Caldara Marina, Charlier Daniel, Cunin Raymond
Laboratorium voor Erfelijkheidsleer en Microbiologie, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium.
Microbiology (Reading). 2006 Nov;152(Pt 11):3343-3354. doi: 10.1099/mic.0.29088-0.
Analysis of the response to arginine of the Escherichia coli K-12 transcriptome by microarray hybridization and real-time quantitative PCR provides the first coherent quantitative picture of the ArgR-mediated repression of arginine biosynthesis and uptake genes. Transcriptional repression was shown to be the major control mechanism of the biosynthetic genes, leaving only limited room for additional transcriptional or post-transcriptional regulation. The art genes, encoding the specific arginine uptake system, are subject to ArgR-mediated repression, with strong repression of artJ, encoding the periplasmic binding protein of the system. The hisJQMP genes of the histidine transporter (part of the lysine-arginine-ornithine uptake system) were discovered to be a part of the arginine regulon. Analysis of their control region with reporter gene fusions and electrophoretic mobility shift in the presence of pure ArgR repressor showed the involvement in repression of the ArgR protein and an ARG box 120 bp upstream of hisJ. No repression of the genes of the third uptake system, arginine-ornithine, was observed. Finally, comparison of the time course of arginine repression of gene transcription with the evolution of the specific activities of the cognate enzymes showed that while full genetic repression was achieved 2 min after arginine addition, enzyme concentrations were diluted at the rate of cell division. This emphasizes the importance of feedback inhibition of the first enzymic step in the pathway in controlling the metabolic flow through biosynthesis in the period following the onset of repression.
通过微阵列杂交和实时定量PCR分析大肠杆菌K-12转录组对精氨酸的反应,首次提供了ArgR介导的精氨酸生物合成和摄取基因抑制的连贯定量图景。转录抑制被证明是生物合成基因的主要控制机制,留给额外转录或转录后调控的空间有限。编码特定精氨酸摄取系统的art基因受到ArgR介导的抑制,其中编码该系统周质结合蛋白的artJ受到强烈抑制。组氨酸转运蛋白的hisJQMP基因(赖氨酸-精氨酸-鸟氨酸摄取系统的一部分)被发现是精氨酸调控子的一部分。用报告基因融合分析其控制区域,并在存在纯ArgR阻遏物的情况下进行电泳迁移率变动分析,结果表明ArgR蛋白和hisJ上游120 bp处的一个ARG框参与了抑制作用。未观察到第三个摄取系统(精氨酸-鸟氨酸)的基因受到抑制。最后,将基因转录的精氨酸抑制时间进程与同源酶的比活性变化进行比较,结果表明,虽然在添加精氨酸后2分钟实现了完全的基因抑制,但酶浓度以细胞分裂的速率被稀释。这强调了在抑制开始后的时期内,该途径中第一个酶促步骤的反馈抑制在控制生物合成代谢流方面的重要性。