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由Tn9介导的共整合体形成。II. IS1的活性受外部DNA序列调控。

Cointegrate formation mediated by Tn9. II. Activity of IS1 is modulated by external DNA sequences.

作者信息

Chandler M, Galas D J

出版信息

J Mol Biol. 1983 Oct 15;170(1):61-91. doi: 10.1016/s0022-2836(83)80227-7.

Abstract

We have studied the effect on the transposition activity of IS1 of the position and orientation of the element in the donor replicon. Previous studies have shown that the IS1s in the compound transposon Tn9 have different activities in forming plasmid cointegrates. In this study, designed to investigate the sources of this differential activity, we have cloned Tn9 (together with 132 base-pairs of flanking DNA) into several sites in pBR322 and created various derivatives of these plasmids to be used as donor molecules in plasmid fusion experiments. These pBR322-Tn9 plasmids were allowed to form cointegrates with a conjugative, F-derived plasmid, and a large collection of independently formed cointegrates was isolated. The relative activities of the two IS1 elements of Tn9 were estimated by examining the structures of the cointegrates for the frequency of usage of each of the IS1s in cointegrate formation. The results suggest that IS1 activity is modulated by the transcription activity of adjacent DNA sequences in the donor plasmids. Transcription directed into an IS1 inhibits its activity. Confirmatory evidence for this hypothesis is provided by the observation that deletion of adjacent promoters of transcription relieves the inhibitory effect on IS1 activity.

摘要

我们研究了供体复制子中IS1元件的位置和方向对其转座活性的影响。先前的研究表明,复合转座子Tn9中的IS1在形成质粒共整合体时具有不同的活性。在本研究中,为了探究这种差异活性的来源,我们将Tn9(连同132个碱基对的侧翼DNA)克隆到pBR322的几个位点,并构建了这些质粒的各种衍生物,用作质粒融合实验中的供体分子。让这些pBR322-Tn9质粒与一个接合性的、F衍生的质粒形成共整合体,并分离出大量独立形成的共整合体。通过检查共整合体的结构中每个IS1在共整合体形成中的使用频率,来估计Tn9的两个IS1元件的相对活性。结果表明,IS1活性受供体质粒中相邻DNA序列转录活性的调节。转录进入IS1会抑制其活性。相邻转录启动子的缺失可消除对IS1活性的抑制作用,这一观察结果为该假设提供了确证。

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