Ohta N, Chen L S, Swanson E, Newton A
J Mol Biol. 1985 Nov 5;186(1):107-15. doi: 10.1016/0022-2836(85)90261-x.
Temporal regulation of flagellar gene expression in Caulobacter crescentus has been examined by a detailed analysis of the flbG-flaJ-flbH-flaK hook operon. The approximate location of the promoter for this 4.4 X 10(3) base-pair transcriptional unit was determined by deletion mapping, and the flaK gene was shown by nucleotide sequencing to code for the hook protein. flaK messenger RNA was quantified by S1 nuclease mapping with an internal restriction fragment of the gene as the 5'-labeled DNA probe. The results of these assays provide the first direct evidence that periodic expression of a flagellar gene in the C. crescentus cell cycle is regulated at the transcriptional level. The effect of altering the time of gene duplication in the cell cycle was examined by subcloning the complete hook operon on a plasmid that replicates throughout the S phase. The normal periodicity of flaK transcription and translation was maintained in this merodiploid strain, which suggests that replication alone is not sufficient to initiate flagellar gene expression. We also show that the three adjacent transcriptional units III, IV and V are required in trans for transcription of the book operon, and we discuss the possible role of these genes in the hierarchical regulation of the flagellar gene expression.
通过对flbG-flaJ-flbH-flaK钩形操纵子进行详细分析,研究了新月柄杆菌鞭毛基因表达的时间调控。通过缺失作图确定了这个4.4×10³碱基对转录单位启动子的大致位置,核苷酸测序表明flaK基因编码钩形蛋白。用该基因的内部限制性片段作为5'-标记的DNA探针,通过S1核酸酶作图对flaK信使RNA进行定量。这些测定结果提供了首个直接证据,表明新月柄杆菌细胞周期中鞭毛基因的周期性表达在转录水平受到调控。通过将完整的钩形操纵子亚克隆到在整个S期都能复制的质粒上,研究了改变细胞周期中基因复制时间的影响。在这种部分二倍体菌株中,flaK转录和翻译的正常周期性得以维持,这表明仅复制不足以启动鞭毛基因表达。我们还表明,三个相邻的转录单位III、IV和V对于钩形操纵子的转录是反式作用所必需的,并且我们讨论了这些基因在鞭毛基因表达分级调控中的可能作用。