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首页> 外文期刊>Annual review of ecology, evolution, and systematics >The Evloution of Multicellularity: A Minor Major Transition?
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The Evloution of Multicellularity: A Minor Major Transition?

机译:多细胞性的演变:重大的过渡?

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Benefits of increased size and functional specialization of qells have repeatedly promoted the evolution of multicellular organisms from unicellular ancestors. Many requirements for multicellulajjjorganization (cell adhesion, cell-cell communication and coorj|lna-tion, programmed cell death) likely evolved in ancestral unicellular organisms. However, the evolution of multicellular organisms from unicellular ancestors may be opposed by genetic conflicts that arise when mutant cell lineages promote their own increase at the expense of the integrity of the multicellular organism. Numerous defenses limit such genetic conflicts, perhaps the most important being development from a unicell, which minimizes conflicts from selection among cell lineages, and redistributes genetic variation arising within multicellular individuals between individuals. With a unicellular bottleneck, defecting cell lineages rarely succeed beyond the life span of the multicellular individual. When multicellularity arises through aggregation of scattered cells or when multicellulai organisms fuse to form genetic chimeras, there are more opportunities foi propagation of defector cell lineages. Intraorganismal competition may partly explain why multicellular organisms that develop by aggregation generally exhibit less differentiation than organisms that develop clonally.
机译:qells大小增加和功能专业化的好处反复促进了单细胞祖先对多细胞生物的进化。在祖先的单细胞生物中可能会发展出许多对多细胞组织的要求(细胞粘附,细胞间通讯和协调,程序性细胞死亡)。然而,当突变细胞谱系以牺牲多细胞生物的完整性为代价来促进其自身的增长时,遗传冲突可能会阻止由单细胞祖先进化而来的多细胞生物的进化。许多防御限制了这种遗传冲突,也许最重要的是单细胞的发展,这使来自细胞谱系选择的冲突最小化,并重新分布了个体之间在多细胞个体中产生的遗传变异。具有单细胞瓶颈,有缺陷的细胞谱系很少会超过多细胞个体的寿命而成功。当通过分散细胞的聚集产生多细胞性时,或者当多细胞生物融合形成遗传嵌合体时,缺陷细胞谱系的繁殖机会就更多。体内竞争可能部分解释了为什么通过聚集发育的多细胞生物通常表现出比克隆生长的生物少的分化。

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