Genetic Databases and Gene Editing Tools for Enhancing Crop Resistance against Abiotic Stress

Simple Summary Plants are subjected to various environmental stresses that negatively impact growth and development and limit crop productivity. Therefore, in order to meet the requirements of the growing world population and food security, it is essential to develop cultivars resistant to abiotic stresses. In recent years, with the availability of genetic databases and the advancement in genome editing techniques, it is feasible to edit target genes with precision and create new opportunities for crop improvement that conventional breeding methods could not achieve. The genome-editing method using CRISPR-Cas systems is very powerful and confers exceptional versatility to develop improved cultivars at abiotic stresses. These efficient gene editing techniques facilitate the cultivation of superior-performing genotypes in challenging environmental conditions without compromising yield. Abstract Abiotic stresses extensively reduce agricultural crop production globally. Traditional breeding technology has been the fundamental approach used to cope with abiotic stresses. The development of gene editing technology for modifying genes responsible for the stresses and the related genetic networks has established the foundation for sustainable agriculture against environmental stress. Integrated approaches based on functional genomics and transcriptomics are now expanding the opportunities to elucidate the molecular mechanisms underlying abiotic stress responses. This review summarizes some of the features and weblinks of plant genome databases related to abiotic stress genes utilized for improving crops. The gene-editing tool based on clustered, regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) has revolutionized stress tolerance research due to its simplicity, versatility, adaptability, flexibility, and broader applications. However, off-target and low cleavage efficiency hinder the successful application of CRISPR/Cas systems. Computational tools have been developed for designing highly competent gRNA with better cleavage efficiency. This powerful genome editing tool offers tremendous crop improvement opportunities, overcoming conventional breeding techniques’ shortcomings. Furthermore, we also discuss the mechanistic insights of the CRISPR/Cas9-based genome editing technology. This review focused on the current advances in understanding plant species’ abiotic stress response mechanism and applying the CRISPR/Cas system genome editing technology to develop crop resilience against drought, salinity, temperature, heavy metals, and herbicides.


Introduction
Agricultural production faces global challenges due to climate change, insufficient arable land, population growth, and abiotic and biotic stresses.Abiotic stress adversely impacts plant growth and development by hampering essential biochemical and physiological activities [1,2].Climate change, such as extreme temperature, drought, water logging, flooding, and increased soil salinity, adversely affect global agricultural crop production.The production of excessive greenhouse gases is the most significant contributor to global climate change, resulting in intense drought, infrequent rain, and high temperatures.Drought stress negatively impacts crop plants by modifying physiological and biochemical processes such as plant growth habit and duration, metabolism, and resistance mechanisms [3][4][5].Salinity stress is one of the significant constraints to crop production because it causes oxidative stress due to the generation of reactive oxygen species (ROS) that damage plant cells [6,7].Similarly, plants respond to heat stress by producing reactive oxygen species (ROS), heat shock proteins (HSPs), and genes encoding scavenger proteins [8,9].Temperature stress strongly impacts grain filling, leading to poor grain yield [5,10].In addition, overusing chemical fertilizers/herbicides contaminates agricultural fields with heavy metals such as arsenic (As), copper (Cu), cobalt (Co), cadmium (Cd), iron (Fe), manganese (Mn), nickel (Ni) zinc (Zn), mercury (Hg), lead (Pb) accumulating inside plants, reducing grain fullness, and increasing risk to human and animal health.Arsenic causes a loss of functionality in plant cells, and cadmium inhibits plant growth, as evidenced by stunted plant growth, a decrease in leaf size, shoot growth, and root dry matter [11][12][13][14].Plants have evolved several defense mechanisms to withstand stress by activating stress-responsive genes via secondary messengers and finally activating several stress-responsive genes and their products [15].
Conventional breeding approaches, including cross-breeding and mutation breeding, have enhanced crop performance under climate change scenarios.However, even with marker-assisted selection, breeding programs can be time-consuming and laborintensive [16].Therefore, more efficient and advanced technologies with immediate effects are needed to overcome the drawbacks of traditional breeding methods.The availability of genome sequence data of numerous crop plants and precise genome editing tools has revolutionized plant breeding programs.By genome editing tools, desired changes are possible within the DNAs by the formation of an insertion/deletion (indel) and mutation in the sequences of particular genes via recruiting specific nucleases such as zinc-finger nucleases (ZFNs) and transcription activator-like effector nucleases (TALENs) or Clustered regularly interspaced palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) system [17].CRISPR/Cas comprises single-guide RNA (sgRNA) and RNA-guided Cas endonuclease that protects bacteria and archaea from being invaded by mobile genetic elements and bacteriophages [18].During the process of genome editing, sgRNA recruits Cas endonuclease to a specific site of the genome to catalyze a DNA double-stranded break (DSB), which can be repaired by various DNA repair mechanisms, including non-homologous end joining (NHEJ), homology-directed repairs (HDR), and microhomology-mediated end joining [MMEJ], leading to gene knockout, DNA fragment insertion, deletion, and replacement [19][20][21][22].Different Cas enzymes recognize Protospacer-Adjacent Motif (PAM) sequences and show unique specificity [23].Moreover, the gRNA spacer sequence could be readily programmed using online tools to target DNA sites with PAM.The online computational tools also minimize off-target effect (guide specificity) and maximize on-target effect (guide efficiency) by avoiding gRNA sequences showing significant homology with genomic loci at multiple sites [24].

Genome Databases of Abiotic Stress Gene
Genome databases dedicated to plant abiotic stress genes and genome data provide helpful information on essential plant species.The availability of a genome database of agronomically important plant species facilitates targeted genome modification using gene editing tools, which offers tremendous opportunities to develop improved cultivars with higher yield and resistance to abiotic stress.The publicly available specialized bioinformatics database resources contain valuable information on plant stress genes, such as PlantStress, Plant Stress Gene, Plant Stress Proteome (PlantPReS), Plant miRNA ENcyclopedia (PmiREN), Network-based Rice Expression Analysis (NetREx), PncStress, and Pearl Millet Drought Transcriptome (PMDTDb) databases.

PlantStress
The PlantStress (https://plantstress.com/, accessed on 31 October 2023) website was launched in the year 2000 to serve as a web-based information resource for a meeting place and a consultation facility, and a source of professional updates on the most important issues of plant environmental abiotic stress, including drought, salinity, heat, mineral deficiency, oxidative stress, cold, water logging, and stress combination [43].
It is an open online proteomic database comprising >35,086 entries from 577 manually curated articles containing >10,600 unique stress-responsive proteins.A customized BLAST tool has been made available, which is helpful in retrieving the homologous sequences from the database.The interface is user-friendly and features several analysis tools such as a gene ontology, cross-referencing, and information on the expression patterns of stressresponsive proteins.

Plant miRNA ENcyclopedia (PmiREN)
PmiREN (Plant miRNA Encyclopedia) is a functional plant miRNA database available at https://www.pmiren.com/,accessed on 23 August 2023.PmiREN contains 38,186 miRNA loci belonging to 7838 families, 141,327 predicted miRNA-target pairs and phylogenetic trees of conserved miRNA families in 179 species spanning from chlorophytes to angiosperms.It also provides tools for in-depth data mining.Additionally, 116 PARE-Seq libraries were utilized to confirm predicted miRNA-target pairs, and 2331 fully sequenced small RNA libraries were used to quantify miRNA expression patterns [46,47].

Network-Based Rice Expression Analysis (NetREx)
Network-based Rice Expression Analysis server (NetREx) provides information on the expression and interaction of rice genes under various environmental stress and hor-monal treatment conditions.NetREx is a web-based server available at https://bioinf.iiit.ac.in/netrex/index.html,accessed on 23 August 2023.It offers a choice of interactable data viewers and modules for analyzing genes under drought, flood, cold conditions, and hormonal treatments (abscisic and jasmonic acid).The server can also explore the expression fold change, gene annotations, and gene pathway analysis.This web server also allows the search of orthologous genes from A. thaliana, T. aestivum, Z. mays, H. vulgare, and S. bicolor [48].

Pearl Millet Drought Transcriptome Database (PMDTDb)
PMDTDb (Pearl Millet Drought Transcriptome Database) is the database of the drought transcriptome of pearl millet available at http://webtom.cabgrid.res.in/pmdtdb/,accessed on 23 August 2023.It catalogs the differentially expressed genes in leaf and root tissues of millet in response to drought, along with transcription factors (TFs), gene regulatory networks (GRNs) with hub genes, and discovery of putative gene region markers such as simple sequence repeats (SSRs), single nucleotide polymorphism (SNP) and, InDels (insertions and deletions).This database is based on a 3-tier architecture developed in PHP and MySQL [50].

Functional Genomic Approaches and Abiotic Stress Tolerance
Functional genomics approaches have been employed to understand the precise regulatory gene networks associated with complex abiotic stress responses, benefiting crop improvement programs.Several stress-related genes/pathways and regulatory networks have been worked out in the past decades using various functional genomic approaches, including expressed sequence tags (ESTs), transcriptome analysis, and targeted random mutagenesis.Recently advanced sequencing technologies have provided a cost-effective and high-throughput method for generating DNA/RNA sequence data, facilitating the identification of genes/transcription factors mediating stress tolerance.The identified genes can be successfully used in the programs for crop improvement by employing a transgenic method or exploiting genetic variation indicating the trait of interest.Additionally, functional validation of stress-related genes may facilitate unraveling the stress-tolerance networks and designing different functional markers for crop improvement programs.

Sequencing-Based Approaches
The single-pass sequencing of cDNA clones generates partial gene coding sequences, which are the Expressed Sequence Tags (ESTs) [51].EST databases are efficient tools for discovering genes, comparing interspecies sequences, and providing markers for physical and genetic mapping and clones for expression analysis.Functional genomics studies utilize ESTs due to their quick and cost-effectiveness compared to the whole genome sequencing method.Currently, over a million ESTs of different crop species are available in the EST database at the National Center for Biotechnological Information (NCBI) (http://www.ncbi.nlm.nih.gov/dbEST/,accessed on 31 October 2023), which serves as the reservoir of differentially expressed genes.Additionally, the relative abundance of cDNA libraries created from various plant species and organs under various physiological situations offers early insights into the expression patterns for the more abundant transcripts [15].Several functional genomics studies have been performed to identify the abiotic stress-responsive transcripts using EST sequencing, Serial analysis of gene expression (SAGE), Super serial analysis of gene expression (SuperSAGE), and massively parallel signature sequencing (MPPS).Plant cDNA libraries were screened for identifying genes involved in abiotic stress response.Screening of the cDNA library from a salttolerant rice genotype showed differential expression of two genes in response to multiple stresses [52].In Cicer arietinum (Chickpea), to identify differentially expressed genes in drought-tolerant and -susceptible genotypes, 5494 high-quality drought-responsive EST sequence was generated by suppression subtraction hybridization (SSH) [53].
The SAGE is a highly competent technology that isolates unique sequence tags from individual mRNAs for transcriptome research.Although SAGE is not widely utilized in plants, it is more sensitive than EST in detecting rarely expressed transcripts [54].SAGE helps to identify a set of specific genes to the cellular conditions and study the gene expression profile of a particular type of cells or organs.By transcriptome analysis using SuperSAGE and high-throughput sequencing, 17,493 SAGE UniTags have been generated from the roots of the drought-tolerant C. arietinum variety [55].Another tag-based method, massively parallel signature sequencing (MPSS), is an open-ended platform for conducting in-depth expression profiling [56].MPSS allows the identification of millions of signatures per experiment, surpassing even the most extensive SAGE applications, covering hundreds of thousands of tags.Due to more extended tags and high-throughput analysis, MPSS identifies genes with greater specificity and sensitivity [57].Plant MPSS databases contain publicly available MPSS expression data for many plant species, including A. thaliana, rice, grape, Z. mays, and soybean [58].MPSS databases quantify the absolute expression level of most genes.It also provides information about novel transcripts, including regulatory intergenic transcripts, alternative splice isoforms, and antisense transcripts [59].

Genome-Wide Association Studies (GWAS)
Genome-wide association studies (GWAS) have emerged as a powerful tool in identifying variations at the DNA level related to stress tolerance.GWAS provides a robust and potent tool successfully applied in germplasm collections that identifies the regulatory loci associated with resistant phenotypic traits [51].The two major approaches were used to study the interaction between genotype and phenotype (trait) based on mapping populations, including linkage mapping and association mapping [60][61][62][63][64][65][66].GWAS can be effectively used for fine genome-wide mapping and also enables finding a higher diversity of alleles at the corresponding loci, which exploits historical recombination events in a population, leading to a better association between the marker and the phenotype with a desired trait.GWAS has identified 155 significant SNPs and 275 genes associated with salt sensitivity in O. sativa [67].Combining QTL mapping and GWAS with transcriptome profiling complements the identification of differentially expressed candidate genes in various crop species.GWAS combination with Meta-QTL analysis can be used to investigate the critical genomic regions and major quantitative traits in T aestivum [68,69].In T. aestivum, meta-analysis was performed using previously identified QTLs associated with abiotic stress, including drought, heat, salinity, temperature, and aluminum stress, resulting in 76 meta-QTLs verified using genome-wide association studies [70].In Z. mays, 86 candidate genes and 5 SNPs related to salt tolerance were identified by GWAS [71].Phosphorus (P) is the essential macronutrient in crop growth and production, and its deficiency is one of the major limiting factors in G. max production, especially at the reproductive stage.GWAS and a combination of high-density SoySNP analysis identified 27 P-efficiency-related single nucleotide polymorphisms (SNPs), which can be utilized in breeding high-P-efficiency varieties of G. max [72].GWAS has been used in detecting genetic variations underlying diverse, complex traits in barley, such as cadmium stress [73], cold tolerance [74], drought tolerance [75,76], aluminum tolerance [77,78], and salinity tolerance [79,80].Heat stress caused a significant decrease in grain nutrient content in C. arietinum.GWAS revealed that grain yield negatively correlated with Fe and Zn content and non-significantly with protein content.In C. arietinum, 181 marker-trait associated with grain nutrient content (Fe, Zn, and protein) under drought and stress conditions was identified using GWAS [81].Similarly, GWAS revealed SNPs associated with QTLs involved in drought stress by evaluating the drought tolerance ability of horsegram (Macrotyloma uniflorum) germplasms [82].

Mechanisms of CRISPR/CAS9 Genome Editing
The CRISPR/Cas system relies on an adaptive immune system found in the genomes of bacteria and archaea to protect against the invasion of foreign plasmids or viral DNA [30].CRISPR/Cas9 is composed of two components of Cas9 and a single guide RNA (sgRNA).The CRISPR/Cas system can be divided into two classes based on the structure and functions of Cas-proteins: Class I (type I, III, and IV) and Class II (type II, V, and VI) [83].Class I systems contain multi-subunit protein complexes, whereas Class II systems include single effector proteins.Due to its relatively simple structure, type II CRISPR/Cas9 has been well-studied and widely used in genetic engineering.The first Cas protein (Cas9) used in genome editing was originated from Streptococcus pyogenes (SpCas9).The Cas9 is a large multi-domain DNA endonuclease, composed of 1368 amino acids, that cleaves the target DNA to generate a double-strand break (DSB) [84].The genome editing mechanism of CRISPR/Cas9 is generally divided into three steps: recognition, cleavage, and repair.The designed sgRNA guides Cas9 and identifies the target sequence within the interest gene through its complementary base pair of 5 crRNA.As a component of the sgRNA/Cas9 complex, 20 nucleotides at the 5' end of a sgRNA bind to the target site.Without sgRNA, the Cas9 protein remains inactive.The Cas9 nuclease-induced double-strand break (DSB) is formed at a three-base pair upstream site to the protospacer adjacent motif (PAM).This specific target location should be immediately at the upstream of PAM, a conserved DNA sequence downstream of the cleavage site.The most commonly used nuclease in the genome-editing tool, Cas9 protein recognizes the PAM sequence at 5 -NGG-3 .Several studies have been conducted to improve the efficiency of the CRISPR/Cas system.For example, plants' unique PAM sites (NGG and NG) were discovered using SpCas9-NG and Cas9-NG variants [85].SpCas9 orthologues have been recognized from Streptococcus thermophiles (St1Cas9) [86] and Staphylococcus aureus (SaCas9) [87].Engineered SaCas9 has been developed to target plant genomic loci with the PAM sequence of NNNRRT [88].Additionally, engineered SpCas9 has been developed to amend plant genomic loci with PAM sequences of NGG, NG, NRNH, NGN, NRN, or NYN [89][90][91][92][93][94][95] [Table 1].
Two mechanisms repair DSBs created by Cas9 protein: homology-directed repair (HDR) and non-homologous end joining (NHEJ) (Figure 1).The HDR is exact and requires a homologous DNA donor template with a target sequence.The HDR mechanism is primarily active in the G2 and late S phases of the cell cycle.HDR executes the specific gene insertion or gene replacement by adding a donor DNA template with sequence homology at the predicted DSB site [21].The NHEJ is the leading and most efficient cellular repair mechanism and is active in all cell cycle phases.Unlike HDR, NHEJ is an error-prone mechanism that may result in indels (short insertions and deletions) at the cleavage site, leading to frameshift mutation or premature stop codon in the sequence.NHEJ accelerates the repairs created by DSBs by joining the cleaved DNAs through an enzymatic activity in the absence of exogenous homologous DNA [19,20,22]."N" is any nucleotide ["A", "T", "G', "C"]."R" is "A" or "G"."H" is "A", "C" or "T"."Y" is "C" or "T"."W" is "A" or "T".Cas13 targets RNA sequences instead of DNA; Cas14 targets single-stranded DNA (ssDNAs) instead of double-stranded DNA (dsDNAs) and does not require a Protospacer-Adjacent Motif (PAM).Note: Adapted from Zhang et al. [96].

Impact of CRISPR/Cas9-Based Genome Editing on Abiotic Stress Tolerance
Due to abiotic stresses, plant growth and development are affected, which can cause crop yield reduction at approximately 50% [113].Though productivity increases to a large extent by traditional breeding, it may cause a loss of genetic variety and fitness.In addition to the development time period, it relies on natural allelic variants, which makes it challenging to develop the desired characteristic and to ensure the sustainability of production.Genome editing must include precise modifications at specific sites to perform desired changes to the DNA sequence [20,21,30].Therefore, genome-editing techniques employing sequence-specific nucleases (SSNs) have become popular in plant research to develop improved cultivars in terms of yield, nutrition content, and resistance to environmental stresses.The SSNs introduce DNA DSBs at a target site, stimulating the cellular DNA repair and resulting in genome alterations, including targeted mutagenesis, gene insertion, and gene replacement [114].In recent years, three types of genome-editing techniques have been widely used, such as zinc finger nucleases (ZFNs), transcription activator-like effector nucleases (TALENs), and clustered regularly interspaced palindromic repeat CRISPR/Cas protein systems.Due to complex procedures and high failure rates, ZFN and TALEN have not been utilized extensively, whereas CRISPR/Cas was successfully used in various crop improvement programs.CRISPR/Cas9-based genome editing is accurate because it targets specific sites of particular genes involved in stress response pathways and modifies genes to develop plants' ability to withstand environmental stress [30,115].Additionally, the CRISPR/Cas system has been used to introduce critical agricultural traits, including plant resistance against abiotic and biotic stress, and other agronomically important traits (increased grain size and grain weight) into many economically important crops, such as O. sativa, T. aestivum, Z. mays, L. esculentum, S. tuberosum, N. tabacum, Gossypium spp., G. max, Brassica sp., S. italica, and Saccharum spp.[5,[30][31][32][33][34]37,39,40].

Improvement in Drought Stress Tolerance using CRISPR/Cas System
Drought stress can reduce crop yields by 50-70% in different crops due to significant reductions in plant growth and development.For example, a 27-40% yield reduction has been observed in C. arietinum, 42% in G. max, 50% in O. sativa, 21% in T. aestivum, 68% in V. unguiculata, and 40% in Z. mays [5].Plants experience morphological, physiological, biochemical, and molecular changes in response to drought stress.CRISPR/Cas technique was successfully applied to enhance the drought resistance of rice crops by modifying the expression of drought and other stress-related genes [116].The potential of CRISPR/Cas gene editing has been documented in various crop species against drought stress (Table 3).Researchers aimed to enhance plants' ability to withstand drought stress and reduce crop losses by altering drought-related genes.A truncated version of gRNAs (<20 nucleotides) with target sequences in plant cells was used to improve the specificity of CRISPR/Cas9 and eventually generate altered alleles for OST2 (Open Stomata 2).The novel mutant alleles for OST2 exhibited drought tolerance by altered stomatal closing in response to environmental stress in A. thaliana [117].Similarly, the remodeled CRISPR/Cas9 activation system activates vacuolar H+-pyro phosphatase AVP1, leading to an increase in single-leaf area, an increase in leaf numbers, and an enhancement of stress tolerance to drought [3].Improved drought resistance was found in homozygous CRISPR/Cas9-edited MIR169a T3 plants using a combinatory dual-sgRNA/Cas9 vector containing deleted miRNA gene regions (MIR169a and MIR827a) [118].Histone acetyltransferase (HAT) modifies chromatin histone, exposing DNA to the transcriptional machinery and regulating gene expression.Stable transgenic plants expressing chimeric dCas9HAT in A. thaliana showed higher chlorophyll content, faster stomatal aperture, and an improved survival rate under drought-stress conditions [119].Trehalase (TRE1) gene silencing through the use of the CRISPR/Cas9 system developed drought tolerance in A. thaliana [120].Transcriptome analysis using microarray technology is the best technique that has proven helpful in discovering many stress-inducible genes/stress-inducible transcription factors including the DRE-binding protein (DREB) members, ethylene-responsible element binding factor (ERF), zinc-finger, WRKY, MYB, basic helix-loop-helix (bHLH), basic-domain leucine zipper (bZIP), NAC (NAM, ATAF1, and CUC2), and homeodomain transcription factor families [4].Overexpressing AtNAC07, AtNAC019, and AtNAC055 can enhance tolerance to drought in A. thaliana [121].Dehydration-responsive element binding (DREB) proteins are one of the most prominent transcription factors and have a significant role in signaling networks regulating various plant development processes and stress responses.The overexpression of DREB1A/CBF3 (C-repeat binding factor) under the stress-inducible RD29A promoter improved drought tolerance in transgenic T. aestivum [122].Drought tolerance in T. aestivum was enhanced by altering Dehydration-responsive element binding 2 (TaDREB2) and Ethylene Responsive Factor 3 (TaERF3) using the CRISPR/Cas system [123].
Abscisic acid (ABA) plays a vital role in drought tolerance by regulating the expression of many drought-related genes.ABA regulates the expression of genes through ABAresponsive element (ABRE) binding protein/ABRE binding factor (AREB/ABF). Drought stress tolerance has been demonstrated by over-expression of AREB1, as compared to the AREB1 knockout mutant [124].In A. thaliana, ABF1, ABF3, AREB1/ABF2, and AREB2/ABF4 are expressed in response to ABA and drought stress in vegetative tissues, whereas ABI5, AREB3, DPBF2, and EEL are expressed during seed maturation [124][125][126].Abscisic acid (ABA) signaling is regulated by ABA-induced transcription repressors (AITRs).The CRISPR/Cas9 system was used in soybean (Glycine max) to target the six GmAITR genes and generated Cas9-free gmaitr36 double and gmaitr23456 quintuple mutants, enhancing salinity tolerance [41].Similarly, the Dehydration-responsive element [DREB1]/CBF is responsible for the ABA-independent induction of several genes in response to osmotic and cold stress, for example, RD29A/COR78/LTI78 gene in A. thaliana.The lateral organ boundaries domain (LBD) genes play essential roles in lateral organ development.CRISPR/Cas9 knockout of SlLBD40 improved drought tolerance in L. esculentum compared with overexpressing transgenic and wild-type plants [127].Mitogen-activated protein kinases (MAPKs) are important signaling molecules that respond to drought stress.Similarly, the CRISPR-Cas knockout mutant for the SlMAPK3 gene down-regulated the expressions of drought stress-responsive genes: SlLOX, SlGST, and SlDREB [128,129].The CRISPR-Cas9 mediated dst ∆184-305 mutation in the DST (drought and salt tolerance) gene of O. indica cv.MTU1010 produced mutants having broader leaves and reduced stomatal density, resulting in improved leaf water retention under drought stress [130].The SNF1-related protein kinase 2 (SnRK2) is the primary regulator of hyper-osmotic stress signaling and abscisic acid (ABA)-dependent plant development.A knockout mutant of the SAPK2 gene improved drought tolerance in O. sativa by affecting ABA signaling [131].The CRISPR/Cas9-mediated knockout of SRL1 and SRL2 (Semi-rolled leaf 1, 2) and ERA1 (Enhanced Response to ABA1) genes improved drought tolerance in O. sativa.OSERA1 mutant lines display similar leaf growth as wild-type plants but enhanced primary root growth [132].The SRL1 and SRL12 knockout mutants had fewer stomata, a slower rate of transpiration, less chlorophyll, vascular bundles, and rolled leaves than the wild type [133].Plant ITPKs (Inositol trisphosphate 5/6 kinases) participate in abiotic stress signaling, and the itpk1 mutant created using programmable nuclease Cas9 displayed higher tolerance to salinity stress than deletion mutants in H. vulgare [134].In B. napus, the bnaa6.rgamutant generated through CRISPR/Cas9 showed enhanced tolerance to drought stress by promoting stomatal closure through increased ABA sensitivity [40].
ARGOS is a negative regulator of the ethylene response, and CRISPR/Cas9-mediated editing of the ethylene response factor ARGOS8 improved drought tolerance in Z. mays [135].WRKY are plant-specific transcription factors that play essential roles in abiotic stress response.Several WRKY transcription factors were identified in plant species, including A. thaliana, O. sativa, G. max, T. aestivum, and H. vulgare [136][137][138].Overexpression of ZmWRKY40 promoted root growth and reduced the water loss rates in transgenic A. thaliana under drought stress [137].Overexpression of the T. aestivum TaWRKY33 enhanced the drought and heat tolerance in transgenic A. thaliana [136].OsWRKY5 is expressed in developing leaves at the seedling and heading stages of O. sativa.It is the negative regulator of drought, and its expression was reduced under drought stress and by treatment with NaCl, mannitol, and abscisic acid (ABA) [138].These studies indicated the efficiency of the CRISPR/Cas system in developing drought-tolerant cultivars by knocking out or overexpressing target genes through precise genome editing.

Improvement in Salinity Stress Tolerance Using CRISPR/Cas System
Genome editing and genetic engineering tools have been utilized to target genes involved in ion transport for regulating osmotic adjustment under salt stress.Soil salinity is a critical abiotic stress affecting crop productivity worldwide.Plant salt tolerance is the ultimate manifestation of several physiologic processes, including Na + uptake and exclusion, ionic balance (especially Na + /K + ratio), and distribution [6].Salt Overly Sensitive 1 (SOS1) is an extensively characterized Na+ efflux transporter in G. max, A. thaliana, and T. aestivum.The gmsos1 mutants were generated using the CRISPR-Cas9 system in G. max, and the resulting mutant displays a significant accumulation of Na+ in the roots and increased salt sensitivity [139].In A. thaliana, the SOS signal transduction pathway (including SOS1, SOS2, and SOS3 genes) is essential for ion homeostasis and salt tolerance.The SOS1 gene isolated from durum wheat (T.durum) conferred salinity tolerance to the sos1 mutant of A. thaliana [140].Similarly, the CRISPR/Cas9 knockout of the AITR family genes (AITR3 and AITR4) in A. thaliana enhanced tolerance to drought and salinity stress without fitness costs [7].A gene cluster containing (T5G46490, AT5G46500, AT5G46520) and (NLRs; AT5G46510) is involved in osmotic stress tolerance.CRISPR/Cas9-mediated mutagenesis generated single and double knockout lines for ACQOS alleles in A. thaliana.A. thaliana plants containing complete deletions or pseudogenization-induced polymorphisms in ACQOS and AT5G46510 show considerable tolerance to salt stress, suggesting the role of ACQOS in salt stress tolerance [141].
Nitric oxide (NO) plays a vital role in cytoprotection by regulating the level of ROS and inducing transcriptional changes, leading to the modulation of protein function [142].Reactive oxygen species (ROS) are highly reactive molecules typically produced in response to environmental stress, such as salinity and drought.Histone acetyltransferase TaHAG1 is a vital regulator to strengthen the salt tolerance of T. aestivum.TaHAG1 contributed to salt tolerance by modulating ROS production and signal specificity.CRISPR-mediated mutagenesis of TaHAG1 validated the role of TaHAG1 in salt tolerance in T. aestivum [143].Salt stress increases ROS production and is responsible for oxidative damage, membrane injury, lipid peroxidation (malondialdehyde), and ultimately cell death.CRISPR/Cas9mediated mutagenesis of the osbhlh024 gene negatively regulates the functions of Na + and K + transporter genes, suppressing the higher accumulation of MDA and H 2 O 2 , leading to salt tolerance in O. sativa [144].
Hormones like Gibberellic and Absiscic acid signaling pathways significantly affect salt stress.OsPIL14-SLR1 (Phytochrome Interacting Factor-Like14-DELLA protein, SLEN-DER RICE1) controls seedling growth in response to salt stress.CRISPR/Cas9 mediated ospil14 mutants produce normal mesocotyls and longer roots than wild-type plants [169].ZmWRKY114 is a negative regulator of salt-stress responses, and overexpressed WRKY114 exhibited enhanced salt-stress sensitivity and reduced ABA sensitivity [170].Salinity stress tolerance was identified in several stress-related genes like HyPRP1 (Hybrid proline-rich protein 1), HKT1, HKT1 (High-affinity potassium transporter1;2), RAD51/54 (DNA repair and recombination protein 51/54) and PR-1 (Pathogenesis-related protein 1) [37,151].HyPRP1 is a negative regulator of salt stress responses, and CRISPR-Cas9 mediated genome editing of HyPRP1 in L. esculentum resulted in the elimination of the functional domain of proline-rich protein.Plants carrying such variants, PR1v1 lacking proline-rich domain, PR2v2 and PR2v3 lacking eight cysteine motifs, showed improved germination compared to wild type under osmosis stress [37].A significant improvement in Homology-directed repair (HDR) using CRISPR/LbCpf1-geminiviral multi-replicons was reported to target marker-free salt-tolerant HKT1, HKT2 alleles in L. esculentum [151].Self-pollinated offspring plants carrying the HKT1, and HKT2 allele showed stable inheritance and germination tolerance under salt stress conditions (100 mm NaCl concentration).In Z. mays, Na + Con-tent1 (ZmNC1) encodes an HKT-type transporter ZmHKT1, preferentially expressed in root stele.CRISPR/Cas9 knockout lines of ZmHKT1 increase Na + concentration in xylem sap and cause increased root-to-shoot Na + delivery, indicating that ZmHKT1 promotes leaf Na + exclusion and salt tolerance by withdrawing Na + from the xylem sap [150].Mutations in genes OsRR9 and OsRR10 generated using the CRISPR/Cas9 system enhanced salinity tolerance but reduced panicle and spikelet numbers per panicle in O. sativa [171].CRISPR/Cas9 mediated mutagenesis of the ARF (Auxin Response Factors) gene generates a slarf4 mutant that displayed salinity and drought tolerance in L. esculentum by stimulating root development and stomatal function [172] (Table 3).These studies demonstrate the potential role of CRISPR/Cas mutagenesis in knocking out genes responsible for salinity tolerance in plants.

Improvement in Heat Stress Tolerance Using CRISPR/Cas System
Heat stress is the third most crucial abiotic factor that adversely affects the yield and quality of plants during entire growth stages, from germination to harvesting.Plants respond to heat stress in various ways, including alterations in enzymes that generate reactive oxygen species (ROS), heat shock proteins (HSPs), and genes encoding scavenger proteins [8].The advancement of structural and functional genomics technologies in plants has led to the identification and characterization of various temperature-stress-related genes to enhance plant ability to withstand heat [9].The heat-shock-induced CRISPR/Cas9mediated genome editing efficiently produces heritable targeted mutations.In O. sativa, a heat-shock-inducible CRISPR/Cas9 system was employed to generate targeted and heritable mutations [173].Similarly, CRISPR/Cas9-based genome editing targeted the heat-sensitive gene, Slagamous-Like 6 (SIAGL6), resulting in increased fruit setting under heat stress conditions in L. esculentum [174].Calcium-dependent protein kinase 28 (cpk28) mutant was generated using CRISPR/Cas9 mediated editing and displayed thermotolerance in L. esculentum [175].Brassinazole Resistant 1 (BZR1) is involved in thermotolerance by regulating the Feronia (FER) homologs.CRISPR/Cas9-based bzr1 mutant reduced apoplastic reactive oxygen species (H 2 O 2 ) production and enhanced heat tolerance L. esculentum [176].Photosynthetic apparatus is highly susceptible to thermal damage.Heat-sensitive albino1 (hsa1) mutant harbors a recessive mutation in a gene encoding fructokinase-like protein2 (FLN2), resulting in a severe albino phenotype with defects in early chloroplast development.In O. sativa, hsa1 mutants showed increased sensitivity to heat stress but had a faster greening phenotype than wild-type plants [177].Knockout of the ZmTMS5 gene of Z. mays using the CRISPR/Cas9 system generated homozygous T1 tms5 thermosensitive male-sterile plants that are male-sterile at 32 • C but are male-fertile at 24 • C [178].NCED4 (9-cis-Epoxycarotenoid Dioxygenase4) is a key regulatory enzyme in the biosynthesis of abscisic acid (ABA).Similarly, stable homozygous NCED4 mutants generated using CRISPR/Cas9 were capable of germinating seeds at a higher temperature (>70% germination at 37 • ) in Lettuce (Lactuca sativa) [179].Another transcription factor, OsNAC006, is regulated by temperature stress, hormones (abscisic acid, indole-3-acetic acid, and gibberellin), NaCl, polyethylene glycol, and reactive oxygen species.Furthermore, CRISPR-Cas9 mediated knockout of OsNAC006 causes drought and heat sensitivity in O. sativa [180] (Table 3).These studies highlight the application of the CRISPR/Cas9 system to target heat-sensitive genes for developing plant resistance against heat stress.

Improvement in Cold Stress Tolerance Using CRISPR/Cas System
Cold stress due to chilling and freezing temperatures hinders plant growth and development.Low temperature inhibited plant metabolic activities, producing osmotic and oxidative stress [5].Mechanical damage and metabolic dysfunction caused by freezing temperatures reduced plant growth and development.In A. thaliana, the two subclasses, namely DREB1/CBF and DREB2, are induced by cold and dehydration, respectively [4].Expression of T. aestivum TaICE41 and TaICE87 in transgenic A. thaliana activated the ex-pression of COR genes and consequently led to the enhancement of cold tolerance, but only after cold acclimation [181].The overexpression of AtDREB1A under the RD29A promoter conferred increased drought and freezing tolerance to transgenic A. thaliana plants without affecting growth and development [182].Several studies have demonstrated that WRKY transcription factors are essential in cold, heat, drought, and salinity stress [183].In Cucumber (Cucumis sativus), CsWRKY46 is a WRKY transcription factor that confers cold resistance in transgenic plants by controlling cold-stress responsive genes in an ABAdependent manner.Overexpression of CsWRKY46 regulates freezing and chilling resistance and increases the expression of stress-inducible genes, including RD29A and COR47 [184].In strawberries (Fragaria vesca), FvICE1 is a positive regulator of cold and drought resistances, and the overexpressed FvICE1 gene improved cold and drought tolerance at the phenotypic and physiological levels.Mutant (fvice1) generated using the CRISPR/Cas9 system demonstrated lower tolerance to cold and drought.This study indicates the potential of CRISPR/Cas9 system in understanding the function of stress-related genes [185]. A. thaliana HOS1 (High Expression of Osmotically Responsive Genes 1) is a Ring finger E3 ubiquitin ligase, a key regulator of cold signaling.CRISPR/Cas9-mediated knockout of the HOS1 gene showed abiotic stress tolerance, accumulation of secondary metabolites, and expression of the biosynthetic genes [10].
The C-repeat binding factors (CBF) are highly conserved CBF cold-response-system components in many plant species.It has a major role in cold acclimation and freezing tolerance in response to low temperatures.CRISPR-Cas9-mediated SlCBF1 mutagenesis reduced chilling tolerance of L. esculentum because of higher electrolyte leakage, increased indole acetic acid contents, decreased abscisic acid, methyl jasmonate, and down-regulated CBF-related genes [186].Similarly, CRISPR-Cas9-mediated mutagenesis of CGFS-type GRXs (SlGRXS14, SlGRXS15, SlGRXS16, and SlGRXS17) genes showed the sensitivity of Slgrxs mutants to various abiotic stresses as compared to wild-type in L. esculentum [187].Plant annexins are Ca2+-dependent phospholipid-binding proteins that play a role in development and protection from environmental stresses.CRISPR/Cas9-mediated knockout mutant of annexin gene OsAnn3 decreased cold tolerance in O sativa [188].OsMYB30 confers cold sensitivity by interacting with an OsJAZ9 protein and downregulating the expression of β-amylase genes in O. sativa [189].Novel mutants were generated by simultaneously editing three genes, OsPIN5b (panicle length gene), GS3 (grain size gene), and OsMYB30, using the CRISPR-Cas9 system showed higher yield and excellent cold tolerance [190].PYR1]/PYR1-like [PYL]/regulatory components of the ABA receptor detects abscisic acid during abiotic stress.CRISPR/Cas9 technology was used to edit PYL1-PYL6 and PYL12 (group I) and PYL7-PYL11 and PYL13 (group II) genes of O. sativa [191].A knockout mutant of the OsPRP1 gene of O. sativa generated by CRISPR/Cas9 demonstrated less antioxidant enzyme activity and accumulated lower levels of proline, chlorophyll, abscisic acid (ABA), and ascorbic acid (AsA) content relative to wild-type plants under low-temperature stress [192].CRISPR/Cas9-mediated base editing technology generated the point mutations in two genes (OsWSL5 and OsZEBRA3) in protoplasts and regenerated plants of O. sativa.OsWSL5 encodes a novel chloroplast-targeted pentatricopeptide repeat protein essential in rice chloroplast biogenesis under cold stress [193,194] (Table 3).These studies indicated the potential of CRISPR/Cas9-mediated mutagenesis in developing resistance to chilling and freezing temperatures in drought-tolerant cultivars by knocking out or overexpressing target genes through precise genome editing.

Improvement in Metal and Herbicide Stress Tolerance Using CRISPR/Cas System
Heavy metals, including arsenic (As), copper (Cu), cobalt (Co), cadmium (Cd), iron (Fe), manganese (Mn), nickel (Ni), zinc (Zn), mercury (Hg), lead (Pb) have accumulated in soils as a result of various human activities such as the overuse of agricultural chemicals (fertilizer, herbicides, and pesticides), improper disposal of industrial and sewage waste [11].Heavy metals are responsible for causing oxidative stress in plants and generate reactive oxygen species, leading to cellular injury.CRISPR-Cas9-mediated mutagenesis was used to improve heat metal stress in plants.OXP1 is one of the enzymes involved in 5-oxoproline metabolism and the pathway for glutathione recycling.The oxp1/CRISPR tolerated plants tolerated heavy metals, such as Cd and amisulbrom (a sulfonamide) [13].Cadmium stress activates the antioxidant defense system and increases the production of abscisic acid (ABA), glutathione (GSH), salicylic acid (SA), jasmonic acid (JA), and nitric oxide (NO) [195,196].Absorption of Cd by the roots is mediated by O. sativa genes (Os-Nramp1, OsCd1, and OsNramp5).In O. sativa, OsHMA2, OsCCX2, and CAL1 regulate Cd transport to the xylem, and OsHMA3 negatively regulates Cd xylem loading.Manipulation in the expression of these genes through CRISPR/Cas9 can minimize the Cd concentration in O. sativa [197].CRISPR/Cas9 knockout mutants of OsLCT1 and OsNramp5 exhibited reduced levels of Cd in O. sativa [198].OsNRAMP1 modulates metal ion and reactive oxygen species (ROS) homeostasis.Osnramp1 mutants generated through CRISPR/Cas9 displayed reduced levels of heavy metals (Cd and Pb) in leaves and grains of O. sativa [14].The OsHAK1 gene encodes a Cs + -permeable K + transporter that regulates the absorption and translocation of cesium [Cs + ] in O. sativa.CRISPR/Cas9 knockout mutant of OsHAK1 exhibited a significant reduction in Cs + uptake in O. sativa [199].Potassium [K + ] is a critical macronutrient for plant growth and development.ROS was strongly induced and accumulated in K + -deficient plants.Gene Prxs have been involved in the toxic reduction and intracellular H 2 O 2 scavenging.The overexpressed OsPRX2 gene improved tolerance to K + deficiency by affecting stomatal movement in O. sativa [200].OsARM1 (Arsenite-Responsive MYB1) is the R2R3 MYB transcription factor that regulates arsenicassociated transporters genes in O. sativa, and the knockout mutant (osarm1) generated using CRISPR/Cas system displayed improved tolerance to arsenic [201].
Herbicides destroy weeds and crop plants by interfering with or altering their metabolic processes, resulting in low yields.Thus, tolerance to herbicides can be one of the essential traits for crop plants that could improve farming practices and crop productivity.CRISPR/Cas-based genome editing techniques efficiently modify target genes and hold great potential in engineering plants with herbicide resistance [202].In recent years, CRISPR-Cas9-based technology has been used to generate herbicide-tolerant crops, including O. sativa, Z. mays, and G. max [203][204][205][206]. Acetolactate synthase (ALS) catalyzes the step in the biosynthesis of the branched-chain amino acids, including leucine (Leu), isoleucine (Ile), and valine (Val).Enzyme ALS is the target enzyme for two classes of herbicides: sulfonylurea and imidazolinone.Tolerance to ALS-inhibiting herbicides has been developed using a genome editing system in A. thaliana, O. sativa, T. aestivum, Z. mays, S. lycopersicon, and Saccharum spp.[42,[203][204][205][206][207][208].Herbicide-resistant plants were generated through CRISPR/Cas9-mediated homologous recombination of ALS in O. sativa [204].Similarly, chlorsulfuron resistance was enhanced in Z. mays by editing the ALS2 gene (substitution P165 with Ser) using either single-strand oligonucleotides or double-strand DNA vectors as repair templates [203].Moreover, P171F substitution in the OsALS1 allele was performed in the O. sativa cultivar Nangeng 46 by precise base editing, resulting in tolerance to the herbicide bispyribac-sodium [208].Four different missense mutations (P171S, P171A, P171Y, and P171F) in the P171 codon of the ALS gene showed different degrees of tolerance towards five typical herbicides (Sulfonylurea, imidazolinone, triazolopyrimidine, pyr-imidinyl-thiobenzoates, and sulfonyl-aminocarbonyl-triazolinone) belongs to five chemical families of ALS inhibitors in O. sativa [206].A novel allele (G628W) was developed from a G-to-T transversion at position 1882 of the OsALS gene and conferred resistance to herbicide stress.These mutants of rice plants conferred resistance to herbicides of imazethapyr (IMT) and imazapic (IMP) [209].The CRISPR/Cas9 system was also successfully used to edit the ALS1 gene of G. max to obtain chlorsulfuron-resistant plants [207].Mutation of the Proline-186 residue in the ALS gene conferred chlorsulfuron resistance in L. esculentum [210].An enzyme of activation-induced cytidine deaminase (AID) converts C to U in DNA/RNA by deamination.A synthetic complex of nuclease-deficient Cas9 fused to an AID, which is target-AID enables targeted nucleotide substitutions (C to T or G to A).The point mutation C287T of the ALS gene in rice plants resisted the herbicide imazamox [211].In T. aestivum, herbicide-tolerant plants were produced by nucleotide editing of the acetolactate synthase (ALS) gene and acetyl-coenzyme A carboxylase gene, which conferred resistance to sulfonylurea, imidazolinone-, and aryloxy phenoxy propionate-type herbicides [205].Co-editing three copies of the ALS gene resulted in herbicide tolerance in Saccharum spp.[42].
Glyphosate is one of the well-known and broad-spectrum herbicides used in the weed management of resistant crops, such as C. annum, G. max, O. sativa, and Z. mays.Glyphosate inhibits the enzyme EPSPS (5-enolpyruvylshikimate-3-phosphate synthase), involved in the biosynthesis of aromatic amino acids and secondary metabolites.Site-specific gene replacements and insertions in the rice endogenous EPSPS gene resulted in glyphosate-resistant plants [212,213].The CRISPR/Cas9 tool creates a structural variation (genomic duplication or inversion) in chromosomes.The resulting mutant developed through CRISPR/Cas technology showed the increased accumulation of transcripts of CP12 and Ubiquitin2 genes and the 10-fold upregulated expression of HPPD (4-hydroxyphenyl pyruvate dioxygenase) and PPO1 (protoporphyrinogen oxidase) resulted in herbicide resistance without affecting the yield and other agronomically important traits in O. sativa [214].CRISPR-Cas9 system was used to edit the target genes of herbicides (ALS and EPSPS) in L. esculentum cv.Micro-Tom [215].Another herbicide resistance gene, Bentazon Sensitive Lethal (BEL), gives resistance to herbicides of bentazon and sulfonylurea in O. sativa.CRISPR/Cas9-based mutation of the BEL gene was evaluated in rice using the Agrobacterium-mediated stable transformation [216].The efficiency of mutagenesis ranged from 2% to 16%, and the phenotypic analysis indicated that the mutated plant was sensitive to the herbicide bentazon.Precise editing of the endogenous α-tubulin homolog gene OsTubA2 using CRIPSR-mediated adenine base editors at the T1981 site.The point mutation in the OsTubA2 gene transformed the O. sativa cultivar into a herbicide (dinitroaniline) tolerant cultivar [217] (Table 3).These studies summarised the application of CRISPR/Cas-mediated editing of genes responsible for metal and herbicide stress tolerance in plants.

Conclusions
The CRISPR/Cas genome editing tool provides a unique and innovative approach to producing crops with enhanced tolerance to environmental stress.It is considered the best genome editing method compared to ZFNs and TALENs due to its simplicity, low cost, and high efficiency.CRISPR/Cas can be used for gene knockout, knockdown, point mutation, replacement, and insertion to develop abiotic stress-tolerant plants.Multiplex genome editing systems can edit a single gene or a few genes, but editing polyploid crops is challenging because their entire genomes have been duplicated or triplicated.The availability of plant genome sequences allows researchers to tailor the genome precisely, facilitating the use of CRISPR/Cas9 in resistance breeding.However, some limitations are associated with this CRISPR/Cas system, such as off-target, which can be reduced by carefully designing sgRNAs and using specific nucleases.Also, PAM sequences provide target specificity and a guide to the genome editing sites.The application of the CRISPR/Cas system will increase with the development of the PAM-independent CRISPR/Cas systems in crop improvement.Numerous studies demonstrate that Cas enzyme modifications may decrease the PAM requirement and create a novel tool for gene functional studies.Several efficient computational tools, including CRISPR-GE, CRISPR-P, and CRISPR-PLANT-V2, have been developed to design the guide RNA precisely.
Genetic modification can integrate with efficient plant transformation and regeneration systems to attain the desired improvement.Efficient and robust transformation techniques are essential for introducing the CRISPR-Cas system into plant cells.Several methods, including Agrobacterium-mediated transformation or particle bombardment, are used for genetic manipulation, but many crops are recalcitrant or exceptionally hard to transform.In order to build an effective tissue culture and plant regeneration system, an attempt has been made to culture immature embryos that can transform into a complete plant.The commercialization and regulation of genome-edited crops are highly debated and vary across countries.Moreover, the generation of transgene-free crops takes longer due to several repeated back-crossings of the edited plant.The development of a DNA-free CRISPR/Cas system is expanding the usefulness and effectiveness of genome editing technology.However, the DNA-free genome editing technique is still evolving, and innovative strategies are urgently required to effectively implement in crop improvement.
The CRISPR/Cas-based genome editing technology presents excellent potential for fundamental and applied research, becoming a sustainable tool for resolving important biological and agricultural problems.The fundamental areas of plant research and improvement will depend on accurate information about the various aspects of the CRISPR/Cas9 system, such as the high-throughput genome sequencing method, guide RNA designing tools, and plant cell transformation and regeneration protocols.

Figure 1 .
Figure 1.Schematic illustration of the mechanism of genome editing using CRISPR/Cas9 system.The single guide RNA (sgRNA)/CRISPR-associated protein 9 (Cas9) complex binds to the target site at a complementary region of the genomic DNA.The protospacer adjacent motif (PAM) is recognized by Cas9 nuclease, which introduces the double-stranded breaks (DSBs) within the target DNA at a site three base pair upstream to the PAM.Double-stranded breaks (DSBs) of the target DNA are repaired by non-homologous end joining (NHEJ), resulting InDel mutations (insertion or deletion) or homology-directed repair (HDR) in the presence of a donor DNA, resulting in precise gene editing.

Figure 1 .
Figure 1.Schematic illustration of the mechanism of genome editing using CRISPR/Cas9 system.The single guide RNA (sgRNA)/CRISPR-associated protein 9 (Cas9) complex binds to the target site at a complementary region of the genomic DNA.The protospacer adjacent motif (PAM) is recognized by Cas9 nuclease, which introduces the double-stranded breaks (DSBs) within the target DNA at a site three base pair upstream to the PAM.Double-stranded breaks (DSBs) of the target DNA are repaired by non-homologous end joining (NHEJ), resulting InDel mutations (insertion or deletion) or homology-directed repair (HDR) in the presence of a donor DNA, resulting in precise gene editing.

Table 3 .
Application of the CRISPR-based genome editing approach in tailoring abiotic stress tolerant plants.