Unlocking Fungal Potential: The CRISPR-Cas System as a Strategy for Secondary Metabolite Discovery.

IF 4.2 2区 生物学 Q2 MICROBIOLOGY
Karla Leal, Edwind Rojas, David Madariaga, María José Contreras, Kattia Nuñez-Montero, Leticia Barrientos, Olman Goméz-Espinoza, Isabel Iturrieta-González
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Abstract

Natural products (NPs) are crucial for the development of novel antibiotics, anticancer agents, and immunosuppressants. To highlight the ability of fungi to produce structurally diverse NPs, this article focuses on the impact of genome mining and CRISPR-Cas9 technology in uncovering and manipulating the biosynthetic gene clusters (BGCs) responsible for NP synthesis. The CRISPR-Cas9 system, originally identified as a bacterial adaptive immune mechanism, has been adapted for precise genome editing in fungi, enabling targeted modifications, such as gene deletions, insertions, and transcription modulation, without altering the genomic sequence. This review elaborates on various CRISPR-Cas9 systems used in fungi, notably the Streptococcus pyogenes type II Cas9 system, and explores advancements in different Cas proteins for fungal genome editing. This review discusses the methodologies employed in CRISPR-Cas9 genome editing of fungi, including guide RNA design, delivery methods, and verification of edited strains. The application of CRISPR-Cas9 has led to enhanced production of secondary metabolites in filamentous fungi, showcasing the potential of this system in biotechnology, medical mycology, and plant pathology. Moreover, this article emphasizes the integration of multi-omics data (genomics, transcriptomics, proteomics, and metabolomics) to validate CRISPR-Cas9 editing effects in fungi. This comprehensive approach aids in understanding molecular changes, identifying off-target effects, and optimizing the editing protocols. Statistical and machine learning techniques are also crucial for analyzing multi-omics data, enabling the development of predictive models and identification of key molecular pathways affected by CRISPR-Cas9 editing. In conclusion, CRISPR-Cas9 technology is a powerful tool for exploring fungal NPs with the potential to accelerate the discovery of novel bioactive compounds. The integration of CRISPR-Cas9 with multi-omics approaches significantly enhances our ability to understand and manipulate fungal genomes for the production of valuable secondary metabolites and for promising new applications in medicine and industry.

释放真菌潜能:CRISPR-Cas系统作为次生代谢物的发现策略。
天然产物(NPs)对于新型抗生素、抗癌剂和免疫抑制剂的开发至关重要。为了突出真菌生产结构多样的 NPs 的能力,本文重点介绍基因组挖掘和 CRISPR-Cas9 技术在发现和操纵负责合成 NPs 的生物合成基因簇 (BGC) 方面的影响。CRISPR-Cas9系统最初被认为是一种细菌适应性免疫机制,现在已被用于真菌的精确基因组编辑,可在不改变基因组序列的情况下进行基因缺失、插入和转录调控等靶向修改。本综述阐述了真菌中使用的各种 CRISPR-Cas9 系统,特别是化脓性链球菌 II 型 Cas9 系统,并探讨了用于真菌基因组编辑的不同 Cas 蛋白的进展。这篇综述讨论了真菌 CRISPR-Cas9 基因组编辑所采用的方法,包括引导 RNA 的设计、传递方法和编辑菌株的验证。CRISPR-Cas9 的应用提高了丝状真菌次生代谢产物的产量,展示了这一系统在生物技术、医学真菌学和植物病理学方面的潜力。此外,本文还强调整合多组学数据(基因组学、转录组学、蛋白质组学和代谢组学)来验证 CRISPR-Cas9 在真菌中的编辑效果。这种综合方法有助于了解分子变化、识别脱靶效应和优化编辑方案。统计和机器学习技术也是分析多组学数据的关键,有助于开发预测模型和识别受 CRISPR-Cas9 编辑影响的关键分子通路。总之,CRISPR-Cas9 技术是探索真菌 NPs 的强大工具,具有加速发现新型生物活性化合物的潜力。CRISPR-Cas9 与多组学方法的整合大大提高了我们了解和操纵真菌基因组的能力,从而生产出有价值的次生代谢物,并在医学和工业领域实现有前景的新应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Fungi
Journal of Fungi Medicine-Microbiology (medical)
CiteScore
6.70
自引率
14.90%
发文量
1151
审稿时长
11 weeks
期刊介绍: Journal of Fungi (ISSN 2309-608X) is an international, peer-reviewed scientific open access journal that provides an advanced forum for studies related to pathogenic fungi, fungal biology, and all other aspects of fungal research. The journal publishes reviews, regular research papers, and communications in quarterly issues. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on paper length. Full experimental details must be provided so that the results can be reproduced.
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