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MrpC, a CRP/Fnr homolog, functions as a negative autoregulator during the Myxococcus xanthus Myxococcus xanthus multicellular developmental program

机译:Myxococcus Xanthus myxococccus Xanthus多细胞发育计划中的MRPC,CRP / FNR同源物,用作阴性自动调节器

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Summary MrpC, a member of the CRP/Fnr superfamily of transcriptional regulators, plays a key role in coordination of the multicellular developmental program inMyxococcus xanthus . Previous reports suggest MrpC is subject to complex regulation including activation by an unusual LonDdependent proteolytic processing event that removes its unique Nterminal peptide, producing the isoform MrpC2. MrpC2 is proposed to positively autoregulate and regulate transcription of hundreds of genes necessary for both the aggregation and sporulation phases of the developmental program. We demonstrate here thatmrpC expression bifurcates corresponding to different cell populations within the developmental program. During our analysis of regulatory events controlling this process, we demonstrate that MrpC2 is not an active isoform; rather, the Nterminal peptide is instead essential for MrpC functionin vivo . We also demonstrate that MrpC is instead a negative autoregulator and represses its own expression by specifically competing with its enhancer binding protein, MrpB. These results provide an additional rare example of CRP/EBP coordinated regulation, and significantly revise the model for control of the central developmental transcriptional activator of theM. xanthus developmental program.
机译:总结MRPC是转录调节因子的CRP / FNR超家族的成员,在多细胞发育计划中素Xanthus的协调起关键作用。之前的报道表明MRPC受复杂的调节,包括通过一种不寻常的Lond依赖性蛋白水解加工事件来激活,该处理事件除去其独特的缠绕肽,产生同种型MRPC2。提出MRPC2以积极仿状和调节发育计划的聚集和孢子阶段所需的数百个基因的转录。我们在这里展示了与发育计划中的不同小区群体相对应的分叉分叉。在我们对控制此过程的监管事件分析期间,我们证明MRPC2不是活跃的同种型;相反,缠绕肽是MRPC功能体内必需的。我们还证明MRPC代替阴性自身调节剂,并通过特别竞争其增强剂结合蛋白MRPB来抑制自己的表达。这些结果提供了额外的CRP / EBP协调规则的罕见举例,并显着修改了控制中央发育转录激活物的模型。 Xanthus发展计划。

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