Department of Biology and Biochemistry, University of Houston, Houston, TX, 77204-5001, USA.
Mol Microbiol. 2013 Oct;90(1):181-94. doi: 10.1111/mmi.12357. Epub 2013 Aug 23.
Sporulation initiation in Bacillus subtilis is controlled by the phosphorylated form of the master regulator Spo0A which controls transcription of a multitude of sporulation genes. In this study, we investigated the importance of temporal dynamics of phosphorylated Spo0A (Spo0A∼P) accumulation by rewiring the network controlling its phosphorylation. We showed that simultaneous induction of KinC, a kinase that can directly phosphorylate Spo0A, and Spo0A itself from separately controlled inducible promoters can efficiently trigger sporulation even under nutrient rich conditions. However, the sporulation efficiency in this artificial two-component system was significantly impaired when KinC and/or Spo0A induction was too high. Using mathematical modelling, we showed that gradual accumulation of Spo0A∼P is essential for the proper temporal order of the Spo0A regulon expression, and that reduction in sporulation efficiency results from the reversal of that order. These insights led us to identify premature repression of DivIVA as one possible explanation for the adverse effects of accelerated accumulation of Spo0A∼P on sporulation. Moreover, we found that positive feedback resulting from autoregulation of the native spo0A promoter leads to robust control of Spo0A∼P accumulation kinetics. Thus we propose that a major function of the conserved architecture of the sporulation network is controlling Spo0A activation dynamics.
枯草芽孢杆菌的孢子形成起始由主调控因子 Spo0A 的磷酸化形式控制,该因子控制着大量孢子形成基因的转录。在本研究中,我们通过重新布线控制其磷酸化的网络,研究了磷酸化 Spo0A(Spo0A∼P)积累的时间动态的重要性。我们表明,通过分别从可诱导启动子中同时诱导激酶 KinC(可直接磷酸化 Spo0A 的激酶)和 Spo0A 本身,可以有效地触发孢子形成,即使在营养丰富的条件下也是如此。然而,当 KinC 和/或 Spo0A 的诱导过高时,这种人工双组分系统的孢子形成效率显著受损。通过数学建模,我们表明 Spo0A∼P 的逐渐积累对于 Spo0A 调控子表达的适当时间顺序是必不可少的,并且孢子形成效率的降低是由于该顺序的逆转造成的。这些见解使我们能够将过早抑制 DivIVA 鉴定为 Spo0A∼P 积累加速对孢子形成产生不利影响的一种可能解释。此外,我们发现,由于天然 spo0A 启动子的自身调控产生的正反馈导致 Spo0A∼P 积累动力学得到稳健控制。因此,我们提出,孢子形成网络保守结构的主要功能之一是控制 Spo0A 激活动力学。