蘑菇功能基因组学应运而生

L. Nagy
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With the advent of high-throughput -omics, the field has quickly embraced new technologies, including genome and transcriptome sequencing or proteomics. However, important stepping stones both in terms of technology and knowledge for linking the genes and gene expression patterns to phenotypes, have been missing. A handful of studies, all published recently, forecast a change in this respect and portrays mushroom developmental biology coming of age. Genomic and transcriptomic resources have, as of today, been generated for many of the important mushroom-forming species in the Agaricomycetes, with a focus on fruiting body development and wood-decay, among others, and overall yielded information on the gene repertoires of most major species utilized by the mushroom industry, as well as related modeland non-model species (reviewed recently ). However, both approaches have their limitations in revealing precise gene function. 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引用次数: 0

摘要

匈牙利塞格德生物化学研究所生物研究中心合成与系统生物学单元*通讯:lnagy@fungenomelab.com (l.n.)收稿日期:2023年3月1日;录用日期:2023年5月6日;在线发布:2023年6月5日;https://doi.org/10.59717/j.xinn-life.2023.100005©2023作者。这是一篇基于CC BY-NC-ND许可(http://creativecommons.org/licenses/by-nc-nd/4.0/)的开放获取文章。引用本文:Nagy LG。(2023)。蘑菇功能基因组学应运而生。创新生活1(1),2005。蘑菇科学及其应用最广泛的方面,即食用和药用蘑菇的生产,传统上综合了发育生物学、遗传学、真菌代谢研究和数百年来在蘑菇生产实践中积累的大量经验知识。随着高通量组学的出现,该领域迅速接受了包括基因组和转录组测序或蛋白质组学在内的新技术。然而,在技术和知识方面,将基因和基因表达模式与表型联系起来的重要垫脚石一直缺失。最近发表的一些研究预测了这方面的变化,并描绘了蘑菇发育生物学的成熟。到目前为止,已经对许多重要的蘑菇形成菌种进行了基因组和转录组资源的研究,重点是子实体发育和木材腐烂等,并总体上获得了蘑菇产业利用的大多数主要物种的基因库信息,以及相关的模式和非模式物种(最近进行了综述)。然而,这两种方法在揭示精确的基因功能方面都有其局限性。子实体发育是一个涉及细胞事件时空协调的发育过程,因此了解基因表达调控模式和揭示基因的精确功能是关键。这反过来又需要正向/反向遗传学和功能基因组学方法(图1),这是最近一波论文取得重大进展的领域。在最近发表在mBio上的一篇论文中,2在裂生菌(Schizophyllum commune)的担子菌(Basidiomycota)中发现了第一个纤维素降解相关的转录因子Roc1。他们通过比较木质和纤维素培养物的RNA-Seq图谱来识别它,发现该基因在真菌中是保守的(尽管它可能更保守,并且与里氏木霉的ACE3同源)。考虑到Roc1的早期出现,它的起源可能早于大约3亿年前有效的木材腐烂系统的出现。roc1基因敲除突变体在纤维素(Avicel)、纤维素二糖和木聚糖上的生长高度降低,但在其他碳源上没有,这表明roc1调控了参与这些碳源利用的基因。事实上,当突变体生长在纤维素上时,一些CAZyme基因不再上调,ChIP-Seq分析发现了几个CAZyme编码基因相关的峰,如水解多糖单加氧酶GH3和GH5,这些基因通常与纤维素降解有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mushroom functional genomics springs up
Synthetic and Systems Biology Unit, Institute of Biochemistry Biological Research Center, Szeged, Hungary *Correspondence: lnagy@fungenomelab.com (L. N.) Received: March 1, 2023; Accepted: May 6, 2023; Published Online: June 5, 2023; https://doi.org/10.59717/j.xinn-life.2023.100005 © 2023 The Author(s). This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). Citation: Nagy LG. (2023). Mushroom functional genomics springs up. The Innovation Life 1(1), 100005. Mushroom science and its most broadly applied aspect, the production of edible and medicinal mushrooms, has traditionally synthesized knowledge from developmental biology, genetics, studies of fungal metabolism and a great deal of empirical knowledge accumulated over the centuries of practice in mushroom production. With the advent of high-throughput -omics, the field has quickly embraced new technologies, including genome and transcriptome sequencing or proteomics. However, important stepping stones both in terms of technology and knowledge for linking the genes and gene expression patterns to phenotypes, have been missing. A handful of studies, all published recently, forecast a change in this respect and portrays mushroom developmental biology coming of age. Genomic and transcriptomic resources have, as of today, been generated for many of the important mushroom-forming species in the Agaricomycetes, with a focus on fruiting body development and wood-decay, among others, and overall yielded information on the gene repertoires of most major species utilized by the mushroom industry, as well as related modeland non-model species (reviewed recently ). However, both approaches have their limitations in revealing precise gene function. Since a considerable portion of research on mushroom-forming fungi focuses on fruiting body development, which is a developmental process involving the temporal and spatial coordination of cellular events, understanding patterns of gene expression regulation and revealing the precise function of genes is key. This in turn requires forward/reverse genetics and functional genomics approaches (Figure 1), a field where a recent wave of papers have made significant progress. In a paper published recently in mBio, 2 identified the first cellulose-degradation related transcription factor in the Basidiomycota, Roc1 of Schizophyllum commune. They identified it by comparing RNA-Seq profiles of woodgrown and cellulose-grown cultures and found that the gene is conserved in the Agaricomycetes (although its possibly even more conserved and orthologous to ACE3 from Trichoderma reesei). Given the early emergence of Roc1, its origin may precede the emergence of efficient wood decay systems some ~300 million years ago. The roc1 knockout mutant showed highly reduced growth on cellulose (Avicel), cellobiose and xylan, but not on other carbon sources, suggesting that Roc1 is regulating genes involved in the utilization of these carbon sources. Indeed, several CAZyme genes were no longer upregulated when the mutant was grown on cellulose and ChIP-Seq analyses identified peaks associated with several CAZyme-encoding genes such as lytic polysaccharide monooxygenases, GH3 and GH5, which are typically associated with cellulose degradation.
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