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通过过表达 CREB1 抑制人巨细胞病毒复制。

Inhibition of human cytomegalovirus replication by overexpression of CREB1.

机构信息

Expression Engineering, Bioprocessing Technology Institute, Agency for Science, Technology and Research (A(∗)STAR), 20 Biopolis Way, #06-01 Centros, Singapore 138668, Singapore.

Department of Microbiology, University of Iowa, 51 Newton Rd., 3-772 Bowen Science Building, Iowa City, IA 52242, USA.

出版信息

Antiviral Res. 2014 Feb;102:11-22. doi: 10.1016/j.antiviral.2013.11.012. Epub 2013 Dec 5.

Abstract

Expression of the human cytomegalovirus (HCMV) major immediate-early (MIE) genes is regulated by a strong enhancer-containing promoter with multiple binding sites for various transcription factors, including cyclic AMP response element binding protein 1 (CREB1). Here we show that overexpression of CREB1 potently blocked MIE transcription and HCMV replication. Surprisingly, CREB1 still exhibited strong inhibition of the MIE promoter when all five CREB binding sites within the enhancer were mutated, suggesting that CREB1 regulated the MIE gene expression indirectly. Promoter deletion analysis and site-directed mutagenesis identified the region between -130 and -50 upstream of the transcription start site of the MIE gene as the "CREB1 responsive region". Mutations of SP1/3 and NF-κB binding sites within this region interrupted the inhibitory effect induced by CREB1 overexpression. Our findings suggest that overexpression of CREB1 can cause repression of HCMV replication and may contribute to the development of new anti-HCMV strategies.

摘要

人巨细胞病毒(HCMV)的主要早期(MIE)基因的表达受一个含有强增强子的启动子调控,该启动子具有多个转录因子结合位点,包括环磷酸腺苷反应元件结合蛋白 1(CREB1)。在这里,我们发现 CREB1 的过表达可强烈阻断 MIE 转录和 HCMV 复制。令人惊讶的是,即使在增强子内的五个 CREB 结合位点全部突变的情况下,CREB1 仍对 MIE 启动子表现出强烈的抑制作用,这表明 CREB1 是间接调节 MIE 基因表达的。启动子缺失分析和定点突变鉴定了 MIE 基因转录起始位点上游-130 至-50 之间的区域为“CREB1 反应区”。该区域内 SP1/3 和 NF-κB 结合位点的突变中断了 CREB1 过表达诱导的抑制作用。我们的研究结果表明,CREB1 的过表达可导致 HCMV 复制的抑制,可能有助于开发新的抗 HCMV 策略。

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