{"title":"Pleurotus ostreatus mek1 is essential for meiosis and basidiospore production","authors":"Takehito Nakazawa , Takeshi Kobukata , Fuga Yamasaki , Junko Sugano , Minji Oh , Moriyuki Kawauchi , Yoichi Honda","doi":"10.1016/j.funbio.2025.101562","DOIUrl":null,"url":null,"abstract":"<div><div>Breeding strains without basidiospores is important for the mushroom industry. However, target genes for sporeless breeding remain limited. To identify a new gene essential for basidiospore production in <em>Pleurotus ostreatus</em>, the RNA sequencing data obtained in our previous study were re-analyzed. Among the 36 <em>P. ostreatus</em> genes that are exclusively expressed in the gills where basidiospores are formed and produced, candidate genes were narrowed down using transcriptome data during the fruiting stage of <em>Coprinopsis cinerea</em>, in which the meiotic steps progress synchronously. Three <em>C. cinerea</em> genes homologous to the gill-specific <em>P. ostreatus</em> genes were upregulated during meiosis. One of these three genes encodes a protein homologous to <em>Saccharomyces cerevisiae</em> Mek1p, a protein kinase important in the meiotic recombination checkpoint. Plasmids containing expression cassettes for hygromycin B-resistance screening, Cas9, and single-guide RNA targeting <em>mek1</em> were introduced into the protoplasts of the dikaryotic <em>P. ostreatus</em> strain PC9×#64, which showed that the obtained dikaryotic gene disruptant produced no basidiospores. Microscopic analysis suggests that meiosis is suspended during telophase I. These results suggested that <em>P. ostreatus</em> Mek1 is essential for meiosis II progression and basidiospore production. In addition, disturbed orientation and loss of negative gravitropism during fruiting were observed.</div></div>","PeriodicalId":12683,"journal":{"name":"Fungal biology","volume":"129 3","pages":"Article 101562"},"PeriodicalIF":2.9000,"publicationDate":"2025-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fungal biology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1878614625000285","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MYCOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
培育无基生孢子的菌株对蘑菇产业非常重要。然而,无孢子育种的目标基因仍然有限。为了确定一个对口蘑产生基孢子至关重要的新基因,我们对之前研究中获得的 RNA 测序数据进行了重新分析。在 36 个只在基生孢子形成和产生的鳃中表达的 P. ostreatus 基因中,我们利用减数分裂同步进行的 Coprinopsis cinerea 果实期的转录组数据缩小了候选基因的范围。在减数分裂过程中,有三个与鳃特异性 P. ostreatus 基因同源的 C. cinerea 基因被上调。这三个基因中有一个编码与酿酒酵母 Mek1p 同源的蛋白,Mek1p 是一种蛋白激酶,在减数分裂重组检查点中非常重要。将含有表达盒的质粒(用于抗百菌清 B 筛选)、Cas9 和靶向 mek1 的单导 RNA 导入到二核菌 P. ostreatus 菌株 PC9×#64 的原生质体中,结果表明所获得的二核菌基因干扰物不产生基生孢子。显微镜分析表明,减数分裂在端期 I 暂停。这些结果表明,大孔菌 Mek1 对减数分裂 II 的进行和基生孢子的产生至关重要。此外,在结实过程中还观察到定向紊乱和负引力丧失。
Pleurotus ostreatus mek1 is essential for meiosis and basidiospore production
Breeding strains without basidiospores is important for the mushroom industry. However, target genes for sporeless breeding remain limited. To identify a new gene essential for basidiospore production in Pleurotus ostreatus, the RNA sequencing data obtained in our previous study were re-analyzed. Among the 36 P. ostreatus genes that are exclusively expressed in the gills where basidiospores are formed and produced, candidate genes were narrowed down using transcriptome data during the fruiting stage of Coprinopsis cinerea, in which the meiotic steps progress synchronously. Three C. cinerea genes homologous to the gill-specific P. ostreatus genes were upregulated during meiosis. One of these three genes encodes a protein homologous to Saccharomyces cerevisiae Mek1p, a protein kinase important in the meiotic recombination checkpoint. Plasmids containing expression cassettes for hygromycin B-resistance screening, Cas9, and single-guide RNA targeting mek1 were introduced into the protoplasts of the dikaryotic P. ostreatus strain PC9×#64, which showed that the obtained dikaryotic gene disruptant produced no basidiospores. Microscopic analysis suggests that meiosis is suspended during telophase I. These results suggested that P. ostreatus Mek1 is essential for meiosis II progression and basidiospore production. In addition, disturbed orientation and loss of negative gravitropism during fruiting were observed.
期刊介绍:
Fungal Biology publishes original contributions in all fields of basic and applied research involving fungi and fungus-like organisms (including oomycetes and slime moulds). Areas of investigation include biodeterioration, biotechnology, cell and developmental biology, ecology, evolution, genetics, geomycology, medical mycology, mutualistic interactions (including lichens and mycorrhizas), physiology, plant pathology, secondary metabolites, and taxonomy and systematics. Submissions on experimental methods are also welcomed. Priority is given to contributions likely to be of interest to a wide international audience.