Hill C W, Harnish B W
J Bacteriol. 1982 Feb;149(2):449-57. doi: 10.1128/jb.149.2.449-457.1982.
We have constructed several mutants of Escherichia coli which have the chromosomal segment between the directly repeated rrnB and rrnE genes deleted from the normal position and transposed into another one of the seven redundant rRNA genes. We have examples where the transposition has been into rrnC, rrnD, rrnG, and rrnH. Included in the evidence for each of these transpositions was the finding that each transposition specifically affected a different one of the seven BamHI-PstI restriction nuclease fragments known to correspond to the seven rrn genes. The transposition mutants were generally healthy, but sensitive mixed-growth experiments revealed that most of them grew somewhat more slowly than the parental control in rich medium. The maximal detrimental effect was a 4 to 5% reduction in growth rate when the transposition of the rrnB-rrnE segment was into rrnG. We have found that a rrnF gene, reported by others to be linked to malA, does not exist in our standard strain, a derivative of Cavalli Hfr. Instead of rrnF, we identified a new rrn gene, rrnH, which mapped near min 5.
我们构建了几种大肠杆菌突变体,这些突变体缺失了正常位置上直接重复的rrnB和rrnE基因之间的染色体片段,并将其转座到七个冗余rRNA基因中的另一个基因处。我们有转座到rrnC、rrnD、rrnG和rrnH的实例。这些转座的证据包括发现每个转座都特异性地影响了已知对应于七个rrn基因的七个BamHI - PstI限制性核酸酶片段中的不同片段。转座突变体通常健康,但敏感混合生长实验表明,它们中的大多数在丰富培养基中比亲本对照生长得稍慢。当rrnB - rrnE片段转座到rrnG时,最大的有害影响是生长速率降低4%至5%。我们发现,其他人报道与malA连锁的rrnF基因在我们的标准菌株(Cavalli Hfr的衍生物)中不存在。我们鉴定出一个新的rrn基因rrnH,而不是rrnF,它位于5分钟附近。