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Cells
2022 Aug 24;1117:. doi: 10.3390/cells11172636.
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A New Model Organism to Investigate Extraocular Photoreception: Opsin and Retinal Gene Expression in the Sea Urchin Paracentrotus lividus.
Paganos P
,
Ullrich-Lüter E
,
Caccavale F
,
Zakrzewski A
,
Voronov D
,
Fournon-Berodia I
,
Cocurullo M
,
Lüter C
,
Arnone MI
.
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Molecular research on the evolution of extraocular photoreception has drawn attention to photosensitive animals lacking proper eye organs. Outside of vertebrates, little is known about this type of sensory system in any other deuterostome. In this study, we investigate such an extraocular photoreceptor cell (PRC) system in developmental stages of the sea urchin Paracentrotus lividus. We provide a general overview of the cell type families present at the mature rudiment stage using single-cell transcriptomics, while emphasizing the PRCs complexity. We show that three neuronal and one muscle-like PRC type families express retinal genes prior to metamorphosis. Two of the three neuronal PRC type families express a rhabdomeric opsin as well as an echinoderm-specific opsin (echinopsin), and their genetic wiring includes sea urchin orthologs of key retinal genes such as hlf, pp2ab56e, barh, otx, ac/sc, brn3, six1/2, pax6, six3, neuroD, irxA, isl and ato. Using qPCR, in situ hybridization, and immunohistochemical analysis, we found that the expressed retinal gene composition becomes more complex from mature rudiment to juvenile stage. The majority of retinal genes are expressed dominantly in the animals' podia, and in addition to the genes already expressed in the mature rudiment, the juvenile podia express a ciliary opsin, another echinopsin, and two Go-opsins. The expression of a core of vertebrate retinal gene orthologs indicates that sea urchins have an evolutionarily conserved gene regulatory toolkit that controls photoreceptor specification and function, and that their podia are photosensory organs.
Figure 1. Cell type atlas of the P. lividus mature rudiment. (A) ScRNA-seq pipeline from larvae collection, rudiment dissection and dissociation to 10Ã capturing and computational analysis. (B) Overlay UMAP showing the overlap of the libraries originating from the two biological replicates. (C) Dotplot showing the average expression of genes used as markers to identify specific cell clusters. (D) UMAP showing mature rudiment cell types, colored by their assignment to the initial set of 20 distinct cell clusters. Average expression gradient for opsin genes is depicted in purple, and for the rest of the genes, in red.
Figure 2. Photoreceptor cell type families and retinal molecular signature. (A) Heatmap and Venn diagram showing the differentially expressed marker genes between the two opsin2/opsin4 double positive clusters (PCRs 2 and PCRs 3). (B) Dotplot showing the averaged scaled expression of common marker genes of the two opsin2/opsin4 double positive clusters against the whole P. lividus mature rudiment atlas.
Figure 3. Distinct molecular signature of the two opsin2/opsin4 double positive cell type families. (A) Sub-clustering analysis of the two opsin2/opsin4 double positive cell type families resulted in the generation of the three and two distinct sub-clusters, respectively. (B) Dotplot showing the average scaled expression of sea urchin orthologues of retinal genes distributed in the different sub-clusters. Average expression gradient for opsin genes is depicted in purple, while the rest of the genes expressed in PRCs 2 and PRCs 3 sub-clusters are shown in green and magenta, respectively.
Figure 4. Immunolocalization (IHC) of sea urchin Opsin4 and expression of opsin4 mRNA (FISH) in mature rudiments and juveniles. (A) Immunohistochemical detection of Opsin4 at the 8-arm mature rudiment stage. (B) FISH using an antisense probe against Pl-opsin4 at the mature rudiment stage. (C) Immunohistochemical detection of Opsin4 protein at juvenile stage. (DâF) FISH using a specific antisense probe for Pl-opsin4 paired with IHC for Opsin4 protein at juvenile stage. (G,H) IHC detection of antigens indicative of the nervous system (1e11), musculature (MHC) and PRCs (Opsin4). (G,H) are a result of compilation of different stacks corresponding to the same individual. (I) Podium close-up showing the immunolocalization of Opsin4 and the pan-neuronal marker 1e11. (JâL) IHC detection of antigens indicative of the nervous system (1e11), musculature (MHC) and PRCs (Opsin4) focusing on a podium and the surrounding spines. DAPI was used to visualize nuclei (gray). Orientation: (A), the specimen is viewed from the top; (B), the specimen is viewed from the side; (D,G,H), juveniles are in oral view.
Figure 5. Retinal transcription factors pax6, neuroD1 and six3 RNA: expression in whole mount mature rudiments and juveniles. (AâE) FISH using a specific antisense probe against Pl-pax6 at rudiment (A,B) and juvenile (CâE) stages. In B and E, FISH are also paired with IHC detection of Opsin4. (F) FISH detection of the neuroD transcripts at juvenile stage. (GâI) FISH using an antisense probe for six3 at rudiment (G) and juvenile (H,I) stages. In I, FISH is paired with IHC for Opsin4. DAPI was used to visualize nuclei (gray). Orientation: (A), the specimen is viewed from the top; (B,G) the specimens are viewed from the side; (CâF,H,I) juveniles are in oral view.
Figure 6. Expression analysis of Opsins in P. lividus juveniles. (A) Relative gene expression of different opsins in juveniles as revealed by qRT-PCR. Sample size: 3 biological replicates; Statistical significance cut-off criteria: * p < 0.05; ** p <0.01. (B) Gene expression visualization of Opsin1, opsin2 and Opsin4 at juvenile stage. (B1âB3) double IHC detection of Opsin1 (magenta) and acetylated tubulin labeling ciliated structures (green). (B4) FISH using a specific antisense probe for Pl-opsin2 (cyan) paired with IHC for acetylated tubulin (green). (B5,B6) FISH for Pl-Opsin2 (cyan) transcripts paired with IHC detection of Opsin4 (red). DAPI was used to visualize nuclei (gray).
Figure 7. Schemes with the opsin expression on them and the molecular signature of the 2 clusters of PRC identified at mature rudiment stage. Nervous system in magenta, Opsin4+ PRCs in green, opsin2+ PRCs in cyan, Opsin1+PRCs in yellow.
Agca,
Neurosensory and neuromuscular organization in tube feet of the sea urchin Strongylocentrotus purpuratus.
2011, Pubmed,
Echinobase
Agca,
Neurosensory and neuromuscular organization in tube feet of the sea urchin Strongylocentrotus purpuratus.
2011,
Pubmed
,
Echinobase
Arendt,
Reconstructing the eyes of Urbilateria.
2001,
Pubmed
Arendt,
Ciliary photoreceptors with a vertebrate-type opsin in an invertebrate brain.
2004,
Pubmed
Arendt,
Evolution of eyes and photoreceptor cell types.
2003,
Pubmed
Ayers,
A Go-type opsin mediates the shadow reflex in the annelid Platynereis dumerilii.
2018,
Pubmed
Belecky-Adams,
Pax-6, Prox 1, and Chx10 homeobox gene expression correlates with phenotypic fate of retinal precursor cells.
1997,
Pubmed
Bernardos,
Notch-Delta signaling is required for spatial patterning and Müller glia differentiation in the zebrafish retina.
2005,
Pubmed
Brown,
Math5 is required for retinal ganglion cell and optic nerve formation.
2001,
Pubmed
Burke,
Neuron-specific expression of a synaptotagmin gene in the sea urchin Strongylocentrotus purpuratus.
2006,
Pubmed
,
Echinobase
Burke,
A genomic view of the sea urchin nervous system.
2006,
Pubmed
,
Echinobase
Buscone,
A new path in defining light parameters for hair growth: Discovery and modulation of photoreceptors in human hair follicle.
2017,
Pubmed
Byrne,
Expression of genes and proteins of the pax-six-eya-dach network in the metamorphic sea urchin: Insights into development of the enigmatic echinoderm body plan and sensory structures.
2018,
Pubmed
,
Echinobase
Caccavale,
Crosstalk between nitric oxide and retinoic acid pathways is essential for amphioxus pharynx development.
2021,
Pubmed
Cary,
Systematic comparison of sea urchin and sea star developmental gene regulatory networks explains how novelty is incorporated in early development.
2020,
Pubmed
,
Echinobase
Conte,
Proper differentiation of photoreceptors and amacrine cells depends on a regulatory loop between NeuroD and Six6.
2010,
Pubmed
Czerny,
DNA-binding and transactivation properties of Pax-6: three amino acids in the paired domain are responsible for the different sequence recognition of Pax-6 and BSAP (Pax-5).
1995,
Pubmed
,
Echinobase
D'Aniello,
Opsin evolution in the Ambulacraria.
2015,
Pubmed
,
Echinobase
Díaz-Balzac,
The catecholaminergic nerve plexus of Holothuroidea.
2010,
Pubmed
,
Echinobase
Ding,
BARHL2 differentially regulates the development of retinal amacrine and ganglion neurons.
2009,
Pubmed
Edgar,
Gene Expression Omnibus: NCBI gene expression and hybridization array data repository.
2002,
Pubmed
Elphick,
NGFFFamide and echinotocin: structurally unrelated myoactive neuropeptides derived from neurophysin-containing precursors in sea urchins.
2009,
Pubmed
,
Echinobase
Feuda,
Metazoan opsin evolution reveals a simple route to animal vision.
2012,
Pubmed
Frankfort,
Senseless is required for pupal retinal development in Drosophila.
2004,
Pubmed
Frankfort,
R8 development in the Drosophila eye: a paradigm for neural selection and differentiation.
2002,
Pubmed
Gehring,
New perspectives on eye development and the evolution of eyes and photoreceptors.
2005,
Pubmed
Halford,
Characterization of a novel human opsin gene with wide tissue expression and identification of embedded and flanking genes on chromosome 1q43.
2001,
Pubmed
Hsieh,
Dynamic Pax6 expression during the neurogenic cell cycle influences proliferation and cell fate choices of retinal progenitors.
2009,
Pubmed
Hsiung,
Retinal development in Drosophila: specifying the first neuron.
2002,
Pubmed
Hughes,
Zfhx3 modulates retinal sensitivity and circadian responses to light.
2021,
Pubmed
Inoue,
Math3 and NeuroD regulate amacrine cell fate specification in the retina.
2002,
Pubmed
Kingston,
Diverse Distributions of Extraocular Opsins in Crustaceans, Cephalopods, and Fish.
2016,
Pubmed
Kirwan,
The sea urchin Diadema africanum uses low resolution vision to find shelter and deter enemies.
2018,
Pubmed
,
Echinobase
Kitamura,
Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans.
2002,
Pubmed
Kojima,
A novel Go-mediated phototransduction cascade in scallop visual cells.
1997,
Pubmed
Lesser,
Sea urchin tube feet are photosensory organs that express a rhabdomeric-like opsin and PAX6.
2011,
Pubmed
,
Echinobase
Liu,
All Brn3 genes can promote retinal ganglion cell differentiation in the chick.
2000,
Pubmed
Lu,
Single-Cell Analysis of Human Retina Identifies Evolutionarily Conserved and Species-Specific Mechanisms Controlling Development.
2020,
Pubmed
Mao,
Substituting mouse transcription factor Pou4f2 with a sea urchin orthologue restores retinal ganglion cell development.
2016,
Pubmed
,
Echinobase
Marquardt,
Pax6 is required for the multipotent state of retinal progenitor cells.
2001,
Pubmed
Martinez-Morales,
Otx genes are required for tissue specification in the developing eye.
2001,
Pubmed
Martín-Partido,
The role of Islet-1 in cell specification, differentiation, and maintenance of phenotypes in the vertebrate neural retina.
2015,
Pubmed
Massri,
Developmental single-cell transcriptomics in the Lytechinus variegatus sea urchin embryo.
2021,
Pubmed
,
Echinobase
Mathers,
The Rx homeobox gene is essential for vertebrate eye development.
1997,
Pubmed
Milito,
Antioxidant and immune response of the sea urchin Paracentrotus lividus to different re-suspension patterns of highly polluted marine sediments.
2020,
Pubmed
,
Echinobase
Millott,
The podial pit--a new structure in the echinoid Diadema antillarum Philippi.
1969,
Pubmed
,
Echinobase
Motahari,
Tbx3 represses bmp4 expression and, with Pax6, is required and sufficient for retina formation.
2016,
Pubmed
Moutsaki,
Teleost multiple tissue (tmt) opsin: a candidate photopigment regulating the peripheral clocks of zebrafish?
2003,
Pubmed
Musser,
Profiling cellular diversity in sponges informs animal cell type and nervous system evolution.
2021,
Pubmed
Paganos,
FISH for All: A Fast and Efficient Fluorescent In situ Hybridization (FISH) Protocol for Marine Embryos and Larvae.
2022,
Pubmed
,
Echinobase
Paganos,
Single-cell RNA sequencing of the Strongylocentrotus purpuratus larva reveals the blueprint of major cell types and nervous system of a non-chordate deuterostome.
2021,
Pubmed
,
Echinobase
Pan,
The Rx-like homeobox gene (Rx-L) is necessary for normal photoreceptor development.
2006,
Pubmed
Panda,
Illumination of the melanopsin signaling pathway.
2005,
Pubmed
Pappu,
Genetic control of retinal specification and determination in Drosophila.
2004,
Pubmed
Perillo,
Regulation of dynamic pigment cell states at single-cell resolution.
2020,
Pubmed
,
Echinobase
Perillo,
Methodology for Whole Mount and Fluorescent RNA In Situ Hybridization in Echinoderms: Single, Double, and Beyond.
2021,
Pubmed
,
Echinobase
Plachetzki,
New insights into the evolutionary history of photoreceptor cells.
2005,
Pubmed
Raible,
Opsins and clusters of sensory G-protein-coupled receptors in the sea urchin genome.
2006,
Pubmed
,
Echinobase
Rentzsch,
Modern genomic tools reveal the structural and cellular diversity of cnidarian nervous systems.
2019,
Pubmed
Rorick,
PP2A:B56epsilon is required for eye induction and eye field separation.
2007,
Pubmed
Schmidt,
Intrinsically photosensitive retinal ganglion cells: many subtypes, diverse functions.
2011,
Pubmed
Sebé-Pedrós,
Cnidarian Cell Type Diversity and Regulation Revealed by Whole-Organism Single-Cell RNA-Seq.
2018,
Pubmed
Silver,
Signaling circuitries in development: insights from the retinal determination gene network.
2005,
Pubmed
Smith,
Differences in Small Molecule Neurotransmitter Profiles From the Crown-of-Thorns Seastar Radial Nerve Revealed Between Sexes and Following Food-Deprivation.
2018,
Pubmed
,
Echinobase
Stuart,
Comprehensive Integration of Single-Cell Data.
2019,
Pubmed
Tsironis,
Coup-TF: A maternal factor essential for differentiation along the embryonic axes in the sea urchin Paracentrotus lividus.
2021,
Pubmed
,
Echinobase
Ullrich-Lüter,
Unique system of photoreceptors in sea urchin tube feet.
2011,
Pubmed
,
Echinobase
Ullrich-Lüter,
C-opsin expressing photoreceptors in echinoderms.
2013,
Pubmed
,
Echinobase
Valencia,
Ciliary photoreceptors in sea urchin larvae indicate pan-deuterostome cell type conservation.
2021,
Pubmed
,
Echinobase
Wood,
Neuropeptidergic Systems in Pluteus Larvae of the Sea Urchin Strongylocentrotus purpuratus: Neurochemical Complexity in a "Simple" Nervous System.
2018,
Pubmed
,
Echinobase
Wu,
Opsin 3-Gαs Promotes Airway Smooth Muscle Relaxation Modulated by G Protein Receptor Kinase 2.
2021,
Pubmed
Yim,
Activation of an Endogenous Opsin 3 Light Receptor Mediates Photo-Relaxation of Pre-Contracting Late Gestation Human Uterine Smooth Muscle Ex Vivo.
2020,
Pubmed
Yim,
Airway smooth muscle photorelaxation via opsin receptor activation.
2019,
Pubmed
Zagozewski,
The role of homeobox genes in retinal development and disease.
2014,
Pubmed
Zeisel,
Brain structure. Cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq.
2015,
Pubmed
Zelhof,
Transforming the architecture of compound eyes.
2006,
Pubmed
Zhu,
The expression of NOTCH2, HES1 and SOX9 during mouse retinal development.
2013,
Pubmed