Sathee Lekshmy, Jagadhesan B, Pandesha Pratheek H, Barman Dipankar, Adavi B Sandeep, Nagar Shivani, Krishna G K, Tripathi Shailesh, Jha Shailendra K, Chinnusamy Viswanathan
Division of Plant Physiology, ICAR-Indian Agricultural Research Institute, New Delhi, India.
Roy and Diana Vagelos Division of Biology and Biomedical Sciences, Washington University in St. Louis, St. Louis, MO, United States.
Front Genet. 2022 Jun 14;13:900897. doi: 10.3389/fgene.2022.900897. eCollection 2022.
In recent years, the development of RNA-guided genome editing (CRISPR-Cas9 technology) has revolutionized plant genome editing. Under nutrient deficiency conditions, different transcription factors and regulatory gene networks work together to maintain nutrient homeostasis. Improvement in the use efficiency of nitrogen (N), phosphorus (P) and potassium (K) is essential to ensure sustainable yield with enhanced quality and tolerance to stresses. This review outlines potential targets suitable for genome editing for understanding and improving nutrient use (NtUE) efficiency and nutrient stress tolerance. The different genome editing strategies for employing crucial negative and positive regulators are also described. Negative regulators of nutrient signalling are the potential targets for genome editing, that may improve nutrient uptake and stress signalling under resource-poor conditions. The promoter engineering by CRISPR/dead (d) Cas9 (dCas9) cytosine and adenine base editing and prime editing is a successful strategy to generate precise changes. CRISPR/dCas9 system also offers the added advantage of exploiting transcriptional activators/repressors for overexpression of genes of interest in a targeted manner. CRISPR activation (CRISPRa) and CRISPR interference (CRISPRi) are variants of CRISPR in which a dCas9 dependent transcription activation or interference is achieved. dCas9-SunTag system can be employed to engineer targeted gene activation and DNA methylation in plants. The development of nutrient use efficient plants through CRISPR-Cas technology will enhance the pace of genetic improvement for nutrient stress tolerance of crops and improve the sustainability of agriculture.
近年来,RNA引导的基因组编辑技术(CRISPR-Cas9技术)的发展彻底改变了植物基因组编辑。在营养缺乏条件下,不同的转录因子和调控基因网络协同作用以维持营养稳态。提高氮(N)、磷(P)和钾(K)的利用效率对于确保产量可持续、品质提高以及增强胁迫耐受性至关重要。本综述概述了适合基因组编辑的潜在靶点,以了解和提高养分利用(NtUE)效率及养分胁迫耐受性。还描述了采用关键负调控因子和正调控因子的不同基因组编辑策略。养分信号的负调控因子是基因组编辑的潜在靶点,这可能会在资源匮乏条件下改善养分吸收和胁迫信号。通过CRISPR/失活(d)Cas9(dCas9)胞嘧啶和腺嘌呤碱基编辑以及引导编辑进行启动子工程是产生精确变化的成功策略。CRISPR/dCas9系统还具有以靶向方式利用转录激活因子/抑制因子过表达感兴趣基因的额外优势。CRISPR激活(CRISPRa)和CRISPR干扰(CRISPRi)是CRISPR的变体,其中实现了依赖dCas9的转录激活或干扰。dCas9-SunTag系统可用于在植物中设计靶向基因激活和DNA甲基化。通过CRISPR-Cas技术培育养分利用高效的植物将加快作物养分胁迫耐受性的遗传改良步伐,并提高农业的可持续性。