Schuetze Christopher, Peters Michelle, Duong Jia-Jen, Cavey Matthieu, Dörig Ruth, Lasko Paul, Suter Beat
Department of Biology, McGill University, 1205 avenue Docteur Penfield, Montreal, QC H3A 1B1, Canada.
Genome. 2004 Oct;47(5):832-8. doi: 10.1139/g04-052.
Chromosomal mutations induced by ethyl methanesulfonate (EMS) treatment can cause female sterility or maternal-effect lethality in Drosophila. EMS is particularly useful to researchers because it creates mutations independent of position effects. However, because researchers have little control over the chromosomal site of mutation, post-mutagenic genetic mapping is required to determine the cytological location of the mutation. To make a valuable set of mutants more useful to the research community, we have mapped the uncharacterized part of the female-sterile - maternal-effect lethal Tubingen collection. We mapped 49 female-sterile - maternal-effect lethal alleles and 72 lethal alleles to individual deficiency intervals on the third chromosome. In addition, we analyzed the phenotype of ovaries resulting from female sterile mutations. The observed phenotypes range from tumorous ovaries and early blocks in oogenesis, to later blocks, slow growth, blocks in stage 10, to apparently full development of the ovary. The mapping and phenotypic characterization of these 121 mutations provide the necessary information for the researcher to consider a specific mutant as a candidate for their gene of interest.
甲磺酸乙酯(EMS)处理诱导的染色体突变可导致果蝇雌性不育或母性效应致死。EMS对研究人员特别有用,因为它能产生与位置效应无关的突变。然而,由于研究人员几乎无法控制突变的染色体位点,因此需要在诱变后进行遗传定位,以确定突变的细胞学位置。为了使一组有价值的突变体对研究群体更有用,我们对雌性不育-母性效应致死的图宾根品系中未表征的部分进行了定位。我们将49个雌性不育-母性效应致死等位基因和72个致死等位基因定位到第三条染色体上的各个缺失区间。此外,我们分析了雌性不育突变产生的卵巢表型。观察到的表型范围从肿瘤性卵巢和卵子发生早期阻滞,到后期阻滞、生长缓慢、第10阶段阻滞,再到卵巢明显完全发育。这121个突变的定位和表型特征为研究人员将特定突变体视为其感兴趣基因的候选者提供了必要信息。