Guarente Leonard
Paul F Glenn Laboratory and Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Cold Spring Harb Symp Quant Biol. 2011;76:81-90. doi: 10.1101/sqb.2011.76.010629. Epub 2011 Nov 23.
Sirtuins are nicotinamide adenine dinucleotide (NAD)-dependent protein deacetylases that link protein acetylation, metabolism, aging, and diseases of aging. Sirtuins were initially found to slow aging in lower organisms and more recently shown to mediate many effects of calorie restriction on metabolism and longevity in mammals. This chapter focuses on two key mammalian sirtuins, SIRT1 (which resides mainly in the nucleus) and SIRT3 (which is mitochondrial). I discuss the many protein substrates of these sirtuins and how they determine the metabolic strategy most efficacious under scarce or abundant food supplies. I also discuss the logic by which sirtuins link protein acetylation and metabolism. Finally, I discuss emerging data showing protection by sirtuins against most of the common diseases of aging. It is possible that sirtuins will be novel targets to combat these diseases pharmacologically.
沉默调节蛋白是烟酰胺腺嘌呤二核苷酸(NAD)依赖性蛋白脱乙酰酶,它将蛋白质乙酰化、新陈代谢、衰老以及衰老相关疾病联系起来。沉默调节蛋白最初被发现可延缓低等生物的衰老,最近又被证明介导了热量限制对哺乳动物新陈代谢和寿命的许多影响。本章重点介绍两种关键的哺乳动物沉默调节蛋白,即SIRT1(主要存在于细胞核中)和SIRT3(存在于线粒体中)。我将讨论这些沉默调节蛋白的众多蛋白质底物,以及它们如何决定在食物供应稀缺或充足的情况下最有效的代谢策略。我还将讨论沉默调节蛋白将蛋白质乙酰化与新陈代谢联系起来的逻辑。最后,我将讨论新出现的数据,这些数据表明沉默调节蛋白对大多数常见的衰老相关疾病具有保护作用。沉默调节蛋白有可能成为对抗这些疾病的新型药理学靶点。
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