4.7 Article

When Bigger Is Better: 3D RNA Profiling of the Developing Head in the Catshark Scyliorhinus canicula

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2021.744982

Keywords

RNA tomography; catshark; forebrain patterning; correlation; auto-correlation

Funding

  1. Agence Nationale de la Recherche [ANR-16-CE13-0013-02]
  2. Region Occitanie [156393]
  3. Ministere de la Recherche [ED515]
  4. Agence Nationale de la Recherche (ANR) [ANR-16-CE13-0013] Funding Source: Agence Nationale de la Recherche (ANR)

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This study adapts RNA tomography to analyze gene expression in the embryonic head of the catshark, providing detailed spatial information for developmental processes. The technique generates a genome-wide 3D atlas of gene expression data, allowing for comparative analysis across gnathostomes and offering new opportunities for evo-devo research in larger organism sizes.
We report the adaptation of RNA tomography, a technique allowing spatially resolved, genome-wide expression profiling, to a species occupying a key phylogenetic position in gnathostomes, the catshark Scyliorhinus canicula. We focused analysis on head explants at an embryonic stage, shortly following neural tube closure and of interest for a number of developmental processes, including early brain patterning, placode specification or the establishment of epithalamic asymmetry. As described in the zebrafish, we have sequenced RNAs extracted from serial sections along transverse, horizontal and sagittal planes, mapped the data onto a gene reference taking advantage of the high continuity genome recently released in the catshark, and projected read counts onto a digital model of the head obtained by confocal microscopy. This results in the generation of a genome-wide 3D atlas, containing expression data for most protein-coding genes in a digital model of the embryonic head. The digital profiles obtained for candidate forebrain regional markers along antero-posterior, dorso-ventral and left-right axes reproduce those obtained by in situ hybridization (ISH), with expected relative organizations. We also use spatial autocorrelation and correlation as measures to analyze these data and show that they provide adequate statistical tools to extract novel expression information from the model. These data and tools allow exhaustive searches of genes exhibiting any predefined expression characteristic, such a restriction to a territory of interest, thus providing a reference for comparative analyses across gnathostomes. This methodology appears best suited to species endowed with large embryo or organ sizes and opens novel perspectives to a wide range of evo-devo model organisms, traditionally counter-selected on size criterion.

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