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枯草芽孢杆菌中 NsrR 的全局转录控制。

Global transcriptional control by NsrR in Bacillus subtilis.

机构信息

Division of Environmental and Biomolecular Systems, Institute of Environmental Health, Oregon Health and Science University, Beaverton, OR, USA.

出版信息

J Bacteriol. 2012 Apr;194(7):1679-88. doi: 10.1128/JB.06486-11. Epub 2012 Jan 27.

DOI:10.1128/JB.06486-11
PMID:22287527
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3302466/
Abstract

The NO-sensitive NsrR repressor of Bacillus subtilis, which carries a [4Fe-4S] cluster, controls transcription of nasD and hmp (class I regulation) under anaerobic conditions. Here, we describe another class of NsrR regulation (class II regulation) that controls a more diverse collection of genes. Base substitution analysis showed that [4Fe-4S]-NsrR recognizes a partial dyad symmetry within the class I cis-acting sites, whereas NO-insensitive interaction of NsrR with an A+T-rich class II regulatory site showed relaxed sequence specificity. Genome-wide transcriptome studies identified genes that are under the control of the class II NsrR regulation. The class II NsrR regulon includes genes controlled by both AbrB and Rok repressors, which also recognize A+T-rich sequences, and by the Fur repressor. Transcription of class II genes was elevated in an nsrR mutant during anaerobic fermentative growth with pyruvate. Although NsrR binding to the class II regulatory sites was NO insensitive in vitro, transcription of class II genes was moderately induced by NO, which involved reversal of NsrR-dependent repression, suggesting that class II repression is also NO sensitive. In all NsrR-repressed genes tested, the loss of NsrR repressor activity was not sufficient to induce transcription as induction required the ResD response regulator. The ResD-ResE signal transduction system is essential for activation of genes involved in aerobic and anaerobic respiration. This study indicated coordinated regulation between ResD and NsrR and uncovered a new role of ResD and NsrR in transcriptional regulation during anaerobiosis of B. subtilis.

摘要

枯草芽孢杆菌的 NsrR 阻遏蛋白对 NO 敏感,它携带一个 [4Fe-4S] 簇,在厌氧条件下控制 nasD 和 hmp 的转录(I 类调控)。在这里,我们描述了 NsrR 调控的另一种类型(II 类调控),它控制着更多种类的基因。碱基取代分析表明,[4Fe-4S]-NsrR 识别 I 类顺式作用位点中的部分二分对称结构,而 NsrR 与富含 A+T 的 II 类调节位点的非 NO 敏感相互作用显示出宽松的序列特异性。全基因组转录组研究确定了受 II 类 NsrR 调控的基因。II 类 NsrR 调控子包括受 AbrB 和 Rok 阻遏物控制的基因,它们也识别富含 A+T 的序列,以及 Fur 阻遏物。在厌氧发酵生长过程中,丙酮酸作为碳源时,II 类基因的转录在 nsrR 突变体中升高。尽管 NsrR 与 II 类调节位点的结合在体外对 NO 不敏感,但 II 类基因的转录被 NO 适度诱导,这涉及到 NsrR 依赖性抑制的逆转,表明 II 类抑制也是对 NO 敏感的。在所测试的所有受 NsrR 抑制的基因中,NsrR 抑制活性的丧失不足以诱导转录,因为诱导需要 ResD 响应调节子。ResD-ResE 信号转导系统对于激活参与需氧和厌氧呼吸的基因是必不可少的。本研究表明 ResD 和 NsrR 之间存在协调调控,并揭示了 ResD 和 NsrR 在枯草芽孢杆菌厌氧条件下转录调控中的新作用。

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Proteomics. 2011 Aug;11(15):2992-3001. doi: 10.1002/pmic.201000790. Epub 2011 Jun 28.
2
Nitric oxide-sensitive and -insensitive interaction of Bacillus subtilis NsrR with a ResDE-controlled promoter.枯草芽孢杆菌 NsrR 与 ResDE 控制的启动子的一氧化氮敏感和不敏感相互作用。
Mol Microbiol. 2010 Dec;78(5):1280-93. doi: 10.1111/j.1365-2958.2010.07407.x. Epub 2010 Oct 8.
3
The transcriptional regulator Rok binds A+T-rich DNA and is involved in repression of a mobile genetic element in Bacillus subtilis.转录调节因子 Rok 结合富含 A+T 的 DNA,并参与枯草芽孢杆菌中移动遗传元件的抑制。
PLoS Genet. 2010 Nov 11;6(11):e1001207. doi: 10.1371/journal.pgen.1001207.
4
Genome-wide binding profiles of the Bacillus subtilis transition state regulator AbrB and its homolog Abh reveals their interactive role in transcriptional regulation.枯草芽孢杆菌过渡态调控因子 AbrB 及其同源物 Abh 的全基因组结合谱揭示了它们在转录调控中的相互作用。
Nucleic Acids Res. 2011 Jan;39(2):414-28. doi: 10.1093/nar/gkq780. Epub 2010 Sep 3.
5
The alternative oxidase (AOX) gene in Vibrio fischeri is controlled by NsrR and upregulated in response to nitric oxide.费氏弧菌中的交替氧化酶(AOX)基因受NsrR调控,并在一氧化氮的作用下上调表达。
Mol Microbiol. 2010 Jul 1;77(1):44-55. doi: 10.1111/j.1365-2958.2010.07194.x. Epub 2010 May 4.
6
There's NO stopping NsrR, a global regulator of the bacterial NO stress response.NsrR 是细菌一氧化氮应激反应的全球调节剂,无法对其进行抑制。
Trends Microbiol. 2010 Apr;18(4):149-56. doi: 10.1016/j.tim.2009.12.009. Epub 2010 Feb 16.
7
NsrR targets in the Escherichia coli genome: new insights into DNA sequence requirements for binding and a role for NsrR in the regulation of motility.大肠杆菌基因组中的NsrR靶点:对结合所需DNA序列要求的新见解以及NsrR在运动性调节中的作用
Mol Microbiol. 2009 Aug;73(4):680-94. doi: 10.1111/j.1365-2958.2009.06799.x. Epub 2009 Jul 27.
8
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Nucleic Acids Res. 2009 Jul;37(Web Server issue):W202-8. doi: 10.1093/nar/gkp335. Epub 2009 May 20.
9
Sequence-specific binding to a subset of IscR-regulated promoters does not require IscR Fe-S cluster ligation.对IscR调控启动子子集的序列特异性结合不需要IscR铁硫簇连接。
J Mol Biol. 2009 Mar 20;387(1):28-41. doi: 10.1016/j.jmb.2009.01.055. Epub 2009 Jan 31.
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Mol Microbiol. 2009 Jan;71(1):227-39. doi: 10.1111/j.1365-2958.2008.06522.x.