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大肠杆菌 sigma 70 启动子 TATAAT 框上游碱基通过改变 DNA 的弯曲角度显著影响模型启动子的活性。

Bases immediate upstream of the TATAAT box of the sigma 70 promoter of Escherichia coli significantly influence the activity of a model promoter by altering the bending angle of DNA.

机构信息

School of Biotechnology, Jawaharlal Nehru University, New Delhi, India.

Department of Chemistry & Kusuma School of Biological Sciences, Indian Institute of Technology, New Delhi, India; Present address, Computational Biochemistry, University of Duisburg Essen, Germany.

出版信息

Gene. 2023 Jan 30;851:146968. doi: 10.1016/j.gene.2022.146968. Epub 2022 Oct 17.

Abstract

Different workers have found different bases of the spacer of the sigma 70 promoter of Escherichia coli to be important, depending on the base sequence of the two hexameric boxes of the naturally occurring promoter they were working on. Besides, there was no clue as to why particular bases worked better than others in particular positions. This necessitated a fresh look at the spacer region of a model promoter comprising all the consensus promoter elements. Randomisation of the three bases of the spacer in positions -15 to -13 with respect to the transcription initiation site, has elicited more than 50-fold variation in activity of the promoter, the highest and the lowest activities being 14,391(the three bases being GCA) and 264 Miller units (the three bases being AAA) respectively. Pairs of promoters of very similar activities were observed, even when the bases in these three positions were very different. The promoters with similar activities had similar three dimensional structures of the promoter DNA, as determined by molecular dynamics simulations. Randomisation of the three bases in positions -18 to -16 of the promoter that contained the triplet GCA in positions -15 to -13, resulted in promoters with highest activity of 15,759 (the triplet upstream of GCA being TAT) and lowest activity of 1,882 (the triplet upstream of GCA being AAA). Good correlation between the bending angles of the promoter DNAs and promoter activities could be observed, the R value being 0.8724. Retardation of electrophoretic mobility of the promoter DNAs correlated well with activity.

摘要

不同的工作者发现大肠杆菌 sigma70 启动子的间隔子的不同碱基很重要,这取决于他们正在研究的天然启动子的两个六聚体盒的碱基序列。此外,为什么特定的碱基在特定位置比其他碱基更好地发挥作用,这一点也没有线索。这就需要重新审视一个包含所有共识启动子元件的模型启动子的间隔区。在转录起始位点的-15 到-13 位上,对间隔子的三个碱基进行随机化,会使启动子的活性增加 50 多倍,最高和最低活性分别为 14391(三个碱基为 GCA)和 264 米勒单位(三个碱基为 AAA)。即使在这三个位置的碱基非常不同的情况下,也观察到了活性非常相似的成对启动子。具有相似活性的启动子具有相似的启动子 DNA 的三维结构,这是通过分子动力学模拟确定的。在包含-15 到-13 位的 GCA 三核苷酸的启动子的-18 到-16 位上对三个碱基进行随机化,导致最高活性为 15759(上游 GCA 的三核苷酸为 TAT)和最低活性为 1882(上游 GCA 的三核苷酸为 AAA)的启动子。可以观察到启动子 DNA 的弯曲角度与启动子活性之间的良好相关性,R 值为 0.8724。启动子 DNA 的电泳迁移率的滞后与活性很好地相关。

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