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噬菌体λ的ninR区域编码的基因产物参与Red介导的重组。

Gene products encoded in the ninR region of phage lambda participate in Red-mediated recombination.

作者信息

Tarkowski Trudee A, Mooney Duane, Thomason Lynn C, Stahl Franklin W

机构信息

Institute of Molecular Biology, University of Oregon, Eugene, OR 97403-1229, USA.

出版信息

Genes Cells. 2002 Apr;7(4):351-63. doi: 10.1046/j.1365-2443.2002.00531.x.

Abstract

BACKGROUND

The ninR region of phage lambda contains two recombination genes, orf (ninB) and rap (ninG), that were previously shown to have roles when the RecF and RecBCD recombination pathways of E. coli, respectively, operate on phage lambda.

RESULTS

When lambda DNA replication is blocked, recombination is focused at the termini of the virion chromosome. Deletion of the ninR region of lambda decreases the sharpness of the focusing without diminishing the overall rate of recombination. The phenotype is accounted for in large part by the deletion of rap and of orf. Mutation of the recJ gene of the host partially suppresses the Rap- phenotype.

CONCLUSION

ninR functions Orf and Rap participate in Red recombination, the primary pathway operating when wild-type lambda grows lytically in rec+ cells. The ability of recJ mutation to suppress the Rap- phenotype indicates that RecJ exonuclease can participate in Red-mediated recombination, at least in the absence of Rap function. A model is presented for Red-mediated RecA-dependent recombination that includes these newly identified participants.

摘要

背景

噬菌体λ的ninR区域包含两个重组基因,即orf(ninB)和rap(ninG),先前的研究表明,当大肠杆菌的RecF和RecBCD重组途径分别作用于噬菌体λ时,这两个基因发挥作用。

结果

当λDNA复制受阻时,重组集中在病毒粒子染色体的末端。删除λ的ninR区域会降低这种集中的尖锐程度,但不会降低总体重组率。这种表型在很大程度上是由rap和orf的缺失导致的。宿主recJ基因的突变部分抑制了Rap-表型。

结论

ninR功能的Orf和Rap参与Red重组,这是野生型λ在rec+细胞中进行裂解生长时的主要途径。recJ突变抑制Rap-表型的能力表明,RecJ核酸外切酶可以参与Red介导的重组,至少在没有Rap功能的情况下是这样。本文提出了一个Red介导的RecA依赖性重组模型,其中包括这些新发现的参与者。

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