Department of Zoology, University of Oxford, Oxford, United Kingdom.
Department of Biochemistry, University of Oxford, Oxford, United Kingdom.
PLoS Biol. 2022 Jun 3;20(6):e3001626. doi: 10.1371/journal.pbio.3001626. eCollection 2022 Jun.
The evolution of cooperation in cellular groups is threatened by lineages of cheaters that proliferate at the expense of the group. These cell lineages occur within microbial communities, and multicellular organisms in the form of tumours and cancer. In contrast to an earlier study, here we show how the evolution of pleiotropic genetic architectures-which link the expression of cooperative and private traits-can protect against cheater lineages and allow cooperation to evolve. We develop an age-structured model of cellular groups and show that cooperation breaks down more slowly within groups that tie expression to a private trait than in groups that do not. We then show that this results in group selection for pleiotropy, which strongly promotes cooperation by limiting the emergence of cheater lineages. These results predict that pleiotropy will rapidly evolve, so long as groups persist long enough for cheater lineages to threaten cooperation. Our results hold when pleiotropic links can be undermined by mutations, when pleiotropy is itself costly, and in mixed-genotype groups such as those that occur in microbes. Finally, we consider features of multicellular organisms-a germ line and delayed reproductive maturity-and show that pleiotropy is again predicted to be important for maintaining cooperation. The study of cancer in multicellular organisms provides the best evidence for pleiotropic constraints, where abberant cell proliferation is linked to apoptosis, senescence, and terminal differentiation. Alongside development from a single cell, we propose that the evolution of pleiotropic constraints has been critical for cooperation in many cellular groups.
细胞群体中的合作进化受到以牺牲群体为代价而增殖的骗子谱系的威胁。这些细胞谱系存在于微生物群落中,以及以肿瘤和癌症形式存在的多细胞生物中。与早期的一项研究不同,在这里我们展示了多效性遗传结构的进化如何保护合作免受骗子谱系的影响,并允许合作进化。我们建立了一个细胞群体的年龄结构模型,并表明与不将表达与私有特征联系起来的群体相比,将合作与私有特征联系起来的群体中合作的崩溃速度更慢。然后,我们表明这导致了群体对多效性的选择,这通过限制骗子谱系的出现强烈促进了合作。这些结果表明,只要群体持续足够长的时间以使骗子谱系威胁到合作,多效性就会迅速进化。当多效性联系可以被突变破坏时,当多效性本身是昂贵的时,以及在混合基因型群体中,例如那些发生在微生物中的群体中,我们的结果仍然成立。最后,我们考虑了多细胞生物的特征-生殖系和延迟的生殖成熟性-并表明多效性对于维持合作再次是重要的。多细胞生物中癌症的研究提供了多效性约束的最佳证据,其中异常细胞增殖与细胞凋亡、衰老和终末分化有关。除了单细胞发育外,我们还提出多效性约束的进化对于许多细胞群体中的合作至关重要。