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首页> 外文期刊>Journal of bacteriology >Nutrient-Regulated Proteolysis of MrpC Halts Expression of Genes Important for Commitment to Sporulation during Myxococcus xanthus Development
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Nutrient-Regulated Proteolysis of MrpC Halts Expression of Genes Important for Commitment to Sporulation during Myxococcus xanthus Development

机译:营养调控的MrpC的蛋白水解过程停止了在粘球菌发展过程中重要参与孢子形成的基因的表达。

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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.
机译:饥饿的黄色粘球菌细胞滑向聚集中心并形成子实体,其中杆状细胞分化为卵形孢子。通过在饥饿后的特定时间添加营养素并确定发育是停止还是进行来研究对发育的承诺。饥饿后24小时,一些杆状细胞被定型为随后的形状改变并成为抗超声处理的孢子,但营养导致子实体的部分分解。饥饿后30小时,有10倍以上的细胞被定为抗超声处理的孢子,并且在添加营养物后,紧密的子实体仍然存在。在饥饿后大约24至30小时的关键承诺期内,转录因子MrpC和FruA协同调节对孢子形成重要的基因。 FruA响应短时C信号,该信号随着细胞形成子实体而增加。在承诺孢子形成的关键时期之前和之中,发现MrpC对营养调节的蛋白水解高度敏感。营养物添加到发育中的细胞后,Mrpc的快速周转使 dev 操纵子的表达停止,这对于孢子形成很重要。 MrpC的调节蛋白水解似乎涉及不依赖ATP的金属蛋白酶活性,并且可能提供一种机制来监测饥饿是否持续以及如果养分重新出现则中止对孢子的形成。

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