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酵母活性可以替代海拉细胞的TATA盒因子。

A yeast activity can substitute for the HeLa cell TATA box factor.

作者信息

Cavallini B, Huet J, Plassat J L, Sentenac A, Egly J M, Chambon P

机构信息

Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Strasbourg, France.

出版信息

Nature. 1988 Jul 7;334(6177):77-80. doi: 10.1038/334077a0.

Abstract

Most class B (II) promoter regions from higher eukaryotes contain the TATA box and upstream and enhancer elements. Both the upstream and enhancer elements and their cognate factors have regulatory functions, whereas the TATA sequence interacts with the TATA box factor BTF1 to position RNA polymerase B and its ancillary initiation factors (STF, BTF2 and BTF3) to direct the initiation of transcription approximately 30 base pairs downstream. In many respects, class B promoter regions from the unicellular eukaryote Saccharomyces cerevisiae are similarly organized, containing upstream activating sequences that bear many similarities to enhancers. Although they are essential for initiation, the yeast TATA sequences are located at variable distances and further from the start sites (40-120 base pairs), whose locations are primarily determined by an initiator element. The basic molecular mechanisms that control initiation of transcription are known to be conserved from yeast to man: the yeast transcriptional transactivator GAL4 can activate a minimal TATA box-containing promoter in human HeLa cells, and a human inducible enhancer factor, the oestrogen receptor, can activate a similar minimal promoter in yeast. This striking evolutionary conservation prompted us to look for the presence in yeast of an activity that could possibly substitute for the human TATA box factor. We report here the existence of such an activity in yeast extracts.

摘要

大多数高等真核生物的B类(II)启动子区域包含TATA盒以及上游元件和增强子元件。上游元件和增强子元件及其相关因子都具有调控功能,而TATA序列与TATA盒因子BTF1相互作用,将RNA聚合酶B及其辅助起始因子(STF、BTF2和BTF3)定位在下游约30个碱基对处,以指导转录起始。在许多方面,单细胞真核生物酿酒酵母的B类启动子区域组织方式类似,包含与增强子有许多相似之处的上游激活序列。尽管酵母TATA序列对起始至关重要,但它们与起始位点的距离可变且更远(40 - 120个碱基对),起始位点的位置主要由起始子元件决定。已知从酵母到人类,控制转录起始的基本分子机制是保守的:酵母转录反式激活因子GAL4可以激活人类HeLa细胞中含最小TATA盒的启动子,而人类诱导型增强子因子雌激素受体可以激活酵母中类似的最小启动子。这种显著的进化保守性促使我们寻找酵母中可能替代人类TATA盒因子的活性。我们在此报告酵母提取物中存在这种活性。

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