Vicente Cláudia M, Girardet Jean-Michel, Hôtel Laurence, Aigle Bertrand
Université de Lorraine, INRAE, DynAMic, Nancy, France.
Université de Lorraine, INRAE, IAM, Nancy, France.
Front Microbiol. 2020 Jul 2;11:1255. doi: 10.3389/fmicb.2020.01255. eCollection 2020.
Signaling molecule receptors play a central role in quorum sensing and in the coordination onset of specialized metabolite biosynthesis in due to their dual function in signal detection and gene expression control through DNA-binding in the promoter region of their target genes. In the biosynthetic gene cluster includes the signaling molecule receptor AlpZ that negatively regulates through a complex regulatory cascade the expression of key genes involved in the kinamycin antibiotic production until its cognate ligand, a yet unidentified signaling molecule, prompts its release from target promoters. Here we use an original molecular dynamics method to evaluate the DNA-binding properties of AlpZ to its target DNA sequence and the impact the signaling molecule has on the interaction. It is the first time this approach is used to characterize a regulator from the γ-butyrolactone receptor family. The observed K in the nanomolar range indicates that AlpZ-DNA constitute a particularly stable complex. The signaling molecule ably disturbs this binding while kinamycin has no effect on the activity of AlpZ. Regulator size was determined and found to be considerably large regarding protein sequence, indicating that AlpZ regulates gene expression by binding the DNA as a homodimer, and structural modeling comparison with closely related γ-butyrolactone receptors supports this conclusion.
信号分子受体在群体感应以及特定代谢物生物合成的协调起始过程中发挥着核心作用,这是由于它们在信号检测和通过与靶基因启动子区域的DNA结合来控制基因表达方面具有双重功能。在[具体情况]中,生物合成基因簇包含信号分子受体AlpZ,它通过复杂的调控级联反应对参与奇霉素抗生素生产的关键基因的表达进行负调控,直到其同源配体(一种尚未鉴定的信号分子)促使它从靶启动子上释放。在这里,我们使用一种原始的分子动力学方法来评估AlpZ与其靶DNA序列的DNA结合特性,以及信号分子对这种相互作用的影响。这是首次使用这种方法来表征γ-丁内酯受体家族的一种调节因子。在纳摩尔范围内观察到的[解离常数]表明AlpZ-DNA构成了一种特别稳定的复合物。信号分子能够干扰这种结合,而奇霉素对AlpZ的活性没有影响。确定了调节因子的大小,发现就蛋白质序列而言相当大,这表明AlpZ通过作为同二聚体结合DNA来调节基因表达,并且与密切相关的γ-丁内酯受体的结构建模比较支持这一结论。