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大肠杆菌K-12 recR基因座的鉴定及其在重组和DNA修复中的作用分析。

Identification of the recR locus of Escherichia coli K-12 and analysis of its role in recombination and DNA repair.

作者信息

Mahdi A A, Lloyd R G

机构信息

Department of Genetics, University of Nottingham, Queens Medical Centre, UK.

出版信息

Mol Gen Genet. 1989 Apr;216(2-3):503-10. doi: 10.1007/BF00334397.

Abstract

A new recombination gene called recR has been identified and located near dnaZ at minute 11 on the current linkage map of Escherichia coli. The gene was detected after transposon mutagenesis of a recB sbcB strain and screening for insertion mutants that had a reduced efficiency of recombination in Hfr crosses. The recR insertions obtained conferred a recombination deficient and extremely UV sensitive phenotype in both recB recC sbcA and recB recC sbcB sbcC genetic backgrounds. recR derivatives of recBC+ sbc+ strains were proficient in conjugational and transductional recombination but deficient in plasmid recombination and sensitive to UV light. Strains carrying recR insertions combined with mutations in uvrA and other rec genes revealed that the gene is involved in a recombinational process of DNA repair that relies also on recF and recO, and possibly recJ, but which is independent of recB, recC and recD. The properties of two other insertions, one located near pyrE and the other near guaA, are discussed in relation to their proximity to recG and xse (the gene for exonuclease VII), respectively.

摘要

一个名为recR的新重组基因已被鉴定出来,并位于大肠杆菌当前连锁图谱上第11分钟处的dnaZ附近。该基因是在对recB sbcB菌株进行转座子诱变并筛选在Hfr杂交中重组效率降低的插入突变体后检测到的。获得的recR插入在recB recC sbcA和recB recC sbcB sbcC遗传背景中均赋予了重组缺陷和极高的紫外线敏感性表型。recBC+ sbc+菌株的recR衍生物在接合和转导重组方面表现正常,但在质粒重组方面存在缺陷且对紫外线敏感。携带recR插入并与uvrA和其他rec基因突变相结合的菌株表明,该基因参与了一种DNA修复的重组过程,该过程还依赖于recF和recO,可能还有recJ,但独立于recB、recC和recD。还讨论了另外两个插入的特性,一个位于pyrE附近,另一个位于guaA附近,分别涉及它们与recG和xse(核酸外切酶VII的基因)的接近程度。

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