Quiñones A, Messer W
Wissenschaftsbereich Genetik, Martin-Luther-Universität, Halle (Saale), German Democratic Republic.
Mol Gen Genet. 1988 Jul;213(1):118-24. doi: 10.1007/BF00333407.
The dnaN gene of Escherichia coli encodes the beta-subunit of the DNA polymerase III holoenzyme. Previous work has established that dnaN lies immediately downstream of dnaA and that both genes may be cotranscribed from the dnaA promoters; no promoter for dnaN has been described. We investigated the in vivo regulation of transcription of the dnaN gene by transcriptional fusions to the galK gene, translational fusion to the lacZ gene and S1 mapping analysis. We found that there are at least three dnaN promoters residing entirely in the reading frame of the preceding dnaA gene, and that transcription from these promoters can occur independently of dnaA transcription which, however, extends at least up to dnaN. Furthermore, we found evidence for the inducibility of the dnaN promoters in a dam background under conditions of simultaneously reduced dnaA transcription. These results are consistent with the hypothesis that although dnaA and dnaN are organized in an operon considerable discoordinate transcription can occur, thus uncoupling dnaN and dnaA regulation, when needed.
大肠杆菌的dnaN基因编码DNA聚合酶III全酶的β亚基。先前的研究已确定dnaN位于dnaA的紧邻下游,且这两个基因可能从dnaA启动子共转录;尚未描述dnaN的启动子。我们通过与galK基因的转录融合、与lacZ基因的翻译融合以及S1图谱分析,研究了dnaN基因转录的体内调控。我们发现至少有三个dnaN启动子完全位于前一个dnaA基因的阅读框内,并且这些启动子的转录可以独立于dnaA的转录发生,不过dnaA的转录至少延伸到dnaN。此外,我们发现有证据表明在同时降低dnaA转录的条件下,dam背景中dnaN启动子具有可诱导性。这些结果与以下假设一致:尽管dnaA和dnaN以操纵子形式组织,但仍可能发生相当程度的不协调转录,从而在需要时使dnaN和dnaA的调控解偶联。