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酵母U6小核仁RNA基因的转录需要一个位于新位置的聚合酶III启动子元件。

Transcription of a yeast U6 snRNA gene requires a polymerase III promoter element in a novel position.

作者信息

Brow D A, Guthrie C

机构信息

Department of Biochemistry and Biophysics, University of California, San Francisco 94143-0448.

出版信息

Genes Dev. 1990 Aug;4(8):1345-56. doi: 10.1101/gad.4.8.1345.

Abstract

Vertebrate genes coding for U6 small nuclear RNA are transcribed by RNA polymerase III (pol III), using only upstream promoter elements rather than the A and B block internal control regions typical of most pol III transcription units. We show that expression of the U6 gene from the yeast Saccharomyces cerevisiae has two unexpected features: it requires a B block promoter element, and this element is located in a novel position, 120 bp downstream of the coding region. In tRNA genes, the B block is the primary binding site for transcription factor (TF) IIIC, whose function is to promote the subsequent binding of TFIIIB. Both factors are thus implicated in yeast U6 gene transcription. We present a model of the U6 transcription complex based on the structure of yeast and vertebrate U6 promoters.

摘要

编码U6小核RNA的脊椎动物基因由RNA聚合酶III(pol III)转录,仅使用上游启动子元件,而非大多数pol III转录单位典型的A和B框内部控制区域。我们发现,来自酿酒酵母的U6基因的表达有两个意外特征:它需要一个B框启动子元件,且该元件位于一个新位置,即编码区下游120 bp处。在tRNA基因中,B框是转录因子(TF)IIIC的主要结合位点,其功能是促进TFIIIB随后的结合。因此,这两个因子都与酵母U6基因转录有关。我们基于酵母和脊椎动物U6启动子的结构提出了一个U6转录复合体模型。

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