Yoon Young Geol, Haug Christopher L, Koob Michael D
Department of Laboratory Medicine and Pathology, Institute of Human Genetics, University of Minnesota School of Medicine, Moos Tower 5-214, MMC 206, 420 Delaware Street S.E., Minneapolis, MN 55455, USA.
Mitochondrion. 2007 May;7(3):223-9. doi: 10.1016/j.mito.2006.11.022. Epub 2006 Dec 9.
A detailed molecular understanding of mitochondrial fusion and fission in mammalian cells is rapidly emerging. In this report, we demonstrate for the first time cross-species mitochondrial fusion between distantly related species using green and red fluorescent proteins targeted to the mitochondrial matrix. We found that mouse mitochondria were able to efficiently fuse to unmodified mitochondria of human cells and that the contents of the mitochondrial matrix were completely mixed in less than 4h. We also observed that mitochondria from the mtDNA-less (rho(0)) mouse cells can homogeneously fuse to the mitochondria of human cells. We were, however, unable to maintain human mitochondrial DNA in the mouse cells. These results indicate that mitochondrial fusion proteins in mouse and human cells have enough functional homology to mediate efficient cross-species mitochondrial fusion, but mouse nuclear and human mitochondrial genomes have not retained functional compatibility with one another.
对哺乳动物细胞中线粒体融合与分裂的详细分子理解正在迅速形成。在本报告中,我们首次使用靶向线粒体基质的绿色和红色荧光蛋白,证明了远缘物种之间的跨物种线粒体融合。我们发现小鼠线粒体能够有效地与人类细胞的未修饰线粒体融合,并且线粒体基质的内容物在不到4小时内完全混合。我们还观察到来自无mtDNA(rho(0))小鼠细胞的线粒体可以与人类细胞的线粒体均匀融合。然而,我们无法在小鼠细胞中维持人类线粒体DNA。这些结果表明,小鼠和人类细胞中的线粒体融合蛋白具有足够的功能同源性来介导高效的跨物种线粒体融合,但小鼠核基因组和人类线粒体基因组彼此之间没有保留功能兼容性。