• 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

由解离酶确定的转座子靶向

Transposon targeting determined by resolvase.

作者信息

Kamali-Moghaddam M, Sundström L

机构信息

Department of Pharmaceutical Biosciences, Division of Microbiology, Uppsala University, Biomedicum, SE-751 23, Uppsala, Sweden.

出版信息

FEMS Microbiol Lett. 2000 May 1;186(1):55-9. doi: 10.1111/j.1574-6968.2000.tb09081.x.

DOI:10.1111/j.1574-6968.2000.tb09081.x
PMID:10779712
Abstract

The Mu-related transposon Tn5090, also called Tn402, was observed to be highly selective for targets clustered in or close to recombination sites of serine-type recombinases in plasmids R388 and RP1. Transposition to the par area of RP1 responded strongly to a deletion in the gene of resolvase ParA. A search in sequence databanks revealed further insertions of Tn5090/Tn402 close to different genes of resolvases. These results imply that the target selection of Tn5090 depends on a property that is shared among several serine recombinases.

摘要

与Mu相关的转座子Tn5090,也称为Tn402,被观察到对聚集在质粒R388和RP1中丝氨酸型重组酶的重组位点内或附近的靶标具有高度选择性。向RP1的par区域转座对解离酶ParA基因中的缺失有强烈反应。在序列数据库中搜索发现Tn5090/Tn402在解离酶的不同基因附近有进一步插入。这些结果表明Tn5090的靶标选择取决于几种丝氨酸重组酶共有的一种特性。

相似文献

1
Transposon targeting determined by resolvase.由解离酶确定的转座子靶向
FEMS Microbiol Lett. 2000 May 1;186(1):55-9. doi: 10.1111/j.1574-6968.2000.tb09081.x.
2
Transposon Tn5090 of plasmid R751, which carries an integron, is related to Tn7, Mu, and the retroelements.携带整合子的质粒R751的转座子Tn5090与Tn7、Mu及逆转录元件相关。
J Bacteriol. 1994 Jun;176(11):3257-68. doi: 10.1128/jb.176.11.3257-3268.1994.
3
Tn5053 family transposons are res site hunters sensing plasmidal res sites occupied by cognate resolvases.Tn5053家族转座子是寻找质粒上同源解离酶占据的res位点的res位点猎手。
Mol Microbiol. 1999 Sep;33(5):1059-68. doi: 10.1046/j.1365-2958.1999.01548.x.
4
The resolvase encoded by Xanthomonas campestris transposable element ISXc5 constitutes a new subfamily closely related to DNA invertases.由野油菜黄单胞菌转座元件ISXc5编码的解离酶构成了一个与DNA转化酶密切相关的新亚家族。
Genes Cells. 1998 Apr;3(4):221-33. doi: 10.1046/j.1365-2443.1998.00182.x.
5
Stability by multimer resolution of pJHCMW1 is due to the Tn1331 resolvase and not to the Escherichia coli Xer system.pJHCMW1通过多聚体解离实现的稳定性归因于Tn1331解离酶,而非大肠杆菌Xer系统。
Microbiology (Reading). 2000 Mar;146 ( Pt 3):581-589. doi: 10.1099/00221287-146-3-581.
6
Transposition of Tn4451 and Tn4453 involves a circular intermediate that forms a promoter for the large resolvase, TnpX.Tn4451和Tn4453的转座涉及一个环状中间体,该中间体形成了大型解离酶TnpX的启动子。
Mol Microbiol. 2000 Nov;38(3):588-601. doi: 10.1046/j.1365-2958.2000.02154.x.
7
The large resolvase TndX is required and sufficient for integration and excision of derivatives of the novel conjugative transposon Tn5397.大型解离酶TndX对于新型接合转座子Tn5397衍生物的整合和切除是必需的且足够的。
J Bacteriol. 2000 Dec;182(23):6577-83. doi: 10.1128/JB.182.23.6577-6583.2000.
8
Chimeric recombinases with designed DNA sequence recognition.具有设计的DNA序列识别功能的嵌合重组酶。
Proc Natl Acad Sci U S A. 2003 Jul 22;100(15):8688-91. doi: 10.1073/pnas.1533177100. Epub 2003 Jul 1.
9
Mutants of Tn3 resolvase which do not require accessory binding sites for recombination activity.Tn3 解离酶的突变体,其重组活性不需要辅助结合位点。
EMBO J. 1999 Mar 1;18(5):1407-14. doi: 10.1093/emboj/18.5.1407.
10
Arrayed transposase-binding sequences on the ends of transposon Tn5090/Tn402.转座子Tn5090/Tn402末端的阵列转座酶结合序列。
Nucleic Acids Res. 2001 Feb 15;29(4):1005-11. doi: 10.1093/nar/29.4.1005.

引用本文的文献

1
Restoration and functional analysis of the SGI1 resolution system - SGI1 multimers are eliminated by the reactivated resolution.SGI1 解离系统的恢复与功能分析 - 重新激活的解离作用可消除 SGI1 多聚体。
Sci Rep. 2025 Jul 1;15(1):20550. doi: 10.1038/s41598-025-06025-6.
2
A programmable seekRNA guides target selection by IS1111 and IS110 type insertion sequences.可编程的 seekRNA 通过 IS1111 和 IS110 型插入序列引导目标选择。
Nat Commun. 2024 Jun 19;15(1):5235. doi: 10.1038/s41467-024-49474-9.
3
Tn, a Carrier of Tn Family Transposons, Occurs in the Chromosome and in a Genomic Island of Clinical Strains.
Tn,Tn家族转座子的载体,存在于临床菌株的染色体和一个基因组岛中。
Microorganisms. 2020 Dec 15;8(12):1997. doi: 10.3390/microorganisms8121997.
4
Tn6249, a new Tn6162 transposon derivative carrying a double-integron platform and involved with acquisition of the blaVIM-1 metallo-β-lactamase gene in Pseudomonas aeruginosa.Tn6249,一种新型Tn6162转座子衍生物,携带双整合子平台,与铜绿假单胞菌中blaVIM-1金属β-内酰胺酶基因的获得有关。
Antimicrob Agents Chemother. 2015 Mar;59(3):1583-7. doi: 10.1128/AAC.04047-14. Epub 2014 Dec 29.
5
IMP-1 encoded by a novel Tn402-like class 1 integron in clinical Achromobacter xylosoxidans, China.中国临床木糖氧化无色杆菌中由一种新型Tn402样1类整合子编码的IMP-1
Sci Rep. 2014 Nov 27;4:7212. doi: 10.1038/srep07212.
6
The complete nucleotide sequence of the carbapenem resistance-conferring conjugative plasmid pLD209 from a Pseudomonas putida clinical strain reveals a chimeric design formed by modules derived from both environmental and clinical bacteria.来自恶臭假单胞菌临床菌株的携带碳青霉烯抗性的接合质粒pLD209的完整核苷酸序列揭示了一种嵌合结构,该结构由源自环境细菌和临床细菌的模块组成。
Antimicrob Agents Chemother. 2014;58(3):1816-21. doi: 10.1128/AAC.02494-13. Epub 2014 Jan 6.
7
Molecular characterization of blaNDM-1 in a sequence type 235 Pseudomonas aeruginosa isolate from France.法国分离的一株 235 型铜绿假单胞菌携带 blaNDM-1 的分子特征。
Antimicrob Agents Chemother. 2013 Jul;57(7):3408-11. doi: 10.1128/AAC.02334-12. Epub 2013 Apr 22.
8
Integrons: Vehicles and pathways for horizontal dissemination in bacteria.整合子:细菌中水平传播的载体与途径
Mob Genet Elements. 2012 Sep 1;2(5):211-223. doi: 10.4161/mge.22967.
9
pJIE137 carrying blaCTX-M-62 is closely related to p271A carrying blaNDM-1.携带 blaCTX-M-62 的 pJIE137 与携带 blaNDM-1 的 p271A 密切相关。
Antimicrob Agents Chemother. 2012 Apr;56(4):2166-8. doi: 10.1128/AAC.05796-11. Epub 2012 Jan 17.
10
Tn502 and Tn512 are res site hunters that provide evidence of resolvase-independent transposition to random sites.Tn502 和 Tn512 是 res 位点猎手,它们为可在随机位点发生的、不依赖于切离酶的转座提供了证据。
J Bacteriol. 2010 Apr;192(7):1865-74. doi: 10.1128/JB.01322-09. Epub 2010 Jan 29.