An analysis of expression patterns of genes encoding proteins with catalytic activities        
Yazarlar (14)
Murat Cankaya
Max Planck Institute For Biophysical Chemistry, Almanya
Ana Martinez Hernandez
Max Planck Institute For Biophysical Chemistry, Almanya
Mehmet Ciftci
Atatürk Üniversitesi, Türkiye
Sukru Beydemir
Atatürk Üniversitesi, Türkiye
Hasan Ozdemir
Atatürk Üniversitesi, Türkiye
Harun Budak
Max Planck Institute For Biophysical Chemistry, Almanya
Ilhami Gulcin
Atatürk Üniversitesi, Türkiye
Veysel Comakli
Atatürk Üniversitesi, Türkiye
Tufan Emircupani
Atatürk Üniversitesi, Türkiye
Deniz Ekinci
Atatürk Üniversitesi, Türkiye
Prof. Dr. Müslüm KUZU Atatürk Üniversitesi, Türkiye
Qiuhong Jiang
Max Planck Institute For Biophysical Chemistry, Almanya
Gregor Eichele
Max Planck Institute For Biophysical Chemistry, Almanya
Omer Irfan Kufrevioglu
Atatürk Üniversitesi, Türkiye
Makale Türü Açık Erişim Özgün Makale
Makale Alt Türü SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale
Dergi Adı BMC Genomics
Dergi ISSN 1471-2164 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili İngilizce
Basım Tarihi 07-2007
Cilt No 8
Sayı 1
Sayfalar 232 / 246
DOI Numarası 10.1186/1471-2164-8-232
Makale Linki http://www.biomedcentral.com/1471-2164/8/232
Özet
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. 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. 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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