Boontawon Tatpong, Nakazawa Takehito, Inoue Chikako, Osakabe Keishi, Kawauchi Moriyuki, Sakamoto Masahiro, Honda Yoichi
Graduate School of Agriculture, Kyoto University, Oiwakecho, Kitashirakawa, Sakyo-ku, 606-8502, Kyoto, Japan.
Graduate School of Technology, Industrial and Social Sciences, Tokushima University, 770-8503, Tokushima, Japan.
AMB Express. 2021 Feb 20;11(1):30. doi: 10.1186/s13568-021-01193-w.
Pleurotus ostreatus is one of the most commercially produced edible mushrooms worldwide. Improved cultivated strains with more useful traits have been obtained using classical breeding, which is laborious and time-consuming. Here, we attempted efficient gene mutagenesis using plasmid-based CRISPR/Cas9 as the first step for non-genetically modified (non-GM) P. ostreatus generation. Plasmids harboring expression cassettes of Cas9 and different single guide RNAs targeting fcy1 and pyrG were individually transferred into fungal protoplasts of the PC9 strain, which generated some strains exhibiting resistance to 5-fluorocytosine and 5-fluoroorotic acid, respectively. Genomic PCR followed by sequencing revealed small insertions/deletions or insertion of a fragment from the plasmid at the target site in some of the drug-resistant strains. The results demonstrated efficient CRISPR/Cas9-assisted genome editing in P. ostreatus, which could contribute to the molecular breeding of non-GM cultivated strains in the future. Furthermore, a mutation in fcy1 via homology-directed repair using this CRISPR/Cas9 system was also efficiently introduced, which could be applied not only for precise gene disruption, but also for insertions leading to heterologous gene expression in this fungus.
糙皮侧耳是全球商业化生产最多的食用菌之一。利用经典育种方法已经获得了具有更多有用性状的改良栽培菌株,但这种方法既费力又耗时。在此,我们尝试使用基于质粒的CRISPR/Cas9进行高效基因诱变,作为非转基因糙皮侧耳培育的第一步。携带Cas9表达盒和靶向fcy1和pyrG的不同单向导RNA的质粒分别转入PC9菌株的真菌原生质体中,分别产生了一些对5-氟胞嘧啶和5-氟乳清酸具有抗性的菌株。随后进行的基因组PCR和测序显示,在一些耐药菌株的靶位点处有小的插入/缺失或质粒片段的插入。结果证明了CRISPR/Cas9辅助的糙皮侧耳基因组编辑是有效的,这可能有助于未来非转基因栽培菌株的分子育种。此外,利用该CRISPR/Cas9系统通过同源定向修复在fcy1中也成功引入了突变,这不仅可用于精确的基因破坏,还可用于在该真菌中导致异源基因表达的插入。