Matsumoto Emi, Sasaki Taeko, Higashiyama Tetsuya, Sasaki Narie
Department of Biological Sciences, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
Laboratory of Molecular Membrane Biology, Institute for Molecular and Cellular Regulation, Gunma University, 3-39-15 Showa-machi, Maebashi, Gunma, 371-8512, Japan.
Sci Rep. 2025 Apr 21;15(1):13811. doi: 10.1038/s41598-025-98397-y.
Mitochondrial DNA (mtDNA) is organized with proteins into mitochondrial nucleoid (mt-nucleoid). The mt-nucleoid is a unit for the maintenance and function of mtDNA. The regulator of chromosome condensation 1-like protein (RCC1L) performs various functions in mitochondria, including translation, but its involvement in regulating mt-nucleoid maintenance is unknown. Herein, we found that human RCC1L was required to maintain mt-nucleoids and mtDNA. Human RCC1L has three splicing isoforms: RCC1L, RCC1L, and RCC1L. Knockout (KO) cells lacking all RCC1L isoforms, which were lethal without pyruvate and uridine, exhibited a decrease in mt-nucleoids and mtDNA, along with swollen and fragmented mitochondria. Among the three RCC1L isoforms, only RCC1L recovered all phenotypes observed in RCC1L KO cells. As the treatment of wild-type cells with chloramphenicol, a mitochondrial translation inhibitor, did not lead to the decrease in mt-nucleoids accompanied by mtDNA depletion, the decrease in mt-nucleoids and mtDNA in RCC1L KO cells was not solely attributed to impaired mitochondrial translation. Using conditional RCC1L KO cells, we observed a rapid decrease in mt-nucleoids and mtDNA during a specific period following RCC1L loss. Our findings indicate that RCC1L regulates the maintenance of mt-nucleoids and mtDNA besides its role in mitochondrial translational regulation.
线粒体DNA(mtDNA)与蛋白质组装成线粒体类核(mt - 类核)。mt - 类核是mtDNA维持和功能的一个单位。染色体凝聚调节因子1样蛋白(RCC1L)在线粒体中发挥多种功能,包括翻译,但它在调节mt - 类核维持方面的作用尚不清楚。在此,我们发现人类RCC1L是维持mt - 类核和mtDNA所必需的。人类RCC1L有三种剪接异构体:RCC1L、RCC1L和RCC1L。缺乏所有RCC1L异构体的基因敲除(KO)细胞在没有丙酮酸和尿苷的情况下是致死的,这些细胞表现出mt - 类核和mtDNA减少,同时线粒体肿胀和碎片化。在这三种RCC1L异构体中,只有RCC1L恢复了在RCC1L KO细胞中观察到的所有表型。由于用线粒体翻译抑制剂氯霉素处理野生型细胞不会导致伴随mtDNA耗竭的mt - 类核减少,因此RCC1L KO细胞中mt - 类核和mtDNA的减少并不完全归因于线粒体翻译受损。使用条件性RCC1L KO细胞,我们观察到在RCC1L缺失后的特定时期内,mt - 类核和mtDNA迅速减少。我们的研究结果表明,RCC1L除了在线粒体翻译调节中的作用外,还调节mt - 类核和mtDNA的维持。