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鲁夫基因和recG基因以及大肠杆菌中Tn10的诱导精确切除

Ruv and recG genes and the induced precise excision of Tn10 in Escherichia coli.

作者信息

Nagel R, Chan A, Rosen E

机构信息

CEFYBO, CONICET, Buenos Aires, Argentina.

出版信息

Mutat Res. 1994 Nov 1;311(1):103-9. doi: 10.1016/0027-5107(94)90078-7.

Abstract

Induction of precise excision of Tn10 by UV or mitomycin C (MMC) is dependent on the expression of the SOS system. Ruv mutants of Escherichia coli, which are defective in DNA repair and recombination, showed diminished frequencies of both spontaneous and UV- or MMC-induced excision of Tn10 inserted in gal. RecG mutants, which are also defective in DNA repair and recombination, showed decreased induction of Tn10 excision with MMC, but not after UV treatment. A recG ruv double mutant showed a greater decrease in induction of excision with MMC than either single mutant. One can speculate that the Ruv proteins, which are known to be involved in the resolution of Holliday junctions, might also be involved in the resolution of putative intermediates generated during the precise excision of Tn10. RecG protein, whose function partially overlaps those of Ruv proteins, might also have some role in this process.

摘要

通过紫外线或丝裂霉素C(MMC)诱导Tn10的精确切除依赖于SOS系统的表达。大肠杆菌的Ruv突变体在DNA修复和重组方面存在缺陷,其插入gal中的Tn10的自发切除频率以及紫外线或MMC诱导的切除频率均降低。RecG突变体在DNA修复和重组方面也存在缺陷,其MMC诱导的Tn10切除诱导率降低,但紫外线处理后未降低。recG ruv双突变体的MMC诱导切除诱导率下降幅度比任何一个单突变体都更大。可以推测,已知参与霍利迪连接点拆分的Ruv蛋白可能也参与了Tn10精确切除过程中产生的假定中间体的拆分。RecG蛋白的功能与Ruv蛋白部分重叠,在这个过程中可能也发挥了一定作用。

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