• 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

大肠杆菌中应对染色体过度复制的生存对策。

Countermeasures to survive excessive chromosome replication in Escherichia coli.

作者信息

Charbon Godefroid, Riber Leise, Løbner-Olesen Anders

机构信息

Department of Biology, University of Copenhagen, Ole Maaløes Vej 5, 2200, Copenhagen N, Denmark.

出版信息

Curr Genet. 2018 Feb;64(1):71-79. doi: 10.1007/s00294-017-0725-4. Epub 2017 Jun 29.

DOI:10.1007/s00294-017-0725-4
PMID:28664289
Abstract

In Escherichia coli, like all organisms, DNA replication is coordinated with cell cycle progression to ensure duplication of the genome prior to cell division. Chromosome replication is initiated from the replication origin, oriC, by the DnaA protein associated with ATP. Initiations take place once per cell cycle and in synchrony at all cellular origins. DnaA also binds ADP with similar affinity as ATP and in wild-type cells the majority of DnaA molecules are ADP bound. In cells where the DnaA/DnaA ratio increases or in cells where DnaA has increased access to oriC, premature initiations take place, often referred to as overinitiation. Overinitiating cells are generally characterized by their slow growth and in the most severe cases lethal accumulation of DNA strand breaks. Here, we review the different strategies adopted by E. coli to survive overinitiation. We propose a unifying model where all mutations that suppress overinitiation keep replication forks separated in time and, thereby, reduce the formation of strand breaks. One group of mutations does so by lowering the activity of oriC and/or DnaA to reduce the frequency of initiations to an acceptable level. In the other group of mutations, replication forks are kept apart by preventing formation of damages that would otherwise cause replication blocks, by allowing bypass of replication blocks and/or by slowing down replication forks. This group of suppressors restores viability despite excessive chromosome replication and provides new insights into mechanisms that safeguard DNA integrity.

摘要

在大肠杆菌中,与所有生物体一样,DNA复制与细胞周期进程相协调,以确保在细胞分裂之前基因组得以复制。染色体复制由与ATP结合的DnaA蛋白从复制起点oriC起始。每个细胞周期起始事件发生一次,且在所有细胞起点同步进行。DnaA还能以与ATP相似的亲和力结合ADP,在野生型细胞中,大多数DnaA分子结合的是ADP。在DnaA/DnaA比值增加的细胞中,或者在DnaA更容易接近oriC的细胞中,会发生过早起始,通常称为过度起始。过度起始的细胞通常生长缓慢,在最严重的情况下,DNA链断裂会致命性累积。在此,我们综述了大肠杆菌为在过度起始情况下存活所采取的不同策略。我们提出了一个统一模型,即所有抑制过度起始的突变都会使复制叉在时间上保持分离,从而减少链断裂的形成。一组突变通过降低oriC和/或DnaA的活性来实现这一点,将起始频率降低到可接受的水平。在另一组突变中,通过防止形成否则会导致复制停滞的损伤、允许绕过复制停滞和/或减缓复制叉,使复制叉保持分开。尽管染色体复制过度,这组抑制子仍能恢复细胞活力,并为保障DNA完整性的机制提供了新的见解。

相似文献

1
Countermeasures to survive excessive chromosome replication in Escherichia coli.大肠杆菌中应对染色体过度复制的生存对策。
Curr Genet. 2018 Feb;64(1):71-79. doi: 10.1007/s00294-017-0725-4. Epub 2017 Jun 29.
2
Suppressors of DnaA(ATP) imposed overinitiation in Escherichia coli.抑制物 DnaA(ATP) 在大肠杆菌中引发起始。
Mol Microbiol. 2011 Feb;79(4):914-28. doi: 10.1111/j.1365-2958.2010.07493.x. Epub 2010 Dec 19.
3
Re-wiring of energy metabolism promotes viability during hyperreplication stress in E. coli.能量代谢的重新布线促进了大肠杆菌在超复制应激期间的生存能力。
PLoS Genet. 2017 Jan 27;13(1):e1006590. doi: 10.1371/journal.pgen.1006590. eCollection 2017 Jan.
4
Coordinated replication and sequestration of oriC and dnaA are required for maintaining controlled once-per-cell-cycle initiation in Escherichia coli.在大肠杆菌中,oriC和dnaA的协同复制与隔离是维持每个细胞周期仅起始一次的控制所必需的。
J Bacteriol. 2005 Aug;187(16):5605-13. doi: 10.1128/JB.187.16.5605-5613.2005.
5
Thymineless Death in Is Unaffected by Chromosomal Replication Complexity.胸腺嘧啶缺乏致死不受染色体复制复合体复杂性的影响。
J Bacteriol. 2019 Apr 9;201(9). doi: 10.1128/JB.00797-18. Print 2019 May 1.
6
Negative control of DNA replication by hydrolysis of ATP bound to DnaA protein, the initiator of chromosomal DNA replication in Escherichia coli.通过水解与DnaA蛋白结合的ATP对DNA复制进行负调控,DnaA蛋白是大肠杆菌中染色体DNA复制的起始因子。
EMBO J. 1997 Jun 16;16(12):3724-30. doi: 10.1093/emboj/16.12.3724.
7
Suppression of temperature-sensitive chromosome replication of an Escherichia coli dnaX(Ts) mutant by reduction of initiation efficiency.通过降低起始效率抑制大肠杆菌 dnaX(Ts) 突变体的温度敏感型染色体复制。
J Bacteriol. 2003 Jun;185(12):3583-95. doi: 10.1128/JB.185.12.3583-3595.2003.
8
Robust control of initiation of prokaryotic chromosome replication: essential considerations for a minimal cell.原核生物染色体复制起始的稳健控制:最小细胞的基本考量
Biotechnol Bioeng. 2004 Dec 5;88(5):575-84. doi: 10.1002/bit.20223.
9
Overproduction of DnaA protein stimulates initiation of chromosome and minichromosome replication in Escherichia coli.DnaA蛋白的过量产生会刺激大肠杆菌中染色体和微型染色体复制的起始。
Mol Gen Genet. 1987 Jan;206(1):51-9. doi: 10.1007/BF00326535.
10
Low Affinity DnaA-ATP Recognition Sites in Make Non-equivalent and Growth Rate-Dependent Contributions to the Regulated Timing of Chromosome Replication.基因组中低亲和力的DnaA-ATP识别位点对染色体复制的调控时间做出了不等同且依赖生长速率的贡献。
Front Microbiol. 2018 Jul 26;9:1673. doi: 10.3389/fmicb.2018.01673. eCollection 2018.

引用本文的文献

1
Targeting synthesis of the Chromosome Replication Initiator Protein DnaA by antisense PNA-peptide conjugates in .通过反义肽核酸-肽缀合物靶向合成染色体复制起始蛋白DnaA 于……中
Front Antibiot. 2024 Apr 8;3:1384390. doi: 10.3389/frabi.2024.1384390. eCollection 2024.
2
Open Questions about the Roles of DnaA, Related Proteins, and Hyperstructure Dynamics in the Cell Cycle.关于DnaA、相关蛋白以及超结构动力学在细胞周期中作用的开放性问题。
Life (Basel). 2023 Sep 10;13(9):1890. doi: 10.3390/life13091890.
3
Multiple mechanisms for overcoming lethal over-initiation of DNA replication.

本文引用的文献

1
Invariance of Initiation Mass and Predictability of Cell Size in Escherichia coli.大肠杆菌中起始质量的不变性和细胞大小的可预测性。
Curr Biol. 2017 May 8;27(9):1278-1287. doi: 10.1016/j.cub.2017.03.022. Epub 2017 Apr 13.
2
Insufficient levels of the nrdAB-encoded ribonucleotide reductase underlie the severe growth defect of the Δhda E. coli strain.由nrdAB编码的核糖核苷酸还原酶水平不足是Δhda大肠杆菌菌株严重生长缺陷的根本原因。
Mol Microbiol. 2017 May;104(3):377-399. doi: 10.1111/mmi.13632. Epub 2017 Mar 13.
3
Re-wiring of energy metabolism promotes viability during hyperreplication stress in E. coli.
克服 DNA 复制起始致死的多种机制。
Mol Microbiol. 2022 Oct;118(4):426-442. doi: 10.1111/mmi.14976. Epub 2022 Sep 11.
4
Single-Molecule Insights Into the Dynamics of Replicative Helicases.对复制解旋酶动力学的单分子见解
Front Mol Biosci. 2021 Aug 26;8:741718. doi: 10.3389/fmolb.2021.741718. eCollection 2021.
5
Arresting chromosome replication upon energy starvation in Escherichia coli.在大肠杆菌中,能量饥饿时染色体复制被抑制。
Curr Genet. 2021 Dec;67(6):877-882. doi: 10.1007/s00294-021-01202-2. Epub 2021 Aug 3.
6
HdaB: a novel and conserved DnaA-related protein that targets the RIDA process to stimulate replication initiation.HdaB:一种新型且保守的 DnaA 相关蛋白,可将 RIDA 过程作为靶标来刺激复制起始。
Nucleic Acids Res. 2020 Mar 18;48(5):2412-2423. doi: 10.1093/nar/gkz1193.
7
Nucleoid-mediated positioning and transport in bacteria.细菌中拟核介导的定位和运输。
Curr Genet. 2020 Apr;66(2):279-291. doi: 10.1007/s00294-019-01041-2. Epub 2019 Nov 5.
8
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.
9
Coping with Reactive Oxygen Species to Ensure Genome Stability in .应对活性氧以确保……中的基因组稳定性
Genes (Basel). 2018 Nov 21;9(11):565. doi: 10.3390/genes9110565.
10
Iron chelation increases the tolerance of Escherichia coli to hyper-replication stress.铁螯合作用提高了大肠杆菌对过度复制压力的耐受性。
Sci Rep. 2018 Jul 12;8(1):10550. doi: 10.1038/s41598-018-28841-9.
能量代谢的重新布线促进了大肠杆菌在超复制应激期间的生存能力。
PLoS Genet. 2017 Jan 27;13(1):e1006590. doi: 10.1371/journal.pgen.1006590. eCollection 2017 Jan.
4
Control of bacterial chromosome replication by non-coding regions outside the origin.通过复制起点以外的非编码区域控制细菌染色体复制
Curr Genet. 2017 Aug;63(4):607-611. doi: 10.1007/s00294-016-0671-6. Epub 2016 Dec 9.
5
DNA Replication Control Is Linked to Genomic Positioning of Control Regions in Escherichia coli.DNA复制控制与大肠杆菌中控制区域的基因组定位相关。
PLoS Genet. 2016 Sep 2;12(9):e1006286. doi: 10.1371/journal.pgen.1006286. eCollection 2016 Sep.
6
Chromosomal location of the DnaA-reactivating sequence DARS2 is important to regulate timely initiation of DNA replication in Escherichia coli.DnaA 激活序列 DARS2 的染色体定位对于调控大肠杆菌中 DNA 复制的适时起始很重要。
Genes Cells. 2016 Sep;21(9):1015-23. doi: 10.1111/gtc.12395. Epub 2016 Jul 25.
7
Multiple DNA Binding Proteins Contribute to Timing of Chromosome Replication in E. coli.多种 DNA 结合蛋白有助于大肠杆菌中染色体的复制定时。
Front Mol Biosci. 2016 Jun 28;3:29. doi: 10.3389/fmolb.2016.00029. eCollection 2016.
8
The Escherichia coli Cryptic Prophage Protein YfdR Binds to DnaA and Initiation of Chromosomal Replication Is Inhibited by Overexpression of the Gene Cluster yfdQ-yfdR-yfdS-yfdT.大肠杆菌隐蔽前噬菌体蛋白YfdR与DnaA结合,基因簇yfdQ - yfdR - yfdS - yfdT的过表达会抑制染色体复制的起始。
Front Microbiol. 2016 Mar 3;7:239. doi: 10.3389/fmicb.2016.00239. eCollection 2016.
9
Single-strand gap repair involves both RecF and RecBCD pathways.单链缺口修复涉及RecF和RecBCD两条途径。
Curr Genet. 2016 Aug;62(3):519-21. doi: 10.1007/s00294-016-0575-5. Epub 2016 Feb 13.
10
A balanced perspective on unbalanced growth and thymineless death.关于不平衡生长和胸腺嘧啶饥饿死亡的平衡观点。
Front Microbiol. 2015 Jun 5;6:504. doi: 10.3389/fmicb.2015.00504. eCollection 2015.