Szklarczyk Radek, Nooteboom Marco, Osiewacz Heinz D
Centre for Molecular and Biomolecular Informatics, Radboud University Medical Centre, 6500 HB Nijmegen, The Netherlands Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, 6200 MD Maastricht, The Netherlands
Department of Biochemistry (286), Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, 6500 HB Nijmegen, The Netherlands.
Philos Trans R Soc Lond B Biol Sci. 2014 Jul 5;369(1646):20130439. doi: 10.1098/rstb.2013.0439.
Various molecular and cellular pathways are active in eukaryotes to control the quality and integrity of mitochondria. These pathways are involved in keeping a 'healthy' population of this essential organelle during the lifetime of the organism. Quality control (QC) systems counteract processes that lead to organellar dysfunction manifesting as degenerative diseases and ageing. We discuss disease- and ageing-related pathways involved in mitochondrial QC: mtDNA repair and reorganization, regeneration of oxidized amino acids, refolding and degradation of severely damaged proteins, degradation of whole mitochondria by mitophagy and finally programmed cell death. The control of the integrity of mtDNA and regulation of its expression is essential to remodel single proteins as well as mitochondrial complexes that determine mitochondrial functions. The redundancy of components, such as proteases, and the hierarchies of the QC raise questions about crosstalk between systems and their precise regulation. The understanding of the underlying mechanisms on the genomic, proteomic, organellar and cellular levels holds the key for the development of interventions for mitochondrial dysfunctions, degenerative processes, ageing and age-related diseases resulting from impairments of mitochondria.
真核生物中有多种分子和细胞途径来控制线粒体的质量和完整性。这些途径参与在生物体的生命周期中维持这种重要细胞器的“健康”群体。质量控制(QC)系统可对抗导致细胞器功能障碍的过程,这些功能障碍表现为退行性疾病和衰老。我们讨论了线粒体QC中与疾病和衰老相关的途径:线粒体DNA修复和重组、氧化氨基酸的再生、严重受损蛋白质的重折叠和降解、通过线粒体自噬对整个线粒体的降解,以及最终的程序性细胞死亡。线粒体DNA完整性的控制及其表达的调节对于重塑决定线粒体功能的单个蛋白质以及线粒体复合物至关重要。蛋白酶等成分的冗余以及质量控制的层次结构引发了关于系统间相互作用及其精确调节的问题。在基因组、蛋白质组、细胞器和细胞水平上对潜在机制的理解是开发针对线粒体功能障碍、退行性过程、衰老以及由线粒体损伤引起的与年龄相关疾病的干预措施的关键。