School of Biological Sciences, University of Northern Colorado, 501 20th Street, Greeley, CO 80639-0017, USA.
Biotechniques. 2018 Dec;65(6):339-345. doi: 10.2144/btn-2018-0096.
DNA barcoding is a simple technique used to develop a large-scale system of classification that is broadly applicable across a wide variety of taxa. DNA-based analysis of snake venoms can provide a system of classification independent of currently accepted taxonomic relationships by generating DNA barcodes specific to each venom sample. DNA purification from dried snake venoms has previously required large amounts of starting material, has resulted in low yields and inconsistent amplification, and was possible with front-fanged snakes only. Here, we present a modified DNA extraction protocol applied to venoms of both front- and rear-fanged snakes that requires significantly less starting material (1 mg) and yields sufficient amounts of DNA for successful PCR amplification of regions commonly used for DNA barcoding. [Formula: see text].
DNA 条形码技术是一种简单的技术,用于开发一种广泛适用于多种分类群的大规模分类系统。基于 DNA 的蛇毒分析可以通过生成每个毒液样本特有的 DNA 条形码,提供一种独立于当前公认的分类关系的分类系统。从干燥的蛇毒液中提取 DNA 以前需要大量的起始材料,产量低且扩增不一致,并且只能从前牙蛇中获得。在这里,我们提出了一种改良的 DNA 提取方案,适用于前牙和后牙蛇的毒液,所需起始材料(1mg)明显减少,并且可以获得足够量的 DNA,成功地对常用于 DNA 条形码的区域进行 PCR 扩增。