Institute for Mitochondrial Diseases and Ageing, Faculty of Medicine and University Hospital Cologne, Cluster of Excellence Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany.
Department of Medical Biochemistry and Cell Biology, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.
Nat Rev Mol Cell Biol. 2024 Feb;25(2):119-132. doi: 10.1038/s41580-023-00661-4. Epub 2023 Oct 2.
The expression of mitochondrial genes is regulated in response to the metabolic needs of different cell types, but the basic mechanisms underlying this process are still poorly understood. In this Review, we describe how different layers of regulation cooperate to fine tune initiation of both mitochondrial DNA (mtDNA) transcription and replication in human cells. We discuss our current understanding of the molecular mechanisms that drive and regulate transcription initiation from mtDNA promoters, and how the packaging of mtDNA into nucleoids can control the number of mtDNA molecules available for both transcription and replication. Indeed, a unique aspect of the mitochondrial transcription machinery is that it is coupled to mtDNA replication, such that mitochondrial RNA polymerase is additionally required for primer synthesis at mtDNA origins of replication. We discuss how the choice between replication-primer formation and genome-length RNA synthesis is controlled at the main origin of replication (OriH) and how the recent discovery of an additional mitochondrial promoter (LSP2) in humans may change this long-standing model.
线粒体基因的表达受不同细胞类型代谢需求的调节,但这一过程的基本机制仍知之甚少。在这篇综述中,我们描述了不同层次的调节如何协同作用,精细调节人类细胞中线粒体 DNA(mtDNA)转录和复制的起始。我们讨论了我们目前对驱动和调节 mtDNA 启动子转录起始的分子机制的理解,以及 mtDNA 包装成核小体如何控制可用于转录和复制的 mtDNA 分子数量。事实上,线粒体转录机制的一个独特方面是它与 mtDNA 复制偶联,使得线粒体 RNA 聚合酶在 mtDNA 复制起点的引物合成中也是必需的。我们讨论了在主要复制起点(OriH)如何控制复制引物形成和基因组长度 RNA 合成之间的选择,以及最近在人类中发现的另一个线粒体启动子(LSP2)如何可能改变这一长期存在的模型。