Smit-McBride Z, Moya A, Ayala F J
Department of Ecology and Evolutionary Biology, University of California, Irvine 92717.
Genetics. 1988 Dec;120(4):1043-51. doi: 10.1093/genetics/120.4.1043.
We have studied linkage disequilibrium in Drosophila melanogaster in two samples from a wild population and in four large laboratory populations derived from the wild samples. We have assayed four polymorphic enzyme loci, fairly closely linked in the third chromosome: Sod Est-6, Pgm, and Odh. The assay method used allows us to identify the allele associations separately in each of the two homologous chromosomes from each male sampled. We have detected significant linkage disequilibrium between two loci in 16.7% of the cases in the wild samples and in 27.8% of the cases in the experimental populations, considerably more than would be expected by chance alone. We have also found three-locus disequilibria in more instances than would be expected by chance. Some disequilibria present in the wild samples disappear in the experimental populations derived from them, but new ones appear over the generations. The effective population sizes required to generate the observed disequilibria by randomness range from 40 to more than 60,000 individuals in the natural population, depending on which locus pair is considered, and from 100 to more than 60,000 in the experimental populations. These population sizes are unrealistic; the fact that different locus-pairs yield disparate estimates within the same population argues against the likelihood that the disequilibria may have arisen as a consequence of population bottlenecks. Migration, or population mixing, cannot be excluded as the process generating the disequilibria in the wild samples, but can in the experimental populations. We conclude that linkage disequilibrium in these populations is most likely due to natural selection acting on the allozymes, or on loci very tightly linked to them.
我们在来自野生种群的两个样本以及从野生样本衍生而来的四个大型实验室种群中研究了黑腹果蝇的连锁不平衡。我们检测了四个多态性酶基因座,它们在第三条染色体上紧密连锁:超氧化物歧化酶(Sod)、酯酶-6(Est-6)、磷酸葡萄糖变位酶(Pgm)和苹果酸脱氢酶(Odh)。所使用的检测方法使我们能够在每个采样雄性的两条同源染色体中的每一条上分别识别等位基因关联。我们在野生样本中16.7%的案例以及实验种群中27.8%的案例中检测到两个基因座之间存在显著的连锁不平衡,大大超过了仅由偶然因素预期的比例。我们还发现三基因座不平衡的情况比偶然预期的更多。野生样本中存在的一些不平衡在由它们衍生而来的实验种群中消失了,但新的不平衡在几代中出现。通过随机性产生观察到的不平衡所需的有效种群大小在自然种群中根据所考虑的基因座对不同,范围从40到超过60000个个体,在实验种群中从100到超过60000个个体。这些种群大小是不现实的;同一种群内不同基因座对产生不同估计这一事实表明,不平衡不太可能是由于种群瓶颈导致的。迁移或种群混合不能被排除为野生样本中产生不平衡的过程,但在实验种群中可以排除。我们得出结论,这些种群中的连锁不平衡很可能是由于自然选择作用于等位酶或与其紧密连锁的基因座。