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果蝇RNA聚合酶I启动子的一个组件位于rRNA转录单元内。

A component of Drosophila RNA polymerase I promoter lies within the rRNA transcription unit.

作者信息

Kohorn B D, Rae P M

出版信息

Nature. 1983;304(5922):179-81. doi: 10.1038/304179a0.

Abstract

Genes transcribed by RNA polymerase II have been characterized as having several control regions upstream of the site at which transcription is initiated, and the 'CAAT' and 'TAATA' regulatory sequences are conserved in content and location in diverse eukaryotes. The transcription of 5S RNA and tRNA by polymerase III is regulated by promoters that are actually within the genes; these are also conserved in diverse eukaryotes. In addition, sequences upstream of tRNA genes can affect RNA synthesis. Recently, it has been determined that DNA sequences influencing the expression of the 18S and 28S ribosomal RNA genes (rDNA) lie upstream of the site of transcription initiation. We have shown that a major component of the promoter of Drosophila rRNA polymerase I activity involves the region -43 to -27, where initiation is at +1. Here we present evidence that another major component of the polymerase I promoter lies within the first four nucleotides of the external transcribed spacer (ETS). Drosophila polymerase I control signals, therefore, lie both upstream of and within the rRNA transcription unit.

摘要

由RNA聚合酶II转录的基因,其特征是在转录起始位点上游有几个控制区域,并且“CAAT”和“TAATA”调控序列在不同真核生物中的含量和位置都是保守的。聚合酶III对5S RNA和tRNA的转录由实际上位于基因内部的启动子调控;这些启动子在不同真核生物中也具有保守性。此外,tRNA基因上游的序列可以影响RNA合成。最近已经确定,影响18S和28S核糖体RNA基因(rDNA)表达的DNA序列位于转录起始位点的上游。我们已经表明,果蝇rRNA聚合酶I活性启动子的一个主要成分涉及-43至-27区域,转录起始于+1处。在此我们提供证据表明,聚合酶I启动子的另一个主要成分位于外部转录间隔区(ETS)的前四个核苷酸内。因此,果蝇聚合酶I的控制信号既位于rRNA转录单元的上游,也位于其内部。

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