Grey Michelle J, Freeman Jackie, Rudd Jason, Irish Naomi, Canning Gail, Chancellor Tania, Palma-Guerrero Javier, Hill Rowena, Hall Neil, Hammond-Kosack Kim E, McMullan Mark
Department of Organisms and Ecosystems, Earlham Institute, Norwich, England.
Rothamsted Research, Strategic Areas: Protecting Crops and the Environment, Plant Sciences for the Bioeconomy, West Common, Harpenden, UK.
Bio Protoc. 2025 Mar 20;15(6):e5245. doi: 10.21769/BioProtoc.5245.
This manuscript details two modified protocols for the isolation of long-stranded or high molecular weight (HMW) DNA from Magnaporthaceae (Ascomycota) fungal mycelium intended for whole genome sequencing. The Cytiva Nucleon PhytoPure and the Macherey-Nagel NucleoBond HMW DNA kits were selected because the former requires lower amounts of starting material and the latter utilizes gentler methods to maximize DNA length, albeit at a higher requirement for input material. The Cytiva Nucleon PhytoPure kit successfully recovered HMW DNA for half of our fungal species by increasing the amount of RNase A treatment and adding in a proteinase K treatment. To reduce the impact of pigmentation development, which occurs toward later stages of culturing, extractions were run in quadruplicate to increase overall DNA concentration. We also adapted the Macherey-Nagel NucleoBond HMW DNA kit for high-quality HMW DNA by grinding the sample to a fine powder, overnight lysis, and splitting the sample before washing the precipitated DNA. For both kits, precipitated DNA was spooled out pre-washing, ensuring a higher percentage of high-integrity long strands. The Macherey-Nagel protocol offers advantages over the first through the utilization of gravity columns that provide gentler treatment, yielding >50% of high-purity DNA strands exceeding 40 kbp. The limitation of this method is the requirement for a large quantity of starting material (1 g). By triaging samples based on the rate of growth relative to the accumulation of secondary metabolites, our methodologies hold promise for yielding reliable and high-quality HMW DNA from a variety of fungal samples, improving sequencing outcomes. Key features • Modified protocols for the extraction of high molecular weight fungal DNA suitable for long-read whole genome sequencing. • Approximately 4 h to complete four samples in parallel (excluding lysis time). • Optimized for the mycelium of Magnaporthaceae fungi, harvested before melanin (or secondary metabolite) buildup, but readily adaptable for other ascomycetes.
本手稿详细介绍了两种改良方案,用于从稻瘟病菌科(子囊菌门)真菌菌丝体中分离长链或高分子量(HMW)DNA,以用于全基因组测序。选择了赛多利斯公司的Nucleon PhytoPure试剂盒和默克密理博公司的NucleoBond HMW DNA试剂盒,因为前者所需的起始材料量较少,而后者采用更温和的方法来最大化DNA长度,尽管对输入材料的要求较高。赛多利斯公司的Nucleon PhytoPure试剂盒通过增加核糖核酸酶A处理量并加入蛋白酶K处理,成功为一半的真菌物种回收了HMW DNA。为了减少培养后期出现的色素沉着的影响,提取过程进行了四次重复以提高总体DNA浓度。我们还对默克密理博公司的NucleoBond HMW DNA试剂盒进行了改进,通过将样品研磨成细粉、过夜裂解以及在洗涤沉淀的DNA之前将样品分开,以获得高质量的HMW DNA。对于这两种试剂盒,沉淀的DNA在洗涤前绕成线轴,确保了更高比例的高完整性长链。默克密理博公司的方案通过使用提供更温和处理的重力柱,比第一种方案具有优势,可产生超过50%的纯度高于40 kbp的DNA链。该方法的局限性是需要大量的起始材料(1 g)。通过根据相对于次生代谢物积累的生长速率对样品进行分类,我们的方法有望从各种真菌样品中产生可靠且高质量的HMW DNA,改善测序结果。关键特性• 改良方案用于提取适用于长读长全基因组测序的高分子量真菌DNA。• 大约4小时可并行完成四个样品(不包括裂解时间)。• 针对稻瘟病菌科真菌的菌丝体进行了优化,在黑色素(或次生代谢物)积累之前收获,但也易于适用于其他子囊菌。