Zhang Jin-Jing, Chen Hui, Xie Min-Ying, Chen Ming-Jie, Hao Hai-Bo, Wang Hong, Feng Zhi-Yong
Institute of Edible Fungi, Shanghai Academy of Agricultural Sciences, Key Laboratory of Agricultural Genetics and Breeding, Ministry of Agriculture, National Engineering Research Center for Edible Fungi, National R&D Center for Edible Fungi Processing, Key Laboratory of Agricultural Genetics and Breeding of Shanghai, Shanghai, China; College of Life Sciences, Nanjing Agricultural University, Nanjing, China.
Institute of Edible Fungi, Shanghai Academy of Agricultural Sciences, Key Laboratory of Agricultural Genetics and Breeding, Ministry of Agriculture, National Engineering Research Center for Edible Fungi, National R&D Center for Edible Fungi Processing, Key Laboratory of Agricultural Genetics and Breeding of Shanghai, Shanghai, China.
Int J Med Mushrooms. 2017;19(2):179-189. doi: 10.1615/IntJMedMushrooms.v19.i2.100.
To understand the fruiting process of Hypsizygus marmoreus, a synthetic liquid medium (SLM) was optimized to induce fruiting body initiation. Dependent on the SLM, the effect of a monofactor (glucose) on the fruiting bodies of H. marmoreus was studied at different concentrations (10 and 40 g/L). Primordia appeared approximately 10 days earlier in low-glucose media (LGM) than in high-glucose media (HGM), whereas mature fruiting bodies formed on mushrooms approximately 7 days earlier and more primordia developed into mature fruiting bodies when cultured in HGM. In addition, the morphogenesis of the primordia was clustered in HGM, which was different than what was observed in LGM. Furthermore, differentially expressed genes (DEGs) that encoded various proteins involved in cell structure, general metabolism, signal transduction, and transcription and translation were analyzed by transcriptome sequencing. Six DEGs were detected by quantitative reverse-transcriptase polymerase chain reaction, and the results were consistent with the altered patterns of gene expression revealed by the transcriptome. This study not only identifies new candidate genes involved in the development of H. marmoreus but also provides a new research platform for studying the development of other edible mushrooms.
为了解玉蕈的出菇过程,对一种合成液体培养基(SLM)进行了优化以诱导子实体起始。基于该SLM,研究了单因素(葡萄糖)在不同浓度(10和40 g/L)下对玉蕈子实体的影响。在低葡萄糖培养基(LGM)中,原基出现的时间比高葡萄糖培养基(HGM)中早约10天,而在HGM中培养时,蘑菇上形成成熟子实体的时间早约7天,且有更多原基发育成成熟子实体。此外,原基的形态发生在HGM中呈聚集状态,这与在LGM中观察到的情况不同。此外,通过转录组测序分析了编码参与细胞结构、一般代谢、信号转导以及转录和翻译的各种蛋白质的差异表达基因(DEG)。通过定量逆转录聚合酶链反应检测到6个DEG,结果与转录组揭示的基因表达变化模式一致。本研究不仅鉴定了参与玉蕈发育的新候选基因,还为研究其他食用菌的发育提供了新的研究平台。