Graduate School of Agriculture, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan.
Mushroom Division, National Institute of Horticultural and Herbal Science, Rural Development Administration, Bisan-ro, Eumseong-gun, Chungcheongbuk-do 22709, Republic of Korea.
Fungal Genet Biol. 2024 Jun;172:103890. doi: 10.1016/j.fgb.2024.103890. Epub 2024 Mar 17.
A sporeless strain is an important breeding target in the mushroom industry. However, basidiospore production in the oyster mushroom Pleurotus ostreatus has been shown to be impaired by single-gene mutations in only two meiosis-related genes, mer3 and msh4. This study proposed a strategy for identifying the genes essential for basidiospore formation after meiotic division to determine new targets for molecular breeding. RNA-seq analysis was performed to identify P. ostreatus genes that are specifically expressed in the gill tissue of fruiting bodies, where basidiospore formation occurs. Transcriptome data during fruiting development of Coprinopsis cinerea, in which the meiotic steps progress synchronously, were then used to identify genes that are active in the postmeiotic stages. Based on these comparative analyses, five P. ostreatus genes were identified. Plasmids containing expression cassettes for hygromycin B-resistance screening, Cas9, and single-guide RNA targeting each gene were introduced into the protoplasts of dikaryotic strain, PC9×#64, to generate dikaryotic gene disruptants. Among the obtained transformants, three dikaryotic pcl1 disruptants and two cro6c disruptants did not produce basidiospores. Microscopic analyses indicated that spore formation was arrested at particular stages in these gene disruptants. These results indicate that these two genes are essential for mature spore formation in this fungus.
无孢子菌株是蘑菇产业的重要育种目标。然而,在牡蛎蘑菇(Pleurotus ostreatus)中,仅在两个减数分裂相关基因 mer3 和 msh4 中发生单基因突变,就会导致担子孢子的产生受损。本研究提出了一种在减数分裂后鉴定对担子孢子形成至关重要的基因的策略,以确定分子育种的新目标。进行了 RNA-seq 分析,以鉴定在担子果组织(担子孢子形成的地方)中特异性表达的 P. ostreatus 基因。然后,使用在 Coprinopsis cinerea 中进行的有丝分裂步骤同步进行的果实发育的转录组数据来鉴定在减数分裂后阶段活跃的基因。基于这些比较分析,鉴定了五个 P. ostreatus 基因。将含有潮霉素 B 抗性筛选、Cas9 和针对每个基因的单导向 RNA 表达盒的质粒导入二倍体菌株 PC9×#64 的原生质体中,以产生二倍体基因敲除体。在所获得的转化体中,三个 pcl1 二倍体敲除体和两个 cro6c 敲除体不产生担子孢子。显微镜分析表明,在这些基因敲除体中,孢子形成在特定阶段被阻断。这些结果表明,这两个基因是该真菌中成熟孢子形成所必需的。