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丝状真菌中的CRISPR系统:当前成果与未来方向。

CRISPR system in filamentous fungi: Current achievements and future directions.

作者信息

Deng Huaxiang, Gao Ruijie, Liao Xiangru, Cai Yujie

机构信息

The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, 1800 Lihu Road, Wuxi, Jiangsu 214122, People's Republic of China.

The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, 1800 Lihu Road, Wuxi, Jiangsu 214122, People's Republic of China.

出版信息

Gene. 2017 Sep 5;627:212-221. doi: 10.1016/j.gene.2017.06.019. Epub 2017 Jun 16.

Abstract

As eukaryotes, filamentous fungi share many features with humans, and they produce numerous active metabolites, some of which are toxic. Traditional genetic approaches are generally inefficient, but the clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 system that has been widely used for basic research on bacteria, mammals and plants offers a simple, fast, versatile technology for systemic research on filamentous fungi. In this review, we summarized the current knowledge on Cas9 and its variants, various selective markers used to screen positive clones, different ways used to detect off-target mutations, and different approaches used to express and transform the CRISPR complex. We also highlight several methods that improve the nuclease specificity and efficiency, and discuss current and potential applications of CRISPR/Cas9 system in filamentous fungi for pathogenesis decoding, confirmation of the gene and pathway, bioenergy process, drug discovery, and chromatin dynamics. We also describe how the synthetic gene circuit of CRISPR/Cas9 systems has been used in the response to various complex environmental signals to redirect metabolite flux and ensure continuous metabolite biosynthesis.

摘要

作为真核生物,丝状真菌与人类有许多共同特征,它们能产生大量活性代谢产物,其中一些具有毒性。传统的遗传方法通常效率低下,但广泛应用于细菌、哺乳动物和植物基础研究的成簇规律间隔短回文重复序列(CRISPR)/Cas9系统为丝状真菌的系统研究提供了一种简单、快速、通用的技术。在这篇综述中,我们总结了关于Cas9及其变体的现有知识、用于筛选阳性克隆的各种选择标记、检测脱靶突变的不同方法以及表达和转化CRISPR复合物的不同方法。我们还重点介绍了几种提高核酸酶特异性和效率的方法,并讨论了CRISPR/Cas9系统在丝状真菌中用于致病机制解码、基因和途径确认、生物能源过程、药物发现以及染色质动力学的当前和潜在应用。我们还描述了CRISPR/Cas9系统的合成基因回路如何用于响应各种复杂环境信号,以重定向代谢物通量并确保代谢物的持续生物合成。

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