Abstract
We report an efficient procedure for in situ hybridization with a multi-well format on Caenorhabditis elegans embryos for large scale screening of gene expression patterns in this organism. Each hybridization well contains embryos at various stages throughout embryogenesis. The validity of the method was confirmed through results with control genes whose expression patterns have been reported; glp-1 in very early embryos, myo-2 in pharyngeal muscle and unc-54 in body wall muscle. Several collagen genes and a pepsinogen gene were also examined to establish a set of lineage-specific markers. As a pilot project, we examined approximately 100 unique cDNA species classified by our cDNA project, finding that approximately 10% of the cDNA groups were expressed in specific cells and at specific stages.
MeSH Terms
Animals
Base Sequence
Caenorhabditis elegans/embryology,genetics
Caenorhabditis elegans Proteins
Collagen/genetics
DNA Probes
DNA, Helminth/analysis
Gene Expression
Helminth Proteins/genetics
In Situ Hybridization/methods
Membrane Glycoproteins/genetics
Molecular Sequence Data
Muscles/chemistry,embryology
Pepsinogens/genetics
Pilot Projects
Receptors, Notch
Chemicals
Caenorhabditis elegans Proteins
DNA Probes
DNA, Helminth
Glp-1 protein, C elegans
Helminth Proteins
Membrane Glycoproteins
Pepsinogens
Receptors, Notch
Collagen
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Tabara H
Department of Genetics, The Graduate University of Advanced Studies, Japan.
Motohashi T
Kohara Y
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