Single-Cell Transcriptomic Analysis Reveals the Molecular Profile of Go-Opsin Photoreceptor Cells in Sea Urchin Larvae

Cells. 2023 Aug 23;12(17):2134. doi: 10.3390/cells12172134.

Abstract

The ability to perceive and respond to light stimuli is fundamental not only for spatial vision but also to many other light-mediated interactions with the environment. In animals, light perception is performed by specific cells known as photoreceptors and, at molecular level, by a group of GPCRs known as opsins. Sea urchin larvae possess a group of photoreceptor cells (PRCs) deploying a Go-Opsin (Opsin3.2) which have been shown to share transcription factors and morphology with PRCs of the ciliary type, raising new questions related to how this sea urchin larva PRC is specified and whether it shares a common ancestor with ciliary PRCs or it if evolved independently through convergent evolution. To answer these questions, we combined immunohistochemistry and fluorescent in situ hybridization to investigate how the Opsin3.2 PRCs develop in the sea urchin Strongylocentrotus purpuratus larva. Subsequently, we applied single-cell transcriptomics to investigate the molecular signature of the Sp-Opsin3.2-expressing cells and show that they deploy an ancient regulatory program responsible for photoreceptors specification. Finally, we also discuss the possible functions of the Opsin3.2-positive cells based on their molecular fingerprint, and we suggest that they are involved in a variety of signaling pathways, including those entailing the thyrotropin-releasing hormone.

Keywords: evolution; opsin; photoreceptors; sea urchin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • In Situ Hybridization, Fluorescence
  • Larva / genetics
  • Opsins* / genetics
  • Photoreceptor Cells
  • Sea Urchins / genetics
  • Transcriptome* / genetics

Substances

  • Opsins

Grants and funding

M.C. was supported by SZN PhD fellowships for the Open University and by the Human Frontiers Science Program grant number (RGP0002/2019). P.P. was supported by Marie Curie ITN EvoCELL (H2020 Grant Number: 766053 to M.I.A.) and by the Human Frontiers Science Program grant number (RGP0002/2019).