Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9434323 | Neuroscience Research | 2005 | 8 Pages |
Abstract
To understand the neuronal cell type-specific expression of Ca2+/calmodulin-dependent protein kinase II (CaM kinase II), we investigated binding proteins that specifically activated the promoter of the α isoform of CaM kinase II (α CaM kinase II). Proteins that bind the promoter sequence were found in rat brain nuclear extract by electrophoretic mobility shift assay. Then, we screened for binding proteins in a mouse brain cDNA library using the yeast one-hybrid system. Zic2, a Zic family zinc finger transcription factor, was identified as one of the binding proteins. To investigate the effect of Zic2 on the promoter activity, Zic2 cDNA was expressed with a luciferase reporter gene containing a neuronal cell type-specific promoter of α CaM kinase II in neuronal and non-neuronal cells. The promoter activity of α CaM kinase II was enhanced 1.3-5-fold in cultured neuronal cells by Zic2. The activation was varied among neuronal cell types. Zic2 also increased the promoter activity in non-neuronal cells, although the relative luciferase activites in non-neuronal cells were lower than those in neuronal cell lines. These results indicated that Zic2 was one of the proteins binding to, and regulating the activity of, the promoter of α CaM kinase II.
Keywords
DMEMCa2+/calmodulin-dependent protein kinase II (CaM kinase II)EMSAYeast one-hybrid systemCaM kinase II3ATZic2RT-PCRPSDFBS3-amino-1,2,4-triazoleCa2+/calmodulin-dependent protein kinase IIDulbecco's modified Eagle's mediumElectrophoretic mobility shift assayGene expressionpostsynaptic densityCNSfetal bovine serumNeuronal cellcentral nervous systemReverse transcriptase-polymerase chain reactionZinc finger proteinHAT
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Authors
Takumi Sakurada, Kazuko Mima, Akira Kurisaki, Hiromu Sugino, Takashi Yamauchi,