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Genome editing in the mushroom-forming basidiomycete Coprinopsis cinerea optimized by a high-throughput transformation system

机译:通过高通量转化系统优化了形成蘑菇的拟南芥鸡腿菇的基因组编辑

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摘要

Mushroom-forming basidiomycetes produce a wide range of metabolites and have great value not only as food but also as an important global natural resource. Here, we demonstrate CRISPR/Cas9-based genome editing in the model species Coprinopsis cinerea. Using a high-throughput reporter assay with cryopreserved protoplasts, we identified a novel promoter, CcDED1 pro, with seven times stronger activity in this assay than the conventional promoter GPD2. To develop highly efficient genome editing using CRISPR/Cas9 in C. cinerea, we used the CcDED1 pro to express Cas9 and a U6-snRNA promoter from C. cinerea to express gRNA. Finally, CRISPR/Cas9-mediated GFP mutagenesis was performed in a stable GFP expression line. Individual genome-edited lines were isolated, and loss of GFP function was detected in hyphae and fruiting body primordia. This novel method of high-throughput CRISPR/Cas9-based genome editing using cryopreserved protoplasts should be a powerful tool in the study of edible mushrooms.
机译:形成蘑菇的担子菌可产生多种代谢产物,不仅作为食物而且作为重要的全球自然资源都具有巨大价值。在这里,我们展示了模型物种灰粉蛇蝎中基于CRISPR / Cas9的基因组编辑。使用具有低温保存的原生质体的高通量报告基因检测方法,我们确定了一种新型启动子CcDED1 pro,其活性比常规启动子GPD2强7倍。为了在灰葡萄中使用CRISPR / Cas9开发高效的基因组编辑,我们使用了CcDED1 pro表达Cas9,并使用了灰葡萄的U6-snRNA启动子来表达gRNA。最后,在稳定的GFP表达系中进行了CRISPR / Cas9介导的GFP诱变。分离单个基因组编辑的品系,并在菌丝和子实体原基中检测到GFP功能的丧失。这种使用低温保存的原生质体进行基于CRISPR / Cas9的高通量基因组编辑的新颖方法,应该是研究可食用蘑菇的有力工具。

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