Suppr超能文献

果蝇线粒体转录因子B2调节施奈德细胞中的线粒体DNA拷贝数和转录。

Drosophila mitochondrial transcription factor B2 regulates mitochondrial DNA copy number and transcription in schneider cells.

作者信息

Matsushima Yuichi, Garesse Rafael, Kaguni Laurie S

机构信息

Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan 48824-1319, USA.

出版信息

J Biol Chem. 2004 Jun 25;279(26):26900-5. doi: 10.1074/jbc.M401643200. Epub 2004 Apr 1.

Abstract

We report the cloning and molecular analysis of Drosophila mitochondrial transcription factor B2 (d-mt-TFB2), a protein that plays a role in mitochondrial transcription and mitochondrial DNA (mtDNA) replication in Drosophila. An RNA interference (RNAi) construct was designed that reduces expression of d-mtTFB2 to 5% of its normal level in Schneider cells. RNAi knock-down of d-mtTFB2 reduces the abundance of specific mitochondrial RNA transcripts 2- to 8-fold and decreases the copy number of mtDNA approximately 3-fold. In a corollary manner, we find that overexpression of d-mtTFB2 increases both the abundance of mitochondrial RNA transcripts and the copy number of mtDNA. In a comparative experiment, we find that overexpression of Drosophila mitochondrial transcription factor A (d-TFAM) increases mtDNA copy number with no significant effect on mitochondrial transcripts. This argues for a direct role for mtTFB2 in mitochondrial transcription and suggests that, if TFAM serves a role in transcription, its endogenous level limits mtDNA copy number but not transcription. Furthermore, we suggest that mtTFB2 increases mtDNA copy number by increasing the frequency of initiation of DNA replication, whereas TFAM serves to stabilize and package mtDNA in mitochondrial nucleoids. Our work represents the first study to document the function of mtTFB2 in vivo, establishing a dual role in regulation of both transcription and replication, and provides a benchmark for comparative biochemical studies in various animal systems.

摘要

我们报告了果蝇线粒体转录因子B2(d-mt-TFB2)的克隆及分子分析,该蛋白在果蝇的线粒体转录和线粒体DNA(mtDNA)复制中发挥作用。设计了一种RNA干扰(RNAi)构建体,可将施奈德细胞中d-mtTFB2的表达水平降低至正常水平的5%。d-mtTFB2的RNAi敲低使特定线粒体RNA转录本的丰度降低了2至8倍,并使mtDNA的拷贝数减少了约3倍。相应地,我们发现d-mtTFB2的过表达增加了线粒体RNA转录本的丰度和mtDNA的拷贝数。在一项对比实验中,我们发现果蝇线粒体转录因子A(d-TFAM)的过表达增加了mtDNA拷贝数,但对线粒体转录本没有显著影响。这表明mtTFB2在线粒体转录中起直接作用,并表明,如果TFAM在转录中起作用,其内源水平限制了mtDNA拷贝数而非转录。此外,我们认为mtTFB2通过增加DNA复制起始频率来增加mtDNA拷贝数,而TFAM则用于稳定和包装线粒体类核中的mtDNA。我们的工作是首次记录mtTFB2体内功能的研究,确立了其在转录和复制调控中的双重作用,并为各种动物系统中的比较生化研究提供了基准。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验