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本文引用的文献

1
Chromosomal toxin-antitoxin loci can diminish large-scale genome reductions in the absence of selection.染色体毒素-抗毒素基因座在缺乏选择的情况下可减少大规模的基因组缩减。
Mol Microbiol. 2007 Mar;63(6):1588-605. doi: 10.1111/j.1365-2958.2007.05613.x.
2
Escherichia coli dinJ-yafQ genes act as a toxin-antitoxin module.大肠杆菌dinJ-yafQ基因作为一种毒素-抗毒素模块。
FEMS Microbiol Lett. 2007 Mar;268(1):112-9. doi: 10.1111/j.1574-6968.2006.00563.x.
3
Functional interactions between coexisting toxin-antitoxin systems of the ccd family in Escherichia coli O157:H7.大肠杆菌O157:H7中ccd家族共存毒素-抗毒素系统之间的功能相互作用。
J Bacteriol. 2007 Apr;189(7):2712-9. doi: 10.1128/JB.01679-06. Epub 2007 Jan 26.
4
par genes and the pathology of chromosome loss in Vibrio cholerae.霍乱弧菌中的par基因与染色体丢失的病理学
Proc Natl Acad Sci U S A. 2007 Jan 9;104(2):630-5. doi: 10.1073/pnas.0608341104. Epub 2006 Dec 29.
5
Characterization of a higBA toxin-antitoxin locus in Vibrio cholerae.霍乱弧菌中一个higBA毒素-抗毒素位点的特征分析
J Bacteriol. 2007 Jan;189(2):491-500. doi: 10.1128/JB.00909-06. Epub 2006 Nov 3.
6
Two higBA loci in the Vibrio cholerae superintegron encode mRNA cleaving enzymes and can stabilize plasmids.霍乱弧菌超级整合子中的两个higBA基因座编码mRNA切割酶,并能稳定质粒。
Mol Microbiol. 2006 Oct;62(2):397-411. doi: 10.1111/j.1365-2958.2006.05385.x.
7
Role of DNA replication and repair in thymineless death in Escherichia coli.DNA复制与修复在大肠杆菌无胸腺嘧啶死亡中的作用
J Bacteriol. 2006 Jul;188(14):5286-8. doi: 10.1128/JB.00543-06.
8
Shutdown decay of mRNA.信使核糖核酸的关闭衰减
Mol Microbiol. 2006 Aug;61(3):573-83. doi: 10.1111/j.1365-2958.2006.05270.x. Epub 2006 Jun 27.
9
Ectopic overexpression of wild-type and mutant hipA genes in Escherichia coli: effects on macromolecular synthesis and persister formation.野生型和突变型hipA基因在大肠杆菌中的异位过表达:对大分子合成和持留菌形成的影响。
J Bacteriol. 2006 Jun;188(11):3826-36. doi: 10.1128/JB.01740-05.
10
Induction of Escherichia coli chromosomal mazEF by stressful conditions causes an irreversible loss of viability.应激条件下诱导大肠杆菌染色体mazEF会导致生存能力的不可逆丧失。
J Bacteriol. 2006 May;188(9):3420-3. doi: 10.1128/JB.188.9.3420-3423.2006.

大肠杆菌基因组中拥有多个毒素-抗毒素系统对其有什么益处?

What is the benefit to Escherichia coli of having multiple toxin-antitoxin systems in its genome?

作者信息

Tsilibaris Virginie, Maenhaut-Michel Geneviève, Mine Natacha, Van Melderen Laurence

机构信息

Laboratoire de Génétique des Procaryotes, Institut de Biologie et Médecine Moléculaires, Université Libre de Bruxelles, 12 rue des Professeurs Jeener et Brachet, B-6041 Gosselies, Belgium.

出版信息

J Bacteriol. 2007 Sep;189(17):6101-8. doi: 10.1128/JB.00527-07. Epub 2007 May 18.

DOI:10.1128/JB.00527-07
PMID:17513477
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1951899/
Abstract

The Escherichia coli K-12 chromosome encodes at least five proteic toxin-antitoxin (TA) systems. The mazEF and relBE systems have been extensively characterized and were proposed to be general stress response modules. On one hand, mazEF was proposed to act as a programmed cell death system that is triggered by a variety of stresses. On the other hand, relBE and mazEF were proposed to serve as growth modulators that induce a dormancy state during amino acid starvation. These conflicting hypotheses led us to test a possible synergetic effect of the five characterized E. coli TA systems on stress response. We compared the behavior of a wild-type strain and its derivative devoid of the five TA systems under various stress conditions. We were unable to detect TA-dependent programmed cell death under any of these conditions, even under conditions previously reported to induce it. Thus, our results rule out the programmed-cell-death hypothesis. Moreover, the presence of the five TA systems advantaged neither recovery from the different stresses nor cell growth under nutrient-limited conditions in competition experiments. This casts a doubt on whether TA systems significantly influence bacterial fitness and competitiveness during non-steady-state growth conditions.

摘要

大肠杆菌K-12染色体编码至少五种蛋白质毒素-抗毒素(TA)系统。mazEF和relBE系统已得到广泛研究,并被认为是一般应激反应模块。一方面,mazEF被认为是一种程序性细胞死亡系统,可由多种应激触发。另一方面,relBE和mazEF被认为是生长调节剂,在氨基酸饥饿期间诱导休眠状态。这些相互矛盾的假设促使我们测试五种已鉴定的大肠杆菌TA系统对应激反应可能的协同作用。我们比较了野生型菌株及其缺失这五种TA系统的衍生物在各种应激条件下的行为。在任何这些条件下,我们都无法检测到TA依赖性程序性细胞死亡,即使在先前报道可诱导其发生的条件下也是如此。因此,我们的结果排除了程序性细胞死亡假说。此外,在竞争实验中,这五种TA系统的存在既没有促进从不同应激中恢复,也没有在营养有限的条件下促进细胞生长。这使人怀疑TA系统在非稳态生长条件下是否会显著影响细菌的适应性和竞争力。