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IscR 依赖的基因表达将铁硫簇组装与大肠杆菌中氧气调节基因的控制联系起来。

IscR-dependent gene expression links iron-sulphur cluster assembly to the control of O2-regulated genes in Escherichia coli.

作者信息

Giel Jennifer L, Rodionov Dmitry, Liu Mingzhu, Blattner Frederick R, Kiley Patricia J

机构信息

Microbiology Doctoral Training Program, Department of Biomolecular Chemistry, University of Winsconsin, Madison, WI 53706, USA.

出版信息

Mol Microbiol. 2006 May;60(4):1058-75. doi: 10.1111/j.1365-2958.2006.05160.x.

Abstract

IscR is an iron-sulphur (Fe-S) cluster-containing transcription factor that represses transcription of the operon containing its own gene and the iscSUA-hscBA-fdx genes, whose products are involved in Fe-S cluster biogenesis. In this study, global transcriptional profiling of Escherichia coli IscR(+) and IscR(-) strains grown under aerobic and anaerobic conditions indicated that 40 genes in 20 predicted operons were regulated by IscR. DNase I footprinting and/or in vitro transcription reactions identified seven new promoters under direct IscR control. Among these were genes encoding known or proposed functions in Fe-S cluster biogenesis (sufABCDSE, yadR and yhgI) and Fe-S cluster-containing anaerobic respiratory enzymes (hyaABCDEF, hybOABCDEFG and napFDAGHBC). The finding that IscR repressed expression of the hyaA, hybO and napF promoters specifically under aerobic growth conditions suggests a new mechanism to explain their upregulation under anaerobic growth conditions. Phylogenetic footprinting of the DNase I protected regions of seven promoters implies that there are at least two different classes of IscR binding sites conserved among many bacteria. The findings presented here indicate a more general role of IscR in the regulation of Fe-S cluster biogenesis and that IscR contributes to the O(2) regulation of several promoters controlling the expression of anaerobic Fe-S proteins.

摘要

IscR是一种含硫铁(Fe-S)簇的转录因子,它可抑制包含其自身基因以及iscSUA-hscBA-fdx基因的操纵子的转录,这些基因的产物参与Fe-S簇的生物合成。在本研究中,对在有氧和无氧条件下生长的大肠杆菌IscR(+)和IscR(-)菌株进行的全基因组转录谱分析表明,20个预测操纵子中的40个基因受IscR调控。DNA酶I足迹法和/或体外转录反应确定了7个受IscR直接控制的新启动子。其中包括在Fe-S簇生物合成中具有已知或推测功能的基因(sufABCDSE、yadR和yhgI)以及含Fe-S簇的厌氧呼吸酶基因(hyaABCDEF、hybOABCDEFG和napFDAGHBC)。IscR在有氧生长条件下特异性抑制hyaA、hybO和napF启动子的表达这一发现,提示了一种新机制来解释它们在厌氧生长条件下的上调。对7个启动子DNA酶I保护区域的系统发育足迹分析表明,在许多细菌中至少存在两类不同的IscR结合位点。本文的研究结果表明IscR在Fe-S簇生物合成调控中具有更广泛的作用,并且IscR有助于对控制厌氧Fe-S蛋白表达的几个启动子进行氧气调控。

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