Desler C, Munch-Petersen B, Rasmussen L J
Department of Life Sciences and Chemistry, Roskilde University, Roskilde, Denmark.
Nucleosides Nucleotides Nucleic Acids. 2006;25(9-11):1171-5. doi: 10.1080/15257770600894501.
Both the nuclear and mitochondrial DNA (mtDNA) depend on separate balanced pools of dNTPs for correct function of DNA replication and repair of DNA damage. Import of dNTPs from the cytosolic compartment to the mitochondria has been suggested to have the potential of rectifying a mitochondrial dNTP imbalance. Reduced TK2 activity has been demonstrated to result in mitochondrial dNTP imbalance and consequently mutations of mtDNA in non-dividing cells. In this study, the consequences of a reduced thymidine kinase 2 (TK2) activity were measured in proliferating HeLa cells, on both whole-cell as well as mitochondrial dNTP levels. With the exception of increased mitochondrial dCTP level no significant difference was found in cells with reduced TK2 activity. Our results suggest that import of cytosolic dNTPs in mitochondria of proliferating cells can compensate a TK2 induced imbalance of the mitochondrial dNTP pool.
细胞核DNA和线粒体DNA(mtDNA)都依赖于各自平衡的脱氧核苷酸三磷酸(dNTP)库,以实现DNA复制和DNA损伤修复的正确功能。有研究表明,将dNTP从胞质区室导入线粒体有纠正线粒体dNTP失衡的潜力。已证实胸苷激酶2(TK2)活性降低会导致线粒体dNTP失衡,进而导致非分裂细胞中mtDNA发生突变。在本研究中,我们检测了增殖的HeLa细胞中胸苷激酶2(TK2)活性降低对全细胞以及线粒体dNTP水平的影响。除了线粒体dCTP水平升高外,TK2活性降低的细胞中未发现显著差异。我们的结果表明,增殖细胞线粒体中胞质dNTP的导入可以补偿TK2诱导的线粒体dNTP库失衡。