Abstract

BackgroundIn situ hybridization (ISH) is a powerful method for visualizing gene expression patterns at the organismal level with cellular resolution. When automated, it is capable of determining the expression of a large number of genes.ResultsThe expression patterns of 662 genes that encode enzymes were determined by ISH in the mid-gestation mouse embryo, a stage that models the complexity of the adult organism. Forty-five percent of transcripts encoding metabolic enzymes (n = 297) showed a regional expression pattern. A similar percentage was found for the 190 kinases that were also analyzed. Many mRNAs encoding glycolytic and TCA cycle enzymes exhibited a characteristic expression pattern. The annotated expression patterns were deposited on the Genepaint database and are retrievable by user-defined queries including gene name and sites of expression.ConclusionThe 662 expression patterns discussed here comprised gene products with activities associated with catalysis. Preliminary analysis of these data revealed that a significant number of genes encoding housekeeping functions such as biosynthesis and catabolism were expressed regionally, so they could be used as tissue-specific gene markers. We found no difference in tissue specificity between mRNAs encoding housekeeping functions and those encoding components of signal transduction pathways, as exemplified by the kinases.

Highlights

  • In situ hybridization (ISH) is a powerful method for visualizing gene expression patterns at the organismal level with cellular resolution

  • Expression patterns of mouse genes encoding proteins with catalytic activity Under its "Molecular Function" category, Gene Ontology lists approximately 2700 gene products that exhibit activity associated with catalysis [22]

  • Genes were selected on the basis of three not mutually exclusive criteria: (1) the genes scored as 'present' in a duplicate Affymetrix microarray chip (MA) hybridized with mRNA from E14.5 mouse embryos (MA data were deposited at NCBI GEO under accession number GSE6081); (2) all gene products encoding glycolytic and TCA cycle enzymes were selected; (3) for kinases, the intensity of the MA signal was ranked by the raw numerical value, and the 190 most stronglyexpressed transcripts were selected

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Summary

Introduction

In situ hybridization (ISH) is a powerful method for visualizing gene expression patterns at the organismal level with cellular resolution. When automated, it is capable of determining the expression of a large number of genes. When and where genes are expressed provides useful information about their function. This view forms the basis of several genome-scale projects that attempt the systematic localization of mRNAs and/or proteins expressed in tissues and cells [1,2]. Expression sites are annotated and images are made accessible on a public website [3,4]

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