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转录干扰会扰乱Sp1与HIV-1启动子的结合。

Transcriptional interference perturbs the binding of Sp1 to the HIV-1 promoter.

作者信息

Greger I H, Demarchi F, Giacca M, Proudfoot N J

机构信息

Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.

出版信息

Nucleic Acids Res. 1998 Mar 1;26(5):1294-301. doi: 10.1093/nar/26.5.1294.

Abstract

Transcriptional interference between adjacent genes has been demonstrated in a variety of biological systems. To study this process in RNA polymerase II (pol II) transcribed genes we have analysed the effect of transcription on tandem HIV-1 promoters integrated into the genome of HeLa cells. We show that transcriptional activation at the upstream promoter reduces transcription from the downstream promoter, as compared with basal transcription conditions (in the absence of an activator). Furthermore, insertion of a strong transcriptional termination element between the two promoters alleviates this transcriptional interference, resulting in elevated levels of transcription from the downstream promoter. Actual protein interactions with the downstream (occluded) promoter were analysed by in vivo footprinting. Binding of Sp1 transcription factors to the occluded promoter was reduced, when compared with the footprint pattern of the promoter protected by the terminator. This suggests that promoter occlusion is due to disruption of certain transcription factors and that it can be blocked by an intervening transcriptional terminator. Chromatin mapping with DNase I indicates that a factor binds to the termination element under both basal and induced conditions.

摘要

相邻基因之间的转录干扰已在多种生物系统中得到证实。为了在RNA聚合酶II(pol II)转录的基因中研究这一过程,我们分析了转录对整合到HeLa细胞基因组中的串联HIV-1启动子的影响。我们发现,与基础转录条件(无激活剂)相比,上游启动子的转录激活会降低下游启动子的转录。此外,在两个启动子之间插入一个强转录终止元件可减轻这种转录干扰,导致下游启动子的转录水平升高。通过体内足迹法分析了与下游(被阻断的)启动子的实际蛋白质相互作用。与由终止子保护的启动子的足迹模式相比,Sp1转录因子与被阻断启动子的结合减少。这表明启动子阻断是由于某些转录因子的破坏,并且它可以被一个中间转录终止子阻断。用DNase I进行的染色质图谱分析表明,在基础和诱导条件下,一个因子都与终止元件结合。

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