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酵母线粒体RNA聚合酶转录起始的机制

Mechanism of transcription initiation by the yeast mitochondrial RNA polymerase.

作者信息

Deshpande Aishwarya P, Patel Smita S

机构信息

Department of Biochemistry, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway, NJ 08854, USA.

出版信息

Biochim Biophys Acta. 2012 Sep-Oct;1819(9-10):930-8. doi: 10.1016/j.bbagrm.2012.02.003. Epub 2012 Feb 14.

Abstract

Mitochondria are the major supplier of cellular energy in the form of ATP. Defects in normal ATP production due to dysfunctions in mitochondrial gene expression are responsible for many mitochondrial and aging related disorders. Mitochondria carry their own DNA genome which is transcribed by relatively simple transcriptional machinery consisting of the mitochondrial RNAP (mtRNAP) and one or more transcription factors. The mtRNAPs are remarkably similar in sequence and structure to single-subunit bacteriophage T7 RNAP but they require accessory transcription factors for promoter-specific initiation. Comparison of the mechanisms of T7 RNAP and mtRNAP provides a framework to better understand how mtRNAP and the transcription factors work together to facilitate promoter selection, DNA melting, initiating nucleotide binding, and promoter clearance. This review focuses primarily on the mechanistic characterization of transcription initiation by the yeast Saccharomyces cerevisiae mtRNAP (Rpo41) and its transcription factor (Mtf1) drawing insights from the homologous T7 and the human mitochondrial transcription systems. We discuss regulatory mechanisms of mitochondrial transcription and the idea that the mtRNAP acts as the in vivo ATP "sensor" to regulate gene expression. This article is part of a Special Issue entitled: Mitochondrial Gene Expression.

摘要

线粒体是以三磷酸腺苷(ATP)形式提供细胞能量的主要来源。由于线粒体基因表达功能障碍导致正常ATP生成缺陷,是许多线粒体相关疾病和衰老相关疾病的病因。线粒体携带自身的DNA基因组,该基因组由相对简单的转录机制进行转录,该转录机制由线粒体RNA聚合酶(mtRNAP)和一种或多种转录因子组成。mtRNAP在序列和结构上与单亚基噬菌体T7 RNA聚合酶非常相似,但它们需要辅助转录因子来进行启动子特异性起始。比较T7 RNA聚合酶和mtRNAP的机制,为更好地理解mtRNAP和转录因子如何协同工作以促进启动子选择、DNA解链、起始核苷酸结合和启动子清除提供了一个框架。本综述主要聚焦于酿酒酵母mtRNAP(Rpo41)及其转录因子(Mtf1)转录起始的机制特征,借鉴同源的T7和人类线粒体转录系统的相关知识。我们讨论了线粒体转录的调控机制,以及mtRNAP作为体内ATP“传感器”来调节基因表达的观点。本文是名为“线粒体基因表达”的特刊的一部分。

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