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腺病毒E4基因产物通过与E2F直接结合来反式激活E2转录并刺激稳定的E2F结合。

An adenovirus E4 gene product trans-activates E2 transcription and stimulates stable E2F binding through a direct association with E2F.

作者信息

Neill S D, Hemstrom C, Virtanen A, Nevins J R

机构信息

Howard Hughes Medical Institute, Duke University Medical Center, Durham, NC 27710.

出版信息

Proc Natl Acad Sci U S A. 1990 Mar;87(5):2008-12. doi: 10.1073/pnas.87.5.2008.

Abstract

The adenovirus E4 gene encodes a trans-activating function that can stimulate the E2 promoter. E2 promoter sequences required for E4 trans-activation are identical to those required for E1A trans-activation, and these principally are the E2 promoter binding factor (E2F) binding sites. Furthermore, full activation of E2F DNA binding activity requires both E1A and E4 action. Analysis of a series of mutant E4 viruses identifies open reading frame (orf) 6/7 of the E4 transcription unit as that required for activation of E2F binding activity. In addition, the assay of various E4 cDNAs demonstrates that the E4 orf 6/7 also is responsible for the trans-activation of E2 transcription. Translation of the E4 orf 6/7 mRNA, but not a control mRNA, in a reticulocyte extract generates an activity that can stimulate cooperative binding of E2F in vitro, consistent with recent in vivo assays that demonstrate a role for the E4 gene in E2F stable complex formation. This stimulation is due to a direct interaction of the E4 protein with E2F since an antibody that recognizes the E4 orf 6/7 polypeptide detects this E4 protein in the E2F-DNA complex. We conclude that the E4 orf 6/7 product interacts with the E2F factor altering binding to allow formation of a stable complex that results in a stimulation of transcription.

摘要

腺病毒E4基因编码一种反式激活功能,可刺激E2启动子。E4反式激活所需的E2启动子序列与E1A反式激活所需的序列相同,这些序列主要是E2启动子结合因子(E2F)结合位点。此外,E2F DNA结合活性的完全激活需要E1A和E4的共同作用。对一系列E4突变病毒的分析确定E4转录单位的开放阅读框(orf)6/7是激活E2F结合活性所必需的。此外,对各种E4 cDNA的检测表明,E4 orf 6/7也负责E2转录的反式激活。在网织红细胞提取物中翻译E4 orf 6/7 mRNA而非对照mRNA会产生一种能在体外刺激E2F协同结合的活性,这与最近的体内检测结果一致,即证明E4基因在E2F稳定复合物形成中起作用。这种刺激是由于E4蛋白与E2F的直接相互作用,因为识别E4 orf 6/7多肽的抗体可在E2F-DNA复合物中检测到这种E4蛋白。我们得出结论,E4 orf 6/7产物与E2F因子相互作用,改变结合以允许形成稳定复合物,从而刺激转录。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e5f/53614/6e4ffd551fa8/pnas01030-0390-a.jpg

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