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一种以甲基化特异性方式结合P1起始核心和oriC 13聚体区域的蛋白质是宿主seqA基因的产物。

A protein that binds to the P1 origin core and the oriC 13mer region in a methylation-specific fashion is the product of the host seqA gene.

作者信息

Brendler T, Abeles A, Austin S

机构信息

Laboratory of Chromosome Biology, ABL-Basic Research Program, NCI-Frederick Cancer Research and Development Center, MD 21702-1201, USA.

出版信息

EMBO J. 1995 Aug 15;14(16):4083-9. doi: 10.1002/j.1460-2075.1995.tb00080.x.

DOI:10.1002/j.1460-2075.1995.tb00080.x
PMID:7664748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC394487/
Abstract

The P1 plasmid replication origin P1oriR is controlled by methylation of four GATC adenine methylation sites within heptamer repeats. A comparable (13mer) region is present in the host origin, oriC. The two origins show comparable responses to methylation; negative control by recognition of hemimethylated DNA (sequestration) and a positive requirement for methylation for efficient function. We have isolated a host protein that recognizes the P1 origin region only when it is isolated from a strain proficient for adenine methylation. The substantially purified 22 kDa protein also binds to the 13mer region of oriC in a methylation-specific fashion. It proved to be the product of the seqA gene that acts in the negative control of oriC by sequestration. We conclude that the role of the SeqA protein in sequestration is to recognize the methylation state of P1oriR and oriC by direct DNA binding. Using synthetic substrates we show that SeqA binds exclusively to the hemimethylated forms of these origins forms that are the immediate products of replication in a methylation-proficient strain. We also show that the protein can recognize sequences with multiple GATC sites, irrespective of the surrounding sequence. The basis for origin specificity is primarily the persistence of hemimethylated forms that are over-represented in the natural. DNA preparations relative to controls.

摘要

P1 质粒复制起点 P1oriR 受七聚体重复序列内四个 GATC 腺嘌呤甲基化位点的甲基化作用控制。宿主复制起点 oriC 中存在一个类似的(13 聚体)区域。这两个复制起点对甲基化表现出相似的反应:通过识别半甲基化 DNA(隔离)进行负调控,以及甲基化对高效功能的正需求。我们分离出了一种宿主蛋白,该蛋白仅在从腺嘌呤甲基化 proficient 的菌株中分离出 P1 复制起点区域时才会识别它。这种经过大量纯化的 22 kDa 蛋白也以甲基化特异性方式与 oriC 的 13 聚体区域结合。事实证明它是 seqA 基因的产物,通过隔离作用对 oriC 进行负调控。我们得出结论,SeqA 蛋白在隔离中的作用是通过直接结合 DNA 来识别 P1oriR 和 oriC 的甲基化状态。使用合成底物,我们表明 SeqA 仅与这些复制起点的半甲基化形式结合,这些形式是甲基化 proficient 菌株中复制的直接产物。我们还表明,该蛋白可以识别具有多个 GATC 位点的序列,而与周围序列无关。复制起点特异性的基础主要是半甲基化形式的持久性,在天然 DNA 制剂中相对于对照,其含量过高。

相似文献

1
A protein that binds to the P1 origin core and the oriC 13mer region in a methylation-specific fashion is the product of the host seqA gene.一种以甲基化特异性方式结合P1起始核心和oriC 13聚体区域的蛋白质是宿主seqA基因的产物。
EMBO J. 1995 Aug 15;14(16):4083-9. doi: 10.1002/j.1460-2075.1995.tb00080.x.
2
Competition between the replication initiator DnaA and the sequestration factor SeqA for binding to the hemimethylated chromosomal origin of E. coli in vitro.复制起始蛋白DnaA与隔离因子SeqA在体外结合大肠杆菌半甲基化染色体起源位点的竞争。
Genes Cells. 2000 Nov;5(11):873-884. doi: 10.1046/j.1365-2443.2000.00380.x.
3
SeqA, the Escherichia coli origin sequestration protein, can regulate the replication of the pBR322 plasmid. SeqA,一种大肠杆菌起源的隔离蛋白,能够调控 pBR322 质粒的复制。
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4
E. coli SeqA protein binds oriC in two different methyl-modulated reactions appropriate to its roles in DNA replication initiation and origin sequestration.大肠杆菌SeqA蛋白通过两种不同的甲基调节反应与oriC结合,这两种反应与其在DNA复制起始和复制起点隔离中的作用相适应。
Cell. 1995 Sep 22;82(6):927-36. doi: 10.1016/0092-8674(95)90272-4.
5
Binding of SeqA protein to DNA requires interaction between two or more complexes bound to separate hemimethylated GATC sequences.SeqA蛋白与DNA的结合需要两个或更多结合在不同半甲基化GATC序列上的复合物之间相互作用。
EMBO J. 1999 Apr 15;18(8):2304-10. doi: 10.1093/emboj/18.8.2304.
6
Interaction of SeqA and Dam methylase on the hemimethylated origin of Escherichia coli chromosomal DNA replication.SeqA与Dam甲基化酶在大肠杆菌染色体DNA复制的半甲基化起始位点上的相互作用。
J Biol Chem. 1999 Apr 23;274(17):11463-8. doi: 10.1074/jbc.274.17.11463.
7
The Escherichia coli SeqA protein binds specifically and co-operatively to two sites in hemimethylated and fully methylated oriC.大肠杆菌SeqA蛋白能特异性地与半甲基化和完全甲基化的oriC中的两个位点协同结合。
Mol Microbiol. 2000 Jun;36(6):1319-26. doi: 10.1046/j.1365-2958.2000.01943.x.
8
The Escherichia coli SeqA protein binds specifically to two sites in fully and hemimethylated oriC and has the capacity to inhibit DNA replication and affect chromosome topology.大肠杆菌SeqA蛋白能特异性结合完全甲基化和半甲基化oriC中的两个位点,并具有抑制DNA复制和影响染色体拓扑结构的能力。
Biochimie. 2001 Jan;83(1):49-51. doi: 10.1016/s0300-9084(00)01207-4.
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Escherichia coli SeqA protein affects DNA topology and inhibits open complex formation at oriC.大肠杆菌SeqA蛋白影响DNA拓扑结构并抑制oriC处开放复合物的形成。
EMBO J. 1999 Sep 1;18(17):4882-8. doi: 10.1093/emboj/18.17.4882.
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SeqA blocking of DnaA-oriC interactions ensures staged assembly of the E. coli pre-RC.SeqA对DnaA-oriC相互作用的阻断确保了大肠杆菌前复制复合体的阶段性组装。
Mol Cell. 2006 Nov 17;24(4):581-92. doi: 10.1016/j.molcel.2006.09.016.

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Chromosomal replication origin from the marine bacterium Vibrio harveyi functions in Escherichia coli: oriC consensus sequence.来自海洋细菌哈维氏弧菌的染色体复制起点在大肠杆菌中发挥作用:oriC共有序列。
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Enzymatic replication of the origin of the Escherichia coli chromosome.大肠杆菌染色体复制起点的酶促复制
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