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与酿酒酵母转录因子Gal11p发生基因相互作用的蛋白质,突出了其在起始-延伸转变过程中的作用。

Proteins that genetically interact with the Saccharomyces cerevisiae transcription factor Gal11p emphasize its role in the initiation-elongation transition.

作者信息

Badi L, Barberis A

机构信息

Institute of Molecular Biology, University of Zürich, Switzerland.

出版信息

Mol Genet Genomics. 2001 Aug;265(6):1076-86. doi: 10.1007/s004380100505.

Abstract

The GAL11 gene encodes a transcription factor that is a component of the SRB/Mediator sub-complex of the RNA polymerase II holoenzyme in the yeast Saccharomyces cerevisiae. In agreement with this biochemical characterization, Gal11p has been found to be required for optimal production of mRNA from many yeast promoters, and recessive mutations in GAL11 have been shown to cause pleiotropic defects. Despite this progress, the role of Gal11p in gene regulation remains largely unknown. In a multicopy suppressor analysis of a gal11delta mutation we have identified genes encoding proteins that are part of, or can interact with, the RNA polymerase II transcription complex, as well as factors involved in cell cycle regulation. Among the suppressors that are clearly related to the transcriptional apparatus, Gal11p genetically interacts with components of the SRB/Mediator complex, as well as with factors such as TFIIE and TFIIH that are required for promoter clearance and transcription elongation by RNA polymerase II. These findings, taken together with published results of biochemical and genetic analyses, suggest a role for Galllp at the interface between the SRB/Mediator complex and the general transcription factors TFIIE and TFIIH, which modulate, via phosphorylation of the CTD, the activity of the RNA polymerase II during the transition between initiation and elongation.

摘要

GAL11基因编码一种转录因子,它是酿酒酵母中RNA聚合酶II全酶的SRB/中介体亚复合物的一个组成部分。与这种生化特性一致,已发现Gal11p是许多酵母启动子最佳产生mRNA所必需的,并且GAL11中的隐性突变已被证明会导致多效性缺陷。尽管取得了这一进展,但Gal11p在基因调控中的作用仍然很大程度上未知。在对gal11delta突变的多拷贝抑制子分析中,我们鉴定出了编码RNA聚合酶II转录复合物一部分或可与之相互作用的蛋白质的基因,以及参与细胞周期调控的因子。在与转录装置明显相关的抑制子中,Gal11p与SRB/中介体复合物的组分以及RNA聚合酶II进行启动子清除和转录延伸所需的TFIIE和TFIIH等因子发生遗传相互作用。这些发现,连同已发表的生化和遗传分析结果,表明Gal11p在SRB/中介体复合物与通用转录因子TFIIE和TFIIH之间的界面处发挥作用,它们在起始和延伸之间的转变过程中通过CTD的磷酸化来调节RNA聚合酶II的活性。

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