Piskacek Martin, Zotova Ludmila, Zsurka Gábor, Schweyen Rudolf J
Department of Genetics, Vienna University, Austria.
J Cell Mol Med. 2009 Apr;13(4):693-700. doi: 10.1111/j.1582-4934.2008.00328.x. Epub 2008 Mar 31.
The human gene MRS2L encodes a mitochondrial protein distantly related to CorA Mg(2+) transport proteins. Constitutive shRNA-mediated knockdown of hMRS2 in human HEK-293 cell line was found here to cause death. To further study its role in Mg(2+) transport, we have established stable cell lines with conditionally expressing shRNAs directed against hMRS2L. The cells expressing shRNA for several generations exhibited lower steady-state levels of free mitochondrial Mg(2+) (Mg(2+)) and reduced capacity of mitochondrial Mg(2+) uptake than control cells. Long-term expression of shRNAs resulted in loss of mitochondrial respiratory complex I, decreased mitochondrial membrane potential and cell death. We conclude that hMrs2 is the major transport protein for Mg (+) uptake into mitochondria and that expression of hMrs2 is essential for the maintenance of respiratory complex I and cell viability.
人类基因MRS2L编码一种与CorA镁离子转运蛋白有远亲关系的线粒体蛋白。在此发现,在人类HEK - 293细胞系中,组成型短发夹RNA(shRNA)介导的hMRS2敲低会导致细胞死亡。为了进一步研究其在镁离子转运中的作用,我们建立了稳定的细胞系,这些细胞系可条件性表达针对hMRS2L的shRNA。连续几代表达shRNA的细胞与对照细胞相比,游离线粒体镁离子([Mg²⁺]m)的稳态水平较低,线粒体镁离子摄取能力降低。shRNA的长期表达导致线粒体呼吸复合体I丧失、线粒体膜电位降低和细胞死亡。我们得出结论,hMrs2是镁离子摄取进入线粒体的主要转运蛋白,并且hMrs2的表达对于维持呼吸复合体I和细胞活力至关重要。