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An analysis of expression patterns of genes encoding proteins with catalytic activities

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 en...

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Detalles Bibliográficos
Autores principales: Cankaya, Murat, Hernandez, Ana Martinez, Ciftci, Mehmet, Beydemir, Sukru, Ozdemir, Hasan, Budak, Harun, Gulcin, Ilhami, Comakli, Veysel, Emircupani, Tufan, Ekinci, Deniz, Kuzu, Muslum, Jiang, Qiuhong, Eichele, Gregor, Kufrevioglu, Omer Irfan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976134/
https://www.ncbi.nlm.nih.gov/pubmed/17626619
http://dx.doi.org/10.1186/1471-2164-8-232
Descripción
Sumario: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.