• 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FIS蛋白通过阻遏物参与噬菌体μ溶原性的维持:早期转录的控制和转座的抑制

Involvement of Escherichia coli FIS protein in maintenance of bacteriophage mu lysogeny by the repressor: control of early transcription and inhibition of transposition.

作者信息

Bétermier M, Poquet I, Alazard R, Chandler M

机构信息

Molecular Genetics and Microbiology Laboratory, Centre National de la Recherche Scientifique UPR 9007, Toulouse, France.

出版信息

J Bacteriol. 1993 Jun;175(12):3798-811. doi: 10.1128/jb.175.12.3798-3811.1993.

DOI:10.1128/jb.175.12.3798-3811.1993
PMID:8389742
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC204797/
Abstract

The Escherichia coli FIS (factor for inversion stimulation) protein has been implicated in assisting bacteriophage Mu repressor, c, in maintaining the lysogenic state under certain conditions. In a fis strain, a temperature-inducible Mucts62 prophage is induced at lower temperatures than in a wild-type host (M. Bétermier, V. Lefrère, C. Koch, R. Alazard, and M. Chandler, Mol. Microbiol. 3:459-468, 1989). Increasing the prophage copy number rendered Mucts62 less sensitive to this effect of the fis mutation, which thus seems to depend critically on the level of repressor activity. The present study also provides evidence that FIS affects the control of Mu gene expression and transposition. As judged by the use of lac transcriptional fusions, repression of early transcription was reduced three- to fourfold in a fis background, and this could be compensated by an increase in cts62 gene copy number. c was also shown to inhibit Mu transposition two- to fourfold less strongly in a fis host. These modulatory effects, however, could not be correlated to sequence-specific binding of FIS to the Mu genome, in particular to the strong site previously identified on the left end. We therefore speculate that a more general function of FIS is responsible for the observed modulation of Mu lysogeny.

摘要

大肠杆菌FIS(反转刺激因子)蛋白在某些条件下参与协助噬菌体Mu阻遏物c维持溶原状态。在fis菌株中,温度诱导型Mucts62原噬菌体在比野生型宿主更低的温度下被诱导(M. 贝泰米尔、V. 勒弗雷尔、C. 科赫、R. 阿拉扎德和M. 钱德勒,《分子微生物学》3:459 - 468,1989年)。增加原噬菌体拷贝数使Mucts62对fis突变的这种效应不那么敏感,因此这似乎严重依赖于阻遏物活性水平。本研究还提供证据表明FIS影响Mu基因表达和转座的控制。通过使用lac转录融合判断,在fis背景下早期转录的抑制降低了三到四倍,这可以通过增加cts62基因拷贝数来补偿。还表明在fis宿主中,c抑制Mu转座的强度也降低了两到四倍。然而,这些调节作用与FIS与Mu基因组的序列特异性结合无关,特别是与先前在左端鉴定出的强位点无关。因此,我们推测FIS的一个更普遍的功能负责观察到的对Mu溶原性的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8cb/204797/fb36ee89e99f/jbacter00054-0122-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8cb/204797/1b1c7f09c955/jbacter00054-0118-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8cb/204797/2b1941211ee4/jbacter00054-0120-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8cb/204797/734bc12c390d/jbacter00054-0121-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8cb/204797/6efe6211f81b/jbacter00054-0121-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8cb/204797/fb36ee89e99f/jbacter00054-0122-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8cb/204797/1b1c7f09c955/jbacter00054-0118-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8cb/204797/2b1941211ee4/jbacter00054-0120-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8cb/204797/734bc12c390d/jbacter00054-0121-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8cb/204797/6efe6211f81b/jbacter00054-0121-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8cb/204797/fb36ee89e99f/jbacter00054-0122-a.jpg

相似文献

1
Involvement of Escherichia coli FIS protein in maintenance of bacteriophage mu lysogeny by the repressor: control of early transcription and inhibition of transposition.大肠杆菌FIS蛋白通过阻遏物参与噬菌体μ溶原性的维持:早期转录的控制和转座的抑制
J Bacteriol. 1993 Jun;175(12):3798-811. doi: 10.1128/jb.175.12.3798-3811.1993.
2
Inhibition of bacteriophage Mu transposition by Mu repressor and Fis.Mu阻遏蛋白和Fis对噬菌体Mu转座的抑制作用
Mol Microbiol. 1993 Oct;10(2):293-8. doi: 10.1111/j.1365-2958.1993.tb01955.x.
3
Starvation-induced Mucts62-mediated coding sequence fusion: a role for ClpXP, Lon, RpoS and Crp.饥饿诱导的Mucts62介导的编码序列融合:ClpXP、Lon、RpoS和Crp的作用
Mol Microbiol. 1999 Apr;32(2):327-43. doi: 10.1046/j.1365-2958.1999.01352.x.
4
Escherichia coli Fis and DnaA proteins bind specifically to the nrd promoter region and affect expression of an nrd-lac fusion.大肠杆菌Fis蛋白和DnaA蛋白特异性结合到nrd启动子区域,并影响nrd - lac融合基因的表达。
J Bacteriol. 1994 Jan;176(2):378-87. doi: 10.1128/jb.176.2.378-387.1994.
5
Involvement of FIS in the H-NS-mediated regulation of virF gene of Shigella and enteroinvasive Escherichia coli.FIS参与H-NS介导的志贺氏菌和肠侵袭性大肠杆菌virF基因的调控。
Mol Microbiol. 2001 Oct;42(2):439-52. doi: 10.1046/j.1365-2958.2001.02646.x.
6
Integration host factor activates the Ner-repressed early promoter of transposable Mu-like phage D108.整合宿主因子激活了转座子类Mu噬菌体D108中被Ner抑制的早期启动子。
J Biol Chem. 1992 Sep 5;267(25):17827-35.
7
Influence of FIS on the transcription from closely spaced and non-overlapping divergent promoters for an aminoacyl-tRNA synthetase gene (gltX) and a tRNA operon (valU) in Escherichia coli.FIS对大肠杆菌中一个氨酰基-tRNA合成酶基因(gltX)和一个tRNA操纵子(valU)紧密间隔且不重叠的反向启动子转录的影响。
Mol Microbiol. 1998 Mar;27(6):1141-56. doi: 10.1046/j.1365-2958.1998.00745.x.
8
Fis, an accessorial factor for transcriptional activation of the mar (multiple antibiotic resistance) promoter of Escherichia coli in the presence of the activator MarA, SoxS, or Rob.Fis是在存在激活剂MarA、SoxS或Rob的情况下,大肠杆菌mar(多重抗生素抗性)启动子转录激活的辅助因子。
J Bacteriol. 1997 Dec;179(23):7410-9. doi: 10.1128/jb.179.23.7410-7419.1997.
9
The N-terminal part of the E.coli DNA binding protein FIS is essential for stimulating site-specific DNA inversion but is not required for specific DNA binding.大肠杆菌DNA结合蛋白FIS的N端部分对于刺激位点特异性DNA倒位至关重要,但对于特异性DNA结合并非必需。
Nucleic Acids Res. 1991 Nov 11;19(21):5915-22. doi: 10.1093/nar/19.21.5915.
10
Deletion analysis of the fis promoter region in Escherichia coli: antagonistic effects of integration host factor and Fis.大肠杆菌中 fis 启动子区域的缺失分析:整合宿主因子与 Fis 的拮抗作用
J Bacteriol. 1997 Oct;179(20):6367-77. doi: 10.1128/jb.179.20.6367-6377.1997.

引用本文的文献

1
Phage-mediated resolution of genetic conflict alters the evolutionary trajectory of lysogens.噬菌体介导的遗传冲突解决改变了溶原菌的进化轨迹。
mSystems. 2024 Sep 17;9(9):e0080124. doi: 10.1128/msystems.00801-24. Epub 2024 Aug 21.
2
Transposable prophage Mu is organized as a stable chromosomal domain of E. coli.可转移的前噬菌体 Mu 组织为大肠杆菌染色体的稳定结构域。
PLoS Genet. 2013 Nov;9(11):e1003902. doi: 10.1371/journal.pgen.1003902. Epub 2013 Nov 7.
3
Silencing of toxic gene expression by Fis.Fis 沉默毒性基因的表达。

本文引用的文献

1
Acetylornithinase of Escherichia coli: partial purification and some properties.大肠杆菌的乙酰鸟氨酸酶:部分纯化及某些性质
J Biol Chem. 1956 Jan;218(1):97-106.
2
Point mutations change the thermal denaturation profile of a short DNA fragment containing the lactose control elements. Comparison between experiment and theory.点突变改变了包含乳糖控制元件的短DNA片段的热变性图谱。实验与理论的比较。
EMBO J. 1982;1(1):99-105. doi: 10.1002/j.1460-2075.1982.tb01131.x.
3
Methylation regulates the expression of a DNA-modification function encoded by bacteriophage Mu.
Nucleic Acids Res. 2012 May;40(10):4358-67. doi: 10.1093/nar/gks037. Epub 2012 Jan 28.
4
Immunity of replicating Mu to self-integration: a novel mechanism employing MuB protein.复制型 Mu 对自身整合的免疫:一种利用 MuB 蛋白的新机制。
Mob DNA. 2010 Feb 1;1(1):8. doi: 10.1186/1759-8753-1-8.
5
Stimulation of DNA inversion by FIS: evidence for enhancer-independent contacts with the Gin-gix complex.FIS对DNA倒位的刺激作用:与Gin-gix复合物形成不依赖增强子的接触的证据。
Nucleic Acids Res. 1997 Oct 1;25(19):3832-9. doi: 10.1093/nar/25.19.3832.
6
Effects of N-terminal deletions of the Escherichia coli protein Fis on growth rate, tRNA(2Ser) expression and cell morphology.大肠杆菌蛋白Fis的N端缺失对生长速率、tRNA(2Ser)表达及细胞形态的影响。
Mol Gen Genet. 1995 Jan 20;246(2):259-65. doi: 10.1007/BF00294690.
7
Identification of genes negatively regulated by Fis: Fis and RpoS comodulate growth-phase-dependent gene expression in Escherichia coli.由Fis负调控的基因的鉴定:Fis和RpoS共同调节大肠杆菌中生长阶段依赖性基因的表达。
J Bacteriol. 1995 Feb;177(4):938-47. doi: 10.1128/jb.177.4.938-947.1995.
8
Regulation of bacteriophage Mu transposition.噬菌体Mu转座的调控
Genetica. 1994;93(1-3):27-39. doi: 10.1007/BF01435237.
9
Sequence, regulation, and functions of fis in Salmonella typhimurium.鼠伤寒沙门氏菌中fis的序列、调控及功能
J Bacteriol. 1995 Apr;177(8):2021-32. doi: 10.1128/jb.177.8.2021-2032.1995.
甲基化调控由噬菌体Mu编码的一种DNA修饰功能的表达。
Cold Spring Harb Symp Quant Biol. 1983;47 Pt 2:639-46. doi: 10.1101/sqb.1983.047.01.075.
4
Linker tailing: unphosphorylated linker oligonucleotides for joining DNA termini.接头加尾:用于连接DNA末端的未磷酸化接头寡核苷酸。
DNA. 1984;3(2):173-82. doi: 10.1089/dna.1984.3.173.
5
Cointegrate formation mediated by Tn9. II. Activity of IS1 is modulated by external DNA sequences.由Tn9介导的共整合体形成。II. IS1的活性受外部DNA序列调控。
J Mol Biol. 1983 Oct 15;170(1):61-91. doi: 10.1016/s0022-2836(83)80227-7.
6
New M13 vectors for cloning.用于克隆的新型M13载体。
Methods Enzymol. 1983;101:20-78. doi: 10.1016/0076-6879(83)01005-8.
7
Ner, a cro-like function of bacteriophage Mu.Ner,噬菌体Mu的一种cro样功能。
Virology. 1982 Nov;123(1):19-28. doi: 10.1016/0042-6822(82)90291-4.
8
rho Mutations restore lamB expression in E. coli K12 strains with an inactive malB region.rho突变可恢复malB区域无活性的大肠杆菌K12菌株中lamB的表达。
Mol Gen Genet. 1981;184(3):479-83. doi: 10.1007/BF00352526.
9
Two pathways in bacteriophage Mu transposition?噬菌体Mu转座中的两条途径?
Cold Spring Harb Symp Quant Biol. 1981;45 Pt 1:329-36. doi: 10.1101/sqb.1981.045.01.046.
10
Regulation of Mu transposition. II. The escherichia coli HimD protein positively controls two repressor promoters and the early promoter of bacteriophage Mu.Mu转座的调控。II. 大肠杆菌HimD蛋白正向调控噬菌体Mu的两个阻遏物启动子和早期启动子。
Gene. 1984 Dec;32(3):419-26. doi: 10.1016/0378-1119(84)90017-9.