Biochemistry and Biophysics, Texas A&M University, College Station, Texas, United States of America.
PLoS One. 2024 Jul 24;19(7):e0301680. doi: 10.1371/journal.pone.0301680. eCollection 2024.
The development of high molecular weight (HMW) genomic DNA (gDNA) extraction protocols for non-model species is essential to fully exploit long-read sequencing technologies in order to generate genome assemblies that can help answer complex questions about these organisms. Obtaining enough high-quality HMW gDNA can be challenging for these species, especially for tissues rich in polysaccharides such as biomass from species within the Botryococcus genus. The existing protocols based on column-based DNA extraction and biochemical lysis kits can be inefficient and may not be useful due to variations in biomass polysaccharide content. We developed an optimized protocol for the efficient extraction of HMW gDNA from Botryococcus biomass for use in long-read sequencing technologies. The protocol utilized an initial wash step with sorbitol to remove polysaccharides and yielded HMW gDNA concentrations up to 220 ng/μL with high purity. We then demonstrated the suitability of the HMW gDNA isolated from this protocol for long-read sequencing on the Oxford Nanopore PromethION platform for three Botryococcus species. Our protocol can be used as a standard for efficient HMW gDNA extraction in microalgae rich in polysaccharides and may be adapted for other challenging species.
开发高分子量(HMW)基因组 DNA(gDNA)提取方案对于非模式物种至关重要,这对于充分利用长读测序技术以生成能够帮助回答有关这些生物体的复杂问题的基因组组装至关重要。对于这些物种来说,获得足够的高质量 HMW gDNA 可能具有挑战性,特别是对于富含多糖的组织,例如 Botryococcus 属物种的生物质。基于柱式 DNA 提取和生化裂解试剂盒的现有方案可能效率低下,并且由于生物质多糖含量的变化可能没有用。我们开发了一种从 Botryococcus 生物质中高效提取 HMW gDNA 的优化方案,用于长读测序技术。该方案利用山梨醇进行初始洗涤步骤以去除多糖,并产生高达 220 ng/μL 的 HMW gDNA 浓度,纯度高。然后,我们证明了该方案分离的 HMW gDNA 适用于在 Oxford Nanopore PromethION 平台上对三种 Botryococcus 物种进行长读测序。我们的方案可作为富含多糖的微藻中高效 HMW gDNA 提取的标准,并可适用于其他具有挑战性的物种。