Department of Biological Chemistry, Jonsson Comprehensive Cancer Center and Molecular Biology Institute, David Geffen School of Medicine at UCLA, Los Angeles, California 90024
Department of Anesthesiology and Pain Medicine, University of Washington and Center for Developmental Therapeutics, Seattle Children's Research Institute, Washington 98101.
Genetics. 2017 Nov;207(3):843-871. doi: 10.1534/genetics.117.300262.
Mitochondria are best known for harboring pathways involved in ATP synthesis through the tricarboxylic acid cycle and oxidative phosphorylation. Major advances in understanding these roles were made with mutants affecting key components of the metabolic pathways. These mutants have not only helped elucidate some of the intricacies of metabolism pathways, but they have also served as jumping off points for pharmacology, toxicology, and aging studies. The field of mitochondria research has also undergone a renaissance, with the increased appreciation of the role of mitochondria in cell processes other than energy production. Here, we focus on discoveries that were made using , with a few excursions into areas that were studied more thoroughly in other organisms, like mitochondrial protein import in yeast. Advances in mitochondrial biogenesis and membrane dynamics were made through the discoveries of novel functions in mitochondrial fission and fusion proteins. Some of these functions were only apparent through the use of diverse model systems, such as Studies of stress responses, exemplified by mitophagy and the mitochondrial unfolded protein response, have also benefitted greatly from the use of model organisms. Recent developments include the discoveries in of cell autonomous and nonautonomous pathways controlling the mitochondrial unfolded protein response, as well as mechanisms for degradation of paternal mitochondria after fertilization. The evolutionary conservation of many, if not all, of these pathways ensures that results obtained with are equally applicable to studies of human mitochondria in health and disease.
线粒体最著名的功能是通过三羧酸循环和氧化磷酸化途径来合成 ATP。对这些途径关键成分的 突变体的研究取得了对这些作用的重大认识。这些突变体不仅有助于阐明代谢途径的一些复杂性,而且还为药理学、毒理学和衰老研究提供了起点。线粒体研究领域也经历了复兴,人们越来越认识到线粒体在除能量产生以外的细胞过程中的作用。在这里,我们重点介绍使用 发现的结果,偶尔也会涉及在其他生物体中研究得更深入的领域,如酵母中线粒体蛋白的输入。通过发现线粒体分裂和融合蛋白的新功能,在线粒体生物发生和膜动力学方面取得了进展。其中一些功能只有通过使用多种模型系统才能显现出来,例如 。对应激反应的研究,如自噬和线粒体未折叠蛋白反应,也从使用模式生物中受益匪浅。最近的发展包括在 中发现了控制线粒体未折叠蛋白反应的细胞自主和非自主途径,以及受精后父本线粒体降解的机制。如果不是所有这些途径都具有进化保守性,那么用 获得的结果同样适用于研究健康和疾病状态下人线粒体。