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DinI and RecX modulate RecA-DNA structures in Escherichia coli K-12

机译:DinI和RecX调节大肠杆菌K-12中的RecA-DNA结构

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RecA plays a central role in recombination, DNA repair and SOS induction through forming a RecA-DNA helical filament. Biochemical observations show that at low ratios to RecA, DinI and RecX stabilize and destabilize RecA-DNA filaments, respectively, and that the C-terminal 17 residues of RecA are important for RecX function. RecA-DNA filament formation was assayed in vivo using RecA-GFP foci formation in log-phase and UV-irradiated cells. In log-phase cells, dinI mutants have fewer foci than wild type and that recX mutants have more foci than wild type. A recA Delta 17::gfp mutant had more foci like a recX mutant. dinI recX double mutants have the same number of foci as dinI mutants alone, suggesting that dinI is epistatic to recX. After UV treatment, the dinI, recX and dinI recX mutants differed in their ability to form foci. All three mutants had fewer foci than wild type. The dinI mutant's foci persisted longer than wild-type foci. Roles of DinI and RecX after UV treatment differed from those during log-phase growth and may reflect the different DNA substrates, population of proteins or amounts during the SOS response. These experiments give new insight into the roles of these proteins.
机译:RecA通过形成RecA-DNA螺旋细丝在重组,DNA修复和SOS诱导中起着核心作用。生化观察表明,在与RecA,DinI和RecX的比率较低时,RecA-DNA细丝分别稳定和不稳定,并且RecA的C端17个残基对于RecX功能很重要。在对数期和紫外线照射的细胞中,使用RecA-GFP灶的形成在体内测定RecA-DNA细丝的形成。在对数期细胞中,dinI突变体的病灶少于野生型,而recX突变体的病灶却比野生型更多。 recA Delta 17 :: gfp突变体像recX突变体一样具有更多的病灶。 dinI recX双重突变体与单独的dinI突变体具有相同数量的病灶,表明dinI对recX具有上位性。紫外线处理后,dinI,recX和dinI recX突变体形成灶的能力不同。这三个突变体的病灶均少于野生型。 dinI突变体的病灶比野生型病灶持续时间更长。紫外线处理后的DinI和RecX的作用不同于对数生长期期间的作用,并且可能反映了SOS反应期间不同的DNA底物,蛋白质种群或数量。这些实验为这些蛋白质的作用提供了新的见识。

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