通过CRISPR基因编辑对Epichloësp.LpTG-3菌株AR37中环氧janthitrem途径的剖析。

IF 2.1 Q3 MYCOLOGY
Frontiers in fungal biology Pub Date : 2022-08-10 eCollection Date: 2022-01-01 DOI:10.3389/ffunb.2022.944234
Taryn A Miller, Debbie A Hudson, Richard D Johnson, Jaspreet S Singh, Wade J Mace, Natasha T Forester, Paul H Maclean, Christine R Voisey, Linda J Johnson
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引用次数: 3

摘要

Epichloëfestucae var.lolii和Epichloèsp.LpTG-3是多年生黑麦草(Lolium perenne)的丝状真菌内生菌,通过赋予寄主草生物优势,对新西兰的农业经济产生了重大影响。总体而言,Epichloë内生菌每年为新西兰经济贡献2亿新西兰元,AR37菌株估计在20年内为新西兰经济带来36亿新西兰元的贡献。该菌株产生次级代谢产物,包括环氧janthitrems,这是一类吲哚二萜,与观察到的AR37对牲畜和害虫的影响有关。直到最近,AR37还难以进行基因修饰,但随着基于CRISPR-Cas9的基因编辑技术的应用,这种情况发生了变化。在这篇论文中,CRISPR-Cas9的基因失活被用于消除环氧janthitrem生物合成的遗传基础,包括创建一个AR37菌株,该菌株已被编辑以去除所有吲哚二萜的生物合成。我们表明,Epichloë的基因编辑可以在没有脱靶事件或通过同时表达CRISPR-Cas9系统和选择性标记的基于AMA1的质粒引入外源DNA(无足迹)的情况下实现。通过基因组测序和植物化学研究了这些转化体中的遗传修饰事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dissection of the epoxyjanthitrem pathway in <i>Epichloë</i> sp. <i>Lp</i>TG-3 strain AR37 by CRISPR gene editing.

Dissection of the epoxyjanthitrem pathway in <i>Epichloë</i> sp. <i>Lp</i>TG-3 strain AR37 by CRISPR gene editing.

Dissection of the epoxyjanthitrem pathway in <i>Epichloë</i> sp. <i>Lp</i>TG-3 strain AR37 by CRISPR gene editing.

Dissection of the epoxyjanthitrem pathway in Epichloë sp. LpTG-3 strain AR37 by CRISPR gene editing.

Epichloë festucae var. lolii and Epichloë sp. LpTG-3 are filamentous fungal endophytes of perennial ryegrass (Lolium perenne) that have a substantial impact on New Zealand's agricultural economy by conferring biotic advantages to the host grass. Overall, Epichloë endophytes contribute NZ$200 million to the economy annually, with strain AR37 estimated to contribute NZ$3.6 billion to the New Zealand economy over a 20-year period. This strain produces secondary metabolites, including epoxyjanthitrems, which are a class of indole diterpenes, associated with the observed effects of AR37 on livestock and insect pests. Until very recently, AR37 was intractable to genetic modification but this has changed with the application of CRISPR-Cas9 based gene editing techniques. In this paper, gene inactivation by CRISPR-Cas9 was used to deconvolute the genetic basis for epoxyjanthitrem biosynthesis, including creating an AR37 strain that has been edited to remove the biosynthesis of all indole diterpenes. We show that gene editing of Epichloë can be achieved without off-target events or introduction of foreign DNA (footprint-less) through an AMA1-based plasmid that simultaneously expresses the CRISPR-Cas9 system and selectable marker. Genetic modification events in these transformants were investigated through genome sequencing and in planta chemistry.

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CiteScore
2.70
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