4.6 Review

Genome Editing Targets for Improving Nutrient Use Efficiency and Nutrient Stress Adaptation

期刊

FRONTIERS IN GENETICS
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2022.900897

关键词

genome editing; CRISPR-Cas; nutrient stress; nutrient use efficiency; biofortification; abiotic stress

资金

  1. NASF (ICAR), New Delhi [NASF/CRISPR-Cas-7003/2017-18]
  2. DBT, Govt of India [BT/PR25820/GET/119/100/2017]
  3. DST-SERB [ECR/2017/002982]

向作者/读者索取更多资源

This review discusses the development of RNA-guided genome editing technology (CRISPR-Cas9) and its potential applications in improving nutrient use efficiency and stress tolerance in plants. It outlines different targets for genome editing and strategies for enhancing nutrient uptake and stress signaling. The use of CRISPR/dCas9 system also allows for targeted overexpression of genes of interest and DNA methylation in plants.
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.

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