Smiraglia Dominic J, Kulawiec Mariola, Bistulfi Gaia L, Gupta Sampa Ghoshal, Singh Keshav K
Department of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, New York 14263, USA.
Cancer Biol Ther. 2008 Aug;7(8):1182-90. doi: 10.4161/cbt.7.8.6215. Epub 2008 Aug 1.
Epigenetic modification in the nuclear genome plays a key role in human tumorigenesis. In this paper, we investigated whether changes in the mtDNA copy number frequently reported to vary in a number of human tumors induce methylation changes in the nucleus. We utilized the Restriction Landmark Genomic Scanning (RLGS) to identify genes that undergo changes in their methylation status in response to the depletion and repletion of mtDNA. Our study demonstrates that depletion of mtDNA results in significant changes in methylation pattern of a number of genes. Furthermore, our study suggests that methylation changes are reversed by the restoration of mtDNA in cells otherwise lacking the entire mitochondrial genome. These studies provide the first direct evidence that mitochondria regulate epigenetic modification in the nucleus that may contribute to tumorigenesis.
核基因组中的表观遗传修饰在人类肿瘤发生过程中起着关键作用。在本文中,我们研究了在许多人类肿瘤中经常报道的线粒体DNA(mtDNA)拷贝数变化是否会诱导细胞核中的甲基化变化。我们利用限制性地标基因组扫描(RLGS)来识别因mtDNA的消耗和补充而甲基化状态发生变化的基因。我们的研究表明,mtDNA的消耗会导致许多基因的甲基化模式发生显著变化。此外,我们的研究表明,在原本缺乏整个线粒体基因组的细胞中,mtDNA的恢复可逆转甲基化变化。这些研究提供了首个直接证据,证明线粒体可调节细胞核中的表观遗传修饰,这可能有助于肿瘤发生。