Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI, 48824, USA.
Department of Bioengineering, Rice University, Houston, TX, 77030, USA.
Mol Microbiol. 2019 Jun;111(6):1732-1752. doi: 10.1111/mmi.14249. Epub 2019 Apr 6.
Upon starvation Myxococcus xanthus undergoes multicellular development. Rod-shaped cells move into mounds in which some cells differentiate into spores. Cells begin committing to sporulation at 24-30 h poststarvation, but the mechanisms governing commitment are unknown. FruA and MrpC are transcription factors that are necessary for commitment. They bind cooperatively to promoter regions and activate developmental gene transcription, including that of the dev operon. Leading up to and during the commitment period, dev mRNA increased in wild type, but not in a mutant defective in C-signaling, a short-range signaling interaction between cells that is also necessary for commitment. The C-signaling mutant exhibited ~20-fold less dev mRNA than wild type at 30 h poststarvation, despite a similar level of MrpC and only 2-fold less FruA. Boosting the FruA level twofold in the C-signaling mutant had little effect on the dev mRNA level, and dev mRNA was not less stable in the C-signaling mutant. Neither did high cooperativity of MrpC and FruA binding upstream of the dev promoter explain the data. Rather, our systematic experimental and computational analyses support a model in which C-signaling activates FruA at least ninefold posttranslationally in order to commit a cell to spore formation.
当处于饥饿状态时,粘球菌会经历多细胞发育。杆状细胞移动到菌块中,其中一些细胞分化成孢子。细胞在饥饿后 24-30 小时开始进入孢子形成状态,但控制细胞进入这一状态的机制尚不清楚。 FruA 和 MrpC 是转录因子,它们是细胞进入孢子形成状态所必需的。它们协同结合启动子区域,激活发育基因转录,包括 dev 操纵子的转录。在进入和进行孢子形成状态的过程中,dev mRNA 在野生型中增加,但在缺乏 C 信号的突变体中没有增加,C 信号是细胞之间的短程信号相互作用,对细胞进入孢子形成状态也是必需的。尽管 C 信号突变体中的 MrpC 水平相似,且 FruA 仅减少了 2 倍,但在饥饿后 30 小时,C 信号突变体中的 dev mRNA 水平比野生型低约 20 倍。在 C 信号突变体中使 FruA 水平增加两倍对 dev mRNA 水平几乎没有影响,并且在 C 信号突变体中 dev mRNA 也没有减少稳定性。MrpC 和 FruA 在 dev 启动子上游的高协同结合也不能解释这些数据。相反,我们的系统实验和计算分析支持这样一种模型,即 C 信号在翻译后至少将 FruA 激活九倍,以使细胞进入孢子形成状态。