Suppr超能文献

在富含GC的启动子区域,C/EBPδ与Sp1的直接相互作用协同促进小鼠巨噬细胞中IL-10基因的转录。

Direct interaction of C/EBPdelta and Sp1 at the GC-enriched promoter region synergizes the IL-10 gene transcription in mouse macrophage.

作者信息

Chiang Ben-Tzu, Liu Yi-Wen, Chen Ben-Kuen, Wang Ju-Ming, Chang Wen-Chang

机构信息

Department of Pharmacology, College of Medicine, National Cheng Kung University, Tainan, 701, Taiwan.

出版信息

J Biomed Sci. 2006 Sep;13(5):621-35. doi: 10.1007/s11373-006-9101-y. Epub 2006 Jul 27.

Abstract

We previously reported that LPS activates the transcription of the IL-10 gene through the Sp1 and C/EBP binding sites and indicated that Sp1, C/EBPbeta and C/EBPdelta can coactivate the IL-10 gene expression in mouse macrophage cells [Liu Y.-W., Tseng H.-P., Chen L.-C., Chen B.-K., Chang W.-C. J. Immunol. 171: 821-828, 2003]. In the present report, we demonstrated the direct physical interaction between C/EBPdelta and Sp1, and also mapped the interaction domains of these two proteins. C/EBPdelta binds to Sp1 via its basic region leucine zipper domain. The C-terminus of Sp1 was also the major region interacting with C/EBPdelta. However, both glutamine- and serine/threonine-rich homologus regions of Sp1 also interacted with C/EBPdelta. The binding of Sp1 and C/EBPdelta as a complex to the Sp1 binding site on the promoter of IL-10 was further confirmed by using the DNA affinity precipitation assay. By using Sp1-deficient SL2 cells, we also found that the overexpressions of C/EBPdelta and Sp1 synergically activate the transcriptional activity of IL-10 gene. Taken together, our present results revealed a novel mechanism of a superactivation of Sp1 by C/EBPdelta via a direct interaction between these two transcription factors leading to the activation of the IL-10 gene in mouse macrophage cells.

摘要

我们先前报道,脂多糖(LPS)通过Sp1和C/EBP结合位点激活白细胞介素-10(IL-10)基因的转录,并指出Sp1、C/EBPβ和C/EBPδ可在小鼠巨噬细胞中共激活IL-10基因的表达[Liu Y.-W., Tseng H.-P., Chen L.-C., Chen B.-K., Chang W.-C. J. Immunol. 171: 821-828, 2003]。在本报告中,我们证明了C/EBPδ与Sp1之间存在直接的物理相互作用,并绘制了这两种蛋白质的相互作用结构域。C/EBPδ通过其碱性区域亮氨酸拉链结构域与Sp1结合。Sp1的C末端也是与C/EBPδ相互作用的主要区域。然而,Sp1富含谷氨酰胺和丝氨酸/苏氨酸的同源区域也与C/EBPδ相互作用。通过DNA亲和沉淀试验进一步证实了Sp1和C/EBPδ作为复合物与IL-10启动子上的Sp1结合位点的结合。通过使用Sp1缺陷型SL2细胞,我们还发现C/EBPδ和Sp1的过表达协同激活IL-10基因的转录活性。综上所述,我们目前的结果揭示了一种新的机制,即C/EBPδ通过这两种转录因子之间的直接相互作用对Sp1进行超激活,从而导致小鼠巨噬细胞中IL-10基因的激活。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验