Attfield P V, Benson F E, Lloyd R G
J Bacteriol. 1985 Oct;164(1):276-81. doi: 10.1128/jb.164.1.276-281.1985.
The ruv gene of Escherichia coli, which is associated with inducible mechanisms of DNA repair and recombination, has been cloned into the low-copy plasmid vector pHSG415. The recombinant plasmid pPVA101 fully complements the DNA repair-deficient phenotype of ruv mutants. Restriction endonuclease analysis of this plasmid revealed a 10.6-kilobase (kb) HindIII DNA insert which contained a 7.7-kb PstI fragment identified as being from the chromosomal ruv region. Deletion analysis and Tn1000 insertional inactivation of ruv function located the ruv coding region to a 2.2-kb section of the cloned DNA fragment. A comparison of the proteins encoded by ruv wild-type and mutant plasmids identified the gene product as a protein of molecular weight 41,000.
大肠杆菌的ruv基因与DNA修复和重组的诱导机制相关,已被克隆到低拷贝质粒载体pHSG415中。重组质粒pPVA101完全互补ruv突变体的DNA修复缺陷表型。对该质粒的限制性内切酶分析显示,有一个10.6千碱基(kb)的HindIII DNA插入片段,其中包含一个7.7 kb的PstI片段,鉴定为来自染色体ruv区域。通过缺失分析和ruv功能的Tn1000插入失活,将ruv编码区域定位到克隆DNA片段的一个2.2 kb区域。对ruv野生型和突变体质粒所编码蛋白质的比较确定该基因产物为一种分子量为41,000的蛋白质。