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首页> 外文期刊>Nucleic acids research >Imprecise transcription termination within Escherichia coli greA leader gives rise to an array of short transcripts, GraL
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Imprecise transcription termination within Escherichia coli greA leader gives rise to an array of short transcripts, GraL

机译:大肠埃希氏菌greA前导分子内转录终止不精确导致一系列短转录本GraL

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We report that greA expression is driven by two strong, overlapping P1 and P2 promoters. The P1 promoter is σ70-dependent and P2 is σE-dependent. Two-thirds of transcripts terminate within the leader region and the remaining third comprises greA mRNA. Termination efficiency seems to be unaffected by growth phase. Two collections of small 40–50 (initiating from P2) and 50–60 nt (from P1) RNA chains, termed GraL, are demonstrable in vivo and in vitro. We document that GraL arrays arise from an intrinsic terminator with an 11 bp stem followed by an AU7GCU2 sequence. Atypical chain termination occurs at multiple sites; the 3′-ends differ by 1 nt over a range of 10 nt. Transcripts observed are shown to be insensitive to Gre factors and physically released from RNAP–DNA complexes. The abundance of individual chains within each cluster displays a characteristic pattern, which can be differentially altered by oligonucleotide probes. Multiple termination sites are particularly sensitive to changes at the bottom of the stem. Evolutionarily conserved GraL stem structures and fitness assays suggest a biological function for the RNA clusters themselves. Although GraL overexpression induces ≥3-fold transcriptional changes of over 100 genes, a direct target remains elusive.
机译:我们报告greA表达是由两个强大的,重叠的P1和P2启动子驱动的。 P1启动子依赖于σ 70 ,P2启动子依赖于σ E 。转录物的三分之二终止于前导区内,其余三分之一包含greA mRNA。终止效率似乎不受成长阶段的影响。可在体内和体外证实两个收集的小40–50(起始于P2)和50–60 nt(起始于P1)RNA链。我们证明了GraL阵列是由一个具有11 bp茎的内在终止子产生的,随后是一个AU 7 GCU 2 序列。非典型链终止发生在多个位置。 3'端在10 nt的范围内相差1 nt。已显示,观察到的转录本对Gre因子不敏感,并从RNAP-DNA复合物中物理释放。每个簇中单个链的丰度显示出特征性模式,该模式可通过寡核苷酸探针差异性地改变。多个终止位点对茎底部的变化特别敏感。进化上保守的GraL茎结构和适应性测定表明RNA簇本身具有生物学功能。尽管GraL的过表达诱导了100多个基因的≥3倍转录变化,但直接的靶标仍然难以捉摸。

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