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核因子YY1通过两种机制抑制人γ干扰素启动子:抑制AP1结合和激活沉默子元件。

The nuclear factor YY1 suppresses the human gamma interferon promoter through two mechanisms: inhibition of AP1 binding and activation of a silencer element.

作者信息

Ye J, Cippitelli M, Dorman L, Ortaldo J R, Young H A

机构信息

Laboratory of Experimental Immunology, Division of Basic Sciences, National Cancer Institute-Frederick Cancer Research and Developmental Center, Maryland 21702-1201, USA.

出版信息

Mol Cell Biol. 1996 Sep;16(9):4744-53. doi: 10.1128/MCB.16.9.4744.

Abstract

Our group has previously reported that the nuclear factor Yin-Yang 1 (YY1), a ubiquitous DNA-binding protein, is able to interact with a silencer element (BE) in the gamma interferon (IFN-gamma) promoter region. In this study, we demonstrated that YY1 can directly inhibit the activity of the IFN-gamma promoter by interacting with multiple sites in the promoter. In cotransfection assays, a YY1 expression vector significantly inhibited IFN-gamma promoter activity. Mutation of the YY1 binding site in the native IFN-gamma promoter was associated with an increase in the IFN-gamma promoter activity. Analysis of the DNA sequences of the IFN-gamma promoter revealed a second functional YY1 binding site (BED) that overlaps with an AP1 binding site. In this element, AP1 enhancer activity was suppressed by YY1. Since the nuclear level of YY1 does not change upon cell activation, our data support a model that the nuclear factor YY1 acts to suppress basal IFN-gamma transcription by interacting with the promoter at multiple DNA binding sites. This repression can occur through two mechanisms: (i) cooperation with an as-yet-unidentified AP2-like repressor protein and (ii) competition for DNA binding with the transactivating factor AP1.

摘要

我们小组先前曾报道,核因子阴阳1(YY1)是一种普遍存在的DNA结合蛋白,能够与γ干扰素(IFN-γ)启动子区域的一个沉默元件(BE)相互作用。在本研究中,我们证明YY1可通过与启动子中的多个位点相互作用直接抑制IFN-γ启动子的活性。在共转染实验中,YY1表达载体显著抑制了IFN-γ启动子活性。天然IFN-γ启动子中YY1结合位点的突变与IFN-γ启动子活性的增加有关。对IFN-γ启动子DNA序列的分析揭示了第二个功能性YY1结合位点(BED),它与一个AP1结合位点重叠。在这个元件中,YY1抑制了AP1增强子活性。由于YY1的核水平在细胞激活后不会改变,我们的数据支持这样一个模型,即核因子YY1通过与启动子上的多个DNA结合位点相互作用来抑制基础IFN-γ转录。这种抑制可通过两种机制发生:(i)与一种尚未鉴定的AP2样阻遏蛋白合作;(ii)与反式激活因子AP1竞争DNA结合。

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