Levine A, Autret S, Séror S J
Institut de Génétique et Microbiologia, URA CNRS 1354, Université Paris XI, Orsay, France.
Mol Microbiol. 1995 Jan;15(2):287-95. doi: 10.1111/j.1365-2958.1995.tb02243.x.
Regulation of DNA replication in Bacillus subtilis involves a post-initiation mechanism which is subject to control by the Stringent System, an essential regulatory network, mediated by the alarmone, ppGpp. In detailed studies using DNA-DNA hybridization procedures, we have now shown that, following the induction of the Stringent Response, replication is blocked downstream of the origin, on the left, close to the hut marker (-175 kb) and on the right, beyond the soft10 marker (+199 kb). In addition, we provide evidence that inhibition of replication under these conditions requires the replication terminator protein (RTP). In a mutant lacking RTP, a protein normally involved in termination of chromosomal replication through recognition of specific terminator sequences, replication continues past the sites normally blocked by the Stringent Response. These data strengthen the argument that this second level of control of DNA replication occurs at specific sites, the Strigent Terminus (STer) sites, either side of orlC. Such sites are presumably related to the sequence involved in RTP recognition at the terminus, terC. We propose that the binding of RTP must be modulated, perhaps through the action of ppGpp, to recognize post-initiation control sequences during the Stringent Response, in order to block replisome movement. This, therefore, acts as a checkpoint in chromosome elongation.
枯草芽孢杆菌中DNA复制的调控涉及一种起始后机制,该机制受严谨反应系统控制,严谨反应系统是一个由警报素ppGpp介导的重要调控网络。在使用DNA-DNA杂交程序的详细研究中,我们现已表明,在诱导严谨反应后,复制在起始点下游被阻断,在左侧靠近hut标记(-175 kb)处,在右侧超出soft10标记(+199 kb)处。此外,我们提供证据表明,在这些条件下复制的抑制需要复制终止蛋白(RTP)。在缺乏RTP的突变体中,RTP是一种通常通过识别特定终止序列参与染色体复制终止的蛋白质,复制会继续越过通常被严谨反应阻断的位点。这些数据支持了这样一种观点,即DNA复制的这一二级控制发生在特定位点,即oriC两侧的严谨终止(STer)位点。这些位点可能与末端terC处RTP识别所涉及的序列有关。我们提出,RTP的结合必须受到调节,可能是通过ppGpp的作用,以便在严谨反应期间识别起始后控制序列,从而阻断复制体的移动。因此,这充当了染色体延伸过程中的一个检查点。