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枯草芽孢杆菌168中的基因重组:recN、recF、recH和addAB突变对DNA修复和重组的影响

Genetic recombination in Bacillus subtilis 168: effect of recN, recF, recH and addAB mutations on DNA repair and recombination.

作者信息

Alonso J C, Stiege A C, Lüder G

机构信息

Max-Planck-Institut für molekulare Genetik, Berlin, Germany.

出版信息

Mol Gen Genet. 1993 May;239(1-2):129-36. doi: 10.1007/BF00281611.

DOI:10.1007/BF00281611
PMID:8510642
Abstract

A recN- (recN1) strain of Bacillus subtilis was constructed. The effects of this and recF, recH and addAB mutations on recombination proficiency were tested. Mutations in the recN, recF, recH and addAB genes, when present in an otherwise Rec+ B. subtilis strain, did not affect genetic exchange. Strains carrying different combinations of mutations in these genes were constructed and examined for their sensitivity to 4-nitroquinoline-1-oxide (4NQO) and recombination proficiency. The recH mutation did not affect the 4NQO sensitivity of recN and recF cells and it only marginally affected that of addA addB cells. However, it reduced genetic recombination in these cells 10(2)- to 10(4)-fold. The addA addB mutations increased the 4NQO sensitivity of recF and recN cells, but completely blocked genetic recombination of recF cells and marginally affected recombination in recN cells. The recN mutation did not affect the recombinational capacity of recF cells. These data indicate that the recN gene product is required for DNA repair and recombination and that the recF, recH and addAB genes provide overlapping activities that compensate for the effects of single mutants proficiency. We proposed that the recF, recH, recB and addA gene products define four different epistatic groups.

摘要

构建了枯草芽孢杆菌的recN -(recN1)菌株。测试了该菌株以及recF、recH和addAB突变对重组能力的影响。当recN、recF、recH和addAB基因的突变存在于其他方面为Rec⁺的枯草芽孢杆菌菌株中时,并不影响基因交换。构建了携带这些基因不同突变组合的菌株,并检测它们对4 - 硝基喹啉 - 1 - 氧化物(4NQO)的敏感性和重组能力。recH突变不影响recN和recF细胞对4NQO的敏感性,对addA addB细胞的敏感性影响也很小。然而,它使这些细胞中的基因重组减少了10²至10⁴倍。addA addB突变增加了recF和recN细胞对4NQO的敏感性,但完全阻断了recF细胞的基因重组,对recN细胞的重组影响很小。recN突变不影响recF细胞的重组能力。这些数据表明recN基因产物是DNA修复和重组所必需的,并且recF、recH和addAB基因提供了重叠的活性,以补偿单个突变体能力的影响。我们提出recF、recH、recB和addA基因产物定义了四个不同的上位性组。

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本文引用的文献

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Plasmid transformation in Bacillus subtilis: effects of insertion of Bacillus subtilis DNA into plasmid pC194.枯草芽孢杆菌中的质粒转化:将枯草芽孢杆菌DNA插入质粒pC194的影响。
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通过可逆同源重组开关促进基因在[具体对象]中的稳定整合、表达及拷贝数扩增。 (原文中“in through”表述有误,推测可能是“in [具体对象] through”,这里按推测后的内容翻译,若实际并非如此,请根据正确原文调整)
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Processing of stalled replication forks in Bacillus subtilis.枯草芽孢杆菌中停滞复制叉的处理。
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RecA Is Required for the Assembly of RecN into DNA Repair Complexes on the Nucleoid.RecA 对于 RecN 组装到核区的 DNA 修复复合物中是必需的。
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