Harris Nicholas, Bachler Marcus, Costa Vitor, Mollapour Mehdi, Moradas-Ferreira Pedro, Piper Peter W
Department of Molecular Biology and Biotechnology, University of Sheffield, Sheffield S10 2TN, UK.
Aging Cell. 2005 Feb;4(1):41-52. doi: 10.1111/j.1474-9726.2005.00142.x.
Yeast overexpressing SOD1, the gene for Cu,Zn-superoxide dismutase (Cu,Zn-Sod), was used to determine how Sod1p overexpression influences the chronological lifespan [the survival of non-dividing stationary (G0) phase cells over time], the replicative lifespan (the number of buds produced by actively dividing yeast cells) and stress resistance. Increasing the level of active Cu,Zn-Sod in yeast was found to require either growth in the presence of high copper, or the simultaneous overexpression of both SOD1 and CCS1 (the latter being the gene that encodes the chaperone dedicated to Cu(2+)-loading of Sod1p in vivo). Dual SOD1 + CCS1 overexpression elevated the levels of Cu,Zn-Sod activity six- to eight-fold in vegetative cultures. It also increased the optimized survival of stationary cells up to two-fold, showing this chronological lifespan is ultimately limited by oxidative stress. In contrast, several detrimental effects resulted when the SOD1 gene was overexpressed in the absence of either high copper or a simultaneous overexpression of CCS1. Both the chronological and the replicative lifespans were shortened; the cells displayed an abnormally high level of endogenous oxidative stress, resulting in a high rate of spontaneous mutation. Such harmful effects were all reversed through the overexpression of CCS1. It is apparent therefore that they relate to the incomplete Cu(2+)-loading of the overexpressed Sod1p, most probably accumulation of a Cu(2+)-deficient Sod1p to appreciable levels in vivo. The same events may generate the detrimental effects that are frequently, though not universally, observed when Cu,Zn-Sod overexpression is attempted in metazoans.
过表达超氧化物歧化酶1(Cu,Zn -超氧化物歧化酶基因,即Cu,Zn - Sod)的酵母被用于确定Sod1p过表达如何影响时序寿命(非分裂静止期(G0)细胞随时间的存活情况)、复制寿命(活跃分裂的酵母细胞产生的芽数)以及抗逆性。研究发现,要在酵母中提高活性Cu,Zn - Sod的水平,要么在高铜环境中生长,要么同时过表达SOD1和CCS1(后者是编码在体内专门负责将铜离子加载到Sod1p上的伴侣蛋白的基因)。在营养培养物中,同时过表达SOD1和CCS1可使Cu,Zn - Sod活性水平提高6至8倍。它还使静止细胞的最佳存活率提高了两倍,表明这种时序寿命最终受氧化应激限制。相比之下,在没有高铜或未同时过表达CCS1的情况下过表达SOD1基因会产生一些有害影响。时序寿命和复制寿命均缩短;细胞内源性氧化应激水平异常高,导致自发突变率升高。通过过表达CCS1,所有这些有害影响都得到了逆转。因此很明显,它们与过表达的Sod1p铜离子加载不完全有关,很可能是体内铜离子缺乏的Sod1p积累到了相当水平。同样的情况可能会产生在多细胞动物中尝试过表达Cu,Zn - Sod时经常(但并非普遍)观察到的有害影响。