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酵母基因组表达对RNA聚合酶III依赖性转录缺陷的响应调节

Modulation of yeast genome expression in response to defective RNA polymerase III-dependent transcription.

作者信息

Conesa Christine, Ruotolo Roberta, Soularue Pascal, Simms Tiffany A, Donze David, Sentenac André, Dieci Giorgio

机构信息

Service de Biochimie et Génétique Moléculaire, Bâtiment 144, CEA/Saclay, 91191 Gif-sur-Yvette Cedex, France.

出版信息

Mol Cell Biol. 2005 Oct;25(19):8631-42. doi: 10.1128/MCB.25.19.8631-8642.2005.

Abstract

We used genome-wide expression analysis in Saccharomyces cerevisiae to explore whether and how the expression of protein-coding, RNA polymerase (Pol) II-transcribed genes is influenced by a decrease in RNA Pol III-dependent transcription. The Pol II transcriptome was characterized in four thermosensitive, slow-growth mutants affected in different components of the RNA Pol III transcription machinery. Unexpectedly, we found only a modest correlation between altered expression of Pol II-transcribed genes and their proximity to class III genes, a result also confirmed by the analysis of single tRNA gene deletants. Instead, the transcriptome of all of the four mutants was characterized by increased expression of genes known to be under the control of the Gcn4p transcriptional activator. Indeed, GCN4 was found to be translationally induced in the mutants, and deleting the GCN4 gene eliminated the response. The Gcn4p-dependent expression changes did not require the Gcn2 protein kinase and could be specifically counteracted by an increased gene dosage of initiator tRNA(Met). Initiator tRNA(Met) depletion thus triggers a GCN4-dependent reprogramming of genome expression in response to decreased Pol III transcription. Such an effect might represent a key element in the coordinated transcriptional response of yeast cells to environmental changes.

摘要

我们利用酿酒酵母中的全基因组表达分析来探究蛋白质编码的、RNA聚合酶(Pol)II转录的基因表达是否以及如何受到RNA Pol III依赖性转录减少的影响。在四个对RNA Pol III转录机制不同组分有影响的温度敏感型、生长缓慢的突变体中对Pol II转录组进行了表征。出乎意料的是,我们发现Pol II转录基因表达的改变与其与III类基因的接近程度之间只有适度的相关性,对单个tRNA基因缺失突变体的分析也证实了这一结果。相反,所有四个突变体的转录组的特征是已知受Gcn4p转录激活因子控制的基因表达增加。事实上,发现GCN4在突变体中被翻译诱导,删除GCN4基因消除了这种反应。Gcn4p依赖性的表达变化不需要Gcn2蛋白激酶,并且可以通过增加起始tRNA(Met)的基因剂量来特异性抵消。因此,起始tRNA(Met)的消耗会触发GCN4依赖性的基因组表达重编程,以应对Pol III转录的减少。这种效应可能代表酵母细胞对环境变化的协调转录反应中的一个关键因素。

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