Department of Microbiology, University of Helsinki, Viikinkaari 9, 00790 Helsinki, Finland.
Biomolecules. 2021 Oct 15;11(10):1526. doi: 10.3390/biom11101526.
is an emerging reference species that can be used to investigate white-rot fungal plant biomass degradation, as it has flexible physiology to utilize different types of biomass as sources of carbon and energy. Recent comparative (post-) genomic studies on resulted in an increasingly detailed knowledge of the genes and enzymes involved in the lignocellulose breakdown in this fungus and showed a complex transcriptional response in the presence of lignocellulose-derived compounds. To fully utilize this increasing amount of data, efficient and reliable genetic manipulation tools are needed, e.g., to characterize the function of certain proteins in vivo and facilitate the construction of strains with enhanced lignocellulolytic capabilities. However, precise genome alterations are often very difficult in wild-type basidiomycetes partially due to extremely low frequencies of homology directed recombination (HDR) and limited availability of selectable markers. To overcome these obstacles, we assessed various Cas9-single guide RNA (sgRNA) ribonucleoprotein (RNP) -based strategies for selectable homology and non-homologous end joining (NHEJ) -based gene editing in . We also showed an induction of HDR-based genetic modifications by using single-stranded oligodeoxynucleotides (ssODNs) in a basidiomycete fungus for the first time. This paper provides directions for the application of targeted CRISPR/Cas9-based genome editing in and other wild-type (basidiomycete) fungi.
是一种新兴的参考物种,可用于研究白腐真菌对植物生物质的降解,因为它具有灵活的生理学特性,可将不同类型的生物质作为碳和能源的来源。最近对 的比较(后)基因组研究,使人们越来越详细地了解了该真菌中木质纤维素分解所涉及的基因和酶,并显示出在存在木质纤维素衍生化合物时复杂的转录反应。为了充分利用这些不断增加的数据量,需要有效的和可靠的遗传操作工具,例如,在体内表征某些蛋白质的功能,并促进构建具有增强木质纤维素分解能力的菌株。然而,由于同源定向重组(HDR)的频率极低且选择标记的可用性有限,野生型担子菌中的精确基因组改变通常非常困难。为了克服这些障碍,我们评估了各种 Cas9-单指导 RNA(sgRNA)核糖核蛋白(RNP)基于同源性和非同源末端连接(NHEJ)的选择策略,用于 在 中进行基因编辑。我们还首次在担子菌真菌中使用单链寡脱氧核苷酸(ssODN)诱导基于 HDR 的遗传修饰。本文为在 和其他野生型(担子菌)真菌中应用靶向 CRISPR/Cas9 基因组编辑提供了方向。