• 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

KOPS:通过定向FtsK转位酶来控制大肠杆菌染色体分离的DNA基序。

KOPS: DNA motifs that control E. coli chromosome segregation by orienting the FtsK translocase.

作者信息

Bigot Sarah, Saleh Omar A, Lesterlin Christian, Pages Carine, El Karoui Meriem, Dennis Cynthia, Grigoriev Mikhail, Allemand Jean-François, Barre François-Xavier, Cornet François

机构信息

LMGM, CNRS, 118, route de Narbonne, Toulouse, France.

出版信息

EMBO J. 2005 Nov 2;24(21):3770-80. doi: 10.1038/sj.emboj.7600835. Epub 2005 Oct 6.

DOI:10.1038/sj.emboj.7600835
PMID:16211009
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1276719/
Abstract

Bacterial chromosomes are organized in replichores of opposite sequence polarity. This conserved feature suggests a role in chromosome dynamics. Indeed, sequence polarity controls resolution of chromosome dimers in Escherichia coli. Chromosome dimers form by homologous recombination between sister chromosomes. They are resolved by the combined action of two tyrosine recombinases, XerC and XerD, acting at a specific chromosomal site, dif, and a DNA translocase, FtsK, which is anchored at the division septum and sorts chromosomal DNA to daughter cells. Evidences suggest that DNA motifs oriented from the replication origin towards dif provide FtsK with the necessary information to faithfully distribute chromosomal DNA to either side of the septum, thereby bringing the dif sites together at the end of this process. However, the nature of the DNA motifs acting as FtsK orienting polar sequences (KOPS) was unknown. Using genetics, bioinformatics and biochemistry, we have identified a family of DNA motifs in the E. coli chromosome with KOPS activity.

摘要

细菌染色体以相反序列极性的复制子形式组织。这一保守特征表明其在染色体动态变化中发挥作用。事实上,序列极性控制大肠杆菌中染色体二聚体的解离。染色体二聚体通过姐妹染色体之间的同源重组形成。它们通过两种酪氨酸重组酶XerC和XerD在特定染色体位点dif的联合作用以及一种DNA转位酶FtsK来解离,FtsK锚定在分裂隔膜上并将染色体DNA分配到子细胞中。有证据表明,从复制起点朝向dif的DNA基序为FtsK提供了必要信息,使其能够将染色体DNA忠实地分配到隔膜两侧,从而在此过程结束时将dif位点聚集在一起。然而,作为FtsK定向极性序列(KOPS)的DNA基序的性质尚不清楚。通过遗传学、生物信息学和生物化学方法,我们在大肠杆菌染色体中鉴定出了具有KOPS活性的一类DNA基序。

相似文献

1
KOPS: DNA motifs that control E. coli chromosome segregation by orienting the FtsK translocase.KOPS:通过定向FtsK转位酶来控制大肠杆菌染色体分离的DNA基序。
EMBO J. 2005 Nov 2;24(21):3770-80. doi: 10.1038/sj.emboj.7600835. Epub 2005 Oct 6.
2
FtsK, a literate chromosome segregation machine.FtsK,一种有读写能力的染色体分离机器。
Mol Microbiol. 2007 Jun;64(6):1434-41. doi: 10.1111/j.1365-2958.2007.05755.x. Epub 2007 May 18.
3
Oriented loading of FtsK on KOPS.FtsK在KOPS上的定向加载。
Nat Struct Mol Biol. 2006 Nov;13(11):1026-8. doi: 10.1038/nsmb1159. Epub 2006 Oct 15.
4
FtsK actively segregates sister chromosomes in Escherichia coli.FtsK 在大肠杆菌中积极分离姐妹染色体。
Proc Natl Acad Sci U S A. 2013 Jul 2;110(27):11157-62. doi: 10.1073/pnas.1304080110. Epub 2013 Jun 18.
5
Extent of the activity domain and possible roles of FtsK in the Escherichia coli chromosome terminus.FtsK在大肠杆菌染色体末端的活性结构域范围及可能作用
Mol Microbiol. 2005 Jun;56(6):1539-48. doi: 10.1111/j.1365-2958.2005.04633.x.
6
KOPS-guided DNA translocation by FtsK safeguards Escherichia coli chromosome segregation.由FtsK引导的KOPS介导的DNA易位保障了大肠杆菌染色体的分离。
Mol Microbiol. 2009 Feb;71(4):1031-42. doi: 10.1111/j.1365-2958.2008.06586.x. Epub 2009 Jan 1.
7
Delayed activation of Xer recombination at dif by FtsK during septum assembly in Escherichia coli.在大肠杆菌隔膜组装过程中,FtsK在dif位点对Xer重组的延迟激活。
Mol Microbiol. 2008 May;68(4):1018-28. doi: 10.1111/j.1365-2958.2008.06212.x. Epub 2008 Mar 19.
8
FtsK-dependent dimer resolution on multiple chromosomes in the pathogen Vibrio cholerae.霍乱弧菌病原体中依赖FtsK的多染色体上的二聚体解离
PLoS Genet. 2008 Sep 26;4(9):e1000201. doi: 10.1371/journal.pgen.1000201.
9
A defined terminal region of the E. coli chromosome shows late segregation and high FtsK activity.大肠杆菌染色体的定义末端区域表现出晚期分离和高 FtsK 活性。
PLoS One. 2011;6(7):e22164. doi: 10.1371/journal.pone.0022164. Epub 2011 Jul 20.
10
FtsK-dependent and -independent pathways of Xer site-specific recombination.Xer位点特异性重组的FtsK依赖性和非依赖性途径。
EMBO J. 1999 Oct 15;18(20):5724-34. doi: 10.1093/emboj/18.20.5724.

引用本文的文献

1
Linear dicentric chromosomes in bacterial natural isolates reveal common constraints for replicon fusion.细菌自然分离株中的线性双着丝粒染色体揭示了复制子融合的常见限制因素。
mBio. 2025 Jun 11;16(6):e0104625. doi: 10.1128/mbio.01046-25. Epub 2025 May 20.
2
Early onset of septal FtsK localization allows for efficient DNA segregation in SMC-deleted strains.隔膜FtsK定位的早期发生允许在SMC缺失菌株中进行有效的DNA分离。
mBio. 2025 Mar 12;16(3):e0285924. doi: 10.1128/mbio.02859-24. Epub 2025 Jan 28.
3
Interplay between the Xer recombination system and the dissemination of antibioresistance in Acinetobacter baumannii.鲍曼不动杆菌中Xer重组系统与抗生素耐药性传播之间的相互作用。
Nucleic Acids Res. 2025 Jan 7;53(1). doi: 10.1093/nar/gkae1255.
4
MatP local enrichment delays segregation independently of tetramer formation and septal anchoring in Vibrio cholerae.MatP 局部富集可独立于四聚体形成和隔膜锚定延迟霍乱弧菌的分离。
Nat Commun. 2024 Nov 15;15(1):9893. doi: 10.1038/s41467-024-54195-0.
5
Chromosome architecture as a determinant for biosynthetic diversity in .作为生物合成多样性决定因素的染色体结构
Microb Genom. 2024 Nov;10(11). doi: 10.1099/mgen.0.001313.
6
Spatio-temporal organization of the chromosome from base to cellular length scales.从碱基到细胞长度尺度的染色体时空组织。
EcoSal Plus. 2024 Dec 12;12(1):eesp00012022. doi: 10.1128/ecosalplus.esp-0001-2022. Epub 2024 Jun 12.
7
Plasticity in the cell division processes of obligate intracellular bacteria.必需内共生菌的细胞分裂过程中的可塑性。
Front Cell Infect Microbiol. 2023 Oct 9;13:1205488. doi: 10.3389/fcimb.2023.1205488. eCollection 2023.
8
Interplay between chromosomal architecture and termination of DNA replication in bacteria.细菌中染色体结构与DNA复制终止之间的相互作用。
Front Microbiol. 2023 Jun 26;14:1180848. doi: 10.3389/fmicb.2023.1180848. eCollection 2023.
9
DNA Segregation in Enterobacteria.肠杆菌中的DNA分离
EcoSal Plus. 2023 Dec 12;11(1):eesp00382020. doi: 10.1128/ecosalplus.esp-0038-2020. Epub 2023 May 9.
10
Role for DNA double strand end-resection activity of RecBCD in control of aberrant chromosomal replication initiation in Escherichia coli.RecBCD 在控制大肠杆菌异常染色体复制起始中的 DNA 双链末端切除活性的作用。
Nucleic Acids Res. 2022 Aug 26;50(15):8643-8657. doi: 10.1093/nar/gkac670.

本文引用的文献

1
Dancing around the divisome: asymmetric chromosome segregation in Escherichia coli.围绕分裂体翩翩起舞:大肠杆菌中的不对称染色体分离
Genes Dev. 2005 Oct 1;19(19):2367-77. doi: 10.1101/gad.345305.
2
Roles for replichores and macrodomains in segregation of the Escherichia coli chromosome.复制子和宏观结构域在大肠杆菌染色体分离中的作用。
EMBO Rep. 2005 Jun;6(6):557-62. doi: 10.1038/sj.embor.7400428.
3
Analysis of DNA supercoil induction by FtsK indicates translocation without groove-tracking.FtsK对DNA超螺旋诱导的分析表明其易位过程中不存在沟追踪现象。
Nat Struct Mol Biol. 2005 May;12(5):436-40. doi: 10.1038/nsmb926. Epub 2005 Apr 10.
4
Sequence-directed DNA translocation by purified FtsK.纯化的FtsK介导的序列导向DNA易位
Science. 2005 Jan 28;307(5709):586-90. doi: 10.1126/science.1104885.
5
Genetic recombination and the cell cycle: what we have learned from chromosome dimers.基因重组与细胞周期:我们从染色体二聚体中学到的知识。
Mol Microbiol. 2004 Dec;54(5):1151-60. doi: 10.1111/j.1365-2958.2004.04356.x.
6
FtsK activities in Xer recombination, DNA mobilization and cell division involve overlapping and separate domains of the protein.FtsK在Xer重组、DNA转移和细胞分裂中的活性涉及该蛋白质的重叠和独立结构域。
Mol Microbiol. 2004 Nov;54(4):876-86. doi: 10.1111/j.1365-2958.2004.04335.x.
7
Twin DNA pumps of a hexameric helicase provide power to simultaneously melt two duplexes.六聚体解旋酶的双DNA泵提供动力以同时解开两条双链。
Mol Cell. 2004 Aug 13;15(3):453-65. doi: 10.1016/j.molcel.2004.06.039.
8
Fast, DNA-sequence independent translocation by FtsK in a single-molecule experiment.在单分子实验中,FtsK介导的快速、不依赖DNA序列的易位。
EMBO J. 2004 Jun 16;23(12):2430-9. doi: 10.1038/sj.emboj.7600242. Epub 2004 May 27.
9
Asymmetric activation of Xer site-specific recombination by FtsK.FtsK对Xer位点特异性重组的不对称激活
EMBO Rep. 2004 Apr;5(4):399-404. doi: 10.1038/sj.embor.7400116.
10
Decatenation of DNA circles by FtsK-dependent Xer site-specific recombination.通过FtsK依赖的Xer位点特异性重组解开DNA环。
EMBO J. 2003 Dec 1;22(23):6399-407. doi: 10.1093/emboj/cdg589.