Department of Genetics, University of Georgia, Athens, GA 30602, USA.
J Hered. 2010 Mar-Apr;101 Suppl 1:S75-84. doi: 10.1093/jhered/esq007. Epub 2010 Mar 1.
We generated all possible haploid and homozygous diploid genotypes at 6 biosynthetic loci in yeast and scored their fitness to examine whether there was any pattern of weak synergistic epistasis, which is a requirement of the deterministic mutation model for the evolution of sex. We measured 4 components of fitness: haploid growth rate, haploid mating efficiency, diploid growth rate, and diploid sporulation efficiency. We found that in agreement with previous work in yeast, epistasis tended to be small in magnitude and variable in sign, regardless of the fitness component measured. The number of background mutations had either no effect or no consistent effect on epistasis distributions. For every combination of 2 loci in a mutation-free background, we also generated all heterozygous genotypes so that we could partition diploid epistasis into additive x additive, additive x dominance, and dominance x dominance epistasis. Our main interest was in determining whether dominance by dominance epistasis was large and negative, which is a requirement of diploid models with inbreeding to explain high levels of recombination. Dominance by dominance epistasis estimates obtained by partitioning diploid epistasis for growth rates were both positive and negative. With the caveat that our results are based on only 6 biosynthetic loci, epistasis for fitness is not supported as an explanation for the maintenance of sex or the high rate of meiotic recombination in yeast.
我们在酵母的 6 个生物合成基因座上生成了所有可能的单倍体和纯合二倍体基因型,并对其适应性进行了评分,以检验是否存在弱协同上位性模式,这是性进化的确定性突变模型的要求。我们测量了 4 个适应性成分:单倍体生长率、单倍体交配效率、二倍体生长率和二倍体产孢效率。我们发现,与酵母之前的研究一致,无论测量的适应性成分如何,上位性的幅度都很小,而且符号也不同。背景突变的数量对上位性分布没有影响或没有一致的影响。对于无突变背景下的每两个基因座组合,我们还生成了所有杂合基因型,以便将二倍体上位性分为加性 x 加性、加性 x 显性和显性 x 显性上位性。我们的主要兴趣是确定显性 x 显性上位性是否大且为负,这是具有自交的二倍体模型解释高水平重组所必需的。通过对生长速率的二倍体上位性进行划分得到的显性 x 显性上位性估计值既有正有负。需要注意的是,我们的结果仅基于 6 个生物合成基因座,因此适应性的上位性不能作为性或酵母中高减数分裂重组率的维持的解释。