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In vitro evidence that RNA Polymerase acetylation and acetyl phosphate-dependent CpxR phosphorylation affect cpxP transcription regulation

机译:体外证据表明RNA聚合酶乙酰化和依赖乙酰磷酸的CpxR磷酸化影响cpxP转录调控

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摘要

The central metabolite acetyl phosphate (acP) has long been proposed to influence transcription regulation by directly transferring its phosphoryl group to a number of response regulators in many bacterial species. Here, we provide in vitro evidence for this proposition and demonstrate, using an in vitro transcription system, that acP-dependent phosphorylation of aspartate 51 of CpxR induces transcription of one of its regulon members in E. coli, cpxP. We also used this in vitro transcription system to extend our previously reported in vivo data that hypothesized that acetylation of RNA polymerase (RNAP) influences acP-dependent cpxP transcription, using glutamine as a genetic mimic for acetylated arginine 291 of the carboxy-terminal domain of RNAP α subunit. The data we present here lend strong support to the hypothesis that acP has a direct effect on transcription regulation in E. coli via phosphorylation of CpxR, and that RNAP acetylation can modulate this response.
机译:长期以来,人们一直提出将中央代谢物乙酰磷酸(acP)通过直接将其磷酸酯基转移到许多细菌物种中的许多响应调节剂中来影响转录调节。在这里,我们为这一提议提供了体外证据,并使用体外转录系统证明了CpxR的天冬氨酸51的acP依赖性磷酸化诱导了其调控因子之一在大肠杆菌cpxP中的转录。我们还使用该体外转录系统扩展了我们先前报道的体内数据,该数据假设RNA聚合酶(RNAP)的乙酰化影响acP依赖的cpxP转录,使用谷氨酰胺作为糖基化羧基末端结构域的乙酰化精氨酸291的遗传模拟物。 RNAPα亚基。我们在此提供的数据为acP通过CpxR的磷酸化对大肠杆菌中的转录调控具有直接影响,而RNAP乙酰化可以调节这种反应的假设提供了有力支持。

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