Suppr超能文献

体内T:G错配的极短片段修复:背景和辅助蛋白的重要性

Very short patch repair of T:G mismatches in vivo: importance of context and accessory proteins.

作者信息

Lieb M, Rehmat S

机构信息

Department of Microbiology, University of Southern California School of Medicine, Los Angeles 90033.

出版信息

J Bacteriol. 1995 Feb;177(3):660-6. doi: 10.1128/jb.177.3.660-666.1995.

Abstract

In Escherichia coli, T:G mismatches in specific contexts are corrected by a very short patch (VSP) repair system. Previous studies have shown that the product of gene vsr mediates correction of T:G to C:G in the 5'CTAGG/3'GGTCC context and in some related contexts. Amber mutations that arose in CAG sequences in gene cI of bacteriophage lambda were used to determine the effect of flanking bases on the repair of T:G mispairs arising during phage recombination. The experimental findings were combined with published data on mismatch repair of mutations in lambda gene P and E. coli gene lacI. While VSP repair was most efficient in the context 5'CTAGG, there was very significant correction when either the 5'C or the 3' G was replaced by another base. Some mismatch repair of TAG to CAG occurred in all contexts tested. Reduction in VSP repair caused by the lack of MutL or MutS was fully complemented by the addition of vsr+ plasmids when the T:G mispair was in the 5'CTAGG/3'GGTCC context. VSP repair was decreased in bacteria containing mutS+ on a multicopy plasmid. It is suggested that VSP repair maintains sequences such as the repetitive extragenic palindromic (REP) and Chi sequences, which have important roles in E. coli and closely related bacteria.

摘要

在大肠杆菌中,特定环境下的T:G错配可由一个极短片段(VSP)修复系统进行校正。先前的研究表明,基因vsr的产物介导了在5'CTAGG/3'GGTCC环境及一些相关环境中T:G到C:G的校正。利用噬菌体λ基因cI中CAG序列出现的琥珀突变来确定侧翼碱基对噬菌体重组过程中产生的T:G错配修复的影响。实验结果与已发表的关于λ基因P和大肠杆菌基因lacI中突变错配修复的数据相结合。虽然VSP修复在5'CTAGG环境中效率最高,但当5'C或3'G被另一个碱基取代时,也有非常显著的校正。在所有测试环境中都发生了一些TAG到CAG的错配修复。当T:G错配处于5'CTAGG/3'GGTCC环境时,添加vsr + 质粒可完全弥补因缺乏MutL或MutS而导致的VSP修复减少。在多拷贝质粒上含有mutS + 的细菌中,VSP修复减少。有人提出,VSP修复维持了诸如重复基因外回文序列(REP)和Chi序列等序列,这些序列在大肠杆菌及密切相关细菌中具有重要作用。

相似文献

1
Very short patch repair of T:G mismatches in vivo: importance of context and accessory proteins.
J Bacteriol. 1995 Feb;177(3):660-6. doi: 10.1128/jb.177.3.660-666.1995.
3
The Escherichia coli MutL protein stimulates binding of Vsr and MutS to heteroduplex DNA.
Nucleic Acids Res. 1998 Feb 15;26(4):948-53. doi: 10.1093/nar/26.4.948.
6
Bacterial genes mutL, mutS, and dcm participate in repair of mismatches at 5-methylcytosine sites.
J Bacteriol. 1987 Nov;169(11):5241-6. doi: 10.1128/jb.169.11.5241-5246.1987.
7
The Vsr endonuclease of Escherichia coli: an efficient DNA repair enzyme and a potent mutagen.
J Bacteriol. 1997 Oct;179(19):6048-52. doi: 10.1128/jb.179.19.6048-6052.1997.
8
Reconstitution of the very short patch repair pathway from Escherichia coli.
J Biol Chem. 2012 Sep 21;287(39):32953-66. doi: 10.1074/jbc.M112.384321. Epub 2012 Jul 30.
9
Very-short-patch repair in Escherichia coli requires the dam adenine methylase.
J Bacteriol. 2001 Jun;183(12):3631-5. doi: 10.1128/JB.183.12.3631-3635.2001.

引用本文的文献

1
DNA Mismatch Repair.
EcoSal Plus. 2012 Nov;5(1). doi: 10.1128/ecosalplus.7.2.5.
2
Reconstitution of the very short patch repair pathway from Escherichia coli.
J Biol Chem. 2012 Sep 21;287(39):32953-66. doi: 10.1074/jbc.M112.384321. Epub 2012 Jul 30.
3
Neisseria gonorrhoeae FA1090 carries genes encoding two classes of Vsr endonucleases.
J Bacteriol. 2010 Aug;192(15):3951-60. doi: 10.1128/JB.00098-10. Epub 2010 May 28.
4
Properties of HflX, an enigmatic protein from Escherichia coli.
J Bacteriol. 2009 Apr;191(7):2307-14. doi: 10.1128/JB.01353-08. Epub 2009 Jan 30.
5
Mismatch repair proteins collaborate with methyltransferases in the repair of O(6)-methylguanine.
DNA Repair (Amst). 2008 Feb 1;7(2):170-6. doi: 10.1016/j.dnarep.2007.09.003. Epub 2007 Oct 24.

本文引用的文献

1
Significant dispersed recurrent DNA sequences in the Escherichia coli genome. Several new groups.
J Mol Biol. 1993 Feb 20;229(4):833-48. doi: 10.1006/jmbi.1993.1090.
4
Repetitive extragenic palindromic sequences: a major component of the bacterial genome.
Cell. 1984 Jul;37(3):1015-26. doi: 10.1016/0092-8674(84)90436-7.
5
Recombinational hotspot activity of Chi-like sequences.
J Mol Biol. 1984 Dec 5;180(2):371-7. doi: 10.1016/s0022-2836(84)80009-1.
6
Specific mismatch correction in bacteriophage lambda crosses by very short patch repair.
Mol Gen Genet. 1983;191(1):118-25. doi: 10.1007/BF00330898.
7
Hyperrecombination at a specific DNA sequence in pneumococcal transformation.
Proc Natl Acad Sci U S A. 1984 Aug;81(16):5184-8. doi: 10.1073/pnas.81.16.5184.
8
Location of DNA methylation genes on the Escherichia coli K-12 genetic map.
Mol Gen Genet. 1973 Dec 14;127(1):47-55. doi: 10.1007/BF00267782.
9
Pedigrees of some mutant strains of Escherichia coli K-12.
Bacteriol Rev. 1972 Dec;36(4):525-57. doi: 10.1128/br.36.4.525-557.1972.
10
Conservation of Chi cutting activity in terrestrial and marine enteric bacteria.
J Mol Biol. 1986 Jun 20;189(4):585-95. doi: 10.1016/0022-2836(86)90489-4.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验