Department of Plant Sciences, Laboratory of Genetics, Wageningen University , 6708 PB Wageningen , The Netherlands.
Proc Biol Sci. 2019 May 15;286(1902):20190128. doi: 10.1098/rspb.2019.0128.
The mutation rate is a fundamental factor in evolutionary genetics. Recently, mutation rates were found to be strongly reduced at high density in a wide range of unicellular organisms, prokaryotic and eukaryotic. Independently, cell division was found to become more asymmetrical at increasing density in diverse organisms; some 'mother' cells continue dividing, while their 'offspring' cells do not divide further. Here, we investigate how this increased asymmetry in cell division at high density can be reconciled with reduced mutation-rate estimates. We calculated the expected number of mutant cells due to replication errors under various modes of segregation of template-DNA strands and copy-DNA strands, both under symmetrical (exponential) and asymmetrical (linear) growth. We show that the observed reduction in the mutation rate at high density can be explained if mother cells preferentially retain the template-DNA strands, since new mutations are then confined to non-dividing daughter cells, thus reducing the spread of mutant cells. Any other inheritance mode results in an increase in the number of mutant cells at higher density. The proposed hypothesis that patterns of DNA-strand segregation are density-dependent fundamentally challenges our current understanding of mutation-rate estimates and extends the distinction between germline and soma to unicellular organisms.
突变率是进化遗传学中的一个基本因素。最近,在广泛的单细胞生物、原核生物和真核生物中发现,突变率在高密度下会强烈降低。独立地,在不同的生物体中,随着密度的增加,细胞分裂变得越来越不对称;一些“母”细胞继续分裂,而它们的“子”细胞不再进一步分裂。在这里,我们研究了在高密度下细胞分裂的这种增加的不对称性如何与降低的突变率估计值相协调。我们计算了在各种模板-DNA 链和复制-DNA 链分离模式下,在对称(指数)和不对称(线性)生长下,由于复制错误而导致的突变细胞的预期数量。我们表明,如果母细胞优先保留模板-DNA 链,那么在高密度下观察到的突变率降低是可以解释的,因为新的突变随后局限于不分裂的子细胞中,从而减少了突变细胞的扩散。任何其他的遗传模式都会导致在更高的密度下突变细胞数量的增加。所提出的假设,即 DNA 链分离模式是密度依赖性的,从根本上挑战了我们对突变率估计的现有理解,并将 DNA 链分离模式扩展到了单细胞生物的生殖细胞和体细胞之间的区别。