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The PurR regulon in Escherichia coli K-12 MG1655

机译:大肠杆菌K-12 MG1655中的PurR调节子

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The PurR transcription factor plays a critical role in transcriptional regulation of purine metabolism in enterobacteria. Here, we elucidate the role of PurR under exogenous adenine stimulation at the genome-scale using high-resolution chromatin immunoprecipitation (ChIP)-chip and gene expression data obtained under in vivo conditions. Analysis of microarray data revealed that adenine stimulation led to changes in transcript level of about 10% of Escherichia coli genes, including the purine biosynthesis pathway. The E. coli strain lacking the purR gene showed that a total of 56 genes are affected by the deletion. From the ChIP-chip analysis, we determined that over 73% of genes directly regulated by PurR were enriched in the biosynthesis, utilization and transport of purine and pyrimidine nucleotides, and 20% of them were functionally unknown. Compared to the functional diversity of the regulon of the other general transcription factors in E. coli, the functions and size of the PurR regulon are limited.
机译:PurR转录因子在肠细菌中嘌呤代谢的转录调控中起关键作用。在这里,我们使用高分辨率染色质免疫沉淀(ChIP)芯片和在体内条件下获得的基因表达数据,阐明了PurR在基因组规模的外源腺嘌呤刺激下的作用。对微阵列数据的分析表明,腺嘌呤刺激导致包括嘌呤生物合成途径在内的大肠埃希氏大肠杆菌基因约10%的转录水平发生变化。缺乏purR基因的大肠杆菌菌株显示,共有56个基因受到缺失的影响。通过ChIP芯片分析,我们确定PurR直接调控的基因中有73%以上富含嘌呤和嘧啶核苷酸的生物合成,利用和转运,其中20%在功能上未知。与大肠杆菌中其他一般转录因子的调节子的功能多样性相比,PurR调节子的功能和大小受到限制。

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