Osborne Brenna, Cooney Gregory J, Turner Nigel
Diabetes & Obesity Research Program, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
Diabetes & Obesity Research Program, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia; St Vincent's Clinical School, University of New South Wales, Sydney, NSW, Australia.
Biochim Biophys Acta. 2014 Apr;1840(4):1295-302. doi: 10.1016/j.bbagen.2013.08.016. Epub 2013 Aug 27.
In recent years, reversible lysine acylation of proteins has emerged as a major post-translational modification across the cell, and importantly has been shown to regulate many proteins in mitochondria. One key family of deacylase enzymes is the sirtuins, of which SIRT3, SIRT4, and SIRT5 are localised to the mitochondria and regulate acyl modifications in this organelle.
In this review we discuss the emerging role of lysine acylation in the mitochondrion and summarise the evidence that proposes mitochondrial sirtuins are important players in the modulation of mitochondrial energy metabolism in response to external nutrient cues, via their action as lysine deacylases. We also highlight some key areas of mitochondrial sirtuin biology where future research efforts are required.
Lysine deacetylation appears to play some role in regulating mitochondrial metabolism. Recent discoveries of new enzymatic capabilities of mitochondrial sirtuins, including desuccinylation and demalonylation activities, as well as an increasing list of novel protein substrates have identified many new questions regarding the role of mitochondrial sirtuins in the regulation of energy metabolism.
Dynamic changes in the regulation of mitochondrial metabolism may have far-reaching consequences for many diseases, and despite promising initial findings in knockout animals and cell models, the role of the mitochondrial sirtuins requires further exploration in this context. This article is part of a Special Issue entitled Frontiers of mitochondrial research.
近年来,蛋白质的可逆赖氨酸酰化已成为细胞内一种主要的翻译后修饰,重要的是,它已被证明可调节线粒体中的许多蛋白质。去酰基酶的一个关键家族是沉默调节蛋白,其中SIRT3、SIRT4和SIRT5定位于线粒体并调节该细胞器中的酰基修饰。
在本综述中,我们讨论了赖氨酸酰化在 mitochondrion 中的新作用,并总结了相关证据,这些证据表明线粒体沉默调节蛋白作为赖氨酸去酰基酶,在响应外部营养信号调节线粒体能量代谢中是重要参与者。我们还强调了线粒体沉默调节蛋白生物学中一些未来需要研究的关键领域。
赖氨酸去乙酰化似乎在调节线粒体代谢中发挥了一定作用。线粒体沉默调节蛋白新酶活性的最新发现,包括去琥珀酰化和去丙二酰化活性,以及越来越多的新型蛋白质底物,提出了许多关于线粒体沉默调节蛋白在能量代谢调节中作用的新问题。
线粒体代谢调节的动态变化可能对许多疾病产生深远影响,尽管在基因敲除动物和细胞模型中初步研究结果很有前景,但线粒体沉默调节蛋白在这种情况下的作用仍需要进一步探索。本文是名为线粒体研究前沿的特刊的一部分。