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Comparative Analysis of Regulatory Elements between Escherichia coli and Klebsiella pneumoniae by Genome-Wide Transcription Start Site Profiling

机译:通过全基因组转录起始位点分析对大肠杆菌和肺炎克雷伯菌的调控元素进行比较分析

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摘要

Genome-wide transcription start site (TSS) profiles of the enterobacteria Escherichia coli and Klebsiella pneumoniae were experimentally determined through modified 5′ RACE followed by deep sequencing of intact primary mRNA. This identified 3,746 and 3,143 TSSs for E. coli and K. pneumoniae, respectively. Experimentally determined TSSs were then used to define promoter regions and 5′ UTRs upstream of coding genes. Comparative analysis of these regulatory elements revealed the use of multiple TSSs, identical sequence motifs of promoter and Shine-Dalgarno sequence, reflecting conserved gene expression apparatuses between the two species. In both species, over 70% of primary transcripts were expressed from operons having orthologous genes during exponential growth. However, expressed orthologous genes in E. coli and K. pneumoniae showed a strikingly different organization of upstream regulatory regions with only 20% identical promoters with TSSs in both species. Over 40% of promoters had TSSs identified in only one species, despite conserved promoter sequences existing in the other species. 662 conserved promoters having TSSs in both species resulted in the same number of comparable 5′ UTR pairs, and that regulatory element was found to be the most variant region in sequence among promoter, 5′ UTR, and ORF. In K. pneumoniae, 48 sRNAs were predicted and 36 of them were expressed during exponential growth. Among them, 34 orthologous sRNAs between two species were analyzed in depth, and the analysis showed that many sRNAs of K. pneumoniae, including pleiotropic sRNAs such as rprA, arcZ, and sgrS, may work in the same way as in E. coli. These results reveal a new dimension of comparative genomics such that a comparison of two genomes needs to be comprehensive over all levels of genome organization.
机译:大肠杆菌和肺炎克雷伯菌的全基因组转录起始位点(TSS)图谱是通过修饰的5'RACE进行实验确定的,然后对完整的初级mRNA进行深度测序。这分别确定了针对大肠杆菌和肺炎克雷伯菌的3,746和3,143 TSS。然后将实验确定的TSS用于定义启动子区域和编码基因上游的5'UTR。对这些调控元件的比较分析显示,使用了多个TSS,相同的启动子序列基序和Shine-Dalgarno序列,反映了两个物种之间保守的基因表达装置。在这两个物种中,超过70%的初级转录本都是在指数生长过程中从具有直系同源基因的操纵子中表达的。然而,在大肠杆菌和肺炎克雷伯菌中表达的直系同源基因显示出上游调控区的组织显着不同,在两个物种中,它们与TSS的启动子只有20%相同。尽管在其他物种中存在保守的启动子序列,但仍有超过40%的启动子在一个物种中鉴定出TSS。在两个物种中均具有TSS的662个保守启动子产生了相同数量的可比较5'UTR对,并且发现该调控元件是启动子,5'UTR和ORF中序列上变异最大的区域。在肺炎克雷伯菌中,预测有48个sRNA,其中有36个在指数生长过程中表达。其中,对两个物种之间的34个直系同源sRNA进行了深入分析,分析表明,肺炎克雷伯菌的许多sRNA,包括多效性sRNA,如rprA,arcZ和sgrS,都可能以与大肠杆菌相同的方式起作用。这些结果揭示了比较基因组学的新领域,因此两个基因组的比较需要在基因组组织的所有水平上全面进行。

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