Matsushima Yuichi, Kaguni Laurie S
Department of Mental Retardation & Birth Defect Research, National Institute of Neuroscience, National Center of Neurology & Psychiatry, Tokyo 187-8502, Japan.
Biochim Biophys Acta. 2012 Sep-Oct;1819(9-10):1080-7. doi: 10.1016/j.bbagrm.2011.11.008. Epub 2011 Dec 8.
Lon, ClpXP and m-AAA are the three major ATP-dependent proteases in the mitochondrial matrix. All three are involved in general quality control by degrading damaged or abnormal proteins. In addition to this role, they are proposed to serve roles in mitochondrial DNA functions including packaging and stability, replication, transcription and translation. In particular, Lon has been implicated in mtDNA metabolism in yeast, fly and humans. Here, we review the role of Lon protease in mitochondrial DNA functions, and discuss a putative physiological role for mitochondrial transcription factor A (TFAM) degradation by Lon protease. We also discuss the possible roles of m-AAA and ClpXP in mitochondrial DNA functions, and the putative candidate substrates for the three matrix proteases. This article is part of a Special Issue entitled: Mitochondrial Gene Expression.
Lon、ClpXP和m-AAA是线粒体基质中三种主要的ATP依赖性蛋白酶。这三种蛋白酶都通过降解受损或异常蛋白质参与一般质量控制。除了这一作用外,它们还被认为在线粒体DNA功能中发挥作用,包括包装和稳定性、复制、转录和翻译。特别是,Lon已被证明在酵母、果蝇和人类的线粒体DNA代谢中起作用。在这里,我们综述了Lon蛋白酶在线粒体DNA功能中的作用,并讨论了Lon蛋白酶降解线粒体转录因子A(TFAM)的假定生理作用。我们还讨论了m-AAA和ClpXP在线粒体DNA功能中的可能作用,以及这三种基质蛋白酶的假定候选底物。本文是名为“线粒体基因表达”的特刊的一部分。