Lynch Michael
Department of Biology, Indiana University, Bloomington, Indiana 47405, USA.
Genetics. 2008 Oct;180(2):933-43. doi: 10.1534/genetics.108.090456. Epub 2008 Aug 30.
Although the matter has been subject to considerable theoretical study, there are numerous open questions regarding the mechanisms driving the mutation rate in various phylogenetic lineages. Most notably, empirical evidence indicates that mutation rates are elevated in multicellular species relative to unicellular eukaryotes and prokaryotes, even on a per-cell division basis, despite the need for the avoidance of somatic damage and the accumulation of germline mutations. Here it is suggested that multicellularity discourages selection against weak mutator alleles for reasons associated with both the cellular and the population-genetic environments, thereby magnifying the vulnerability to somatic mutations (cancer) and increasing the risk of extinction from the accumulation of germline mutations. Moreover, contrary to common belief, a cost of fidelity need not be invoked to explain the lower bound to observed mutation rates, which instead may simply be set by the inability of selection to advance very weakly advantageous antimutator alleles in finite populations.
尽管该问题已受到大量理论研究,但关于驱动不同系统发育谱系中突变率的机制仍存在众多未解决的问题。最值得注意的是,经验证据表明,即使按每个细胞分裂计算,多细胞物种中的突变率相对于单细胞真核生物和原核生物也有所升高,尽管需要避免体细胞损伤和生殖系突变的积累。本文认为,由于细胞和群体遗传环境相关的原因,多细胞性不利于对弱突变等位基因进行选择,从而放大了对体细胞突变(癌症)的易感性,并增加了因生殖系突变积累而灭绝的风险。此外,与普遍看法相反,无需引入保真度成本来解释观察到的突变率下限,相反,这可能仅仅是由于选择在有限群体中无法推进非常微弱有利的抗突变等位基因所致。