• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

染色体复制起点处双向复制的起始是由解旋酶和引发酶之间的相互作用所引导的。

Initiation of bidirectional replication at the chromosomal origin is directed by the interaction between helicase and primase.

作者信息

Hiasa H, Marians K J

机构信息

Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.

出版信息

J Biol Chem. 1999 Sep 17;274(38):27244-8. doi: 10.1074/jbc.274.38.27244.

DOI:10.1074/jbc.274.38.27244
PMID:10480943
Abstract

Several protein-protein interactions have been shown to be critical for proper replication fork function in Escherichia coli. These include interactions between the polymerase and the helicase, the helicase and the primase, and the primase and the polymerase. We have studied the influence of these interactions on proper initiation at oriC by using mutant primases defective in their interaction with the helicase and DNA polymerase III holoenzyme lacking the tau subunit so that it will not interact with the helicase. We show here that accurate initiation of bidirectional DNA replication from oriC is dependent on proper placement of the primers for leading strand synthesis and is thus governed primarily by the interaction between the helicase and primase.

摘要

几种蛋白质-蛋白质相互作用已被证明对大肠杆菌中正确的复制叉功能至关重要。这些相互作用包括聚合酶与解旋酶之间、解旋酶与引发酶之间以及引发酶与聚合酶之间的相互作用。我们通过使用与解旋酶相互作用有缺陷的突变引发酶以及缺乏τ亚基从而不会与解旋酶相互作用的DNA聚合酶III全酶,研究了这些相互作用对oriC处正确起始的影响。我们在此表明,从oriC进行双向DNA复制的准确起始取决于前导链合成引物的正确定位,因此主要由解旋酶与引发酶之间的相互作用决定。

相似文献

1
Initiation of bidirectional replication at the chromosomal origin is directed by the interaction between helicase and primase.染色体复制起点处双向复制的起始是由解旋酶和引发酶之间的相互作用所引导的。
J Biol Chem. 1999 Sep 17;274(38):27244-8. doi: 10.1074/jbc.274.38.27244.
2
Mechanism and stoichiometry of interaction of DnaG primase with DnaB helicase of Escherichia coli in RNA primer synthesis.大肠杆菌RNA引物合成过程中DnaG引发酶与DnaB解旋酶相互作用的机制和化学计量关系。
J Biol Chem. 2003 Dec 26;278(52):52253-61. doi: 10.1074/jbc.M308956200. Epub 2003 Oct 13.
3
Replication initiation at the Escherichia coli chromosomal origin.大肠杆菌染色体起点的复制起始。
Curr Opin Chem Biol. 2011 Oct;15(5):606-13. doi: 10.1016/j.cbpa.2011.07.016. Epub 2011 Aug 18.
4
Identification of a domain of Escherichia coli primase required for functional interaction with the DnaB helicase at the replication fork.鉴定大肠杆菌引发酶中与复制叉处DnaB解旋酶进行功能相互作用所需的结构域。
J Biol Chem. 1994 Feb 11;269(6):4675-82.
5
Identification of a region of Escherichia coli DnaB required for functional interaction with DnaG at the replication fork.鉴定大肠杆菌DnaB中与复制叉处的DnaG进行功能相互作用所需的区域。
J Biol Chem. 2000 Aug 25;275(34):26187-95. doi: 10.1074/jbc.M001800200.
6
Regulation of bacterial priming and daughter strand synthesis through helicase-primase interactions.通过解旋酶-引发酶相互作用对细菌引发和子链合成的调控。
Nucleic Acids Res. 2006;34(15):4082-8. doi: 10.1093/nar/gkl363. Epub 2006 Aug 25.
7
Helicase action of dnaB protein during replication from the Escherichia coli chromosomal origin in vitro.体外从大肠杆菌染色体复制起点进行复制过程中dnaB蛋白的解旋酶作用。
J Biol Chem. 1987 May 15;262(14):6877-85.
8
Replisome assembly at oriC, the replication origin of E. coli, reveals an explanation for initiation sites outside an origin.大肠杆菌复制起点oriC处的复制体组装揭示了对起点外起始位点的一种解释。
Mol Cell. 1999 Oct;4(4):541-53. doi: 10.1016/s1097-2765(00)80205-1.
9
The interaction between helicase and primase sets the replication fork clock.解旋酶与引发酶之间的相互作用设定了复制叉时钟。
J Biol Chem. 1996 Aug 30;271(35):21398-405. doi: 10.1074/jbc.271.35.21398.
10
Strand-specific loading of DnaB helicase by DnaA to a substrate mimicking unwound oriC.DnaA将DnaB解旋酶特异性加载到模拟解旋oriC的底物上。
Mol Microbiol. 2002 Nov;46(4):1149-56. doi: 10.1046/j.1365-2958.2002.03232.x.

引用本文的文献

1
Establishing a biochemical understanding of the initiation of chromosome replication in bacteria.建立细菌染色体复制起始的生化理解。
Proc Natl Acad Sci U S A. 2024 Jun 4;121(23):e2400667121. doi: 10.1073/pnas.2400667121. Epub 2024 May 17.
2
Blocking the Trigger: Inhibition of the Initiation of Bacterial Chromosome Replication as an Antimicrobial Strategy.阻断触发因素:抑制细菌染色体复制起始作为一种抗菌策略。
Antibiotics (Basel). 2019 Aug 6;8(3):111. doi: 10.3390/antibiotics8030111.
3
Efficient Arrangement of the Replication Fork Trap for In Vitro Propagation of Monomeric Circular DNA in the Chromosome-Replication Cycle Reaction.
用于染色体复制循环反应中单体环状DNA体外增殖的复制叉陷阱的高效排列
Life (Basel). 2018 Sep 25;8(4):43. doi: 10.3390/life8040043.
4
Exponential propagation of large circular DNA by reconstitution of a chromosome-replication cycle.通过重建染色体复制周期实现大型环状DNA的指数增殖。
Nucleic Acids Res. 2017 Nov 16;45(20):11525-11534. doi: 10.1093/nar/gkx822.
5
Replisome Dynamics during Chromosome Duplication.染色体复制过程中的复制体动力学
EcoSal Plus. 2009 Aug;3(2). doi: 10.1128/ecosalplus.4.4.2.
6
SSB as an organizer/mobilizer of genome maintenance complexes.单链结合蛋白作为基因组维持复合物的组织者/动员者。
Crit Rev Biochem Mol Biol. 2008 Sep-Oct;43(5):289-318. doi: 10.1080/10409230802341296.
7
Solution structure of the helicase-interaction domain of the primase DnaG: a model for helicase activation.引发酶DnaG解旋酶相互作用结构域的溶液结构:解旋酶激活模型
Structure. 2005 Apr;13(4):609-16. doi: 10.1016/j.str.2005.01.022.
8
Identification of temperature-sensitive dnaD mutants of Staphylococcus aureus that are defective in chromosomal DNA replication.金黄色葡萄球菌温度敏感型dnaD突变体的鉴定,这些突变体在染色体DNA复制方面存在缺陷。
Mol Genet Genomics. 2004 May;271(4):447-57. doi: 10.1007/s00438-004-0996-6. Epub 2004 Mar 24.
9
Molecular flip-flops formed by overlapping Fis sites.由重叠的Fis位点形成的分子触发器。
Nucleic Acids Res. 2003 Nov 15;31(22):6663-73. doi: 10.1093/nar/gkg877.
10
Measuring motion on DNA by the type I restriction endonuclease EcoR124I using triplex displacement.利用三链置换通过I型限制性内切核酸酶EcoR124I测量DNA上的运动。
EMBO J. 2000 May 2;19(9):2094-102. doi: 10.1093/emboj/19.9.2094.