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本文引用的文献

1
Escherichia coli DNA adenine methyltransferase: the structural basis of processive catalysis and indirect read-out.大肠杆菌DNA腺嘌呤甲基转移酶:持续性催化和间接识别的结构基础。
J Biol Chem. 2009 Jul 3;284(27):18390-400. doi: 10.1074/jbc.M109.005876. Epub 2009 May 5.
2
Growth rate dependent numbers of SeqA structures organize the multiple replication forks in rapidly growing Escherichia coli.生长速度依赖的 SeqA 结构数量组织了快速生长的大肠杆菌中的多个复制叉。
Genes Cells. 2009 May;14(5):643-57. doi: 10.1111/j.1365-2443.2009.01298.x. Epub 2009 Apr 15.
3
Structural insights into the cooperative binding of SeqA to a tandem GATC repeat.SeqA与串联GATC重复序列协同结合的结构见解。
Nucleic Acids Res. 2009 Jun;37(10):3143-52. doi: 10.1093/nar/gkp151. Epub 2009 Mar 20.
4
The Escherichia coli SeqA protein.大肠杆菌SeqA蛋白。
Plasmid. 2009 May;61(3):141-50. doi: 10.1016/j.plasmid.2009.02.004. Epub 2009 Feb 28.
5
The oligomerization of OxyR in Escherichia coli.大肠杆菌中OxyR的寡聚化。
Protein Sci. 2009 Jan;18(1):101-7. doi: 10.1002/pro.5.
6
The initiator protein DnaA contributes to keeping new origins inactivated by promoting the presence of hemimethylated DNA.引发蛋白DnaA通过促进半甲基化DNA的存在,有助于使新的复制起点保持失活状态。
J Mol Biol. 2008 Dec 31;384(5):1076-85. doi: 10.1016/j.jmb.2008.09.042. Epub 2008 Sep 25.
7
Regulation and function of Ag43 (flu).Ag43(流感)的调控与功能
Annu Rev Microbiol. 2008;62:153-69. doi: 10.1146/annurev.micro.62.081307.162938.
8
Competitive Lrp and Dam assembly at the pap regulatory region: implications for mechanisms of epigenetic regulation.在pap调控区域的竞争性Lrp和Dam组装:对表观遗传调控机制的启示
J Mol Biol. 2008 Oct 31;383(1):92-105. doi: 10.1016/j.jmb.2008.07.086. Epub 2008 Aug 6.
9
Modulation of Escherichia coli DNA methyltransferase activity by biologically derived GATC-flanking sequences.生物衍生的GATC侧翼序列对大肠杆菌DNA甲基转移酶活性的调控
J Biol Chem. 2008 Jul 18;283(29):20106-16. doi: 10.1074/jbc.M802502200. Epub 2008 May 23.
10
Clocks and switches: bacterial gene regulation by DNA adenine methylation.时钟与开关:DNA腺嘌呤甲基化对细菌基因的调控
Curr Opin Microbiol. 2008 Apr;11(2):106-12. doi: 10.1016/j.mib.2008.02.012. Epub 2008 Apr 8.

建立并维持大肠杆菌 agn43 相变异的 Dam 靶位点的隔离。

Establishing and maintaining sequestration of Dam target sites for phase variation of agn43 in Escherichia coli.

机构信息

Center for Immunology and Infection, Hull York Medical School, Department of Biology, University of York, York, United Kingdom.

出版信息

J Bacteriol. 2010 Apr;192(7):1937-45. doi: 10.1128/JB.01629-09. Epub 2010 Jan 29.

DOI:10.1128/JB.01629-09
PMID:20118257
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2838033/
Abstract

Phase variation of the outer membrane protein Ag43 encoded by agn43 in Escherichia coli is controlled by an epigenetic mechanism. Sequestration of the regulatory region from Dam-dependent methylation has to be established and maintained throughout a generation to obtain and maintain the OFF phase. This work shows that hemimethylated DNA, which is formed by the passage of the DNA replication fork in an ON-phase cell, can be sequestered from methylation by OxyR binding, which is thus a key event for the switch from ON to OFF. No evidence was found that the protein SeqA, which also binds to the region, is involved in sequestration. To facilitate the dissection of this process further, a novel approach was introduced that does not alter the sequence of the regulatory region or the cellular concentration of Dam or OxyR, which consists of inserting auxiliary OxyR binding sites upstream of the regulatory region. Using this strategy, it was shown that the ON-to-OFF switch frequency can be modulated without changing the OFF-to-ON frequency. The data support a model in which in an ON-phase cell, the subcellular OxyR availability at the replication fork as it passes through the agn43 regulatory region is key for initiating an ON-to-OFF switch. In contrast, this availability is not a determining factor for the switch from OFF to ON. This finding shows that different variables affect these two stochastic events. This provides new insight into the events determining the stochastic nature of epigenetic phase variation.

摘要

大肠杆菌 agn43 编码的外膜蛋白 Ag43 的相位变化受表观遗传机制控制。必须建立并维持调节区域与 Dam 依赖性甲基化的隔离,以获得和维持关闭相位。本工作表明,半甲基化 DNA 可以通过 OxyR 结合从甲基化中隔离出来,这种结合是从 ON 到 OFF 转变的关键事件。没有证据表明同样结合该区域的 SeqA 蛋白参与隔离。为了进一步促进对该过程的剖析,引入了一种不会改变调控区序列或细胞内 Dam 或 OxyR 浓度的新方法,该方法包括在调控区的上游插入辅助的 OxyR 结合位点。使用这种策略,表明可以在不改变关闭到打开频率的情况下调节打开到关闭的转换频率。这些数据支持这样一种模型,即在打开相位的细胞中,复制叉通过 agn43 调控区时亚细胞 OxyR 的可用性对于启动打开到关闭的转换至关重要。相比之下,这种可用性不是从关闭到打开转换的决定因素。这一发现表明,不同的变量会影响这两个随机事件。这为决定表观遗传相位变化的随机性质的事件提供了新的见解。