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Cited 11 time in webofscience Cited 11 time in scopus
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dc.contributor.authorCHAE, HD-
dc.contributor.authorKIM, KT-
dc.date.accessioned2016-03-31T14:33:43Z-
dc.date.available2016-03-31T14:33:43Z-
dc.date.created2009-03-18-
dc.date.issued1995-01-17-
dc.identifier.issn0006-291X-
dc.identifier.other1995-OAK-0000009029-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/21863-
dc.description.abstractTo test the role of cytosolic calcium in the basal expression of a neuronal gene, promoter activity of the rat tyrosine hydroxylase (TH) gene was monitored upon reduced resting level of intracellular calcium. TH promoter activity was decreased by cell-permeable calcium chelator, BAPTA/AM, in SK-N-BE(2)C human neuroblastoma cells. The cAMP response element (CRE) was mapped to the calcium responsible element by mutational and deletional analysis of the 5' upstream promoter region. Gel shift assay showed 2 CRE-specific DNA-protein complexes. The quantities of specific complexes were markedly decreased in BAPTA/AM-treated cells. These data suggest that resting level of intracellular calcium has a critical role in the basal expression of TH gene through the regulation of the binding of nuclear proteins to the CRE motif in the promoter. (C) 1995 Academic Press, Inc.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherACADEMIC PRESS INC JNL-COMP SUBSCRIPT-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.subjectCELL-SPECIFIC EXPRESSION-
dc.subjectNERVE GROWTH-FACTOR-
dc.subjectMEMBRANE DEPOLARIZATION-
dc.subjectCHLORAMPHENICOL ACETYLTRANSFERASE-
dc.subjectREGULATORY ELEMENTS-
dc.subjectRESPONSIVE ELEMENT-
dc.subjectCYCLIC-AMP-
dc.subjectPC12 CELLS-
dc.subjectTRANSCRIPTION-
dc.subjectPHOSPHORYLATION-
dc.titleCYTOSOLIC CALCIUM IS ESSENTIAL IN TBE BASAL EXPRESSION OF TYROSINE-HYDROXYLASE GENE-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.identifier.doi10.1006/bbrc.1995.1093-
dc.author.googleCHAE, HD-
dc.author.googleKIM, KT-
dc.relation.volume206-
dc.relation.issue2-
dc.relation.startpage659-
dc.relation.lastpage666-
dc.contributor.id10104775-
dc.relation.journalBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.206, no.2, pp.659 - 666-
dc.identifier.wosidA1995QC11500032-
dc.date.tcdate2019-01-01-
dc.citation.endPage666-
dc.citation.number2-
dc.citation.startPage659-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume206-
dc.contributor.affiliatedAuthorKIM, KT-
dc.identifier.scopusid2-s2.0-0028931834-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc11-
dc.type.docTypeArticle-
dc.subject.keywordPlusCELL-SPECIFIC EXPRESSION-
dc.subject.keywordPlusNERVE GROWTH-FACTOR-
dc.subject.keywordPlusMEMBRANE DEPOLARIZATION-
dc.subject.keywordPlusCHLORAMPHENICOL ACETYLTRANSFERASE-
dc.subject.keywordPlusREGULATORY ELEMENTS-
dc.subject.keywordPlusRESPONSIVE ELEMENT-
dc.subject.keywordPlusCYCLIC-AMP-
dc.subject.keywordPlusPC12 CELLS-
dc.subject.keywordPlusTRANSCRIPTION-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-

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김경태KIM, KYONG TAI
Dept of Life Sciences
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