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人线粒体 RNA 聚合酶的 DNA 构象依赖性活性。

DNA conformation-dependent activities of human mitochondrial RNA polymerase.

机构信息

Department of Clinical Chemistry and Laboratory Medicine, Kyushu University Graduate School of Medical Sciences, Fukuoka 812-8582, Japan.

出版信息

Genes Cells. 2009 Aug;14(8):1029-42. doi: 10.1111/j.1365-2443.2009.01328.x. Epub 2009 Jul 14.

DOI:10.1111/j.1365-2443.2009.01328.x
PMID:19624753
Abstract

Mitochondrial RNA polymerase (POLRMT) is a core protein for mitochondrial DNA (mtDNA) transcription. In addition, POLRMT is assumed to be involved in replication, although its exact role is not yet clearly elucidated. We have found novel properties of human POLRMT using a reconstituted transcription system. Various lengths of RNA molecules were synthesized from templates even without a defined promoter sequence, when we used supercoiled circular double-stranded DNA as a template. This promoter-independent activity was as strong as the promoter-dependent one. Promoter-independent DNA conformation-dependent transcription required TFB2M. On supercoiled templates, the promoter-independent activity was strongly suppressed by a putatively physiological amount of TFAM, while promoter-dependent transcription was inhibited to a lesser extent. These different inhibition patterns by TFAM may be important for prevention of random RNA synthesis in vivo. Promoter-independent activity was also observed on relaxed circular single-stranded DNA, where its activity no longer required TFB2M. RNA synthesis on single-stranded DNA was weakly suppressed by a putatively physiological amount of TFAM but restored by the addition of mitochondrial single-stranded DNA binding protein. We suggest that these properties of POLRMT could explain the characteristic features of mammalian mtDNA transcription and replication.

摘要

线粒体 RNA 聚合酶 (POLRMT) 是线粒体 DNA (mtDNA) 转录的核心蛋白。此外,POLRMT 被认为参与复制,尽管其确切作用尚未明确阐明。我们使用重组转录系统发现了人类 POLRMT 的新特性。当我们使用超螺旋环状双链 DNA 作为模板时,即使没有定义的启动子序列,也可以合成各种长度的 RNA 分子。这种启动子非依赖性活性与启动子依赖性活性一样强。启动子非依赖性 DNA 构象依赖性转录需要 TFB2M。在超螺旋模板上,启动子非依赖性活性被假定的生理量的 TFAM 强烈抑制,而启动子依赖性转录的抑制程度较小。TFAM 的这种不同抑制模式可能对预防体内随机 RNA 合成很重要。在松弛的环状单链 DNA 上也观察到启动子非依赖性活性,其活性不再需要 TFB2M。假定的生理量的 TFAM 对单链 DNA 上的 RNA 合成有较弱的抑制作用,但添加线粒体单链 DNA 结合蛋白后可恢复。我们认为,POLRMT 的这些特性可以解释哺乳动物 mtDNA 转录和复制的特征。

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