Medical Research Council Mitochondrial Biology Unit, University of Cambridge, Cambridge CB2 0XY, UK.
Department of Chemistry, Seoul National University, Gwanak-ro 1, Seoul 08826, South Korea.
Nucleic Acids Res. 2019 Sep 19;47(16):8720-8733. doi: 10.1093/nar/gkz559.
Expression of human mitochondrial DNA is indispensable for proper function of the oxidative phosphorylation machinery. The mitochondrial genome encodes 22 tRNAs, 2 rRNAs and 11 mRNAs and their post-transcriptional modification constitutes one of the key regulatory steps during mitochondrial gene expression. Cytosine-5 methylation (m5C) has been detected in mitochondrial transcriptome, however its biogenesis has not been investigated in details. Mammalian NOP2/Sun RNA Methyltransferase Family Member 2 (NSUN2) has been characterized as an RNA methyltransferase introducing m5C in nuclear-encoded tRNAs, mRNAs and microRNAs and associated with cell proliferation and differentiation, with pathogenic variants in NSUN2 being linked to neurodevelopmental disorders. Here we employ spatially restricted proximity labelling and immunodetection to demonstrate that NSUN2 is imported into the matrix of mammalian mitochondria. Using three genetic models for NSUN2 inactivation-knockout mice, patient-derived fibroblasts and CRISPR/Cas9 knockout in human cells-we show that NSUN2 is necessary for the generation of m5C at positions 48, 49 and 50 of several mammalian mitochondrial tRNAs. Finally, we show that inactivation of NSUN2 does not have a profound effect on mitochondrial tRNA stability and oxidative phosphorylation in differentiated cells. We discuss the importance of the newly discovered function of NSUN2 in the context of human disease.
人线粒体 DNA 的表达对于氧化磷酸化机制的正常功能是必不可少的。线粒体基因组编码 22 种 tRNA、2 种 rRNA 和 11 种 mRNA,其转录后修饰是线粒体基因表达过程中的关键调节步骤之一。在线粒体转录组中已经检测到胞嘧啶-5 甲基化(m5C),但其生物发生尚未详细研究。哺乳动物 NOP2/Sun RNA Methyltransferase Family Member 2(NSUN2)已被鉴定为一种 RNA 甲基转移酶,可在核编码的 tRNA、mRNA 和 microRNA 中引入 m5C,并与细胞增殖和分化有关,NSUN2 的致病变体与神经发育障碍有关。在这里,我们采用空间限制的邻近标记和免疫检测来证明 NSUN2 被导入哺乳动物线粒体的基质中。使用 NSUN2 失活的三种遗传模型——敲除小鼠、患者来源的成纤维细胞和人类细胞中的 CRISPR/Cas9 敲除——我们表明 NSUN2 对于几个哺乳动物线粒体 tRNA 中位置 48、49 和 50 的 m5C 的产生是必需的。最后,我们表明 NSUN2 的失活对分化细胞中线粒体 tRNA 的稳定性和氧化磷酸化没有深远的影响。我们将 NSUN2 的新发现功能在人类疾病背景下的重要性进行了讨论。