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同源毒素-抗毒素盒 和 的转录抑制研究进展

Insights into Transcriptional Repression of the Homologous Toxin-Antitoxin Cassettes and .

机构信息

Department of Bacterial Molecular Genetics, Faculty of Biology, University of Gdańsk, Wita Stwosza 59, 80-308 Gdańsk, Poland.

出版信息

Int J Mol Sci. 2020 Nov 28;21(23):9062. doi: 10.3390/ijms21239062.

Abstract

Transcriptional repression is a mechanism which enables effective gene expression switch off. The activity of most of type II toxin-antitoxin (TA) cassettes is controlled in this way. These cassettes undergo negative autoregulation by the TA protein complex which binds to the promoter/operator sequence and blocks transcription initiation of the TA operon. Precise and tight control of this process is vital to avoid uncontrolled expression of the toxin component. Here, we employed a series of in vivo and in vitro experiments to establish the molecular basis for previously observed differences in transcriptional activity and repression levels of the and promoters which control expression of two homologous TA systems, YefM-YoeB and Axe-Txe, respectively. Transcriptional fusions of promoters with a reporter, together with in vitro transcription, EMSA and footprinting assays revealed that: (1) the different sequence composition of the -35 promoter element is responsible for substantial divergence in strengths of the promoters; (2) variations in repression result from the TA repressor complex acting at different steps in the transcription initiation process; (3) transcription from an additional promoter upstream of also contributes to the observed inefficient repression of module. This study provides evidence that even closely related TA cassettes with high sequence similarity in the promoter/operator region may employ diverse mechanisms for transcriptional regulation of their genes.

摘要

转录抑制是一种能够有效关闭基因表达的机制。大多数 II 型毒素-抗毒素 (TA) 盒的活性就是通过这种方式进行控制的。这些盒通过 TA 蛋白复合物的负自调控来进行,该复合物结合到启动子/操纵子序列上,并阻止 TA 操纵子的转录起始。这个过程的精确和严格控制对于避免毒素成分的失控表达至关重要。在这里,我们利用一系列体内和体外实验,确定了先前观察到的控制两个同源 TA 系统(YefM-YoeB 和 Axe-Txe)表达的 和 启动子在转录活性和抑制水平上存在差异的分子基础。带有报告基因的启动子转录融合,以及体外转录、EMSA 和足迹实验表明:(1)-35 启动子元件的不同序列组成是导致启动子强度差异的主要原因;(2)抑制作用的差异源于 TA 抑制复合物在转录起始过程的不同步骤上发挥作用;(3)在 上游的额外启动子的转录也导致了观察到的 模块抑制效率低下。这项研究提供了证据,即使是在启动子/操纵子区域具有高度序列相似性的密切相关的 TA 盒,也可能采用不同的机制来调节其基因的转录。

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