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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.

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。

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