Mitochondrial protein transport in health and disease

作者：Kang Yilin; Fielden Laura F; Stojanovski Diana^*

来源：Seminars in Cell & Developmental Biology, 2018, 76: 142-153.

DOI：10.1016/j.semcdb.2017.07.028

• Mitochondria
• Mitochondrial protein import
• Mitochondrial dysfunction and disease
• TOM
• TIM23
• TIM22
• MIA
• SAM

Mitochondria are fundamental structures that fulfil important and diverse functions within cells, including cellular respiration and iron-sulfur cluster biogenesis. Mitochondrial function is reliant on the organelles proteome, which is maintained and adjusted depending on cellular requirements. The majority of mitochondrial proteins are encoded by nuclear genes and must be trafficked to, and imported into the organelle following synthesis in the cytosol. These nuclear-encoded mitochondrial precursors utilise dynamic and multimeric translocation machines to traverse the organelles membranes and be partitioned to the appropriate mitochondrial subcompartment. Yeast model systems have been instrumental in establishing the molecular basis of mitochondrial protein import machines and mechanisms, however unique players and mechanisms are apparent in higher eukaryotes. Here, we review our current knowledge on mitochondrial protein import in human cells and how dysfunction in these pathways can lead to disease.

• 出版日期2018-4