4.4 Article

Identification of the genes encoding candidate septate junction components expressed during early development of the sea urchin, Strongylocentrotus purpuratus, and evidence of a role for Mesh in the formation of the gut barrier

Journal

DEVELOPMENTAL BIOLOGY
Volume 495, Issue -, Pages 21-34

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ydbio.2022.12.007

Keywords

Sea urchin; Epithelial development; Septate junctions; Mesh; Intestinal barrier; CRISPR; Cas9

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In this study, the cell-specific expression of nine candidate septate junction (SJ) genes in the early life stages of the sea urchin Strongylocentrotus purpuratus was investigated. It was found that different cohorts of SJ genes were expressed in different epithelia during embryonic and larval development. Specifically, a gene called SpMesh was highly enriched in the endodermal epithelium of the mid- and hindgut. Functional analysis revealed that loss of SpMesh disrupted the integrity of the gut-paracellular barrier. These findings provide insights into the molecular physiology of SJ during the development of marine organisms and suggest a shared role for Mesh-homologous proteins in forming intestinal barriers in invertebrates.
Septate junctions (SJs) evolved as cell-cell junctions that regulate the paracellular barrier and integrity of epithelia in invertebrates. Multiple morphological variants of SJs exist specific to different epithelia and/or phyla but the biological significance of varied SJ morphology is unclear because the knowledge of the SJ associated proteins and their functions in non-insect invertebrates remains largely unknown. Here we report cell-specific expression of nine candidate SJ genes in the early life stages of the sea urchin Strongylocentrotus purpuratus. By use of in situ RNA hybridization and single cell RNA-seq we found that the expression of selected genes encoding putatively SJ associated transmembrane and cytoplasmic scaffold molecules was dynamically regulated during epithelial development in the embryos and larvae with different epithelia expressing different cohorts of SJ genes. We focused a functional analysis on SpMesh, a homolog of the Drosophila smooth SJ component Mesh, which was highly enriched in the endodermal epithelium of the mid- and hindgut. Functional perturbation of SpMesh by both CRISPR/Cas9 mutagenesis and vivo morpholino-mediated knockdown shows that loss of SpMesh does not disrupt the formation of the gut epithelium during gastrulation. However, loss of SpMesh resulted in a severely reduced gut-paracellular barrier as quantitated by increased permeability to 3-5 kDa FITC-dextran. Together, these studies provide a first look at the molecular SJ physiology during the development of a marine organism and suggest a shared role for Mesh-homologous proteins in forming an intestinal barrier in invertebrates. Results have implications for consideration of the traits underlying species-specific sensitivity of marine larvae to climate driven ocean change.

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