首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Genetic Interactions Between Naturally Occuning Alleles at Quantitative Trait Loci and Mutant Alleles at Candidate Loci Affecting Bristle Number in Drosophila melanogaster
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Genetic Interactions Between Naturally Occuning Alleles at Quantitative Trait Loci and Mutant Alleles at Candidate Loci Affecting Bristle Number in Drosophila melanogaster

机译:数量性状位点上自然存在的等位基因与候选位点上的突变等位基因之间的遗传相互作用影响果蝇的刚毛数。

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Previously, we mapped quantitative trait loci (QTL) affecting response to short-term selection for abdominal bristle number to seven suggestive regions that contain loci involved in bristle development and/or that have adult bristle number mutant phenotypes, and are thus candidates for bristle number QTL in natural populations. To test the hypothesis that the factors contributing to selection response genetically interact with these candidate loci, high and low chromosomes from selection lines were crossed to chromosomes containing wild-type or mutant alleles at the candidate loci, and the numbers of bristles were recorded in trans heterozygotes. Quantitative failure to complement, detected as a significant selection line*cross effect by analysis of variance, can be interpreted as evidence for allelism or epistasis between the factors on selected chromosomes and the candidate loci. Mutations at some candidate loci ( bb, emc, h, Dl, Hairless ) showed strong interactions with selected chromosomes, whereas others interacted weakly ( ASC, abd, Scr ) or not at all ( N, mab, E(spl) ). These results support the hypothesis that some candidate loci, initially identified through mutations of large effect on bristle number, either harbor or are close members in the same genetic pathway as variants that contribute to standing variation in bristle number.
机译:以前,我们将影响对猪鬃数量短期选择的响应的数量性状基因座(QTL)映射到七个提示区域,这些区域包含参与猪鬃发育的场所和/或具有成人猪鬃数量突变表型的人,因此是猪鬃数量的候选者自然种群中的QTL。为了检验这一假设,即导致选择反应的因素与这些候选基因座发生了遗传相互作用,选择线的高低染色体与候选位点上含有野生型或突变等位基因的染色体相交,并在反式中记录刷毛的数量。杂合子。补体定量失败,通过方差分析检测为显着选择线*交叉效应,可以解释为所选染色体上的因子与候选基因座之间存在等位基因或上位性的证据。在某些候选基因座(bb,emc,h,Dl,Hairless)上的突变显示出与选定染色体的强相互作用,而其他突变则弱相互作用(ASC,abd,Scr)或根本不相互作用(N,mab,E(spl))。这些结果支持这样的假设:一些候选位点最初是通过对猪鬃数量产生重大影响的突变而鉴定的,它们与有助于猪鬃数量的长期变异的变体在同一遗传途径中具有相同的亲缘关系或与之接近。

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