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杆状病毒 p35 基因受 Spodoptera frugiperda 中 P53 和 AP-1 样因子的反式调节。

Baculovirus p35 gene is oppositely regulated by P53 and AP-1 like factors in Spodoptera frugiperda.

机构信息

Laboratory of Molecular and Cell Biology, Center for DNA Fingerprinting and Diagnostics, Hyderabad 500001, India.

出版信息

Biochem Biophys Res Commun. 2011 Nov 4;414(4):688-93. doi: 10.1016/j.bbrc.2011.09.133. Epub 2011 Oct 2.

Abstract

Baculovirus p35 belongs to the early class of genes of AcMNPV and requires viral factors like Immediate Early protein-1 for its transcription. To investigate the role of host factors in regulating p35 gene expression, the putative transcription factor binding sites were examined in silico and the role of these factors in influencing the transcription of p35 gene was assessed. We focused our studies on AP-1 and P53-like factors, which are activated under oxidative stress conditions. The AP-1 motif is located at -1401 while P53 motif is at -1912 relative to p35 translation start site. The predicted AP-1 and P53 elements formed specific complexes with Spodoptera frugiperda nuclear extracts. Both AP-1 and P53 motif binding proteins were down regulated as a function of AcMNPV infection in Spodoptera cells. To address the question whether during an oxidative outburst, the p35 transcription is enhanced; we investigated the role of these oxidative stress induced host transcription factors in influencing p35 gene transcription. Reporter assays revealed that AP-1 element enhances the transcription of p35 by a factor of two. Interestingly, P53 element appears to repress the transcription of p35 gene.

摘要

杆状病毒 p35 属于 AcMNPV 的早期基因类,其转录需要病毒因子如早期蛋白-1。为了研究宿主因子在调节 p35 基因表达中的作用,我们对可能的转录因子结合位点进行了计算机分析,并评估了这些因子对 p35 基因转录的影响。我们的研究集中在 AP-1 和 P53 样因子上,它们在氧化应激条件下被激活。AP-1 基序位于-1401,而 P53 基序位于 p35 翻译起始位点的-1912 处。预测的 AP-1 和 P53 元件与草地贪夜蛾核提取物形成特定的复合物。随着 AcMNPV 在 Spodoptera 细胞中的感染,AP-1 和 P53 基序结合蛋白的表达都下调。为了研究在氧化爆发期间,p35 转录是否增强,我们研究了这些氧化应激诱导的宿主转录因子在影响 p35 基因转录中的作用。报告基因实验表明,AP-1 元件将 p35 的转录增强了两倍。有趣的是,P53 元件似乎抑制了 p35 基因的转录。

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