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Emerging role of Lon protease as a master regulator of mitochondrial functions

机译:Lon蛋白酶作为线粒体功能的主要调节剂的新兴作用

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Lon protease is a nuclear-encoded, mitochondrial ATP-dependent protease highly conserved throughout the evolution, crucial for the maintenance of mitochondrial homeostasis. Lon acts as a chaperone of misfolded proteins, and is necessary for maintaining mitochondria( DNA. The impairment of these functions has a deep impact on mitochondrial functionality and morphology. An altered expression of Lon leads to a profound reprogramming of cell metabolism, with a switch from respiration to glycolysis, which is often observed in cancer cells. Mutations of Lon, which likely impair its chaperone properties, are at the basis of a genetic inherited disease named of the cerebral, ocular, dental, auricular, skeletal (CODAS) syndrome. This article is part of a Special Issue entitled 'EBEC 2016: 19th European Bioenergetics Conference, Riva del Garda, Italy, July 2-6, 2016', edited by Prof. Paolo Bernardi. (C) 2016 Elsevier B.V. All rights reserved.
机译:Lon蛋白酶是一种在整个进化过程中高度保守的核编码,线粒体ATP依赖性蛋白酶,对维持线粒体的体内平衡至关重要。 Lon充当错误折叠蛋白的伴侣,是维持线粒体(DNA)所必需的。这些功能的受损对线粒体功能和形态产生深远的影响。Lon表达的改变导致细胞代谢的深刻重编程,并伴随着开关从呼吸到糖酵解(通常在癌细胞中观察到)Lon的突变可能会破坏其分子伴侣的特性,这是遗传遗传疾病的基础,这种疾病被称为脑,眼,牙齿,耳,骨骼(CODAS)综合征。本文是专刊的一部分,标题为“ EBEC 2016:第19届欧洲生物能学会议,2016年7月2日至6日,意大利里瓦德尔加尔达”,由Paolo Bernardi教授编辑(C)2016 Elsevier BV保留所有权利。

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