Silverman M, Simon M
J Bacteriol. 1973 Oct;116(1):114-22. doi: 10.1128/jb.116.1.114-122.1973.
In previous work, at least 10 discrete cistrons involved in the synthesis of flagella in Escherichia coli were described. Six cistrons were located between his and uvrC on the genetic map. These were referred to as hag, flaA, flaB, flaC, flaD, and flaE. Four cistrons referred to as mot, flaG, flaH, and flaI were located between uvrC and aroD. In order to determine whether these genes are organized into transcriptional units, a series of Mu phage-induced flagellar mutants was studied. The mutant strains behaved as if they were carrying strong polar mutations. Of 228 independent Mu-induced mutants, 114 with mutations in the his-aroD region of the genetic map were tested by preparing partial diploid strains with episomes carrying a variety of previously defined mutations. The pattern of complementation that emerged indicated that cistrons flaB, flaC, and flaE form a transcriptional unit. Cistron flaO, defined in the course of this study, is also a member of this transcriptional unit. The order of transcription is B-C-O-E. flaA was found to be complex, and it included four cistrons, flaA, flaP, flaQ, and flaR, with the transcriptional order A-P-Q-R. Cistrons flaG and flaH are cotranscribed with the transcriptional order G-H. The remaining genes, flaD, flaI, hag, and mot do not belong to multicistronic transcriptional units. Complementation analysis suggested that the cheC locus is the same as cistron flaA.
在之前的研究中,描述了至少10个参与大肠杆菌鞭毛合成的离散顺反子。在遗传图谱上,6个顺反子位于his和uvrC之间。这些被称为hag、flaA、flaB、flaC、flaD和flaE。4个顺反子,即mot、flaG、flaH和flaI,位于uvrC和aroD之间。为了确定这些基因是否被组织成转录单元,研究了一系列Mu噬菌体诱导的鞭毛突变体。这些突变菌株的行为就好像它们携带了强极性突变。在228个独立的Mu诱导突变体中,通过用携带各种先前定义突变的附加体制备部分二倍体菌株,对遗传图谱上his-aroD区域有突变的114个突变体进行了测试。出现的互补模式表明,顺反子flaB、flaC和flaE形成一个转录单元。在本研究过程中定义的顺反子flaO也是这个转录单元的成员。转录顺序是B-C-O-E。发现flaA很复杂,它包括4个顺反子,flaA、flaP、flaQ和flaR,转录顺序是A-P-Q-R。顺反子flaG和flaH以G-H的转录顺序共转录。其余的基因,flaD、flaI、hag和mot不属于多顺反子转录单元。互补分析表明,cheC位点与顺反子flaA相同。