Natural Genetic Resources from Diverse Plants to Improve Abiotic Stress Tolerance in Plants

The current agricultural system is biased for the yield increase at the cost of biodiversity. However, due to the loss of precious genetic diversity during domestication and artificial selection, modern cultivars have lost the adaptability to cope with unfavorable environments. There are many reports on variations such as single nucleotide polymorphisms (SNPs) and indels in the stress-tolerant gene alleles that are associated with higher stress tolerance in wild progenitors, natural accessions, and extremophiles in comparison with domesticated crops or model plants. Therefore, to gain a better understanding of stress-tolerant traits in naturally stress-resistant plants, more comparative studies between the modern crops/model plants and crop progenitors/natural accessions/extremophiles are required. In this review, we discussed and summarized recent progress on natural variations associated with enhanced abiotic stress tolerance in various plants. By applying the recent biotechniques such as the CRISPR/Cas9 gene editing tool, natural genetic resources (i.e., stress-tolerant gene alleles) from diverse plants could be introduced to the modern crop in a non-genetically modified way to improve stress-tolerant traits.


Introduction
Since the birth of Agrobacterium tumefaciens-mediated genetic transformation in plant biotechnology [1], many genes have been identified and used to improve crop traits-notably, stress tolerance, which is the main topic of this review. Some genes have been successful, while some have not [2]. However, even a gene successful in one particular crop does not always work for another crop. This indicates the presence of diverse genetic functions and regulation systems in plants. Thus, one approach to overcome this hurdle of crop improvement could be to isolate the diverse alleles from various natural resources.
In the course of the domestication and continuous artificial selection, genetic diversity in the wild cultivars has been lost in many modern crop cultivars [3][4][5]. Crop breeding favored yield over other traits such as stress tolerance, which could be replaced by farmers' care and agricultural techniques [2,6]. Thus, compared to the modern crop varieties, wild ancestors of crops could effectively tolerate and thrive under a wide range of weather fluctuations and unfavorable habitats [2,5,7,8]. Hence, the wild accessions in many crop plants can be considered primary reservoirs of genetic diversity and deserve much more attention to be explored for their stress-tolerant traits.
In this review, we look into the current studies on stress-tolerant gene alleles from various germplasms that render advantageous traits in stress tolerance and provide an opportunity to think about possible applications. In Table 1, we also summarize the stress-tolerant alleles from diverse resources that show superior functions in stress tolerance.

Limited Genetic Diversity in Domesticated Crops
Crop domestication through artificial selection often results in opposition to natural selection [40]. For example, farmers favored the trait of non-shattering seeds, which is obviously an unfavored trait for plants in nature that need to spread their offspring widely [41]. The breeding programs mostly aim to develop high yielding crop varieties [2]. Thus, domestication of crops has resulted in increased productivity but limited genetic diversity, often by losing useful alleles such as stress-tolerant genes [42]. During domestication processes, beneficial traits can be lost by gene loss, changes in gene regulation, and gene activity modification (i.e., sequence variations in coding sequence).

Gene Loss
Munns et al. examined natural diversity in shoot Na + exclusion within ancestral wheat germplasms. An ancestor of modern wheat, Triticum monococcum carries Nax1 and Nax2 loci while modern durum wheat (Triticum turgidum) or bread wheat (Triticum aestivum) does not [31,43]. The introduction of the T. monococcum Nax2 locus encoding TmHKT1;5-A gene to durum wheat by genetic crosses or molecular transformation dramatically decreased Na + accumulation in the leaves and increased grain yield on saline soils [31]. High-affinity K + Transporter (HKT) is one of the genes that is found only in plants, facilitating mostly monovalent cation (i.e., K + and Na + ) transport and playing important roles in the regulation of K + and Na + transport, and hence the salt tolerance in plants [44][45][46][47]. Thus, this gives an example that a gene responsible for stress tolerance in a wheat ancestor was lost during domestication to make durum wheat and bread wheat.

Alterations in Gene Expression
In addition to stress-tolerant gene loss, modifications of gene expression can also occur during domestication by changing the promoter activity. Bian et al. uncovered that the gene expression levels of class-B type heat shock factor, HSFB2b, are correlated with the degrees of salt stress tolerance in soybean (Glycine max) [32]. HSFB2b appeared to promote flavonoid accumulation by activating the expression of flavonoid biosynthetic genes and relieving the inhibition of flavonoid biosynthesis, which led to salt stress tolerance. Among the four haplotypes of the HSFB2b promoters in the analyzed soybeans, ones from salt-tolerant wild accessions displayed higher HSFB2b promoter activity than the domesticated soybean cultivars. This suggests that the strong selection was imposed on the promoter regions of HSFB2b during domestication and that the wild accessions could provide a strong allele to combat against salt stress [32]. In addition, many genome-wide association studies (GWAS) in maize have also revealed the promoter sequences as a genic area of the domestication target (see below).

Variations in Coding Sequence
In addition, natural variations in the open reading frame could also lead to a loss of beneficial traits during crop domestication. After analyzing the differential patterns of heat stress acclimation in the course of domestication between wild tomato (Solanum pennellii) and cultivated tomato (Solanum lycopersicum), Hu et al. found an alternative splicing variation in the HsfA2 gene which encodes a major heat inducible transcription factor [5]. The natural variation in wild species caused alternative splicing of the HsfA2 gene, resulting in the synthesis of a HsfA2-II isoform for rapid heat stress acclimation in wild species compared to the cultivated tomato [5].
In another report, Wang et al. compared the Na + /K + ratios in roots of salt-sensitive and -tolerant tomato cultivars under salt stress and processed the results through GWAS analysis [4]. They found that the gene SlHAK20 was associated with salt stress tolerance: The natural variations in the SlHAK20 coding sequence appeared to be the reason for the different levels of salt tolerance in tomato accessions. The SlHAK20 encoded a member of the clade IV High-Affinity K + /K + Uptake Permease/K + Transporter (HAK/KUP/KT) transporters and functioned in the transport of Na + and K + . Salt-tolerant wild tomato accessions contained a "strong" SlHAK20 allele (haplotype 1) which efficiently lowered the Na + /K + ratio in plants and brought about enhanced salt tolerance. The activity of domesticated tomato SlHAK20 (haplotype 2) was low, indicating the coding sequence variations during domestication caused the loss of SlHAK20 activity, hence the loss of salt tolerance [4].

Arabidopsis
Arabidopsis thaliana accessions (ecotypes) are broadly distributed to the various regions of the world, and this distribution contributes to the genetic variations of Arabidopsis that are crucial for stress adaptation [48]. Thus, genetic variations among the Arabidopsis accessions provide a valuable genetic model to find out both unique stress tolerance mechanisms and important stress-tolerant alleles [49]. For example, Jha et al. found a positive correlation between AtAVP1 transcript levels and salinity tolerance [50]. In comparison to Col and C24, the Ler and Ws accessions displayed higher transcript abundance of AtAVP1 in association with higher salt stress tolerance [50].
The RAS1 allele from the salt-sensitive accession Ler encodes a 230 amino acid-length protein, while the RAS1 allele in Sha only produces a truncated polypeptide with 209 amino acid residues due to the premature stop codon [15]. RNAi-caused RAS1 reduction in Ler reduced salt sensitivity, and overexpression of the Ler RAS1 allele increased salt sensitivity, supporting the correlation of the RAS1 coding sequence variations with salt sensitivity. The RAS1 gene acts as a negative regulator of salt tolerance; hence, the functional loss of RAS1 gene could render the salt tolerance. Thus, it is expected that the allele modification resulting in the C-terminal truncation and loss of its activity enabled Sha to become salt tolerant in the course of its evolution [15].

LRR-KISS
A genome-wide association study (GWAS) with 160 accessions of Arabidopsis identified one single nucleotide polymorphism (SNP) associated with natural variations in dry weight at 500 mM NaCl. The SNP was located in the promoter region of the Leucine-Rich Repeat Kinase Family Protein Induced By Salt Stress (LRR-KISS) gene [16]. Salt stress did not affect the rosette size in Arabidopsis accession with high LRR-KISS expression (Cen-0), while the same stress greatly reduced relative rosette size in the accession with low LRR-KISS expression (HR-5). This suggests that the natural variations in the promoter activity are associated with salt stress tolerance-the higher the LRR-KISS transcript levels, the larger the rosettes under salt stress.

Rice
Rice is originally a chilling-sensitive crop derived from tropical or sub-tropical regions of Asia. Rice cultivars include two subspecies, indica and japonica [55,56]. Compared to indica, the japonica rice cultivars were found to be more cold-tolerant and grow at higher altitudes and latitudes and temperate zones [11,17,57].

Cold-Tolerant Alleles from Japonica Cultivar
To understand the genetic basis of enhanced cold tolerance in japonica, several genes with natural variations were identified and characterized [11,13,17,18]. Some of the superior alleles from japonica in cold tolerance are described below. Some that were not described due to the space limits are included in Table 1.

COLD1
The CHILLING-TOLERANCE DIVERGENCE 1 (COLD1) gene encodes a plasma membrane and endoplasmic reticulum localized regulator of G-protein which activates Ca 2+ influx upon cold sensing [17]. COLD1 was identified through a quantitative trait locus (QTL) analysis in recombinant inbred lines from a cross between chilling-tolerant japonica and chilling-sensitive indica. COLD1 allele from japonica and indica contained several SNPs including an SNP in the fourth exon (SNP2), which was shown to be associated with chilling tolerance. An expanded comparative sequence analysis of japonica cultivars, indica cultivars, and wild rice revealed polymorphism of T/C in chilling-sensitive rice (indica) and A in chilling-tolerant rice (japonica and wild rice Oryza rufipogon) at SNP2, which resulted in Met187/Thr187 in chilling-sensitive rice and Lys187 in chilling-tolerant rice [17]. Thus, it is likely that chilling-tolerant COLD1 allele from O. rufipogon was selected during japonica domestication to confer the chilling tolerance trait in japonica [17].

HAN1
Similarly, a recent report demonstrated the HAN1 gene contribution to chilling tolerance in temperate japonica. The HAN1 gene encodes an oxidase that converts the active jasmonoyl-L-isoleucine (JA-Ile) to an inactive form, 12-hydroxy-JA-Ile (12OH-JA-Ile), and it further modulates the jasmonic acid-mediated chilling responses [13]. Overexpression and mutation analysis of HAN1 suggested that HAN1 negatively regulates chilling tolerance. While both coding sequences of HAN1 alleles from indica cultivar (Teqing) and japonica cultivar (02428) showed the same functional and physiological activities, the allelic variation for chilling tolerance variations was found in the HAN1 promoter [13]. The promoter analysis in 101 rice accessions identified an SNP in MYB cis-elements at the promoter of HAN1 in most chilling-tolerant japonica cultivars, which might be responsible for the adaptation of japonica cultivars to temperate climates, probably by reducing the HAN1 expression.

CTB4a
QTL analysis on recombinant inbred lines from a cross between cold-sensitive Towada and the cold-tolerant japonica landrace KUNMINGXIAOBAIGU (KMXBG) at booting stage identified the cold tolerance at booting stage 4a (CTB4a) encoding a leucine-rich repeat receptor-like kinase [11]. Despite the multiple SNPs and indels both in the promoter regions and the coding regions of the CTB4a alleles from KMXBG and Towada, a strong correlation was found between the CTB4a expression levels and cold tolerance, suggesting that the nucleotide polymorphisms in the promoter regions account for different cold sensitivity. Further analysis revealed that upregulation of CTB4a is positively correlated with ATP synthase activity, ATP contents, seed setting, and yield under cold stress [11].

bZIP73
In rice, there are 89 members of the basic leucine zipper (bZIP) family proteins and some of bZIP proteins have been identified to function in cold stress responses in rice [58,59]. Using association analysis and population genetics of bZIP genes combined with expression profiles under stress, bZIP73 was identified to be associated with low temperature seedling survivability [18]. The bZIP73 contained a single SNP in the coding sequence; at 511 bp, G in japonica and A in indica, resulting in glutamate in japonica and lysine in indica at the one hundred and seventy-first amino acid. This single SNP in bZIP73 was responsible for differences in cold tolerance between japonica and indica as evidenced by overexpression of each allele and the introgression of the indica bZIP73 allele to japonica. The japonica bZIP73 allele, working with its interacting partner bZIP71, is a superior allele in comparison to the indica allele to facilitate cold adaptation during japonica domestication [18].

Heat-and Drought-Tolerant Alleles from Indica Cultivar
Unlike japonica cultivars, indica cultivars predominantly grow in tropical and subtropical regions [18,60]. Wild progenitors from a low moisture region such as O. barthii, O. australiensis, O. glaberrima, O. longistaminata, and O. punctata could be able to provide drought-or heat-tolerant candidate genes to cultivated rice [61].

TT1
CG14 line originated from an African wild rice cultivar O. glaberrima is more tolerant to heat stress than Wuyunjing, an Asian cultivar. Through map-based cloning, Li et al. identified the causal gene at the Os03g0387100 locus and named it as Thermo-tolerance 1 (TT1) [25]. Multiple sequence alignment of the TT1 locus with other species revealed the existence of three SNP variations in the Oryza glaberrima TT1 (OgTT1) allele compared to its counterpart Oryza sativa TT1 (OsTT1). One of the variations in the OgTT1 coding sequence caused the substitution of histidine instead of arginine at the ninety-ninth position in the protein sequence of OsTT1 from Wuyunjing [25]. The OgTT1 overexpressing lines displayed predominantly higher thermal tolerance than the OsTT1 overexpressing lines. This suggests that the OgTT1 is a superior allele to OsTT1 in rendering heat tolerance [25]. TT1 encodes an α2 subunit of the 26S proteasome [25].

OsDREB1F
In rice, dehydration-responsive element binding 1F (DREB1F) gene is known as one of the key drought stress-responsive transcriptional activator genes. To assess the allelic variations and molecular evolution of DREB1F, DREB1F alleles from indica wild rice germplasms and various accessions were compared along with the Oryza sativa DREB1F (OsDREB1F) [26]. The haplotype analysis classified the DREB1F alleles into 8 haplogroups and the alleles from drought-tolerant lines fell into H5 haplogroup with C changed to G at the three hundred and sixty-third nucleotide from the translation start site, resulting in a substitution of glutamate in the place of aspartate. This natural variation is associated with drought tolerance in the H5 haplogroup compared to the other variants [26].

Drought-and Flooding-Tolerant Alleles from Upland Rice and Lowland Rice
Two major rice ecotypes include upland rice and lowland rice [62]. While lowland rice grows on flooded paddies, upland rice grows on dry soil; hence, upland rice cultivars are drought tolerant.

OsLG3 and OsCBL10
Gene association analysis revealed that the natural variation in the OsLG3 promoter is associated with osmotic tolerance [12]. Upon drought stress, OsLG3, an ethylene response factor (ERF) family transcription factor is more highly induced in IRAT109, a japonica upland rice cultivar, than in Nipponbare, a japonica lowland rice cultivar. Introduction of the OsLG3 allele from IRAT109 to rice improved drought tolerance, attributing the IRAT109 variation in the OsLG3 promoter to enhanced drought tolerance [12]. Higher expression of OsLG3 in IRAT109 because of variations in the promoter efficiently induced the transcription of downstream stress-responsive genes and the reactive oxygen species (ROS) scavenging genes under drought, causing increased drought tolerance. Similarly, natural variations in the OsCBL10 promoters of upland and lowland rice are shown to be associated with flooding tolerance [27]. Japonica lowland rice variations in the OsCBL10 promoter suppress the OsCBL10 expression in response to flooding, affecting downstream Ca 2+ mediated signaling toward flooding tolerance in seed germination [27]. These results again recapitulate that the regulation on the promoter activity is one of the selection targets in rice domestication.

ZmDREB2.7
In maize, drought-responsive ZmDREB2.7 displays natural variations in association with drought tolerance. DNA polymorphisms at the 5 untranslated regions of ZmDREB2.7 gene were shown to be important in determining the degrees of drought tolerance in maize varieties. Liu et al. found that the ZmDREB2.7 allele from drought-tolerant tropical or subtropical varieties (TST; CIMBL70, 91, 92 and CML118) was rapidly induced by moderate drought in comparison with the drought-sensitive variety (Shen5003) [28]. In return, the TST ZmDREB2.7 allele was more effective in inducing drought stress tolerance. These data suggest that the tolerant ZmDREB2.7 allele is a beneficial genetic resource for drought-tolerant crop development.

ZmVPP1
In maize, the ZmVPP1 encodes for a vacuolar-type H + pyrophosphatase. A GWAS study of drought tolerance at the maize seedling stage identified 83 genetic variants and uncovered that two variants (indels at -397 (366 bp) and -126 (5 bp) upstream from the translation start site) at the promoter region of ZmVPP1 are significantly associated with drought tolerance [3]. In particular, the 366-bp insertion of ZmVPP1 alleles from drought-tolerant tropical/subtropical cultivars contained three MYB binding cis elements and was important in drought stress-responsive gene induction, hence the enhanced drought tolerance [3].

ZmNAC111
Another GWAS study with 368 inbred lines identified the ZmNAC111 gene associated with drought tolerance at the seedling stage [29]. Among the natural variations in the ZmNAC111 gene, the 82-bp insertion of a miniature inverted-repeat transposable element (MITE) at the promoter was found to be most significantly associated with drought tolerance. The MITE was present in the ZmNAC111 alleles from drought-sensitive B73 and Mo17 inbreds while it was missing in drought-tolerant CIMBL55, 70, 90, and CML118. The MITE insertion in the drought-sensitive ZmNAC111 allele caused a reduction in the ZmNAC111 expression in drought-sensitive cultivars, resulting in lower drought tolerance compared to drought-tolerant cultivars [29].

ZmTIP1
Through a GWAS analysis, Zhang et al. recently established a significant association between the natural variations of ZmTIP1 and drought tolerance [30]. ZmTIP1 encodes an S-acyl transferase and its expression levels are correlated with the degrees of drought tolerance [30]. The ZmTIP1 alleles from drought-tolerant cultivars contained a higher number of transcription factor binding elements in the promoter region than the alleles from drought-sensitive cultivars. These natural variations are responsible for higher ZmTIP1 expression in drought-tolerant cultivars than drought-sensitive lines. However, the natural variations in the ZmTIP1 coding region did not contribute to the levels of drought tolerance. ZmTIP1 may function through S-acylation of a calcium-dependent protein kinase (ZmCPK9) that facilitates the ZmCPK4 association with the plasma membrane.

MBF1c from a Polar Moss
Polytrichastrum alpinum is one type of polar moss that survives extreme conditions in the Antarctic. From this extremophile, a stress-responsive transcriptional coactivator gene, multi-protein bridging factor1c (PaMBF1c), was isolated and compared with Arabidopsis MBF1c (AtMBF1c) [14]. In previous work, the AtMBF1c gene was already identified as a key regulator for thermotolerance responses and the AtMBF1c gene overexpression enhanced heat tolerance in Arabidopsis [63]. When Arabidopsis transgenic plants overexpressing the PaMBF1c gene were compared with AtMBF1c overexpressing Arabidopsis lines, both lines showed high tolerance to heat stress [14]. Interestingly, the PaMBF1c overexpressing lines conferred enhanced tolerance to salt (NaCl) and ionic (LiCl) stresses at both germination and seedling stages in comparison to the WT and AtMBF1c overexpressing lines. In other words, PaMBF1c overexpression brought about tolerance to multiple stresses including heat, salt, and ionic stresses, which was not observed in the AtMBF1c overexpressing Arabidopsis. It is assumed that PaMBF1c might have evolved to adapt P. alpinum to the high salt conditions of the Antarctic, probably by optimizing amino acid residues for the multifunctional activity. PaMBF1c contains 14 amino acid variations different from Triticum aestivum MBF1c and AtMBF1c, the functions of which were shown to be involved in abiotic stress tolerance [64,65]. In conclusion, the data suggest that extremophiles could contain a more "useful" allele for improvement of abiotic stress tolerance in crops.

Galactinol Synthase 1 from a Desert Shrub
Ammopiptanthus nanus is a desert shrub that can survive a wide temperature range, from −30 to 47 • C [66,67]. Galactinol synthase1 (GolS1), a galactinol biosynthesis gene associated with stress tolerance, was shown to be cold-inducible in A. nanus [68,69]. Overexpression of A. nanus GolS1 (AnGolS1) in tomato caused an increase of galactinol contents in young leaves under cold stress, activation of ethylene signaling, and induction of ethylene response factors (ERFs), which led to cold tolerance [33]. Among four tomato GolSs (SlGolS1, SlGolS2, SlGolS3, and SlGolS4) homologous to AnGolS1, only SlGolS2 was cold-inducible, but at low levels, and believed to be a functional homolog of AnGolS1. AnGolS1 showed higher catalytic activity than SlGolS2 [33]. Thus, it is assumable that these features of AnGolS1 such as a higher inducibility and a higher catalytic activity might confer higher cold stress tolerance than SlGolS2.

Sodium Proton Antiporters from Halophytes
Overexpression of the halophyte Suaeda salsa NHX1 (SsNHX1) increased cold and salt tolerance in Arabidopsis [34]. Yadav et al. also reported that transgenic tobacco plants overexpressing the SbSOS1 gene from an extreme halophyte Salicornia brachiata showed higher salt tolerance compared to the WT plants [35]. Although these results were already observed in AtNHX1 or AtSOS1 overexpressing Arabidopsis [70,71], the halophyte SsNHX1 gene overexpressing plants grew normally even after 200 mM NaCl treatment [34]. In contrast, AtNHX1 or AtSOS1 overexpressors showed a limited salt tolerance only up to 200 mM NaCl and could not survive at NaCl concentrations higher than 200 mM [72]. Thus, it is likely that these halophyte genes function better under stress than the glycophyte homologs.

HKT1;1 from Halophytes
High-affinity K + transporter, HKT1;1 (previously known as HKT1), plays an important role in reducing the phytotoxicity of Na + by controlling shoot Na + levels and maintaining the balance between Na + and K + ions under salt stress. Originated from the Namibian desert in Southern Africa, Mesembryanthemum crystallinum (also known as ice plant) is one of the extremophiles and is extremely salt stress tolerant, withstanding up to 0.5 M NaCl [73]. Arabidopsis HKT1;1 homolog gene, McMKT2 (now renamed McMKT1;2) was isolated from M. crystallinum and found to have several distinct features compared to AtHKT1;1 [36]. For instance, the McHKT2 amino acid sequence contains 13 contiguous threonine residues between the first and second transmembrane pore domains as compared to the amino acid sequences of HKT1 from other plant species [36]. AtHKT1-overexpressing Arabidopsis is known to display salt-sensitive phenotypes [74,75]. However, McMKT2 overexpressing Arabidopsis showed significantly high salt tolerance. Thus, it is speculated that the natural variations in McMKT2 from halophyte M. crystallinum are responsible for these functional differences when overexpressed. Indeed, HKT1 orthologs with natural variations from soybean and maize also brought about enhanced salt tolerance in tobacco plants when overexpressed [76][77][78].
Recent studies determined amino acid variations responsible for the HKT1 functional differences between glycophyte and halophyte. AtHKT1;1 from the glycophyte Arabidopsis and TsHKT1;2 from the halophyte Thellungiella salsuginea, a model extremophile plant, share high DNA and protein sequence identities. However, they have different features in terms of ion selectivity and salt stress responses [37,79]. When the two genes were expressed in the Arabidopsis hkt1-1 mutant under control of the AtHKT1;1 promoter, TsHKT1;2 expressing lines showed higher tolerance to salinity, a higher fresh biomass, and a lower shoots/roots Na + ratio than wild-type or AtHKT1;1 expressing lines, exemplifying that the HKT1 allele from an extremophile (TsHKT1;2) is a superior allele in handling salt stress [37,38,79]. By comparative analysis and protein modeling, an amino acid residue important for each activity was found in the second pore loop domain; the two hundred and seventh aspartate residue in TsHKT1;2 and the two hundred and eleventh asparagine residue in AtHKT1;1. When TsHKT1;2 D207N (TsHKT1;2 with Asp at the two hundred and seventh amino acid switched to Asn) was expressed in the K + transporter-deficient yeast, TsHKT1;2 D207N expression resulted in lower salt tolerance than its original TsHKT1;2 expression, but slightly higher than AtHKT1;1 expression. These results indicate the superior function of the TsHKT1;1 allele associated with the amino acid variation [37,38]. A similar functional determinant at the amino acid variation in the second pore loop was identified in another extremophile Eutrema parvula HKT1;2, indicating that the presence of Asn or Asp in the second pore loop determines the cation selectivity in the HKT1 transporters [74]. This finding also fortifies the notion that the extremophiles could contain the functionally superior alleles.
More importantly, AtHKT1;1 N211D (AtHKT1;1 with Asn at the two hundred and eleventh amino acid changed to Asp) expression in the Arabidopsis hkt1-1 mutant showed significantly enhanced growth in comparison to the original AtHKT1;1 expressing hkt1-1 lines [38]. Using this information, Vu et al. applied the CRISPR/Cpf1-mediated homologous recombination technique to replace the original Asn at the two hundred and seventeenth amino acid of the tomato HKT1;2 allele with Asp residue important for the activity of the superior TsHKT1;2 allele in salt stress [39]. This gene edited SlHKT1;2 N217D tomato showed enhanced salt tolerance at the germination stage under 100 mM NaCl and the edited allele was successfully inherited to the next generation [39].

Concluding Remarks
Conventionally, most of the physiological characterization studies, thus far, aimed to elucidate a gene function by relying on genes from model plants or modern cultivars through either mutant or overexpression-based approaches. Recently, many researchers reported the utilization of the genetic resources from wild crop progenitors and extremophiles and proved many of them to be better alleles than alleles from model plants in crop improvement against abiotic stresses. Therefore, it would be needed to expand our efforts to understand the natural genetic variations in the wild progenitors or accessions which have been adapted to extreme environments. Understanding of their stress-evading strategies will enable us to plan and design the breeding and biotechnological programs to generate crop plants with multifaceted stress tolerance [80,81].
The recent bioinformatic technical advancements including whole genome surveys, gene targeted surveys, and genome-wide association studies successfully demonstrated and uncovered the complex causative elements with very high precision in various plant species. They could be highly instrumental to expand our knowledge on the genetic information of untapped stress-tolerant wild ancestors and to learn the selection impact over wild cultivar germplasm during domestication. As we summarized, many natural variations including indels in the promoters and SNPs in the coding sequences have been reported to be determinant factors of the levels of gene activity. To make this genetic resource more useful, it is necessary to carry out comparative studies among the alleles. Thus far, there are not many comparative studies of alleles from the extremophiles and temperate plants.
When combined with genetic resources and natural variations, the revolutionary CRISPR gene editing tool will facilitate crop improvement. For example, the negative regulators of stress tolerance could be deleted by the CRISPR gene editing tool to introduce the stress tolerance in the crop if the crop genome contains the negative regulator gene. In addition, the variations in the promoters and the coding sequences could be edited to be a superior allele. The CRISPR editing variants such as the base editors and the prime editors will be a tool of choice for introducing the favorable natural variations into the target genes. The above-described tomato HKT1 editing study is one example of CRISPR application in crop improvement [39]. One thing to note is that the natural genetic resources might have not been selected during domestication due to its deleterious effects on yield. Thus, detailed characterization of the "superior" alleles must be performed to avoid any yield penalty in crop improvement.