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λ 噬菌体 Red 介导的大肠杆菌 K12 中质粒线性多聚体的合成。

Lambda Red-mediated synthesis of plasmid linear multimers in Escherichia coli K12.

作者信息

Silberstein Z, Maor S, Berger I, Cohen A

机构信息

Department of Molecular Genetics, Hebrew University-Hadassah Medical School, Jerusalem, Israel.

出版信息

Mol Gen Genet. 1990 Sep;223(3):496-507. doi: 10.1007/BF00264459.

Abstract

Expression of the red+ and gam+ genes of bacteriophage lambda in plasmids cloned in Escherichia coli wild-type cells leads to plasmid linear multimer (PLM) formation. In mutants that lack exonuclease I (sbcB sbcC), either of these lambda functions mediates PLM formation. In order to determine whether PLM formation in sbcB sbcC mutants occurs by conservative (break-join) recombination of circular plasmids or by de novo DNA synthesis, thyA sbcB sbcC mutants were transferred from thymine- to 5-bromo-2'-deoxyuridine (BUDR)-supplemented medium, concurrently with induction of red+ or gam+ expression, and the density distribution of plasmid molecular species was analyzed. After a period of less than one generation in the BUDR-supplemented medium, most PLM were of heavy/heavy density. Circular plasmids, as well as chromosomal DNA, were of light/light or light/heavy density. These results indicate that Red or Gam activities mediate de novo synthesis of PLM in sbcB sbcC mutants. Examination of plasmid DNA preparations from sbcB sbcC mutants expressing gam+ or red+ reveals the presence of two molecular species that may represent intermediates in the PLM biosynthesis pathway: single-branched circles (sigma-structures) and PLM with single-stranded DNA tails. While Gam-mediated PLM synthesis in sbcB mutants depends on the activity of the RecF pathway genes, Red-mediated PLM synthesis, like Red-mediated recombination, is independent of recA and recF activities. One of the red+ products, beta protein, suppresses RecA deficiency in plasmid recombination and PLM synthesis in RecBCD- ExoI- cells. The dependence of PLM synthesis on the RecE, RecF or Red recombination pathways and the dependence of plasmid recombination by these pathways on activities that are required for plasmid replication support the proposal that PLM synthesis and recombination by these pathways are mutually dependent. We propose the hypothesis that DNA double-stranded ends, which are produced in the process of PLM synthesis, are involved in plasmid recombination by the RecE, RecF and Red pathways. Conversely, recombination-dependent priming of DNA synthesis at 3' single-stranded DNA ends is hypothesized to initiate PLM synthesis on circular plasmid DNA templates.

摘要

在大肠杆菌野生型细胞中克隆的质粒中,噬菌体λ的red⁺和gam⁺基因的表达会导致质粒线性多聚体(PLM)的形成。在缺乏核酸外切酶I(sbcB sbcC)的突变体中,这两种λ功能中的任何一种都介导PLM的形成。为了确定sbcB sbcC突变体中PLM的形成是通过环状质粒的保守(断裂-连接)重组还是通过从头DNA合成发生的,将thyA sbcB sbcC突变体从胸腺嘧啶补充培养基转移到5-溴-2'-脱氧尿苷(BUDR)补充培养基中,同时诱导red⁺或gam⁺表达,并分析质粒分子种类的密度分布。在补充了BUDR的培养基中培养不到一代的时间后,大多数PLM具有重/重密度。环状质粒以及染色体DNA具有轻/轻或轻/重密度。这些结果表明,Red或Gam活性介导了sbcB sbcC突变体中PLM的从头合成。对表达gam⁺或red⁺的sbcB sbcC突变体质粒DNA制备物的检查揭示了存在两种分子种类,它们可能代表PLM生物合成途径中的中间体:单分支环(σ结构)和具有单链DNA尾巴的PLM。虽然sbcB突变体中Gam介导的PLM合成依赖于RecF途径基因的活性,但Red介导的PLM合成,就像Red介导的重组一样,独立于recA和recF活性。red⁺产物之一β蛋白抑制RecBCD-ExoI⁻细胞中质粒重组和PLM合成中的RecA缺陷。PLM合成对RecE、RecF或Red重组途径的依赖性以及这些途径的质粒重组对质粒复制所需活性的依赖性支持了这样的提议,即这些途径的PLM合成和重组是相互依赖的。我们提出一个假说,即在PLM合成过程中产生的DNA双链末端参与了RecE、RecF和Red途径的质粒重组。相反,据推测,在3'单链DNA末端的重组依赖性DNA合成引发作用会启动环状质粒DNA模板上的PLM合成。

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