Cavener D R, Clegg M T
Genetics. 1978 Nov;90(3):629-44. doi: 10.1093/genetics/90.3.629.
Four replicate populations of Drosophila melanogaster, two reared on medium supplemented with ethanol and two reared on standard medium, were electrophoretically monitored for 28 generations. During the first 12 generations, allelic, genotypic and gametic frequencies were determined for eight polymorphic enzymes: GOT, alpha-GPDH, MDH, ADH, TO, E6, Ec and ODH. Samples from generation 18 and 28 were electrophoretically typed for ADH and alpha-GPDH. In addition, samples from generation 27 were analyzed for the presence of inversion heterozygotes. The experimental results showed rapid gene-frequency divergence between control and treatment populations at the Adh locus in a direction consistent with the activity hierarchy of Adh genotypes. Gene-frequency divergence between control and treatment populations also occurred at the alpha-Gpdh locus, although the agreement among replicates appeared to have broken down by generation 28. No differential gene-frequency change occurred at any of the six remaining marker loci. Furthermore, values of linkage disequilibria among all linked pairs of genes were initially small and remained small throughout the course of the experiment. Taking these facts into account, it is argued that the gene-frequency response observed at ADH is most probably caused by selection at the Adh locus. The gene frequency response at alpha-Gpdh can also be be accounted for in terms of the effect of ethanol on energy metabolism, although other explanations cannot be excluded.
对四组黑腹果蝇进行了28代的电泳监测,其中两组饲养在添加乙醇的培养基上,两组饲养在标准培养基上。在最初的12代中,测定了八种多态性酶(GOT、α-GPDH、MDH、ADH、TO、E6、Ec和ODH)的等位基因、基因型和配子频率。对第18代和第28代的样本进行了ADH和α-GPDH的电泳分型。此外,对第27代的样本进行了倒位杂合子的分析。实验结果表明,对照群体和处理群体在Adh位点的基因频率迅速分化,其方向与Adh基因型的活性等级一致。对照群体和处理群体在α-Gpdh位点也出现了基因频率分化,尽管到第28代时重复实验之间的一致性似乎已经瓦解。其余六个标记位点均未发生基因频率的差异变化。此外,所有连锁基因对之间的连锁不平衡值最初很小,并且在整个实验过程中一直保持很小。考虑到这些事实,可以认为在ADH处观察到的基因频率反应很可能是由Adh位点的选择引起的。α-Gpdh处的基因频率反应也可以用乙醇对能量代谢的影响来解释,尽管不能排除其他解释。