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本文引用的文献

1
Deficiencies in mitochondrial dynamics sensitize Caenorhabditis elegans to arsenite and other mitochondrial toxicants by reducing mitochondrial adaptability.线粒体动力学缺陷通过降低线粒体适应性,使秀丽隐杆线虫对亚砷酸盐和其他线粒体毒物敏感。
Toxicology. 2017 Jul 15;387:81-94. doi: 10.1016/j.tox.2017.05.018. Epub 2017 Jun 8.
2
Transcription factors CEP-1/p53 and CEH-23 collaborate with AAK-2/AMPK to modulate longevity in Caenorhabditis elegans.转录因子CEP-1/p53和CEH-23与AAK-2/AMPK协同作用,调控秀丽隐杆线虫的寿命。
Aging Cell. 2017 Aug;16(4):814-824. doi: 10.1111/acel.12619. Epub 2017 May 30.
3
A Select Subset of Electron Transport Chain Genes Associated with Optic Atrophy Link Mitochondria to Axon Regeneration in .与视神经萎缩相关的电子传递链基因的一个特定子集将线粒体与……中的轴突再生联系起来。
Front Neurosci. 2017 May 10;11:263. doi: 10.3389/fnins.2017.00263. eCollection 2017.
4
A brief history of the discovery of the mitochondrial unfolded protein response in mammalian cells.哺乳动物细胞中线粒体未折叠蛋白反应的发现简史。
J Bioenerg Biomembr. 2017 Aug;49(4):293-295. doi: 10.1007/s10863-017-9703-2.
5
A single biochemical activity underlies the pleiotropy of the aging-related protein CLK-1.单一生化活性是与衰老相关蛋白 CLK-1 多效性的基础。
Sci Rep. 2017 Apr 12;7(1):859. doi: 10.1038/s41598-017-00754-z.
6
Tomatidine enhances lifespan and healthspan in C. elegans through mitophagy induction via the SKN-1/Nrf2 pathway.番茄苷通过 SKN-1/Nrf2 通路诱导自噬来延长秀丽隐杆线虫的寿命和健康跨度。
Sci Rep. 2017 Apr 11;7:46208. doi: 10.1038/srep46208.
7
Mitochondrial Machineries for Protein Import and Assembly.线粒体蛋白输入与组装的分子机制
Annu Rev Biochem. 2017 Jun 20;86:685-714. doi: 10.1146/annurev-biochem-060815-014352. Epub 2017 Mar 15.
8
Integrating the UPR into the mitochondrial maintenance network.将未折叠蛋白反应整合到线粒体维持网络中。
Crit Rev Biochem Mol Biol. 2017 Jun;52(3):304-313. doi: 10.1080/10409238.2017.1291577. Epub 2017 Feb 22.
9
Effects of methyl and inorganic mercury exposure on genome homeostasis and mitochondrial function in Caenorhabditis elegans.甲基汞和无机汞暴露对秀丽隐杆线虫基因组稳态和线粒体功能的影响。
DNA Repair (Amst). 2017 Apr;52:31-48. doi: 10.1016/j.dnarep.2017.02.005. Epub 2017 Feb 13.
10
Mitochondrial Complex I Activity is Conditioned by Supercomplex I-IIIIV Assembly in Brain Cells: Relevance for Parkinson's Disease.线粒体复合体I活性受脑细胞中超复合体I-IIIIV组装的调节:与帕金森病的相关性。
Neurochem Res. 2017 Jun;42(6):1676-1682. doi: 10.1007/s11064-017-2191-2. Epub 2017 Feb 14.

线粒体的细胞生物学。

Cell Biology of the Mitochondrion.

机构信息

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.

出版信息

Genetics. 2017 Nov;207(3):843-871. doi: 10.1534/genetics.117.300262.

DOI:10.1534/genetics.117.300262
PMID:29097398
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5676242/
Abstract

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.

摘要

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。