red) and r-opsin1 (cyan) counterstained for acetylated tubulin (white) in 56-hpf (Q, R) and 72-hpf (S, T) larvae reveals the expression of the two opsins in two adjacent photoreceptor cells of the eyespot (Q–S), and co-expression in the adult eye (T). In (A, C), the eyespot’s pigment was highlighted using the reflection of the laser light in the confocal microscope. In (P–S), asterisks label the dendrites of the photoreceptor cells, in (T) the cell bodies of the photoreceptors. In (P, S), dashed lines mark the boundaries of the photoreceptor cells as revealed by the in situ and the acetylated-tubulin signals. The boxed area in (Q) is shown enlarged in (R). AE, adult eye; ES, eyespot. Scale bars: (B, D, E–O, Q): 30 µm, (P, R, S, T) 5 µm.
Fig. 3
Fig. 3
Summary diagram of the expression patterns of Platynereis r-opsin1 and r-opsin3 in the photoreceptor cells of the adult eyes, eyespots, and parapodia in various larval and adult stages, based on the data in this article and Backfisch et al. (2013).
Fig. 4
Fig. 4
Ultrastructure of eyes and immunohistochemical localization of opsins in Platynereis rhabdomeric photoreceptors. (A–H) Ultrastructure of an eyespot and the projection of the photoreceptor cells in a 72-hpf larva. (A, B) TEM images of an eyespot with the two rhabdomeric photoreceptor cells (orange, green), the pigment cell (yellow) and pigment granules (cyan) in two different layers. (C) TEM image of the apical end of a photoreceptor cell with a cilium. (D, E) TEM images of the eyespot with the reconstructed 3D structure of the two rhabdomers (D) and the pigment granules (E). (F, G) TEM images of the prototroch region. (F) Axon of a photoreceptor cell (orange) in close contact with a prototroch cell (cyan). (G) Close-up image of a synapse between the photoreceptor cell (orange) and the prototroch cell (cyan). (H) TEM image of the prototroch region with the reconstructed photoreceptor cells and their axons. (I) TEM image of an adult eye. Each cell is labeled with a different color. (J) Schematic drawing of the eyes and their projections to the apical nerve plexus. (K–M) Immunostaining for r-opsin3 (red) in 72-hpf larvae counterstained for acetylated tubulin (white). (L) Close-up image of the eyespot, (M) close-up image of the adult eye. In (M), the fluorescent signal is overlaid with the DIC signal in the right panel to show the eye pigment. (N–P) Immunostaining for r-opsin1 (red) in 72-hpf and 5-dpf larvae counterstained for acetylated tubulin (white). (O) Close-up image of the eyespot, (P) close-up image of the adult eye. In (P), the fluorescent signal is overlaid with the DIC signal in the right panel to show the eye pigment. (Q) In situ hybridization for r-opsin1 (red) in a 5-dpf larva counterstained for acetylated tubulin (white) reveals the mRNA signal in the photoreceptor projections in the adult eye. (R) Immunostaining for r-opsin1 (red) in a 5-dpf larva counterstained for acetylated tubulin (white). (S) Close-up image of the right adult eye and the apical nerve plexus. In (B, C), arrowheads indicate the basal body of PRC2 and in (L, O), arrowheads indicate the photoreceptor’s rhabdomeres. Asterisks show the pigment cups (in M, P), the immunostaining signal in the photoreceptor cell-body deeper in the tissue (in O), and the r-opsin1 signal in the apical nerve plexus in the area of the photoreceptor projections (in R, S). AAEN, anterior adult-eye nerve; AE, adult eye; CPC, ciliated prototroch cell; ES, eyespot; PAEN, posterior adult-eye nerve; PC, pigment cell; PRC, photoreceptor cell. Scale bars: (A, B, I) 2 µm, (C, G) 0.5 µm, (F, Q, S) 10 µm, (M) 15 µm, (K, N, R) 30 µm, (L, O, P) 5 µm.

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