Herrmann J M, Stuart R A, Craig E A, Neupert W
Institut für Physiologische Chemie, Universität München, Germany.
J Cell Biol. 1994 Nov;127(4):893-902. doi: 10.1083/jcb.127.4.893.
Mitochondrial heat shock protein 70 (mt-Hsp70) has been shown to play an important role in facilitating import into, as well as folding and assembly of nuclear-encoded proteins in the mitochondrial matrix. Here, we describe a role for mt-Hsp70 in chaperoning proteins encoded by mitochondrial DNA and synthesized within mitochondria. The availability of mt-Hsp70 function influences the pattern of proteins synthesized in mitochondria of yeast both in vivo and in vitro. In particular, we show that mt-Hsp70 acts in maintaining the var1 protein, the only mitochondrially encoded subunit of mitochondrial ribosomes, in an assembly competent state, especially under heat stress conditions. Furthermore, mt-Hsp70 helps to facilitate assembly of mitochondrially encoded subunits of the ATP synthase complex. By interacting with the ATP-ase 9 oligomer, mt-Hsp70 promotes assembly of ATP-ase 6, and thereby protects the latter protein from proteolytic degradation. Thus mt-Hsp70 by acting as a chaperone for proteins encoded by the mitochondrial DNA, has a critical role in the assembly of supra-molecular complexes.
线粒体热休克蛋白70(mt-Hsp70)已被证明在促进核编码蛋白进入线粒体基质以及在其中折叠和组装方面发挥重要作用。在此,我们描述了mt-Hsp70在陪伴线粒体DNA编码并在线粒体内合成的蛋白质方面的作用。mt-Hsp70功能的可用性在体内和体外都会影响酵母线粒体内合成的蛋白质模式。特别是,我们表明mt-Hsp70在维持var1蛋白(线粒体核糖体唯一的线粒体编码亚基)处于组装胜任状态方面发挥作用,尤其是在热应激条件下。此外,mt-Hsp70有助于促进ATP合酶复合体的线粒体编码亚基的组装。通过与ATP酶9寡聚体相互作用,mt-Hsp70促进ATP酶6的组装,从而保护后者蛋白不被蛋白水解降解。因此,mt-Hsp70作为线粒体DNA编码蛋白质的伴侣,在超分子复合物的组装中起关键作用。