Atlung T, Hansen F G
Department of Life Sciences and Chemistry, Roskilde University, DK-4000 Roskilde, Denmark.
J Bacteriol. 2002 Apr;184(7):1843-50. doi: 10.1128/JB.184.7.1843-1850.2002.
Flow cytometric analysis showed that the hns205 and hns206 mutants, lacking the abundant nucleoid-associated protein H-NS, have decreased origin concentration, as well as a low number of origins per cell (ploidy). The most striking observation was that the low ploidy was due to a very short replication time, e.g., at 30 degrees C it was halved compared to that of the hns(+) strain. The decreased origin concentration was not caused by a decreased dnaA gene expression, and the hns206 mutant had normal DnaA protein concentrations. The replication phenotypes of the hns206 mutant were independent of RpoS. Cells overproducing H-NS from a LacI-controlled plasmid had a normal origin concentration, indicating that H-NS is not controlling initiation. A wild-type H-NS concentration is, however, required to obtain a wild-type origin concentration, since cells with an intermediate H-NS concentration had an intermediate origin concentration. Two lines of evidence point to an indirect effect of H-NS on initiation. First, H-NS did not show high-affinity binding to any part of oriC, and H-NS had no effect on transcription entering oriC from the mioC promoter. Second, in a shift experiment with the hns206 mutant, when H-NS protein was induced to wild-type levels within 10 min, it took more than one generation before the origin concentration started to increase.
流式细胞术分析表明,缺乏丰富的类核相关蛋白H-NS的hns205和hns206突变体,其复制起点浓度降低,且每个细胞中的起点数量(倍性)也较低。最引人注目的观察结果是,低倍性是由于复制时间非常短,例如,在30℃时,与hns(+)菌株相比,其复制时间减半。复制起点浓度的降低不是由dnaA基因表达降低引起的,并且hns206突变体具有正常的DnaA蛋白浓度。hns206突变体的复制表型与RpoS无关。从LacI控制的质粒中过量产生H-NS的细胞具有正常的复制起点浓度,这表明H-NS并不控制起始。然而,要获得野生型的复制起点浓度,需要野生型的H-NS浓度,因为具有中等H-NS浓度的细胞具有中等的复制起点浓度。有两条证据表明H-NS对起始有间接影响。第一,H-NS未显示与oriC的任何部分有高亲和力结合,并且H-NS对从mioC启动子进入oriC的转录没有影响。第二,在对hns206突变体的转换实验中,当在10分钟内将H-NS蛋白诱导至野生型水平时,复制起点浓度开始增加之前需要超过一代的时间。