Tsuchiya Mitsuhiro, Dang Nick, Kerr Emily O, Hu Di, Steffen Kristan K, Oakes Jonathan A, Kennedy Brian K, Kaeberlein Matt
Department of Biochemistry, University of Washington, Seattle, WA 98195, USA.
Aging Cell. 2006 Dec;5(6):505-14. doi: 10.1111/j.1474-9726.2006.00240.x.
Two models have been proposed for how calorie restriction (CR) enhances replicative longevity in yeast: (i) suppression of rDNA recombination through activation of the sirtuin protein deacetylase Sir2 or (ii) decreased activity of the nutrient-responsive kinases Sch9 and TOR. We report here that CR increases lifespan independently of all Sir2-family proteins in yeast. Furthermore, we demonstrate that nicotinamide, an inhibitor of Sir2-mediated deacetylation, interferes with lifespan extension from CR, but does so independent of Sir2, Hst1, Hst2, and Hst4. We also find that 5 mm nicotinamide, a concentration sufficient to inhibit other sirtuins, does not phenocopy deletion of HST3. Thus, we propose that lifespan extension by CR is independent of sirtuins and that nicotinamide has sirtuin-independent effects on lifespan extension by CR.
关于卡路里限制(CR)如何延长酵母复制寿命,已提出两种模型:(i)通过激活沉默调节蛋白脱乙酰酶Sir2抑制核糖体DNA(rDNA)重组,或(ii)降低营养响应激酶Sch9和雷帕霉素靶蛋白(TOR)的活性。我们在此报告,CR在酵母中独立于所有Sir2家族蛋白延长寿命。此外,我们证明烟酰胺,一种Sir2介导的脱乙酰化抑制剂,干扰CR介导的寿命延长,但这种干扰独立于Sir2、Hst1、Hst2和Hst4。我们还发现,5 mM烟酰胺,一种足以抑制其他沉默调节蛋白的浓度,不会模拟HST3缺失的表型。因此,我们提出CR介导的寿命延长独立于沉默调节蛋白,且烟酰胺对CR介导的寿命延长具有独立于沉默调节蛋白的作用。