Department of Cellular Biochemistry, University Medical Center Göttingen, D-37073 Göttingen, Germany.
Department of Cellular Biochemistry, University Medical Center Göttingen, D-37073 Göttingen, Germany; Max Planck Institute for Biophysical Chemistry, D-37077 Göttingen, Germany.
Trends Cell Biol. 2017 Oct;27(10):712-721. doi: 10.1016/j.tcb.2017.05.004. Epub 2017 Jun 9.
Mitochondria maintained a genome during evolution to synthesize core subunits of the oxidative phosphorylation system. Expression of the mitochondrial genome requires intraorganellar replication, transcription, and translation. Membrane-associated ribosomes translate mitochondrial-encoded proteins and facilitate co-translational insertion of newly synthesized polypeptides into the inner membrane. Considering that mitochondrial-encoded proteins assemble with imported, nuclear-encoded proteins into enzyme complexes of the oxidative phosphorylation system, it is expected that expression of mitochondrial genes should adapt to the availability of their nuclear-encoded partners. Recent work shows that mitochondrial translation is influenced by the cellular environment. We discuss how mitochondrial translation is affected by the cellular environment and propose models of translational plasticity that modulate mitochondrial translation in response to the availability of imported proteins.
线粒体在进化过程中保持基因组以合成氧化磷酸化系统的核心亚基。线粒体基因组的表达需要细胞器内的复制、转录和翻译。膜结合核糖体翻译线粒体编码的蛋白质,并促进新合成的多肽在向内膜的共翻译插入。考虑到线粒体编码的蛋白质与导入的核编码蛋白组装成氧化磷酸化系统的酶复合物,预计线粒体基因的表达应该适应其核编码伴侣的可用性。最近的工作表明,线粒体翻译受细胞环境的影响。我们讨论了线粒体翻译如何受细胞环境的影响,并提出了翻译可塑性的模型,这些模型可根据导入蛋白质的可用性来调节线粒体翻译。