Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan, USA.
Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan, USA
J Bacteriol. 2014 Aug;196(15):2736-47. doi: 10.1128/JB.01692-14. Epub 2014 May 16.
Starved Myxococcus xanthus cells glide to aggregation centers and form fruiting bodies in which rod-shaped cells differentiate into ovoid spores. Commitment to development was investigated by adding nutrients at specific times after starvation and determining whether development halted or proceeded. At 24 h poststarvation, some rod-shaped cells were committed to subsequent shape change and to becoming sonication-resistant spores, but nutrients caused partial disaggregation of fruiting bodies. By 30 h poststarvation, 10-fold more cells were committed to becoming sonication-resistant spores, and compact fruiting bodies persisted after nutrient addition. During the critical period of commitment around 24 to 30 h poststarvation, the transcription factors MrpC and FruA cooperatively regulate genes important for sporulation. FruA responds to short-range C-signaling, which increases as cells form fruiting bodies. MrpC was found to be highly sensitive to nutrient-regulated proteolysis both before and during the critical period of commitment to sporulation. The rapid turnover of MrpC upon nutrient addition to developing cells halted expression of the dev operon, which is important for sporulation. Regulated proteolysis of MrpC appeared to involve ATP-independent metalloprotease activity and may provide a mechanism for monitoring whether starvation persists and halting commitment to sporulation if nutrients reappear.
饥饿状态下的粘球菌细胞会滑行到聚集中心,并形成子实体,在子实体中,杆状细胞分化成卵形孢子。通过在饥饿后特定时间添加营养物质,并确定发育是否停止或继续,来研究细胞对发育的承诺。饥饿后 24 小时,一些杆状细胞就开始进行后续的形状变化,并成为抗超声处理的孢子,但营养物质会导致子实体部分解体。饥饿后 30 小时,有 10 倍以上的细胞开始成为抗超声处理的孢子,并且在添加营养物质后,紧凑的子实体仍然存在。在饥饿后 24 到 30 小时的关键承诺期,转录因子 MrpC 和 FruA 共同调控对孢子形成很重要的基因。 FruA 对短程 C 信号作出反应,随着细胞形成子实体,C 信号会增加。发现 MrpC 在饥饿前和承诺期对孢子形成的高度敏感,其对营养调节的蛋白水解作用非常敏感。当发育细胞添加营养物质时,MrpC 的快速周转会停止表达 dev 操纵子,该操纵子对孢子形成很重要。MrpC 的调控蛋白水解似乎涉及 ATP 非依赖性金属蛋白酶活性,并且可能为监测是否持续饥饿以及如果营养物质再次出现而停止对孢子形成的承诺提供一种机制。