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DNA 甲基化对变形链球菌毒力基因表达的影响。

Effects of DNA methylation on expression of virulence genes in Streptococcus mutans.

机构信息

Dows Institute for Research, University of Iowa College of Dentistry, N436 Dental Science Building, Iowa City, IA 52242, USA.

出版信息

Appl Environ Microbiol. 2011 Oct;77(20):7236-42. doi: 10.1128/AEM.00543-11. Epub 2011 Aug 12.

Abstract

Bacteria produce a variety of enzymes capable of methylating DNA. In many species, the majority of adenine methylation is accomplished by the DNA adenine methylase Dam. In Escherichia coli the Dam methylase plays roles in the initiation of replication, mismatch repair, and gene regulation. In a number of other bacterial species, mutation or overexpression of Dam leads to attenuation of virulence. Homologues of the dam gene exist in some members of the Firmicutes, including Streptococcus mutans, a dental pathogen. An S. mutans strain inactivated in the dam gene (SMU.504; here designated damA) was engineered, and phenotypes linked to cariogenicity were examined. A prominent observation was that the damA mutant produced greater amounts of glucan than the parental strain. Real-time PCR confirmed upregulation of gtfB. To determine whether other loci were affected by the damA mutation, a microarray analysis was carried out. Seventy genes were upregulated at least 2-fold in the damA mutant, and 33 genes were downregulated at least 2-fold. In addition to gtfB (upregulated 2.6-fold; 1.7-fold when measured by real-time PCR), other upregulated virulence factors included gbpC (upregulated 2.1-fold) and loci predicted to encode bacteriocins (upregulated 2- to 7-fold). Various sugar transport operons were also upregulated, the most extreme being the cellobiose operon (upregulated nearly 40-fold). Expression of sacB, encoding fructosyltransferase, was downregulated 2.4-fold. The sequence 5'-GATC-3' appeared to constitute the recognition sequence for methylation. These results provide evidence that DNA methylation in S. mutans has a global effect on gene expression, including that of genes associated with cariogenic potential.

摘要

细菌产生多种能够甲基化 DNA 的酶。在许多物种中,大多数腺嘌呤甲基化是由 DNA 腺嘌呤甲基酶 Dam 完成的。在大肠杆菌中,Dam 甲基酶在复制起始、错配修复和基因调控中发挥作用。在其他一些细菌物种中,Dam 的突变或过表达导致毒力减弱。Firmicutes 中的一些成员存在 dam 基因的同源物,包括口腔病原体变形链球菌。失活 dam 基因的 S. mutans 菌株(SMU.504;在此指定为 damA)被工程改造,并且研究了与致龋性相关的表型。一个突出的观察结果是,damA 突变体产生的葡聚糖量比亲本菌株多。实时 PCR 证实 gtfB 的上调。为了确定 damA 突变是否影响其他基因座,进行了微阵列分析。damA 突变体中有 70 个基因至少上调 2 倍,33 个基因至少下调 2 倍。除了 gtfB(上调 2.6 倍;通过实时 PCR 测量时为 1.7 倍),其他上调的毒力因子包括 gbpC(上调 2.1 倍)和预测编码细菌素的基因座(上调 2 到 7 倍)。各种糖转运操纵子也上调,最极端的是纤维二糖操纵子(上调近 40 倍)。编码果糖基转移酶的 sacB 的表达下调了 2.4 倍。序列 5'-GATC-3' 似乎构成了甲基化的识别序列。这些结果提供了证据,表明 S. mutans 中的 DNA 甲基化对基因表达具有全局影响,包括与致龋潜力相关的基因表达。

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