Abstract

Traditionally, generation of new plants with improved or desirable features has relied on laborious and time-consuming breeding techniques. Genome-editing technologies have led to a new era of genome engineering, enabling an effective, precise, and rapid engineering of the plant genomes. Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (CRISPR/Cas9) has emerged as a new genome-editing tool, extensively applied in various organisms, including plants. The use of CRISPR/Cas9 allows generating transgene-free genome-edited plants (“null segregants”) in a short period of time. In this review, we provide a critical overview of the recent advances in CRISPR/Cas9 derived technologies for inducing mutations at target sites in the genome and controlling the expression of target genes. We highlight the major breakthroughs in applying CRISPR/Cas9 to plant engineering, and challenges toward the production of null segregants. We also provide an update on the efforts of engineering Cas9 proteins, newly discovered Cas9 variants, and novel CRISPR/Cas systems for use in plants. The application of CRISPR/Cas9 and related technologies in plant engineering will not only facilitate molecular breeding of crop plants but also accelerate progress in basic research.

Highlights

  • While nonhomologous end-joining (NHEJ) is an error-prone repair process and often results in the introduction of mutations, such as small insertions and deletions (Indel), homology-directed repair (HDR) results in a precise repair of Double-strand break (DSB) [1, 2]

  • We summarized the recent approaches for the targeted manipulation of plant genome using Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 nuclease (Cas9), focusing on the ones that lead to heritable genome modifications even in the absence of transgenes and on the production of transgene-free plants, discussing their advantages and disadvantages, and scope for further development

  • The results indicates that multiplex genome editing using CRISPR/Cas9 can be used to mimic the domestication process during evolution in a short time frame, with implications for a rapid and convenient generation of new plants with desirable traits

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Summary

Background

Production of plants with improved traits drives the current reliance of agriculture and various industries on plant resources. The authors first generated parental lines expressing the Cas gene under the control of the egg celland early embryo-specific DD45 promoter from Arabidopsis They introduced the donor DNA fragment and gRNA expression vectors into selected parental plants that exhibited high genome-editing activity, by the floral dip method. In this manner, the authors achieved heritable gene targeting with 5–10% efficiency (according to the number of T2 Arabidopsis populations examined). These are Mendelian segregation, programmed self-elimination of transgenic plants, transient expression of CRISPR/Cas, and ribonucleoprotein (RNP)-mediated genome editing.

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