Promoter analysis of human CC chemokine CCL23 gene in U937 monocytoid cells

Yong-Hyun Shin , Guy Wilhem Lee , Kyung-No Son , Sang Min Lee , Chang Joong Kang , Byoung S. Kwon , Jiyoung Kim
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引用次数: 6

Abstract

Expression of CCL23 is induced by external stimuli including PMA in monocytes, but its transcriptional regulation has not been studied to date. Serial deletion analysis of its 5′ flanking region revealed that the region − 293 to + 31 was important for induction by PMA. Cis-acting elements at the − 269/− 264 (NFAT site), − 167/− 159 (NF-κB site), and − 51/− 43 (AP-1 site) positions were identified as the critical sites for the CCL23 expression in U937 cells. We demonstrated the binding of the transcription factors to the consensus sites. Specific inhibitors for signal pathways reduced PMA-induced expression of CCL23, confirming involvement of these transcription factors.

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人CC趋化因子CCL23基因在U937单核细胞中的启动子分析
CCL23在单核细胞中可被包括PMA在内的外部刺激诱导表达,但其转录调控迄今尚未被研究。对其5 '侧区进行序列缺失分析,发现−293 ~ + 31区域对PMA诱导具有重要意义。在U937细胞中,- 269/−264 (NFAT位点)、- 167/−159 (NF-κB位点)和- 51/−43 (AP-1位点)的顺式作用元件被确定为CCL23表达的关键位点。我们证明了转录因子与共识位点的结合。信号通路的特异性抑制剂降低了pma诱导的CCL23表达,证实了这些转录因子的参与。
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