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首页> 外文期刊>Molecular Genetics and Genomics >Identification of different promoters in the absA1–absA2 two-component system, a negative regulator of antibiotic production in Streptomyces coelicolor
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Identification of different promoters in the absA1–absA2 two-component system, a negative regulator of antibiotic production in Streptomyces coelicolor

机译:鉴定absA1-absA2两组分系统中不同启动子,这是天蓝色链霉菌中抗生素产生的负调节剂

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摘要

The absA1–absA2 genes encode a two-component system that negatively regulates the transcription of multiple antibiotic gene clusters of Streptomyces coelicolor. The microarray dataset time series of a S. coelicolor M145 bioreactor culture indicated that the transcription values of absA2 were approximately four times higher than those of absA1 throughout the time course of the culture. The co-transcription of absA1 and absA2 genes has been previously shown, although an independent absA2 promoter was not detected. In this study, we show by different technical approaches that the absA1–absA2 operon is transcribed from at least two promoters, the first producing a read-through transcript that includes both absA1 and absA2 genes and the second including only the absA2 gene. An absA2 mRNA 5′ end was mapped by primer extension and confirmed as TSS by deep sequencing in combination with TEX. Promoter-probe analyses detected promoter activity in both the absA1 and absA2 upstream regions. The absA2 upstream region showed a higher promoter activity, at least sevenfold higher than that of absA1. Furthermore, the absA2 gene may contain at least two additional promoters as shown by deep sequencing analyses. All together this work contributes to the understanding of the complex transcriptional regulation of these antibiotic regulators genes in S. coelicolor.
机译:absA1-absA2基因编码一个由两部分组成的系统,该系统负调控天蓝色链霉菌的多个抗生素基因簇的转录。 S. coelicolor M145生物反应器培养物的微阵列数据集时间序列表明,在整个培养过程中,absA2的转录值大约是absA1的转录值的四倍。先前已经显示了absA1和absA2基因的共转录,尽管未检测到独立的absA2启动子。在这项研究中,我们通过不同的技术方法证明了absA1–absA2操纵子是从至少两个启动子转录而成的,第一个启动子包含absA1和absA2基因,而第二个则包含absA2基因。通过引物延伸来绘制absA2 mRNA 5'末端,并通过与TEX结合的深度测序确认为TSS。启动子探针分析在absA1和absA2上游区域均检测到启动子活性。 absA2上游区域显示较高的启动子活性,至少比absA1高7倍。此外,如深度测序分析所示,absA2基因可包含至少两个另外的启动子。总之,这项工作有助于理解天蓝色链霉菌中这些抗生素调节基因的复杂转录调节。

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