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非规范启动子元件驱动水平获得的细菌基因的假转录。

A non-canonical promoter element drives spurious transcription of horizontally acquired bacterial genes.

机构信息

Institute of Microbiology and Infection, School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.

出版信息

Nucleic Acids Res. 2020 May 21;48(9):4891-4901. doi: 10.1093/nar/gkaa244.

Abstract

RNA polymerases initiate transcription at DNA sequences called promoters. In bacteria, the best conserved promoter feature is the AT-rich -10 element; a sequence essential for DNA unwinding. Further elements, and gene regulatory proteins, are needed to recruit RNA polymerase to the -10 sequence. Hence, -10 elements cannot function in isolation. Many horizontally acquired genes also have a high AT-content. Consequently, sequences that resemble the -10 element occur frequently. As a result, foreign genes are predisposed to spurious transcription. However, it is not clear how RNA polymerase initially recognizes such sequences. Here, we identify a non-canonical promoter element that plays a key role. The sequence, itself a short AT-tract, resides 5 base pairs upstream of otherwise cryptic -10 elements. The AT-tract alters DNA conformation and enhances contacts between the DNA backbone and RNA polymerase.

摘要

RNA 聚合酶在称为启动子的 DNA 序列上起始转录。在细菌中,最保守的启动子特征是富含 AT 的-10 元件;这是 DNA 解旋所必需的序列。需要进一步的元件和基因调控蛋白来招募 RNA 聚合酶到-10 序列。因此,-10 元件不能孤立发挥作用。许多水平获得的基因也具有高 AT 含量。因此,类似于-10 元件的序列经常出现。结果,外源基因容易发生虚假转录。然而,目前尚不清楚 RNA 聚合酶最初是如何识别这些序列的。在这里,我们确定了一个起关键作用的非典型启动子元件。该序列本身是一个短的 AT 串,位于通常隐匿的-10 元件上游 5 个碱基对处。AT 串改变了 DNA 的构象,并增强了 DNA 骨架和 RNA 聚合酶之间的接触。

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