Institute for Molecular Bioscience, The University of Queensland, Brisbane QLD 4072, Australia.
Cell. 2011 Aug 19;146(4):645-58. doi: 10.1016/j.cell.2011.06.051.
The human mitochondrial genome comprises a distinct genetic system transcribed as precursor polycistronic transcripts that are subsequently cleaved to generate individual mRNAs, tRNAs, and rRNAs. Here, we provide a comprehensive analysis of the human mitochondrial transcriptome across multiple cell lines and tissues. Using directional deep sequencing and parallel analysis of RNA ends, we demonstrate wide variation in mitochondrial transcript abundance and precisely resolve transcript processing and maturation events. We identify previously undescribed transcripts, including small RNAs, and observe the enrichment of several nuclear RNAs in mitochondria. Using high-throughput in vivo DNaseI footprinting, we establish the global profile of DNA-binding protein occupancy across the mitochondrial genome at single-nucleotide resolution, revealing regulatory features at mitochondrial transcription initiation sites and functional insights into disease-associated variants. This integrated analysis of the mitochondrial transcriptome reveals unexpected complexity in the regulation, expression, and processing of mitochondrial RNA and provides a resource for future studies of mitochondrial function (accessed at http://mitochondria.matticklab.com).
人类线粒体基因组包含一个独特的遗传系统,转录为前体多顺反子转录本,随后被切割生成单个 mRNA、tRNA 和 rRNA。在这里,我们对多个细胞系和组织中的人类线粒体转录组进行了全面分析。我们使用定向深度测序和 RNA 末端的平行分析,证明了线粒体转录物丰度的广泛变化,并精确地解析了转录物加工和成熟事件。我们鉴定了以前未描述的转录物,包括小 RNA,并观察到几种核 RNA 在线粒体中的富集。我们使用高通量体内 DNaseI 足迹法,以单核苷酸分辨率建立了整个线粒体基因组中 DNA 结合蛋白占据的全局图谱,揭示了线粒体转录起始位点的调控特征,并为与疾病相关的变异提供了功能见解。对线粒体转录组的综合分析揭示了线粒体 RNA 调控、表达和加工的出人意料的复杂性,并为未来的线粒体功能研究提供了资源(可在 http://mitochondria.matticklab.com 访问)。