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EST sequencing and fosmid library construction in a non-model moth, Mamestra brassicae, for comparative mapping

机译:EST测序和非模型蛾(Mamestra brasicae)中的fosmid文库构建,用于比较定位

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摘要

Genome data are useful for both basic and applied research; however, it is difficult to carry out large-scale genome analyses using species with limited genetic or genomic resources. Here, we describe a cost-effective method to analyze the genome of a non-model species, using the cabbage moth, Mamestra brassicae (Lepidoptera: Noctuidae). First, we conducted expression sequence tag (EST) analysis. In this analysis, we performed PCR-based prescreening of a non-normalized embryonic cDNA library to eliminate already sequenced cDNAs from further sequencing, which significantly increased the percentage of unique genes. Next, we constructed a fosmid library of M. brassicae and isolated 120 clones containing 119 putative single copy genes by PCR-based screening with primer sets designed from the ESTs. Finally, we showed that the isolated fosmid clones could be used as probes for multicolor fluorescence in situ hybridization (FISH) analysis against an M. brassicae chromosome and confirmed conserved gene order between M. brassicae and the silkworm, Bombyx mori. Thus, we developed new genomic resources for comparative genome analysis in M. brassicae using robust and relatively low cost methods that can be applied to any non-model organism.
机译:基因组数据可用于基础研究和应用研究。但是,很难使用遗传或基因组资源有限的物种进行大规模的基因组分析。在这里,我们描述了一种使用白菜蛾Mamestra brasicae(鳞翅目:夜蛾科)分析非模式物种基因组的经济有效的方法。首先,我们进行了表达序列标签(EST)分析。在此分析中,我们对未标准化的胚胎cDNA文库进行了基于PCR的预筛选,以消除进一步测序中已测序的cDNA,从而显着提高了独特基因的百分比。接下来,我们构建了芸苔分枝杆菌的fosmid文库,并通过基于EST的引物对进行了基于PCR的筛选,分离出120个含有119个推定单拷贝基因的克隆。最后,我们证明了分离出的化石克隆可用作探针,用于针对芸苔分枝杆菌染色体进行多色荧光原位杂交(FISH)分析,并证实了芸苔分枝杆菌与家蚕(Bombyx mori)之间的保守基因顺序。因此,我们使用健壮且成本相对较低的方法开发了用于芸苔分枝杆菌比较基因组分析的新基因组资源,该方法可应用于任何非模式生物。

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