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FoxA1 translates epigenetic signatures into enhancer-driven lineage-specific transcription 总被引:1,自引:0,他引:1
Lupien M Eeckhoute J Meyer CA Wang Q Zhang Y Li W Carroll JS Liu XS Brown M 《Cell》2008,132(6):958-970
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Use of chromatin immunoprecipitation to clone novel E2F target promoters 总被引:20,自引:0,他引:20 下载免费PDF全文
Weinmann AS Bartley SM Zhang T Zhang MQ Farnham PJ 《Molecular and cellular biology》2001,21(20):6820-6832
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In vivo interactions of the Acanthamoeba TBP gene promoter 总被引:1,自引:0,他引:1
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Okada Y Nobori H Shimizu M Watanabe M Yonekura M Nakai T Kamikawa Y Wakimura A Funahashi N Naruse H Watanabe A Yamasaki D Fukada S Yasui K Matsumoto K Sato T Kitajima K Nakano T Aird WC Doi T 《PloS one》2011,6(9):e24837
In previous studies on the mechanism underlying megakaryocyte-specific gene expression, several ETS motifs were found in each megakaryocyte-specific gene promoter. Although these studies suggested that several ETS family proteins regulate megakaryocyte-specific gene expression, only a few ETS family proteins have been identified. Platelet factor 4 (PF4) is a megakaryocyte-specific gene and its promoter includes multiple ETS motifs. We had previously shown that ETS-1 binds to an ETS motif in the PF4 promoter. However, the functions of the other ETS motifs are still unclear. The goal of this study was to investigate a novel functional ETS motif in the PF4 promoter and identify proteins binding to the motif. In electrophoretic mobility shift assays and a chromatin immunoprecipitation assay, FLI-1, ELF-1, and GABP bound to the -51 ETS site. Expression of FLI-1, ELF-1, and GABP activated the PF4 promoter in HepG2 cells. Mutation of a -51 ETS site attenuated FLI-1-, ELF-1-, and GABP-mediated transactivation of the promoter. siRNA analysis demonstrated that FLI-1, ELF-1, and GABP regulate PF4 gene expression in HEL cells. Among these three proteins, only FLI-1 synergistically activated the promoter with GATA-1. In addition, only FLI-1 expression was increased during megakaryocytic differentiation. Finally, the importance of the -51 ETS site for the activation of the PF4 promoter during physiological megakaryocytic differentiation was confirmed by a novel reporter gene assay using in vitro ES cell differentiation system. Together, these data suggest that FLI-1, ELF-1, and GABP regulate PF4 gene expression through the -51 ETS site in megakaryocytes and implicate the differentiation stage-specific regulation of PF4 gene expression by multiple ETS factors. 相似文献
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