Literature DB >> 11356200

Overlapping CRE and E-box promoter elements can independently regulate COX-2 gene transcription in macrophages.

J R Mestre, D E Rivadeneira, P J Mackrell, M Duff, P P Stapleton, V Mack-Strong, S Maddali, G P Smyth, T Tanabe, J M Daly.   

Abstract

Macrophage cyclooxygenase-2 (COX-2) transcription is mediated through the collaboration of different promoter elements. Here, the role of an overlapping cyclic AMP responsive element (CRE)/E-box was investigated. Nuclear proteins bound both the CRE and E-box, which synergized with other promoter elements to induce COX-2 transcription. Endotoxin induced binding of nuclear proteins to the CRE and E-box and each element independently induced higher COX-2 transcription levels than the overlapping CRE/E-box. Transcription factors associated with the CRE binding complex included c-Jun and CRE binding protein and with the E-box binding complex USF-1; their overexpression significantly induced COX-2 transcription. Therefore, both CRE and E-box promoter elements regulate COX-2 transcription in macrophages.

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Year:  2001        PMID: 11356200     DOI: 10.1016/s0014-5793(01)02422-x

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  14 in total

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3.  Transcription factor Ets-1 inhibits glucose-stimulated insulin secretion of pancreatic β-cells partly through up-regulation of COX-2 gene expression.

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Journal:  BMC Mol Biol       Date:  2011-07-11       Impact factor: 2.946

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Journal:  PLoS Genet       Date:  2009-09-04       Impact factor: 5.917

10.  The ETS-Domain Transcription Factor Elk-1 Regulates COX-2 Gene Expression and Inhibits Glucose-Stimulated Insulin Secretion in the Pancreatic β -Cell Line INS-1.

Authors:  Xiong-Fei Zhang; Yi Zhu; Wen-Biao Liang; Jing-Jing Zhang
Journal:  Int J Endocrinol       Date:  2013-06-02       Impact factor: 3.257

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