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在U937前单核细胞中,NF-IL6基因最小启动子的转录受CREB/ATF和SP1蛋白调控。

Transcription of a minimal promoter from the NF-IL6 gene is regulated by CREB/ATF and SP1 proteins in U937 promonocytic cells.

作者信息

Berrier A, Siu G, Calame K

机构信息

Department of Microbiology, College of Physicians and Surgeons, Columbia University, New York 10032, USA.

出版信息

J Immunol. 1998 Sep 1;161(5):2267-75.

PMID:9725220
Abstract

NF-IL6 is an important transcriptional regulator of genes induced in activated monocytes/macrophages, and NF-IL6 is the only CCAAT/enhancer-binding protein (C/EBP) family member whose steady-state mRNA levels increase upon activation of monocytes (1). We show that increased transcription of the NF-IL6 gene is responsible, at least in part, for induction of NF-IL6 mRNA following activation of U937 promonocytic cells. We have identified a 104-bp minimal promoter region of the NF-IL6 gene that is sufficient for basal and activation-dependent induction of transcription in U937 cells. This region contains binding sites for the cAMP response element-binding protein/activation transcription factor (CREB/ATF) and Sp1 families of transcription factors. Each site is functionally important and contributes independently to transcription of the NF-IL6 gene in U937 cells.

摘要

NF-IL6是活化单核细胞/巨噬细胞中诱导基因的重要转录调节因子,并且NF-IL6是唯一一种在单核细胞活化后其稳态mRNA水平会升高的CCAAT/增强子结合蛋白(C/EBP)家族成员(1)。我们发现,NF-IL6基因转录的增加至少部分地导致了U937原单核细胞活化后NF-IL6 mRNA的诱导。我们已经鉴定出NF-IL6基因的一个104bp最小启动子区域,该区域足以在U937细胞中进行基础转录和依赖于活化的转录诱导。该区域包含cAMP反应元件结合蛋白/活化转录因子(CREB/ATF)和Sp1转录因子家族的结合位点。每个位点在功能上都很重要,并独立地促进U937细胞中NF-IL6基因的转录。

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