• 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

recD、recJ和recN的重叠功能为大肠杆菌重组和DNA修复中基因的三个上位性组提供了证据。

Overlapping functions of recD, recJ and recN provide evidence of three epistatic groups of genes in Escherichia coli recombination and DNA repair.

作者信息

Lloyd R G, Buckman C

机构信息

Department of Genetics, University of Nottingham, Queens Medical Centre, UK.

出版信息

Biochimie. 1991 Feb-Mar;73(2-3):313-20. doi: 10.1016/0300-9084(91)90218-p.

DOI:10.1016/0300-9084(91)90218-p
PMID:1883889
Abstract

The recD, recJ and recN genes of Escherichia coli K-12 have been shown to be involved in genetic recombination and DNA repair in this organism. Yet, mutation of any one of these genes does not seem to interfere much with the recovery of recombinants from conjugational crosses. Strains carrying all possible combinations of mutations inactivating these genes were constructed and examined for their recombination proficiency and sensitivity to UV light. The recD recJ and recJ recN double mutants are moderately sensitive to UV light and slightly deficient in recombination. A combination of mutations in all 3 genes produced strains that are very deficient in recombination (50- to 100-fold reduction) and strikingly sensitive to UV light. We conclude that these genes provide overlapping activities that compensate for one another in the single mutants. On the basis of these and other data, recombination genes are classified into 3 epistatic groups that define activities which function pre-synaptically or post-synaptically to promote genetic exchanges catalysed by RecA.

摘要

已证明大肠杆菌K-12的recD、recJ和recN基因参与该生物体的基因重组和DNA修复。然而,这些基因中的任何一个发生突变似乎都不会对从接合杂交中获得重组体产生太大干扰。构建了携带使这些基因失活的所有可能突变组合的菌株,并检测了它们的重组能力和对紫外线的敏感性。recD recJ和recJ recN双突变体对紫外线中度敏感,重组能力略有缺陷。所有3个基因的突变组合产生的菌株重组能力非常缺陷(降低50至100倍),并且对紫外线极其敏感。我们得出结论,这些基因提供重叠的活性,在单突变体中相互补偿。基于这些及其他数据,重组基因被分为3个上位性组,这些组定义了在突触前或突触后发挥作用以促进由RecA催化的基因交换的活性。

相似文献

1
Overlapping functions of recD, recJ and recN provide evidence of three epistatic groups of genes in Escherichia coli recombination and DNA repair.recD、recJ和recN的重叠功能为大肠杆菌重组和DNA修复中基因的三个上位性组提供了证据。
Biochimie. 1991 Feb-Mar;73(2-3):313-20. doi: 10.1016/0300-9084(91)90218-p.
2
Effect of recF, recJ, recN, recO and ruv mutations on ultraviolet survival and genetic recombination in a recD strain of Escherichia coli K12.recF、recJ、recN、recO和ruv突变对大肠杆菌K12 recD菌株紫外线存活率和基因重组的影响。
Mol Gen Genet. 1988 May;212(2):317-24. doi: 10.1007/BF00334702.
3
The genetic dependence of recombination in recD mutants of Escherichia coli.大肠杆菌recD突变体中重组的遗传依赖性。
Genetics. 1988 Sep;120(1):37-45. doi: 10.1093/genetics/120.1.37.
4
Effects of recJ, recQ, and recFOR mutations on recombination in nuclease-deficient recB recD double mutants of Escherichia coli.recJ、recQ和recFOR突变对大肠杆菌核酸酶缺陷型recB recD双突变体中重组的影响。
J Bacteriol. 2005 Feb;187(4):1350-6. doi: 10.1128/JB.187.4.1350-1356.2005.
5
Genetic analysis of conjugational recombination in Escherichia coli K12 strains deficient in RecBCD enzyme.对缺乏RecBCD酶的大肠杆菌K12菌株中接合重组的遗传分析。
J Gen Microbiol. 1987 Sep;133(9):2531-8. doi: 10.1099/00221287-133-9-2531.
6
Recombination of bacteriophage lambda in recD mutants of Escherichia coli.噬菌体λ在大肠杆菌recD突变体中的重组
Genome. 1989;31(1):53-67. doi: 10.1139/g89-013.
7
RecFOR function is required for DNA repair and recombination in a RecA loading-deficient recB mutant of Escherichia coli.在大肠杆菌RecA装载缺陷型recB突变体中,DNA修复和重组需要RecFOR功能。
Genetics. 2003 Feb;163(2):485-94. doi: 10.1093/genetics/163.2.485.
8
The hybrid recombinational repair pathway operates in a χ activity deficient recC1004 mutant of Escherichia coli.大肠杆菌 recC1004 突变体中,杂合重组修复途径在 χ 活性缺失的情况下起作用。
Biochimie. 2012 Sep;94(9):1918-25. doi: 10.1016/j.biochi.2012.05.008. Epub 2012 May 19.
9
Influence of uvrA, recJ and recN gene mutations on nucleoid reorganization in UV-treated Escherichia coli cells.uvrA、recJ和recN基因突变对紫外线处理的大肠杆菌细胞中类核重组的影响。
FEMS Microbiol Lett. 2018 Jun 1;365(11). doi: 10.1093/femsle/fny110.
10
Functions of multiple exonucleases are essential for cell viability, DNA repair and homologous recombination in recD mutants of Escherichia coli.多种核酸外切酶的功能对于大肠杆菌recD突变体中的细胞活力、DNA修复和同源重组至关重要。
Genetics. 2006 Apr;172(4):2057-69. doi: 10.1534/genetics.105.052076. Epub 2006 Feb 1.

引用本文的文献

1
The Role of the RecFOR Complex in Genome Stability.RecFOR复合物在基因组稳定性中的作用。
Int J Mol Sci. 2025 Jun 6;26(12):5441. doi: 10.3390/ijms26125441.
2
Spontaneous Genomic Variation as a Survival Strategy of Nosocomial Staphylococcus haemolyticus.自发基因组变异作为医院溶血葡萄球菌的一种生存策略
Microbiol Spectr. 2023 Mar 6;11(2):e0255222. doi: 10.1128/spectrum.02552-22.
3
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.
4
Single strand gap repair: The presynaptic phase plays a pivotal role in modulating lesion tolerance pathways.单链缺口修复:突触前相在调节损伤耐受途径方面起着关键作用。
PLoS Genet. 2022 Jun 2;18(6):e1010238. doi: 10.1371/journal.pgen.1010238. eCollection 2022 Jun.
5
Homologous Recombination-Experimental Systems, Analysis, and Significance.同源重组——实验系统、分析及意义
EcoSal Plus. 2011 Dec;4(2). doi: 10.1128/ecosalplus.7.2.6.
6
Investigation of the genes involved in antigenic switching at the vlsE locus in Borrelia burgdorferi: an essential role for the RuvAB branch migrase.研究伯氏疏螺旋体 vlsE 基因座抗原转换相关基因:RuvAB 分支迁移酶的重要作用。
PLoS Pathog. 2009 Dec;5(12):e1000680. doi: 10.1371/journal.ppat.1000680. Epub 2009 Dec 4.
7
RecBCD enzyme and the repair of double-stranded DNA breaks.RecBCD酶与双链DNA断裂的修复
Microbiol Mol Biol Rev. 2008 Dec;72(4):642-71, Table of Contents. doi: 10.1128/MMBR.00020-08.
8
Deficiency of RecA-dependent RecFOR and RecBCD pathways causes increased instability of the (GAA*TTC)n sequence when GAA is the lagging strand template.当GAA作为后随链模板时,RecA依赖的RecFOR和RecBCD途径的缺陷会导致(GAA*TTC)n序列的不稳定性增加。
Nucleic Acids Res. 2007;35(20):6884-94. doi: 10.1093/nar/gkm810. Epub 2007 Oct 11.
9
Roles of PriA protein and double-strand DNA break repair functions in UV-induced restriction alleviation in Escherichia coli.PriA蛋白和双链DNA断裂修复功能在大肠杆菌紫外线诱导的限制缓解中的作用
Genetics. 2006 Dec;174(4):2137-49. doi: 10.1534/genetics.106.063750. Epub 2006 Oct 8.
10
Bacillus subtilis RecN binds and protects 3'-single-stranded DNA extensions in the presence of ATP.枯草芽孢杆菌RecN在ATP存在的情况下结合并保护3'-单链DNA延伸段。
Nucleic Acids Res. 2005 Apr 22;33(7):2343-50. doi: 10.1093/nar/gki533. Print 2005.