Regamey A, Harry E J, Wake R G
Department of Biochemistry, University of Sydney, NSW 2006, Australia.
Mol Microbiol. 2000 Nov;38(3):423-34. doi: 10.1046/j.1365-2958.2000.02130.x.
We have shown previously that, when spores of a thymine-requiring strain of Bacillus subtilis were grown out in the absence of thymine, mid-cell Z rings formed over the nucleoid and much earlier than might be expected with respect to progression into the round of replication. It is now shown that such conditions allow no replication of oriC. Rather than replication, partial degradation of the oriC region occurs, suggesting that the status of this region is connected with the 'premature' mid-cell Z ring assembly. A correlation was observed between entry into the replication elongation phase and a block to mid-cell Z rings. The conformation of the nucleoid under various conditions of DNA replication inhibition or limitation suggests that relief of nucleoid occlusion is not primarily responsible for mid-cell Z ring formation in the absence of thymine. We propose the existence of a specific structure at mid-cell that defines the Z ring nucleation site (NS). It is suggested that this NS is normally masked by the replisome upon initiation of replication or soon after entry into the elongation phase, and subsequently unmasked relatively late in the round. During spore outgrowth in the absence of thymine, this checkpoint control over mid-cell Z ring assembly breaks down prematurely.
我们之前已经表明,当在无胸腺嘧啶的情况下培养需要胸腺嘧啶的枯草芽孢杆菌菌株的孢子时,中细胞Z环在类核上方形成,且比预期进入复制轮次的时间要早得多。现在表明,这种条件下oriC不进行复制。相反,oriC区域发生部分降解,这表明该区域的状态与“过早”的中细胞Z环组装有关。观察到进入复制延伸阶段与中细胞Z环形成受阻之间存在相关性。在DNA复制抑制或限制的各种条件下类核的构象表明,在无胸腺嘧啶的情况下,类核阻碍的解除并非中细胞Z环形成的主要原因。我们提出在中细胞存在一种特定结构,它定义了Z环成核位点(NS)。有人认为,这个NS在复制起始时或进入延伸阶段后不久通常被复制体掩盖,随后在复制轮次中相对较晚才被揭开。在无胸腺嘧啶的孢子萌发过程中,对中细胞Z环组装的这种检查点控制过早失效。