Steele Laura D, Muir William M, Seong Keon Mook, Valero M Carmen, Rangesa Madhumitha, Sun Weilin, Clark John M, Coates Brad, Pittendrigh Barry R
Department of Entomology, University of Illinois, Urbana-Champaign, Urbana, Illinois, United States of America.
Department of Animal Sciences, Purdue University, West Lafayette, Indiana, United States of America.
PLoS One. 2014 Jun 10;9(6):e98584. doi: 10.1371/journal.pone.0098584. eCollection 2014.
The Drosophila melanogaster 91-R and 91-C strains are of common origin, however, 91-R has been intensely selected for dichlorodiphenyltrichloroethane (DDT) resistance over six decades while 91-C has been maintained as the non-selected control strain. These fly strains represent a unique genetic resource to understand the accumulation and fixation of mutations under laboratory conditions over decades of pesticide selection. Considerable research has been done to investigate the differential expression of genes associated with the highly DDT resistant strain 91-R, however, with the advent of whole genome sequencing we can now begin to develop an in depth understanding of the genomic changes associated with this intense decades-long xenobiotic selection pressure. Here we present the first whole genome sequencing analysis of the 91-R and 91-C fly strains to identify genome-wide structural changes within the open reading frames. Between-strain changes in allele frequencies revealed a higher percent of new alleles going to fixation for the 91-R strain, as compared to 91-C (P<0.0001). These results suggest that resistance to DDT in the 91-R laboratory strain could potentially be due primarily to new mutations, as well as being polygenic rather than the result of a few major mutations, two hypotheses that remain to be tested.
果蝇黑腹种的91-R和91-C品系起源相同,然而,60多年来91-R品系一直因对二氯二苯三氯乙烷(DDT)具有抗性而被强烈选择,而91-C品系则作为未被选择的对照品系保存下来。这些果蝇品系代表了一种独特的遗传资源,可用于了解在数十年农药选择的实验室条件下突变的积累和固定情况。已经开展了大量研究来调查与高抗DDT品系91-R相关的基因差异表达,然而,随着全基因组测序的出现,我们现在可以开始深入了解与这种长达数十年的强烈异源生物选择压力相关的基因组变化。在此,我们展示了91-R和91-C果蝇品系的首次全基因组测序分析,以确定开放阅读框内全基因组范围的结构变化。等位基因频率的品系间变化显示,与91-C品系相比,91-R品系中固定的新等位基因比例更高(P<0.0001)。这些结果表明,91-R实验室品系对DDT的抗性可能主要归因于新突变,并且是多基因的,而非少数主要突变的结果,这两个假设仍有待检验。