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大肠杆菌uvrB基因调控元件的结构与功能

The structure and function of the regulatory elements of the Escherichia coli uvrB gene.

作者信息

van den Berg E, Zwetsloot J, Noordermeer I, Pannekoek H, Dekker B, Dijkema R, van Ormondt H

出版信息

Nucleic Acids Res. 1981 Nov 11;9(21):5623-43. doi: 10.1093/nar/9.21.5623.

Abstract

The construction and properties of recombinant plasmids carrying the Escherichia coli uvrB gene, including its transcriptional- and translational regulatory elements, is reported. The DNA sequence of the region, which governs the expression of the uvrB gene, has been determined. Within this sequence two non-overlapping DNA segments match the model sequence for Escherichia coli promoters (1). The '-10 regions' and the '-35 regions' of the proposed uvrB promoters are, respectively, 5'TAAAAT (P1), 5'TATAAT (P2) and 5'TTGGCA (P1), 5'GTGATG (P2). The existence and the position of these promoters has been established by elimination of one promoter (P2), using molecular cloning procedures, by length measurements of in vitro synthesized 'run-off' transcripts and by protection of the uvrB regulatory region for S1 nuclease digestion using in vivo made RNA. Potential sites of interaction within the uvrB regulatory region with regulatory proteins, such as the LexA protein (2) and the UvrC protein (3) are discussed.

摘要

本文报道了携带大肠杆菌uvrB基因的重组质粒的构建及其特性,包括其转录和翻译调控元件。已确定了该区域中控制uvrB基因表达的DNA序列。在该序列中,有两个不重叠的DNA片段与大肠杆菌启动子的模型序列相匹配(1)。所提出的uvrB启动子的“-10区”和“-35区”分别为5'TAAAAT(P1)、5'TATAAT(P2)以及5'TTGGCA(P1)、5'GTGATG(P2)。这些启动子的存在及其位置已通过以下方法得以确定:利用分子克隆程序去除一个启动子(P2);对体外合成的“延伸”转录本进行长度测量;以及使用体内合成的RNA保护uvrB调控区域免受S1核酸酶消化。文中还讨论了uvrB调控区域内与调控蛋白(如LexA蛋白(2)和UvrC蛋白(3))相互作用的潜在位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aec/327548/e56b9ba06637/nar00414-0131-a.jpg

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