通过基因共表达网络分析揭示Fomes fomentarius在真菌基物质生产过程中的转录景观。

Q1 Agricultural and Biological Sciences
Timothy Cairns, Carsten Freidank-Pohl, Anna Sofia Birke, Carmen Regner, Sascha Jung, Vera Meyer
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引用次数: 0

摘要

背景:真菌基复合材料已经成为一种可再生的高性能生物材料,它是由林业和农业的木质纤维素残流生产的。工业规模的生产有望通过生产可持续、低排放、无毒和可生物降解的建筑、包装、纺织品和其他材料,彻底改变人类居住的世界。多孔Fomes fomentarius是一种用于生物材料生产的担子菌,但在复合材料形成过程中,对底物分解、营养吸收或真菌生长的转录基础一无所知。基于RNA-Seq分析的共表达网络分析使人们对一系列真菌有了深刻的了解,因此我们旨在为F. fomentarius开发这样的资源。结果:我们分析了广泛的实验室培养物(n = 9)或生物材料形成(n = 18)的基因表达,以确定fomentarius在底物分解过程中的转录景观,并确定了以下重要基因:(i)木质纤维素和其他植物基底物的酶降解,(ii)它们的碳单体的吸收,以及(iii)通过菌丝生长和细胞壁生物合成指导菌丝形成的基因。我们生成并测试了用于共表达网络构建的简单脚本,并利用该脚本鉴定了一种真菌特异性转录因子CacA,该转录因子与多个甲壳素和葡聚糖生物合成基因或Rho GTPase编码基因强烈共表达,表明该蛋白是复合生长过程中工程粘附和分支的高优先目标。然后,我们更新了碳水化合物激活酶(CAZymes)编码基因注释,使用系统遗传学来分配假定的摄取系统,并应用网络分析来预测木质纤维素降解的抑制/激活转录因子。最后,我们发现了真菌中从未描述过的全新类型的共表达连续簇,包括预测编码CAZymes,疏水酶,激酶,脂肪酶,F-box结构域,几丁质合成酶等的基因。结论:本研究所获得的系统生物学数据将使我们能够以前所未有的细节了解黄颡鱼生物材料形成的遗传基础。我们为准确的网络衍生预测提供了原理证明,并生成了任何最终用户分析所需的数据和脚本。发现了全新的连续共表达基因簇,并确定了多个转录因子编码基因,这些基因是基因工程的优先目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Uncovering the transcriptional landscape of Fomes fomentarius during fungal-based material production through gene co-expression network analysis.

Background: Fungal-based composites have emerged as renewable, high-performance biomaterials that are produced on lignocellulosic residual streams from forestry and agriculture. Production at an industrial scale promises to revolutionize the world humans inhabit by generating sustainable, low emission, non-toxic and biodegradable construction, packaging, textile, and other materials. The polypore Fomes fomentarius is one of the basidiomycete species used for biomaterial production, yet nothing is known about the transcriptional basis of substrate decomposition, nutrient uptake, or fungal growth during composite formation. Co-expression network analysis based on RNA-Seq profiling has enabled remarkable insights into a range of fungi, and we thus aimed to develop such resources for F. fomentarius.

Results: We analysed gene expression from a wide range of laboratory cultures (n = 9) or biomaterial formation (n = 18) to determine the transcriptional landscape of F. fomentarius during substrate decomposition and to identify genes important for (i) the enzymatic degradation of lignocellulose and other plant-based substrates, (ii) the uptake of their carbon monomers, and (iii) genes guiding mycelium formation through hyphal growth and cell wall biosynthesis. Simple scripts for co-expression network construction were generated and tested, and harnessed to identify a fungal-specific transcription factor named CacA strongly co-expressed with multiple chitin and glucan biosynthetic genes or Rho GTPase encoding genes, suggesting this protein is a high-priority target for engineering adhesion and branching during composite growth. We then updated carbohydrate activated enzymes (CAZymes) encoding gene annotation, used phylogenetics to assign putative uptake systems, and applied network analysis to predict repressing/activating transcription factors for lignocellulose degradation. Finally, we identified entirely new types of co-expressed contiguous clusters not previously described in fungi, including genes predicted to encode CAZymes, hydrophobins, kinases, lipases, F-box domains, chitin synthases, amongst others.

Conclusion: The systems biology data generated in this study will enable us to understand the genetic basis of F. fomentarius biomaterial formation in unprecedented detail. We provided proof-of-principle for accurate network-derived predictions of gene function in F. fomentarius and generated the necessary data and scripts for analysis by any end user. Entirely new classes of contiguous co-expressed gene clusters were discovered, and multiple transcription factor encoding genes which are high-priority targets for genetic engineering were identified.

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来源期刊
Fungal Biology and Biotechnology
Fungal Biology and Biotechnology Agricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
10.20
自引率
0.00%
发文量
17
审稿时长
9 weeks
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