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Accumulation of large non-circular forms of the chromosome in recombination-defective mutants of Escherichia coli

机译:大的非圆形形式的染色体在重组缺陷型大肠杆菌中的积累

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Background Double-strand breakage of chromosomal DNA is obviously a serious threat to cells because various activities of the chromosome depend on its integrity. However, recent experiments suggest that such breakage may occur frequently during "normal" growth in various organisms – from bacteria through vertebrates, possibly through arrest of a replication fork at some endogenous DNA damage. Results In order to learn how the recombination processes contribute to generation and processing of the breakage, large (> 2000 kb) linear forms of Escherichia coli chromosome were detected by pulsed-field gel electrophoresis in various recombination-defective mutants. The mutants were analyzed in a rich medium, in which the wild-type strain showed fewer of these huge broken chromosomes than in a synthetic medium, and the following results were obtained: (i) Several recB and recC null mutants (in an otherwise rec+ background) accumulated these huge linear forms, but several non-null recBCD mutants (recD, recC1001, recC1002, recC1003, recC1004, recC2145, recB2154, and recB2155) did not. (ii) In a recBC sbcA background, in which RecE-mediated recombination is active, recA, recJ, recQ, recE, recT, recF, recO, and recR mutations led to their accumulation. The recJ mutant accumulated many linear forms, but this effect was suppressed by a recQ mutation. (iii) The recA, recJ, recQ, recF and recR mutations led to their accumulation in a recBC sbcBC background. The recJ mutation showed the largest amount of these forms. (iv) No accumulation was detected in mutants affecting resolution of Holliday intermediates, recG, ruvAB and ruvC, in any of these backgrounds. Conclusion These results are discussed in terms of stepwise processing of chromosomal double-strand breaks.
机译:背景技术染色体DNA的双链断裂显然是对细胞的严重威胁,因为染色体的各种活动都取决于其完整性。但是,最近的实验表明,这种断裂可能会在各种生物体的“正常”生长过程中频繁发生-从细菌到脊椎动物,可能是由于复制叉在某些内源性DNA损伤处的阻滞。结果为了了解重组过程如何促进断裂的产生和处理,通过脉冲场凝胶电泳在各种重组缺陷型突变体中检测到大(> 2000 kb)线性大肠埃希氏菌染色体。在丰富的培养基中分析了突变体,其中野生型菌株显示出的这些巨大的断裂染色体少于合成培养基中的突变体,并且获得了以下结果:(i)多个recB和recC null突变体(否则为rec + 背景)积累了这些巨大的线性形式,但没有几个非null recBCD突变体(recD,recC1001,recC1002,recC1003,recC1004,recC2145,recB2154和recB2155)没有。 (ii)在recE介导的重组活跃的recBC sbcA背景下,recA,recJ,recQ,recE,recT,recF,recO和recR突变导致其积累。 recJ突变体积累了许多线性形式,但是该效果被recQ突变所抑制。 (iii)recA,recJ,recQ,recF和recR突变导致它们在recBC sbcBC背景下积累。 recJ突变显示出最大数量的这些形式。 (iv)在任何这些背景下,在影响Holliday中间体,recG,ruvAB和ruvC的分离的突变体中均未检测到积累。结论从逐步处理染色体双链断裂的角度讨论了这些结果。

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