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A chloroplast genomic strategy for designing taxon specific DNA mini-barcodes: a case study on ginsengs

机译:叶绿体基因组学策略设计分类群特异的DNA迷你条形码:以人参为例的研究

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Background Universal conventional DNA barcodes will become more and more popular in biological material identifications. However, in many cases such as processed medicines or canned food, the universal conventional barcodes are unnecessary and/or inapplicable due to DNA degradation. DNA mini-barcode is a solution for such specific purposes. Here we exemplify how to develop the best mini-barcodes for specific taxa using the ginseng genus (Panax) as an example. Results The chloroplast genome of P. notoginseng was sequenced. The genome was compared with that of P. ginseng. Regions of the highest variability were sought out. The shortest lengths which had the same discrimination powers of conventional lengths were considered the best mini-barcodes. The results showed that the chloroplast genome of P. notoginseng is 156,387 bp. There are only 464 (0.30%) substitutions between the two genomes. The intron of rps16 and two regions of the coding gene ycf1, ycf1a and ycf1b, evolved the quickest and served as candidate regions. The mini-barcodes of Panax turned out to be 60 bp for ycf1a at a discrimination power of 91.67%, 100 bp for ycf1b at 100%, and 280 bp for rps16 at 83.33%. Conclusions The strategy by searching the whole chloroplast genomes, identifying the most variable regions, shortening the focal regions for mini-barcodes are believed to be efficient in developing taxon-specific DNA mini-barcodes. The best DNA mini-barcodes are guaranteed to be found following this strategy.
机译:背景技术通用的常规DNA条形码将在生物材料鉴定中变得越来越流行。但是,在许多情况下,例如加工药品或罐头食品,由于DNA降解,通用的常规条形码是不必要的和/或不适用的。 DNA迷你条形码是用于此类特定目的的解决方案。在这里,我们以人参属(Panax)为例,举例说明如何为特定分类群开发最佳的迷你条形码。结果对三七叶绿体基因组进行了测序。将基因组与人参的基因组进行比较。寻找变异性最高的区域。具有与传统长度相同的识别能力的最短长度被认为是最佳的迷你条形码。结果表明,三七的叶绿体基因组为156,387 bp。两个基因组之间只有464个(0.30%)取代。 rps16的内含子和编码基因ycf1的两个区域ycf1a和ycf1b进化最快,可作为候选区域。 Panax的迷你条形码在ycf1a的分辨力为91.67%时为60 bp,在ycf1b的分辨力为100%时为100 bp,对于rps16的分辨力为83.33%时为280 bp。结论通过搜索整个叶绿体基因组,识别最具可变性的区域,缩短迷你条形码的焦点区域,该策略被认为在开发分类群特异性DNA迷你条形码方面是有效的。遵循此策略,可以确保找到最佳的DNA迷你条形码。

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