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1
Mutations of Bacteria from Virus Sensitivity to Virus Resistance.细菌从对病毒敏感到对病毒抗性的突变。
Genetics. 1943 Nov;28(6):491-511. doi: 10.1093/genetics/28.6.491.
2
Locus-specific mutational events in a multilocus variable-number tandem repeat analysis of Escherichia coli O157:H7.大肠杆菌O157:H7多位点可变数目串联重复序列分析中的位点特异性突变事件
J Clin Microbiol. 2006 Feb;44(2):374-7. doi: 10.1128/JCM.44.2.374-377.2006.
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Multiple-locus variable number tandem repeats analysis for genetic fingerprinting of pathogenic bacteria.多位点可变数目串联重复序列分析用于病原菌的基因指纹识别
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Highly diverse variable number tandem repeat loci in the E. coli O157:H7 and O55:H7 genomes for high-resolution molecular typing.大肠杆菌O157:H7和O55:H7基因组中高度多样的可变数目串联重复序列位点用于高分辨率分子分型。
J Appl Microbiol. 2005;98(4):928-40. doi: 10.1111/j.1365-2672.2004.02532.x.
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Identifying sources of human exposure to plague.确定人类接触鼠疫的来源。
J Clin Microbiol. 2005 Feb;43(2):650-6. doi: 10.1128/JCM.43.2.650-656.2005.
6
Microevolution and history of the plague bacillus, Yersinia pestis.鼠疫杆菌耶尔森氏菌的微进化与历史
Proc Natl Acad Sci U S A. 2004 Dec 21;101(51):17837-42. doi: 10.1073/pnas.0408026101. Epub 2004 Dec 14.
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Anthrax molecular epidemiology and forensics: using the appropriate marker for different evolutionary scales.炭疽分子流行病学与法医学:针对不同进化尺度使用合适的标记物。
Infect Genet Evol. 2004 Sep;4(3):205-13. doi: 10.1016/j.meegid.2004.02.005.
8
Differential plague-transmission dynamics determine Yersinia pestis population genetic structure on local, regional, and global scales.不同的鼠疫传播动态决定了鼠疫耶尔森菌在局部、区域和全球尺度上的种群遗传结构。
Proc Natl Acad Sci U S A. 2004 Jun 1;101(22):8408-13. doi: 10.1073/pnas.0401561101. Epub 2004 May 20.
9
DNA mismatch repair and mutation avoidance pathways.DNA错配修复与突变避免途径
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10
Identification and characterization of variable-number tandem repeats in the Yersinia pestis genome.鼠疫耶尔森氏菌基因组中可变数目串联重复序列的鉴定与特征分析。
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重复拷贝数对大肠杆菌O157:H7中可变数目串联重复序列突变的影响。

Effect of repeat copy number on variable-number tandem repeat mutations in Escherichia coli O157:H7.

作者信息

Vogler Amy J, Keys Christine, Nemoto Yoshimi, Colman Rebecca E, Jay Zack, Keim Paul

机构信息

Department of Biological Sciences, Northern Arizona University, Flagstaff, AZ 86011-5640, USA.

出版信息

J Bacteriol. 2006 Jun;188(12):4253-63. doi: 10.1128/JB.00001-06.

DOI:10.1128/JB.00001-06
PMID:16740932
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1482962/
Abstract

Variable-number tandem repeat (VNTR) loci have shown a remarkable ability to discriminate among isolates of the recently emerged clonal pathogen Escherichia coli O157:H7, making them a very useful molecular epidemiological tool. However, little is known about the rates at which these sequences mutate, the factors that affect mutation rates, or the mechanisms by which mutations occur at these loci. Here, we measure mutation rates for 28 VNTR loci and investigate the effects of repeat copy number and mismatch repair on mutation rate using in vitro-generated populations for 10 E. coli O157:H7 strains. We find single-locus rates as high as 7.0 x 10(-4) mutations/generation and a combined 28-locus rate of 6.4 x 10(-4) mutations/generation. We observed single- and multirepeat mutations that were consistent with a slipped-strand mispairing mutation model, as well as a smaller number of large repeat copy number mutations that were consistent with recombination-mediated events. Repeat copy number within an array was strongly correlated with mutation rate both at the most mutable locus, O157-10 (r2= 0.565, P = 0.0196), and across all mutating loci. The combined locus model was significant whether locus O157-10 was included (r2= 0.833, P < 0.0001) or excluded (r2= 0.452, P < 0.0001) from the analysis. Deficient mismatch repair did not affect mutation rate at any of the 28 VNTRs with repeat unit sizes of >5 bp, although a poly(G) homomeric tract was destabilized in the mutS strain. Finally, we describe a general model for VNTR mutations that encompasses insertions and deletions, single- and multiple-repeat mutations, and their relative frequencies based upon our empirical mutation rate data.

摘要

可变数目串联重复序列(VNTR)位点已显示出卓越的能力,能够区分新出现的克隆病原体大肠杆菌O157:H7的分离株,使其成为一种非常有用的分子流行病学工具。然而,对于这些序列的突变率、影响突变率的因素,或这些位点发生突变的机制,我们知之甚少。在此,我们测量了28个VNTR位点的突变率,并使用10株大肠杆菌O157:H7菌株的体外生成群体,研究重复拷贝数和错配修复对突变率的影响。我们发现单一位点的突变率高达7.0×10⁻⁴突变/代,28个位点的综合突变率为6.4×10⁻⁴突变/代。我们观察到与滑链错配突变模型一致的单重复和多重复突变,以及少量与重组介导事件一致的大重复拷贝数突变。在最易突变的位点O157 - 10(r² = 0.565,P = 0.0196)以及所有发生突变的位点,阵列内的重复拷贝数与突变率都密切相关。无论分析中是否包含位点O157 - 10,综合位点模型都具有显著性(包含时r² = 0.833,P < 0.0001;排除时r² = 0.452,P < 0.0001)。对于28个重复单元大小>5 bp的VNTR,错配修复缺陷并不影响突变率,尽管在mutS菌株中聚(G)同聚物序列不稳定。最后,我们基于经验性突变率数据,描述了一个涵盖插入和缺失、单重复和多重复突变及其相对频率的VNTR突变通用模型。