CRISPR activation: identifying and using novel genes for plant disease resistance breeding.

IF 4.4 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Frontiers in genome editing Pub Date : 2025-09-08 eCollection Date: 2025-01-01 DOI:10.3389/fgeed.2025.1596600
John E McLaughlin, Idrice Carther Kue Foka, Michael A Lawton, Rong Di
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引用次数: 0

Abstract

CRISPR-based technologies have revolutionized plant science by enabling precise modulation of gene function, including CRISPR activation (CRISPRa), a recently emerging strategy which shows particular promise for enhancing disease resistance through targeted gene upregulation. Unlike conventional CRISPR editing, which introduces double-stranded DNA breaks and permanent genomic changes, CRISPRa employs a deactivated Cas9 (dCas9) fused to transcriptional activators. This system allows quantitative and reversible gene activation without altering the DNA sequence, offering a gain-of-function (GOF) like enhanced blight resistance in staple crops. Despite its potential, the limited adoption of CRISPRa in plant biology to date underscores the need for future studies to fully harness its capabilities for crop improvement. This review addresses the groundbreaking and relatively underexplored potential of CRISPR activation (CRISPRa) systems for GOF studies in plant biology, and advocates for the adoption of CRISPRa to discover and harness genetic variation for enhancing disease resistance. We present recent advancements in CRISPRa technology, emphasizing its successful application in boosting plant immunity. Moreover, we discuss the synergistic potential of integrating CRISPRa with functional genomics tools such as genome-wide association studies (GWAS) and multi-omics approaches to identify and characterize key resistance genes. Additionally, we highlight ongoing progress in developing plant-specific programmable transcriptional activators (PTAs) to optimize CRISPRa efficiency. Challenges associated with achieving transgene-free overexpression and the deployment of alternative CRISPR systems are also explored. Together, these advances position CRISPRa as a transformative tool for future crop breeding strategies aimed at achieving durable, broad-spectrum disease resistance and sustainability in agriculture.

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CRISPR激活:鉴定和利用新基因进行植物抗病育种。
基于CRISPR的技术通过实现基因功能的精确调节,包括CRISPR激活(CRISPRa),从而彻底改变了植物科学,CRISPR激活(CRISPRa)是最近出现的一种策略,它通过靶向基因上调来增强抗病性。与引入双链DNA断裂和永久性基因组变化的传统CRISPR编辑不同,CRISPRa将失活的Cas9 (dCas9)融合到转录激活剂中。该系统允许在不改变DNA序列的情况下进行定量和可逆的基因激活,提供了一种功能获得(GOF),比如增强了主食作物的抗枯萎病能力。尽管具有潜力,但迄今为止,CRISPRa在植物生物学中的应用有限,这突显了未来研究充分利用其作物改良能力的必要性。本文综述了CRISPR激活(CRISPRa)系统在植物生物学GOF研究中的突破性和相对未被充分开发的潜力,并倡导采用CRISPR来发现和利用遗传变异以增强抗病性。我们介绍了CRISPRa技术的最新进展,重点介绍了其在提高植物免疫力方面的成功应用。此外,我们还讨论了将CRISPRa与功能基因组学工具(如全基因组关联研究(GWAS)和多组学方法)结合起来识别和表征关键抗性基因的协同潜力。此外,我们强调了开发植物特异性可编程转录激活因子(PTAs)以优化CRISPRa效率的持续进展。与实现无转基因过表达和替代CRISPR系统的部署相关的挑战也进行了探讨。总之,这些进展使CRISPRa成为未来作物育种战略的变革性工具,旨在实现农业的持久、广谱抗病和可持续性。
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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CiteScore
7.00
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0.00%
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审稿时长
13 weeks
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