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RuvABC-dependent double-strand breaks in dnaBts mutants require recA.dnaBts突变体中依赖RuvABC的双链断裂需要recA。
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本文引用的文献

1
The sbcC and sbcD genes of Escherichia coli encode a nuclease involved in palindrome inviability and genetic recombination.大肠杆菌的sbcC和sbcD基因编码一种参与回文序列致死性和基因重组的核酸酶。
Genes Cells. 1996 Mar;1(3):285-91. doi: 10.1046/j.1365-2443.1996.23024.x.
2
Overlapping functions for recF and priA in cell viability and UV-inducible SOS expression are distinguished by dnaC809 in Escherichia coli K-12.在大肠杆菌K-12中,recF和priA在细胞活力和紫外线诱导的SOS表达中的重叠功能可通过dnaC809加以区分。
Mol Microbiol. 1996 Feb;19(4):871-80. doi: 10.1046/j.1365-2958.1996.429959.x.
3
Differential suppression of priA2::kan phenotypes in Escherichia coli K-12 by mutations in priA, lexA, and dnaC.在大肠杆菌K-12中,priA、lexA和dnaC基因的突变对priA2::kan表型的差异抑制作用
Genetics. 1996 May;143(1):5-13. doi: 10.1093/genetics/143.1.5.
4
Repair of x-ray-induced DNA double-strand breaks in specific Not I restriction fragments in human fibroblasts: joining of correct and incorrect ends.人成纤维细胞中特定Not I限制片段的X射线诱导DNA双链断裂的修复:正确和错误末端的连接
Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12050-4. doi: 10.1073/pnas.92.26.12050.
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Positional cloning of the Werner's syndrome gene.沃纳综合征基因的定位克隆
Science. 1996 Apr 12;272(5259):258-62. doi: 10.1126/science.272.5259.258.
6
Insertion of inverted Ter sites into the terminus region of the Escherichia coli chromosome delays completion of DNA replication and disrupts the cell cycle.将反向Ter位点插入大肠杆菌染色体的末端区域会延迟DNA复制的完成并扰乱细胞周期。
Mol Microbiol. 1995 Oct;18(1):45-61. doi: 10.1111/j.1365-2958.1995.mmi_18010045.x.
7
Lethality of rep recB and rep recC double mutants of Escherichia coli.大肠杆菌rep recB和rep recC双突变体的致死率。
Mol Microbiol. 1995 Sep;17(6):1177-88. doi: 10.1111/j.1365-2958.1995.mmi_17061177.x.
8
Strand-specific binding to duplex DNA ends by the subunits of the Escherichia coli RecBCD enzyme.大肠杆菌RecBCD酶的亚基对双链DNA末端的链特异性结合。
J Mol Biol. 1993 Jan 5;229(1):67-78. doi: 10.1006/jmbi.1993.1008.
9
DNA helicases: enzymes with essential roles in all aspects of DNA metabolism.DNA解旋酶:在DNA代谢的各个方面都发挥着关键作用的酶。
Bioessays. 1994 Jan;16(1):13-22. doi: 10.1002/bies.950160103.
10
Homologous genetic recombination: the pieces begin to fall into place.同源基因重组:各部分开始各就各位。
Crit Rev Microbiol. 1994;20(2):125-42. doi: 10.3109/10408419409113552.

由复制停滞引起的DNA双链断裂。

DNA double-strand breaks caused by replication arrest.

作者信息

Michel B, Ehrlich S D, Uzest M

机构信息

Laboratoire de Génétique Microbienne, Institut National de la Recherche Agronomique, Jouy en Josas, France.

出版信息

EMBO J. 1997 Jan 15;16(2):430-8. doi: 10.1093/emboj/16.2.430.

DOI:10.1093/emboj/16.2.430
PMID:9029161
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1169647/
Abstract

We report here that DNA double-strand breaks (DSBs) form in Escherichia coli upon arrest of replication forks due to a defect in, or the inhibition of, replicative DNA helicases. The formation of DSBs was assessed by the appearance of linear DNA detected by pulse-field gel electrophoresis. Processing of DSBs by recombination repair or linear DNA degradation was abolished by mutations in recBCD genes. Two E. coli replicative helicases were tested, Rep, which is essential in recBC mutants, and DnaB. The proportion of linear DNA increased up to 50% upon shift of rep recBTS recCTS cells to restrictive temperature. No increase in linear DNA was observed in the absence of replicating chromosomes, indicating that the formation of DSBs in rep strains requires replication. Inhibition of the DnaB helicase either by a strong replication terminator or by a dnaBTS mutation led to the formation of linear DNA, showing that blocked replication forks are prone to DSB formation. In wild-type E. coli, linear DNA was detected in the absence of RecBC or of both RecA and RecD. This reveals the existence of a significant amount of spontaneous DSBs. We propose that some of them may also result from the impairment of replication fork progression.

摘要

我们在此报告,由于复制性DNA解旋酶存在缺陷或受到抑制,导致复制叉停滞时,大肠杆菌中会形成DNA双链断裂(DSB)。通过脉冲场凝胶电泳检测到的线性DNA的出现来评估DSB的形成。recBCD基因的突变消除了通过重组修复或线性DNA降解对DSB的处理。测试了两种大肠杆菌复制性解旋酶,在recBC突变体中必不可少的Rep以及DnaB。将rep recBTS recCTS细胞转移至限制温度后,线性DNA的比例增加至50%。在没有复制染色体的情况下未观察到线性DNA增加,这表明rep菌株中DSB的形成需要复制。强复制终止子或dnaBTS突变对DnaB解旋酶的抑制导致线性DNA的形成,表明停滞的复制叉易于形成DSB。在野生型大肠杆菌中,在没有RecBC或同时没有RecA和RecD的情况下检测到线性DNA。这揭示了存在大量自发DSB。我们认为其中一些也可能是由于复制叉进展受损所致。