National Centre of Applied Human Genetics, School of Life Sciences, Jawaharlal Nehru University, New Delhi, 110067, India.
Sci Rep. 2017 May 8;7(1):1525. doi: 10.1038/s41598-017-01743-y.
Here we demonstrate localization of the isoform3 of DNA Methyltransferase1 (DNMT1) enzyme to mitochondria, instead of isoform1 as reported earlier. The fused DNMT1-isoform1, reported earlier to localize in mitochondria, surprisingly showed its exclusive presence inside the nucleus after its ectopic expression; and failed to localize in mitochondria. On the other hand, ectopically expressed DNMT1-isoform3 targeted itself to mitochondria and subsequently methylated CpG regions in the mitochondrial genome. In addition, overexpression of DNMT1-isoform3 affected mitochondrial biology and regulated its function. Under different conditions of oxidative and nutritional stress, this isoform was down-regulated, resulting in hypomethylation of mitochondrial genome. Our study reveals how DNMT1-isoform3, instead of isoform1, is responsible for mtDNA methylation, influencing its biology.
在这里,我们证明了 DNA 甲基转移酶 1(DNMT1)同工型 3 酶定位于线粒体,而不是早期报道的同工型 1。早期报道的定位于线粒体的融合 DNMT1-同工型 1,在异位表达后出人意料地仅存在于核内,而未能定位于线粒体。另一方面,异位表达的 DNMT1-同工型 3 将自身靶向线粒体,并随后甲基化线粒体基因组中的 CpG 区域。此外,DNMT1-同工型 3 的过表达影响线粒体生物学并调节其功能。在氧化和营养应激的不同条件下,这种同工型下调,导致线粒体基因组的低甲基化。我们的研究揭示了 DNMT1-同工型 3 如何代替同工型 1 负责 mtDNA 甲基化,从而影响其生物学。