Multiple stress signal integration in the regulation of the complex σS-dependent csiD-ygaF-gabDTP operon in Escherichia coli

Multiple stress signal integration in the regulation of the complex σS-dependent csiD-ygaF-gabDTP operon in Escherichia coli
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DOI:
10.1046/j.1365-2958.2003.03867.x
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发表时间:
2004-02-01
影响因子:
3.6
通讯作者:
Hengge, R
Hengge, R
中科院分区:
生物学2区
文献类型:
--
作者:
Metzner, M;Germer, J;Hengge, R

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大肠杆菌基因组中的CSID-YGAF-GABDTP区域代表了Sigma(S)控制基因的簇。在这里,我们研究了所有这些基因的启动子结构,sigma因子依赖性,潜在的共调节和环境调节模式。我们发现该区域构成一个复杂的操纵子,表达受三个差异调节的启动子控制:(i)CSID(p)影响所有五个基因的表达,是CAMP-CRP/SIGMA(S)依赖性且依赖性和激活的。在碳饥饿和静止期; (ii)GABD(p1),它是依赖性的(S)依赖性的,并且表现出多种应力诱导,例如Sigma(S)本身; (iii)GABD(P2)[先前由Schneider,B.L.,Ruback,S.,Kiupakis,A.K.,Kasbarian,H.,Pybus,C。和Reitzer,L。(2002)J。Bacteriol。 184:6976-6986],似乎是NAC/Sigma(70)控制的,并对较差的氮来源做出反应。此外,我们确定了一种新型的阻遏物CSIR,该阻遏物在早期固定阶段以时间方式调节CSID(P)活性。最后,我们提出了Sigma(S)控制的GABT/D介导的γ-氨基丁酸(GABA)分解代谢和谷氨酸在一般应激适应中积累的生理作用。在不同条件下,操纵子内GABD(P1)启动子的激活也反映了这种生理作用,这些条件也诱导了Sigma(S),其中包括转移到酸性pH或高渗透压以及饥饿或固定相。
The csiD-ygaF-gabDTP region in the Escherichia coli genome represents a cluster of sigma(S)-controlled genes. Here, we investigated promoter structures, sigma factor dependencies, potential co-regulation and environmental regulatory patterns for all of these genes. We find that this region constitutes a complex operon with expression being controlled by three differentially regulated promoters: (i) csiD(p), which affects the expression of all five genes, is cAMP-CRP/sigma(S)-dependent and activated exclusively upon carbon starvation and stationary phase; (ii) gabD(p1), which is sigma(S)-dependent and exhibits multiple stress induction like sigma(S) itself; and (iii) gabD(p2)[previously suggested by Schneider, B.L., Ruback, S., Kiupakis, A.K., Kasbarian, H., Pybus, C., and Reitzer, L. (2002) J. Bacteriol. 184: 6976-6986], which appears to be Nac/sigma(70)-controlled and to respond to poor nitrogen sources. In addition, we identify a novel repressor, CsiR, which modulates csiD(p) activity in a temporal manner during early stationary phase. Finally, we propose a physiological role for sigma(S)-controlled GabT/D-mediated gamma-aminobutyrate (GABA) catabolism and glutamate accumulation in general stress adaptation. This physiological role is reflected by the activation of the operon-internal gabD(p1) promoter under the different conditions that also induce sigma(S), which include shifts to acidic pH or high osmolarity as well as starvation or stationary phase.