[No authors listed]
BACKGROUND: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. RESULTS:The 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. CONCLUSION:The 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.
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Rnaset2a, Gck, Aco1, Aco2, Adh1, Aldoa, Aldoc, Car8, Car1, Car11, Car2, Car3, Car4, Car5a, Car6, Car7, Cs, Dld, Eno1, Eno2, Eno3, Fh1, Gapdh, Gapdhs, Gpi1, Hk1, Hk2, Idh1, Idh3g, Loxl3, Idh3b, Mdh2, Mdh1, Ogdh, Pfkl, Pfkm, Pgam1, Pgk1, Pkm, Pklr, Ptgds, Sucla2, Suclg2, Hk3, Tpi1, Aldob, Car14, Pla2g2f, Idh2, Pgam2, Car5b, Pfkp, Suclg1, Sdhc, Sdhd, Sdha, Sdhb, Idh3a, Rnaset2b, Acss1, Csl, Car13, Car10, Car12, Dlst, Car15, Cpn1
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