Madhu Bhoomi, Lakdawala Mohammed Farhan, Gumienny Tina L
Department of Biology, Texas Woman's University.
Department of Biology, Texas Woman's University;
J Vis Exp. 2022 Jun 7(184). doi: 10.3791/63716.
Genomic DNA extraction from single or a few Caenorhabditis elegans has many downstream applications, including PCR for genotyping lines, cloning, and sequencing. The traditional proteinase K-based methods for genomic DNA extraction from C. elegans take several hours. Commercial extraction kits that effectively break open the C. elegans cuticle and extract genomic DNA are limited. An easy, faster (~15 min), and cost-efficient method of extracting C. elegans genomic DNA that works well for classroom and research applications is reported here. This DNA extraction method is optimized to use single or a few late-larval (L4) or adult nematodes as starting material for obtaining a reliable template to perform PCR. The results indicate that the DNA quality is suitable for amplifying gene targets of different sizes by PCR, permitting genotyping of single or a few animals even at dilutions to one-fiftieth of the genomic DNA from a single adult per reaction. The reported protocols can be reliably used to quickly produce DNA template from a single or a small sample of C. elegans for PCR-based applications.
从单个或少数秀丽隐杆线虫中提取基因组DNA有许多下游应用,包括用于品系基因分型的PCR、克隆和测序。传统的基于蛋白酶K从秀丽隐杆线虫中提取基因组DNA的方法需要数小时。能有效打开秀丽隐杆线虫角质层并提取基因组DNA的商业提取试剂盒数量有限。本文报道了一种简便、快速(约15分钟)且经济高效的提取秀丽隐杆线虫基因组DNA的方法,该方法适用于课堂和研究应用。这种DNA提取方法经过优化,以单个或少数晚期幼虫(L4)或成虫线虫作为起始材料,用于获得可靠的模板以进行PCR。结果表明,DNA质量适合通过PCR扩增不同大小的基因靶点,即使在每个反应中将来自单个成虫的基因组DNA稀释至五十分之一的情况下,也能对单个或少数动物进行基因分型。所报道的方案可可靠地用于从单个或少量秀丽隐杆线虫样本中快速制备用于基于PCR应用的DNA模板。