Bonawitz Nicholas D, Clayton David A, Shadel Gerald S
Department of Pathology, Yale University School of Medicine, 310 Cedar Street, P.O. Box 208023, New Haven, Connecticut 06520, USA.
Mol Cell. 2006 Dec 28;24(6):813-25. doi: 10.1016/j.molcel.2006.11.024.
Mitochondria contain their own DNA (mtDNA) that is expressed and replicated by nucleus-encoded factors imported into the organelle. Recently, the core human mitochondrial transcription machinery has been defined, comprising a bacteriophage-related mtRNA polymerase (POLRMT), an HMG-box transcription factor (h-mtTFA), and two transcription factors (h-mtTFB1 and h-mtTFB2) that also serve as rRNA methyltransferases. Here, we describe these transcription components as well as recent insights into the mechanism of human mitochondrial transcription initiation and its regulation. We also discuss novel roles for the mitochondrial transcription machinery beyond transcription initiation, including priming of mtDNA replication, packaging of mtDNA, coordination of ribosome biogenesis, and coupling of transcription to translation.
线粒体含有自己的DNA(mtDNA),其通过导入该细胞器的核编码因子进行表达和复制。最近,已确定了核心人类线粒体转录机制,包括一种与噬菌体相关的mtRNA聚合酶(POLRMT)、一种HMG盒转录因子(h-mtTFA)以及两种也作为rRNA甲基转移酶的转录因子(h-mtTFB1和h-mtTFB2)。在此,我们描述了这些转录成分以及对人类线粒体转录起始机制及其调控的最新见解。我们还讨论了线粒体转录机制在转录起始之外的新作用,包括mtDNA复制的引发、mtDNA的包装、核糖体生物合成的协调以及转录与翻译的偶联。