Otto S P, Orive M E
Institute of Cellular, Animal and Population Biology, University of Edinburgh, United Kingdom.
Genetics. 1995 Nov;141(3):1173-87. doi: 10.1093/genetics/141.3.1173.
Whether in sexual or asexual organisms, selection among cell lineages during development is an effective way of eliminating deleterious mutations. Using a mathematical analysis, we find that relatively small differences in cell replication rates during development can translate into large differences in the proportion of mutant cells within the adult, especially when development involves a large number of cell divisions. Consequently, intraorganismal selection can substantially reduce the deleterious mutation rate observed among offspring as well as the mutation load within a population, because cells rather than individuals provide the selective "deaths" necessary to stem the tide of deleterious mutations. The reduction in mutation rate among offspring is more pronounced in organisms with plastic development than in those with structured development. It is also more pronounced in asexual organisms that produce multicellular rather than unicellular offspring. By effecting the mutation rate, intraorganismal selection may have broad evolutionary implications; as an example, we consider its influence on the evolution of ploidy levels, finding that cell-lineage selection is more effective in haploids and tends to favor their evolution.
无论是有性生殖还是无性生殖的生物体,发育过程中细胞谱系间的选择都是消除有害突变的有效方式。通过数学分析,我们发现发育过程中细胞复制速率相对较小的差异,能够转化为成体中突变细胞比例的巨大差异,尤其是当发育涉及大量细胞分裂时。因此,体内选择能够大幅降低后代中观察到的有害突变率以及种群内的突变负荷,因为是细胞而非个体提供了阻止有害突变浪潮所需的选择性“死亡”。后代中突变率的降低在具有可塑性发育的生物体中比在具有结构化发育的生物体中更为显著。在产生多细胞而非单细胞后代的无性生物体中,这种降低也更为显著。通过影响突变率,体内选择可能具有广泛的进化意义;例如,我们考虑其对倍性水平进化的影响,发现细胞谱系选择在单倍体中更有效,并且倾向于促进其进化。