IST Austria, Klosterneuburg, Austria.
EMBL Heidelberg, Heidelberg, Germany.
Mol Syst Biol. 2019 Feb 14;15(2):e8470. doi: 10.15252/msb.20188470.
Sudden stress often triggers diverse, temporally structured gene expression responses in microbes, but it is largely unknown how variable in time such responses are and if genes respond in the same temporal order in every single cell. Here, we quantified timing variability of individual promoters responding to sublethal antibiotic stress using fluorescent reporters, microfluidics, and time-lapse microscopy. We identified lower and upper bounds that put definite constraints on timing variability, which varies strongly among promoters and conditions. Timing variability can be interpreted using results from statistical kinetics, which enable us to estimate the number of rate-limiting molecular steps underlying different responses. We found that just a few critical steps control some responses while others rely on dozens of steps. To probe connections between different stress responses, we then tracked the temporal order and response time correlations of promoter pairs in individual cells. Our results support that, when bacteria are exposed to the antibiotic nitrofurantoin, the ensuing oxidative stress and SOS responses are part of the same causal chain of molecular events. In contrast, under trimethoprim, the acid stress response and the SOS response are part of different chains of events running in parallel. Our approach reveals fundamental constraints on gene expression timing and provides new insights into the molecular events that underlie the timing of stress responses.
突发应激通常会引发微生物中多样化的、具有时间结构的基因表达反应,但人们在很大程度上并不清楚这些反应在时间上的变化有多大,以及在每个细胞中基因是否以相同的时间顺序作出反应。在这里,我们使用荧光报告基因、微流控技术和延时显微镜来定量测量单个启动子对亚致死抗生素应激的反应的时间变化。我们确定了下限和上限,这对时间变化施加了明确的限制,而时间变化在不同的启动子和条件之间变化很大。可以使用统计动力学的结果来解释时间变化,这使我们能够估计不同反应所涉及的限速分子步骤的数量。我们发现,只有少数关键步骤控制着一些反应,而其他反应则依赖于数十个步骤。为了探究不同应激反应之间的联系,我们随后在单个细胞中跟踪了启动子对之间的时间顺序和反应时间相关性。我们的结果支持这样一种观点,即在细菌暴露于抗生素呋喃妥因时,随之而来的氧化应激和 SOS 反应是同一分子事件因果链的一部分。相比之下,在甲氧苄啶的情况下,酸应激反应和 SOS 反应是不同的平行事件链的一部分。我们的方法揭示了基因表达时间的基本限制,并为应激反应时间背后的分子事件提供了新的见解。