• 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

大肠杆菌中DNA损伤诱导的DNA复制起始位点

DNA damage-inducible origins of DNA replication in Escherichia coli.

作者信息

Magee T R, Asai T, Malka D, Kogoma T

机构信息

Department of Cell Biology, School of Medicine, University of New Mexico, Albuquerque 87131.

出版信息

EMBO J. 1992 Nov;11(11):4219-25. doi: 10.1002/j.1460-2075.1992.tb05516.x.

DOI:10.1002/j.1460-2075.1992.tb05516.x
PMID:1396602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC556933/
Abstract

Upon induction of the SOS response in Escherichia coli, the mode of initiation of DNA replication is altered such that it can occur in the absence of normally required protein synthesis. This type of DNA replication has been termed induced stable DNA replication (iSDR). We examined the origin usage during iSDR and found that the initiation of iSDR occurs primarily in the oriC and terC regions of the chromosome in a manner completely independent of transcription, translation and DnaA protein. Minichromosomes (oriC plasmids) pOC23 and pOC81 were induced to replicate in the absence of DnaA protein and transcription after SOS induction. The results localized one of the iSDR origin activities in a 596 bp region which includes the minimal oriC.

摘要

在大肠杆菌中诱导SOS反应时,DNA复制的起始模式会发生改变,从而使其能够在缺乏正常所需蛋白质合成的情况下发生。这种类型的DNA复制被称为诱导稳定DNA复制(iSDR)。我们研究了iSDR过程中的起始点使用情况,发现iSDR的起始主要发生在染色体的oriC和terC区域,其方式完全独立于转录、翻译和DnaA蛋白。在SOS诱导后,微小染色体(oriC质粒)pOC23和pOC81在没有DnaA蛋白和转录的情况下被诱导复制。结果将其中一个iSDR起始点活性定位在一个596 bp的区域,该区域包括最小oriC。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6d/556933/e7df80872799/emboj00096-0398-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6d/556933/e7df80872799/emboj00096-0398-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6d/556933/e7df80872799/emboj00096-0398-a.jpg

相似文献

1
DNA damage-inducible origins of DNA replication in Escherichia coli.大肠杆菌中DNA损伤诱导的DNA复制起始位点
EMBO J. 1992 Nov;11(11):4219-25. doi: 10.1002/j.1460-2075.1992.tb05516.x.
2
DNA damage-inducible replication of the Escherichia coli chromosome is initiated at separable sites within the minimal oriC.大肠杆菌染色体的DNA损伤诱导复制在最小oriC内的可分离位点起始。
J Mol Biol. 1994 Feb 4;235(5):1459-69. doi: 10.1006/jmbi.1994.1101.
3
Homologous recombination-dependent initiation of DNA replication from DNA damage-inducible origins in Escherichia coli.大肠杆菌中依赖同源重组从DNA损伤诱导型起始点引发DNA复制
EMBO J. 1993 Aug;12(8):3287-95. doi: 10.1002/j.1460-2075.1993.tb05998.x.
4
Escherichia coli PriA protein is essential for inducible and constitutive stable DNA replication.大肠杆菌PriA蛋白对于诱导型和组成型稳定DNA复制至关重要。
EMBO J. 1994 Nov 15;13(22):5338-45. doi: 10.1002/j.1460-2075.1994.tb06868.x.
5
Roles of ruvA, ruvC and recG gene functions in normal and DNA damage-inducible replication of the Escherichia coli chromosome.ruvA、ruvC和recG基因功能在大肠杆菌染色体正常及DNA损伤诱导复制中的作用
Genetics. 1994 Aug;137(4):895-902. doi: 10.1093/genetics/137.4.895.
6
Ordered and sequential binding of DnaA protein to oriC, the chromosomal origin of Escherichia coli.DnaA蛋白与大肠杆菌染色体复制起点oriC的有序且相继结合。
J Biol Chem. 1996 Jul 19;271(29):17035-40. doi: 10.1074/jbc.271.29.17035.
7
Purified dnaA protein in initiation of replication at the Escherichia coli chromosomal origin of replication.纯化的DnaA蛋白在大肠杆菌染色体复制起点处启动复制过程中的作用。
Proc Natl Acad Sci U S A. 1983 Oct;80(19):5817-21. doi: 10.1073/pnas.80.19.5817.
8
dnaA protein-regulated transcription: effects on the in vitro replication of Escherichia coli minichromosomes.DnaA蛋白调控的转录:对大肠杆菌微型染色体体外复制的影响
EMBO J. 1985 Feb;4(2):555-60. doi: 10.1002/j.1460-2075.1985.tb03664.x.
9
Requirement of RecBC enzyme and an elevated level of activated RecA for induced stable DNA replication in Escherichia coli.RecBC酶的需求以及激活的RecA水平升高对大肠杆菌中诱导的稳定DNA复制的作用
J Bacteriol. 1990 Apr;172(4):1834-9. doi: 10.1128/jb.172.4.1834-1839.1990.
10
The RecF pathway of homologous recombination can mediate the initiation of DNA damage-inducible replication of the Escherichia coli chromosome.同源重组的RecF途径可介导大肠杆菌染色体DNA损伤诱导复制的起始。
J Bacteriol. 1994 Nov;176(22):7113-4. doi: 10.1128/jb.176.22.7113-7114.1994.

引用本文的文献

1
Topo IV is required to allow replisomes to converge and complete replication on the chromosome.拓扑异构酶IV是使复制体在染色体上汇聚并完成复制所必需的。
PLoS Genet. 2025 Sep 8;21(9):e1011857. doi: 10.1371/journal.pgen.1011857. eCollection 2025 Sep.
2
The Roles of Bacterial DNA Double-Strand Break Repair Proteins in Chromosomal DNA Replication.细菌 DNA 双链断裂修复蛋白在染色体 DNA 复制中的作用。
FEMS Microbiol Rev. 2020 May 1;44(3):351-368. doi: 10.1093/femsre/fuaa009.
3
RecBCD, SbcCD and ExoI process a substrate created by convergent replisomes to complete DNA replication.

本文引用的文献

1
INDUCTION OF REPLICATION BY THYMINE STARVATION AT THE CHROMOSOME ORIGIN IN ESCHERICHIA COLI.大肠杆菌中染色体起源处胸腺嘧啶饥饿诱导复制
J Mol Biol. 1964 Aug;9:288-307. doi: 10.1016/s0022-2836(64)80208-4.
2
THE EFFECT OF AMINO ACID DEPRIVATION ON SUBSEQUENT DEOXYRIBONUCLEIC ACID REPLICATION.氨基酸剥夺对后续脱氧核糖核酸复制的影响。
Biochim Biophys Acta. 1963 Sep 17;76:9-24.
3
Thymine deficiency and the normal DNA replication cycle. I.胸腺嘧啶缺乏与正常DNA复制周期。I.
RecBCD、SbcCD 和 ExoI 可处理由两个复制叉引发的底物,以完成 DNA 复制。
Mol Microbiol. 2019 Jun;111(6):1638-1651. doi: 10.1111/mmi.14242. Epub 2019 May 6.
4
RecBCD is required to complete chromosomal replication: Implications for double-strand break frequencies and repair mechanisms.RecBCD蛋白是完成染色体复制所必需的:对双链断裂频率和修复机制的影响。
DNA Repair (Amst). 2015 Aug;32:86-95. doi: 10.1016/j.dnarep.2015.04.018. Epub 2015 May 2.
5
Completion of DNA replication in Escherichia coli.大肠杆菌中DNA复制的完成。
Proc Natl Acad Sci U S A. 2014 Nov 18;111(46):16454-9. doi: 10.1073/pnas.1415025111. Epub 2014 Nov 3.
6
Recombinational repair of DNA damage in Escherichia coli and bacteriophage lambda.大肠杆菌和噬菌体λ中DNA损伤的重组修复
Microbiol Mol Biol Rev. 1999 Dec;63(4):751-813, table of contents. doi: 10.1128/MMBR.63.4.751-813.1999.
7
Double-strand end repair via the RecBC pathway in Escherichia coli primes DNA replication.大肠杆菌中通过RecBC途径进行的双链末端修复引发DNA复制。
Genes Dev. 1999 Feb 1;13(3):345-56. doi: 10.1101/gad.13.3.345.
8
The absence of effect of gid or mioC transcription on the initiation of chromosomal replication in Escherichia coli.gid或mioC转录对大肠杆菌染色体复制起始无影响。
Proc Natl Acad Sci U S A. 1997 Nov 11;94(23):12497-502. doi: 10.1073/pnas.94.23.12497.
9
Stable DNA replication: interplay between DNA replication, homologous recombination, and transcription.稳定的DNA复制:DNA复制、同源重组与转录之间的相互作用
Microbiol Mol Biol Rev. 1997 Jun;61(2):212-38. doi: 10.1128/mmbr.61.2.212-238.1997.
10
DNA polymerase I in constitutive stable DNA replication in Escherichia coli.DNA聚合酶I参与大肠杆菌的组成型稳定DNA复制。
J Bacteriol. 1997 Apr;179(7):2109-15. doi: 10.1128/jb.179.7.2109-2115.1997.
J Mol Biol. 1961 Apr;3:144-55. doi: 10.1016/s0022-2836(61)80041-7.
4
The origin of replication, oriC, and the dnaA protein are dispensable in stable DNA replication (sdrA) mutants of Escherichia coli K-12.在大肠杆菌K-12的稳定DNA复制(sdrA)突变体中,复制起点oriC和DnaA蛋白是可有可无的。
EMBO J. 1983;2(3):463-8. doi: 10.1002/j.1460-2075.1983.tb01445.x.
5
Two alternative mechanisms for initiation of DNA replication forks in bacteriophage T4: priming by RNA polymerase and by recombination.噬菌体T4中DNA复制叉起始的两种替代机制:RNA聚合酶引发和重组引发。
Proc Natl Acad Sci U S A. 1982 Feb;79(4):1101-5. doi: 10.1073/pnas.79.4.1101.
6
The dnaA gene product is not required during stable chromosome replication in Escherichia coli.在大肠杆菌稳定染色体复制过程中,并不需要dnaA基因产物。
Mol Gen Genet. 1980;180(3):617-20. doi: 10.1007/BF00268069.
7
Replication origin of the Escherichia coli K-12 chromosome: the size and structure of the minimum DNA segment carrying the information for autonomous replication.大肠杆菌K-12染色体的复制起点:携带自主复制信息的最小DNA片段的大小和结构
Mol Gen Genet. 1980 Apr;178(1):9-20. doi: 10.1007/BF00267207.
8
Multiple origin usage for DNA replication in sdrA(rnh) mutants of Escherichia coli K-12. Initiation in the absence of oriC.大肠杆菌K-12的sdrA(rnh)突变体中DNA复制的多起点使用。在无oriC情况下的起始。
J Mol Biol. 1984 Sep 15;178(2):227-36. doi: 10.1016/0022-2836(84)90141-4.
9
A third defective lambdoid prophage of Escherichia coli K12 defined by the lambda derivative, lambdaqin111.由λ衍生物λqin111定义的大肠杆菌K12的第三种缺陷性λ样原噬菌体。
J Mol Biol. 1983 Nov 5;170(3):611-33. doi: 10.1016/s0022-2836(83)80124-7.
10
Isolation and properties of Tn10 insertions in the rac locus of Escherichia coli.大肠杆菌rac基因座中Tn10插入片段的分离与特性
Mol Gen Genet. 1981;183(2):333-40. doi: 10.1007/BF00270637.