Clegg Robert J, Dyson Rosemary J, Kreft Jan-Ulrich
Centre for Systems Biology, University of Birmingham, Birmingham, UK.
BMC Biol. 2014 Aug 16;12:52. doi: 10.1186/s12915-014-0052-x.
How aging, being unfavourable for the individual, can evolve is one of the fundamental problems of biology. Evidence for aging in unicellular organisms is far from conclusive. Some studies found aging even in symmetrically dividing unicellular species; others did not find aging in the same, or in different, unicellular species, or only under stress. Mathematical models suggested that segregation of non-genetic damage, as an aging strategy, would increase fitness. However, these models failed to consider repair as an alternative strategy or did not properly account for the benefits of repair. We used a new and improved individual-based model to examine rigorously the effect of a range of aging strategies on fitness in various environments.
Repair of damage emerges as the best strategy despite its fitness costs, since it immediately increases growth rate. There is an optimal investment in repair that outperforms damage segregation in well-mixed, lasting and benign environments over a wide range of parameter values. Damage segregation becomes beneficial, and only in combination with repair, when three factors are combined: (i) the rate of damage accumulation is high, (ii) damage is toxic and (iii) efficiency of repair is low. In contrast to previous models, our model predicts that unicellular organisms should have active mechanisms to repair damage rather than age by segregating damage. Indeed, as predicted, all organisms have evolved active mechanisms of repair whilst aging in unicellular organisms is absent or minimal under benign conditions, apart from microorganisms with a different ecology, inhabiting short-lived environments strongly favouring early reproduction rather than longevity.
Aging confers no fitness advantage for unicellular organisms in lasting environments under benign conditions, since repair of non-genetic damage is better than damage segregation.
衰老对个体不利,却能进化,这是生物学的基本问题之一。单细胞生物存在衰老现象的证据远非确凿。一些研究发现,即使在对称分裂的单细胞物种中也存在衰老;另一些研究则未在相同或不同的单细胞物种中发现衰老现象,或者仅在压力条件下发现衰老。数学模型表明,作为一种衰老策略,非遗传损伤的隔离会提高适应性。然而,这些模型未能将修复视为一种替代策略,或者没有恰当地考虑修复的益处。我们使用了一种新的、改进的基于个体的模型,来严格检验一系列衰老策略在各种环境中对适应性的影响。
尽管存在适应性成本,但损伤修复仍是最佳策略,因为它能立即提高生长速率。在参数值范围广泛的充分混合、持久且良性的环境中,存在一个最佳的修复投入,其表现优于损伤隔离。当三个因素同时出现时,损伤隔离才会变得有益,并且仅与修复相结合时才有益:(i)损伤积累速率高,(ii)损伤具有毒性,(iii)修复效率低。与之前的模型不同,我们的模型预测单细胞生物应该具有修复损伤的活跃机制,而不是通过隔离损伤来衰老。事实上,正如预测的那样,所有生物都进化出了活跃的修复机制,而在良性条件下单细胞生物中不存在衰老现象或衰老现象极少,那些具有不同生态习性、栖息在强烈有利于早期繁殖而非长寿的短暂环境中的微生物除外。
在良性条件下的持久环境中,衰老对单细胞生物没有适应性优势,因为非遗传损伤的修复优于损伤隔离。