Division of Biology, Hyogo Medical University, Nishinomiya, Hyogo, 663-8501, Japan.
Evolutionary Morphology Laboratory, RIKEN Cluster for Pioneering Research (CPR), Kobe, 650-0047, Japan.
Biotechniques. 2023 May;74(5):243-278. doi: 10.2144/btn-2023-0004. Epub 2023 May 23.
High-purity total RNA extraction from animal embryos is essential for transcriptome analyses. lampreys, together with hagfish, are the only extant jawless vertebrates or cyclostomes and are thus key organisms for EvoDevo studies. However, extracting uncontaminated RNA from early-stage embryos remains challenging. RNA does not bind to the silica membrane in filter-based extractions, significantly reducing yields; and ethanol/isopropanol precipitation methods lead to contaminants, bringing down the optical density (OD) 260/280 ratio. The RNA extraction protocol was modified using precentrifugation and adding salts before isopropanol precipitation. This modification significantly increased RNA yield, removed contaminants and improved RNA integrity. Egg membrane sources were suspected to cause RNA purification problems because low-quality extraction does not occur in posthatching embryos.
从动物胚胎中提取高纯度的总 RNA 对于转录组分析至关重要。七鳃鳗和盲鳗是现存的无颌脊椎动物或圆口类动物,因此是 EvoDevo 研究的关键生物。然而,从早期胚胎中提取无污染的 RNA 仍然具有挑战性。在基于过滤的提取中,RNA 不会与硅基质膜结合,这会显著降低产量;而乙醇/异丙醇沉淀法会导致杂质的产生,降低 OD260/280 比值。通过在异丙醇沉淀前进行预离心和添加盐的方法对 RNA 提取方案进行了修改。该改进显著提高了 RNA 的产量,去除了杂质并改善了 RNA 的完整性。由于孵化后的胚胎不会出现低质量的提取,因此怀疑卵膜来源会导致 RNA 纯化问题。