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首页> 外文期刊>Molecular and Cellular Biology >RNA Polymerase III Transcription Complexes on Chromosomal 5S rRNA Genes In Vivo: TFIIIB Occupancy and Promoter Opening
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RNA Polymerase III Transcription Complexes on Chromosomal 5S rRNA Genes In Vivo: TFIIIB Occupancy and Promoter Opening

机译:染色体5S rRNA基因上的RNA聚合酶III转录复合物体内:TFIIIB占用和启动子开放。

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Quantitative analysis of multiple-hit potassium permanganate (KMnO4) footprinting has been carried out in vivo onSaccharomyces cerevisiae 5S rRNA genes. The results fix the number of open complexes at steady state in exponentially growing cells at between 8 and 17% of the 150 to 200 chromosomal copies. UV and dimethyl sulfate footprinting set the transcription factor TFIIIB occupancy at 23 to 47%. The comparison between the two values suggests that RNA polymerase III binding or promoter opening is the rate-limiting step in 5S rRNA transcription in vivo. Inhibition of RNA elongation in vivo by cordycepin confirms this result. An experimental system that is capable of providing information on the mechanistic steps involved in regulatory events in S. cerevisiae cells has been established.
机译:已在体内对酿酒酵母 5S rRNA基因进行了多击高锰酸钾(KMnO 4 )足迹的定量分析。结果将成倍增长的细胞中稳定状态下开放复合物的数量固定在150至200个染色体拷贝的8%至17%之间。 UV和硫酸二甲酯的足迹将转录因子TFIIIB的占用率设置为23%至47%。这两个值之间的比较表明,RNA聚合酶III结合或启动子打开是体内5S rRNA转录中的限速步骤。虫草素在体内抑制RNA延长证实了这一结果。一个实验系统,能够提供有关 S中调控事件的机械步骤的信息。啤酒酵母细胞已经建立。

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