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F1 缺失的 HeLa 细胞和酵母细胞中 ATP 合酶亚基的周转率。

Turnover of ATP synthase subunits in F1-depleted HeLa and yeast cells.

机构信息

Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

出版信息

FEBS Lett. 2011 Aug 19;585(16):2582-6. doi: 10.1016/j.febslet.2011.07.011. Epub 2011 Jul 23.

Abstract

Mitochondrial translation of the Saccharomyces cerevisiae Atp6p subunit of F(1)-F(0) ATP synthase is regulated by the F(1) ATPase. Here we show normal expression of Atp6p in HeLa cells depleted of the F(1) β subunit. Instead of being translationally down-regulated, HeLa cells lacking F(1) degrade Atp6p, thereby preventing proton leakage across the inner membrane. Mammalian mitochondria also differ in the way they minimize the harmful effect of unassembled F(1) α subunit. While yeast mutants lacking β subunit have stable aggregated F(1) α subunit in the mitochondrial matrix, the human α subunit is completely degraded in cells deficient in F(1) β subunit. These results are discussed in light of the different properties of the proteins and environments in which yeast and human mitochondria exist.

摘要

酿酒酵母 F(1)-F(0)ATP 合酶 Atp6p 亚基的线粒体翻译受 F(1)ATP 酶调控。在这里,我们展示了在耗尽 F(1)β 亚基的 HeLa 细胞中 Atp6p 的正常表达。HeLa 细胞缺乏 F(1)反而会降解 Atp6p,从而防止质子通过内膜渗漏。哺乳动物线粒体在最小化未组装的 F(1)α亚基的有害影响方面也存在差异。虽然缺乏β亚基的酵母突变体在线粒体基质中有稳定聚集的 F(1)α亚基,但在缺乏 F(1)β亚基的细胞中,人α亚基完全降解。这些结果是根据酵母和人线粒体中存在的蛋白质和环境的不同性质进行讨论的。

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