Loukas M, Vergini Y, Krimbas C B
Genetics. 1981 Feb;97(2):429-41. doi: 10.1093/genetics/97.2.429.
Urea denaturation of allozymes was used to provide finer resolution of allelic states within classes of different electrophoretic mobility. This method gives perfectly repeatable results. About 170 isogenic strains for the O chromosome of Drosophila subobscura, derived from two natural populations, were constructed. Their gene arrangements were studied, as well as eight polymorphic genes located on the O chromosome (Est-5, Odh, Ao, ME, Xdh, Lap, Pept-1 and Acph). Crosses performed indicate that differences in urea sensitivity are genetically controlled by the same genes that control electrophoretic mobility. Twice as many alleles have been detected in comparison to the usual electrophoretic method. However, the effective number of alleles did not increase considerably. Studies of linkage disequilibria, by taking into account the finer resolution of allelic states, gave results nearly identical with those obtained in studies where the usual electrophoretic method was used. Although the power of the test is diminished, the absence of genic associations seems to indicate that there are no hidden linkage disequilibria in electrophoretic studies (because of consolidation effects of real alleles into few electromorph classes). The paucity of linkage disequilibria would indicate that there are no epistatic interactions such as those suggested in the model of FRANKLIN and LEWONTIN (1970).
利用同工酶的尿素变性来更精细地分辨不同电泳迁移率类别内的等位基因状态。该方法可给出完全可重复的结果。构建了约170个源自两个自然种群的暗果蝇O染色体的同基因品系。研究了它们的基因排列,以及位于O染色体上的八个多态基因(Est-5、Odh、Ao、ME、Xdh、Lap、Pept-1和Acph)。进行的杂交表明,尿素敏感性的差异由控制电泳迁移率的相同基因进行遗传控制。与常规电泳方法相比,检测到的等位基因数量增加了一倍。然而,等位基因的有效数量并未显著增加。通过考虑等位基因状态的更精细分辨来研究连锁不平衡,得到的结果与使用常规电泳方法的研究结果几乎相同。尽管检验效能有所降低,但基因关联的缺失似乎表明在电泳研究中不存在隐藏的连锁不平衡(由于实际等位基因合并到少数电泳形态类别中的合并效应)。连锁不平衡的缺乏表明不存在诸如FRANKLIN和LEWONTIN(1970)模型中所提出的上位性相互作用。