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Regulation of human resistin gene expression in cell systems: an important role of stimulatory protein 1 interaction with a common promoter polymorphic site

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dc.contributor.authorChung, S. S.-
dc.contributor.authorChoi, H. H.-
dc.contributor.authorKim, K. W.-
dc.contributor.authorCho, Y. M.-
dc.contributor.authorLee, H. K.-
dc.contributor.authorPark, K. S.-
dc.date.accessioned2009-12-29T04:59:58Z-
dc.date.available2009-12-29T04:59:58Z-
dc.date.issued2005-
dc.identifier.citationDiabetologia 48(6):1150-1158en
dc.identifier.issn0012-186X (Print)-
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=15864531-
dc.identifier.urihttp://hdl.handle.net/10371/23037-
dc.description.abstractAIMS/HYPOTHESIS: Resistin is an adipokine that might link obesity and insulin resistance. A common polymorphism of the human resistin gene, -420C >G, is a major determinant of plasma resistin concentrations as well as resistin mRNA expression in human adipose tissue. In this study, we investigated the regulatory mechanism by which this polymorphism affects resistin expression. METHODS: Electrophoretic mobility shift assay was performed to identify the transcription factors binding to the -420G region. Transient transfection and reporter assay were used to measure promoter activities of the resistin gene. The binding ability of stimulatory protein 1 (Sp1) in response to adipocyte differentiation or high glucose concentrations was also measured. RESULTS: Sp1 and stimulatory protein 3 (Sp3) specifically bound to the region around -420G of the human resistin gene. Overexpression of Sp1 increased the promoter activity regardless of -420 genotypes, while the promoter activity of the -420G construct was two-fold higher than that of the -420C construct. In contrast, overexpression of Sp3 scarcely increased the promoter activity. The binding ability of Sp1 to the -420G region was increased in response to adipocyte differentiation. Mithramycin A, an inhibitor of DNA binding of Sp1, reduced the effect of high glucose on transcription induction of the resistin gene in adipocytes. CONCLUSIONS/INTERPRETATION: These results suggest that Sp1 is an important factor regulating transcription of human resistin gene. A common polymorphism of the human resistin promoter, -420C >G, is critical for the binding of Sp1 and modulates the transcriptional activity of the resistin gene by changing the binding ability of Sp1. In addition, Sp1 may be involved in the increase of resistin expression by hyperglycaemia.en
dc.description.sponsorshipThis study was supported by a grant from the
Korea Health 21 R & D Project, Ministry of Health & Welfare, Republic
of Korea (00-PJ3-PG6-GN07-001).
en
dc.language.isoenen
dc.publisherSpringer Verlagen
dc.subject3T3 Cellsen
dc.subjectAdipocytes/metabolismen
dc.subjectAnimalsen
dc.subjectBase Sequenceen
dc.subjectCell Lineen
dc.subjectDNA Fragmentationen
dc.subjectDNA Primersen
dc.subject*Gene Expression Regulationen
dc.subjectHeat-Shock Proteins/*metabolismen
dc.subjectHormones, Ectopic/*genetics/metabolismen
dc.subjectHumansen
dc.subjectMiceen
dc.subjectMonocytes/metabolismen
dc.subjectPlicamycin/analogs & derivatives/pharmacologyen
dc.subject*Polymorphism, Geneticen
dc.subject*Promoter Regions, Geneticen
dc.subjectRecombinant Fusion Proteins/metabolismen
dc.subjectResistinen
dc.titleRegulation of human resistin gene expression in cell systems: an important role of stimulatory protein 1 interaction with a common promoter polymorphic siteen
dc.typeArticleen
dc.identifier.doi10.1007/s00125-005-1762-y-
Appears in Collections:
College of Medicine/School of Medicine (의과대학/대학원)Internal Medicine (내과학전공)Journal Papers (저널논문_내과학전공)
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