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在无细胞转录系统中对腺病毒12型E1A基因启动子的分析。

Analysis of promoters of adenovirus type 12 E1A gene in a cell-free transcription system.

作者信息

Nakanishi Y, Shibata H, Hase T, Masamune Y

出版信息

Biochem Biophys Res Commun. 1987 Jul 31;146(2):783-90. doi: 10.1016/0006-291x(87)90598-5.

Abstract

Transcription from the E1A gene of adenovirus type 12 initiates at two sites in vivo. In this paper we analyzed the E1A promoter(s) in a cell-free transcription system. Primer extension assay revealed that transcriptions were accurately initiated at two sites apart by 140 bp. The efficiency of transcriptions from two sites was almost equal in the standard reaction. However, when transcription reaction was done following pre-incubation of a nuclear extract and template DNA in the absence of ribonucleotides, transcription from the site proximal to E1A gene significantly decreased with little effect on that from distal site. This suggests the existence of a mechanism which controls the efficiency of transcriptions from two start sites of E1A gene.

摘要

12型腺病毒E1A基因的转录在体内的两个位点起始。在本文中,我们在无细胞转录系统中分析了E1A启动子。引物延伸试验表明,转录在相距140 bp的两个位点准确起始。在标准反应中,两个位点的转录效率几乎相等。然而,当在无核糖核苷酸的情况下对核提取物和模板DNA进行预孵育后进行转录反应时,靠近E1A基因的位点的转录显著减少,而对远端位点的转录影响很小。这表明存在一种机制来控制E1A基因两个起始位点的转录效率。

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