Parker Joel D, Parker Karen M, Sohal Barbara H, Sohal Rajindar S, Keller Laurent
Department of Ecology and Evolution, Biology Building, University of Lausanne, 1015 Lausanne, Switzerland.
Proc Natl Acad Sci U S A. 2004 Mar 9;101(10):3486-9. doi: 10.1073/pnas.0400222101. Epub 2004 Mar 1.
Reactive oxygen species, the by-products of oxidative energy metabolism, are considered a main proximate cause of aging. Accordingly, overexpression of the enzyme Cu-Zn superoxide dismutase 1 (SOD1) can lengthen lifespan of Drosophila melanogaster in the laboratory. However, the role of SOD1 as a main determinant of lifespan has been challenged on the grounds that overexpression might be effective only in compromised genetic backgrounds. Moreover, interspecific comparisons show lower levels of antioxidant activities in longer-lived species, suggesting that life-span extension may evolve through less reactive oxygen species generation from the mitochondria rather than higher expression of SOD1. The tremendous variation in lifespan between ant castes, ranging over 2 orders of magnitude, coupled with the fact that all individuals share the same genome, provides a system to investigate the role of SOD1 in the wild. We used the ant Lasius niger as a model system, because queens can reach the extreme age of 28 years, whereas workers and males live only 1-2 years and a few weeks, respectively. We cloned SOD1 and found that long-lived queens have a lower level of expression than workers and males. Specific enzyme-activity assays also showed higher SOD1 activity levels in males and workers compared with queens, which had SOD1 activity levels similar to that of D. melanogaster. Altogether, these data show that increased expression of SOD1 is not required for the evolution of extreme lifespan, even in a system in which differential gene expression is the only way to express phenotypes with great lifespan differences.
活性氧作为氧化能量代谢的副产物,被认为是衰老的主要直接原因。相应地,在实验室中,铜锌超氧化物歧化酶1(SOD1)的过表达可以延长黑腹果蝇的寿命。然而,SOD1作为寿命主要决定因素的作用受到了挑战,理由是过表达可能仅在受损的遗传背景下才有效。此外,种间比较表明,寿命较长的物种中抗氧化活性水平较低,这表明寿命延长可能是通过线粒体产生较少的活性氧来实现的,而不是通过SOD1的高表达。蚁群之间的寿命差异巨大,相差超过2个数量级,再加上所有个体共享相同的基因组,这提供了一个在自然环境中研究SOD1作用的系统。我们以黑蚁作为模型系统,因为蚁后可以活到28岁的高龄,而工蚁和雄蚁的寿命分别只有1 - 2年和几周。我们克隆了SOD1,发现长寿的蚁后其表达水平低于工蚁和雄蚁。特定的酶活性测定还表明,与蚁后相比,雄蚁和工蚁的SOD1活性水平更高,蚁后的SOD1活性水平与黑腹果蝇的相似。总之,这些数据表明,即使在一个差异基因表达是表达具有巨大寿命差异表型的唯一方式的系统中,极端寿命的进化也不需要SOD1表达增加。