Transcription Factors Interact with ABA through Gene Expression and Signaling Pathways to Mitigate Drought and Salinity Stress

Among abiotic stressors, drought and salinity seriously affect crop growth worldwide. In plants, research has aimed to increase stress-responsive protein synthesis upstream or downstream of the various transcription factors (TFs) that alleviate drought and salinity stress. TFs play diverse roles in controlling gene expression in plants, which is necessary to regulate biological processes, such as development and environmental stress responses. In general, plant responses to different stress conditions may be either abscisic acid (ABA)-dependent or ABA-independent. A detailed understanding of how TF pathways and ABA interact to cause stress responses is essential to improve tolerance to drought and salinity stress. Despite previous progress, more active approaches based on TFs are the current focus. Therefore, the present review emphasizes the recent advancements in complex cascades of gene expression during drought and salinity responses, especially identifying the specificity and crosstalk in ABA-dependent and -independent signaling pathways. This review also highlights the transcriptional regulation of gene expression governed by various key TF pathways, including AP2/ERF, bHLH, bZIP, DREB, GATA, HD-Zip, Homeo-box, MADS-box, MYB, NAC, Tri-helix, WHIRLY, WOX, WRKY, YABBY, and zinc finger, operating in ABA-dependent and -independent signaling pathways.


Introduction
Being sessile, plants are susceptible to various adverse environmental conditions. Plants inherently live in harsh conditions [1], and the natural environment of plants comprises abiotic and biotic stressors [2]. Abiotic stressors are the foremost limiting factors, e.g., drought, high salinity, low temperature, high temperature, nutrient stress, and heavy metals, and are hostile to plant growth and development, ultimately affecting crop productivity and sustainability [3][4][5].
Drought and salinity periods interrupt the ionic and osmotic strength, encourage the redox balance and cellular energy, and cause the loss of photosynthesis [6]. Drought stress is one of the leading aspects of regulating crop production, provoking many physiological, molecular, biochemical, and anatomical changes [7]. Salinity is a significant factor that decreases crop production by deteriorating plant health [8]. There are different transcription factors (TFs) involved in drought and salinity stress responses; for example, MtHB2 in Medicago truncatula [9], Zmhdz10 in maize [10], OsGATA23a in rice [11], and ATHB17 in and helpful approach for developing crop varieties resistant to climate change. It will be a helpful tool for capable and particular genome editing in different plants for several traits, including abiotic stresses [29]. Therefore, some genes are targeted through genome editing based on CRISPR/Cas9 technology in different crops. Another yeast two-hybrid method is a well-established genetics-based system that uses yeast to display binary protein-protein interactions [30]. Using such techniques, the PYL6 and MYC2 interact, and their interaction is enhanced in the presence of ABA [31].
Both drought and salinity are among the most severe abiotic factors restricting plant growth and yield. ABA-dependent (drought-inducible genes were clarified upon their induction by exogenous ABA, which means two different systems in stress-inducible gene expression; later, ABA-dependent genes are regulated by endogenous ABA based on mutant analyses) ABA-independent pathways regulate numerous genes that function in drought response. Many signaling molecules, such as ABA, ROS, H 2 O 2 , NO, Ca 2+ , PAs, and others, have been well known and revealed in plant signaling perception and transduction pathways. Many drought-and salinity-responsive genes are involved in ABA-signaling pathways, such as ABA-inducible (ABA-inducible genes were genes induced by exogenous ABA treatment in the early phase of research; now, ABA-inducible genes are regulated by endogenous ABA, as well), ABA-sensitivity (ABA-sensitivity is phenotypes related to ABA sensitive responses during germination, stress response, and so on; various mutants and ecotypes have been reported to be ABA-sensitive ones based on their responses to ABA), and ABA-mediated (ABA-mediated genes are genes regulated by ABA signaling pathways in stress responses and plant growth). However, several drought-and salinityinduced genes do not respond to ABA signaling, showing that ABA-independent signaling pathways also regulate the response to drought and salinity stress. This review mainly focuses on the recent progress and development of TFs and their upstream and downstream ABA-related genes to emphasize the role of ABA genetic engineering in drought and salinity tolerance in various crops and sheds light on various TF families' functions to orchestrate the tolerance response in crop species.

TFs Regulatory Network in Response to Drought and Salinity Stress
A transcription factor is a protein that binds to DNA and regulates gene expression by promoting or suppressing transcription. The function of TFs is to regulate turn on and off genes and ensure their expression in the suitable cell at the right time and the right amount throughout the life of the cell and the organism [32]. Transcription factors are modular in structure and contain two domains. The first is the DNA-binding domain, which attaches to specific DNA sequences (enhancer or promoter) adjacent to regulated genes. DNA sequences that bind transcription factors are often referred to as response elements [33]. The second is the activation domain, which contains binding sites for other proteins such as transcription coregulatory. These binding sites are frequently referred to as activation functions, transactivation domains, or trans-activating domains but do not mix with the topologically associating domain [32,33]. Generally, a stress signal transduction pathway comprises the following key steps: (1) signal perception, (2) signal transduction, and (3) stress response. The first step in activating a signaling cascade for drought and salinity stress recognizes stress signal via receptors located on the membrane of the plant cell [34]. After recognition, these sensors transmit the signal downstream through phytohormones and second messengers such as Ca 2+ and ROS [35]. The second messengers, such as ROS, trigger another set of ROS-modulated PKs and PPs, including MAPK cascades, CDPKs, CBLs, CIPK, and many other PKs, as well PPs such as some PP2Cs (Figure 1) [34]. ABA is the principal hormone involved in the coordination of abiotic stress in plants [36]. The different stress tolerance responsive TFs usually function independently. However, there is a possibility that some level of cross-link occurs between these TFs (Figure 1). The last step is the expression of functional genes involved in different functions such as stomatal closure, oxidative damage, leaf senescence, or indirectly regulating regulatory genes contributing to signaling cascades and transcriptional regulation of gene expression [34,37]. These abilities Biomolecules 2021, 11,1159 4 of 30 allow them to be excellent candidate genes for genetic manipulation of complex stress tolerance traits [38]. To date, based on genome-wide analysis, a great deal of TFs belonging to different families, such as AP2/ERF, bHLH, bZIP, DREB, GATA, HD-Zip, Homeo-box, MADS-box, MYB, NAC, Tri-helix, WHIRLY, WOX, WRKY, YABBY, and zinc finger, and so on, have been identified in different plant species [39,40].
such as stomatal closure, oxidative damage, leaf senescence, or indirectly regulating regulatory genes contributing to signaling cascades and transcriptional regulation of gene expression [34,37]. These abilities allow them to be excellent candidate genes for genetic manipulation of complex stress tolerance traits [38]. To date, based on genome-wide analysis, a great deal of TFs belonging to different families, such as AP2/ERF, bHLH, bZIP,  DREB, GATA, HD-Zip, Homeo-box, MADS-box, MYB, NAC, Tri-helix, WHIRLY, WOX, WRKY, YABBY, and zinc finger, and so on, have been identified in different plant species [39,40].

AP2/ERF
The AP2/ERF is one of the largest families of TFs, with 140-280 members in several plants [41,42], which regulate multiple responses such as stress, metabolism, and development in plants [43]. In the past, AP2/ERF genes were considered plant-specific, but recently, this domain was reported in non-plants, such as in the protists, ciliate, cyanobacterium, and phages [44,45]. The rice ABA-independent gene OsERF48 directly binds to the promoter of OsCML16 via AP2/ERF cis-acting regulatory elements, thereby activating its transcription. Overexpression of OsERF48 causes regulation of OsCML16, a calmodulinlike protein gene that enhances root growth, drought tolerance, and grain yield and is involved in cell wall proteins, carbohydrate metabolism, and stress signaling in drought conditions in the field [46]. The rice OsERF71 gene is an AP2/ERF TF involved in an ABA-

TFs Involved in Drought and Salinity Stress Responses
The AP2/ERF is one of the largest families of TFs, with 140-280 members in several plants [41,42], which regulate multiple responses such as stress, metabolism, and development in plants [43]. In the past, AP2/ERF genes were considered plant-specific, but recently, this domain was reported in non-plants, such as in the protists, ciliate, cyanobacterium, and phages [44,45]. The rice ABA-independent gene OsERF48 directly binds to the promoter of OsCML16 via AP2/ERF cis-acting regulatory elements, thereby activating its transcription. Overexpression of OsERF48 causes regulation of OsCML16, a calmodulinlike protein gene that enhances root growth, drought tolerance, and grain yield and is involved in cell wall proteins, carbohydrate metabolism, and stress signaling in drought conditions in the field [46]. The rice OsERF71 gene is an AP2/ERF TF involved in an ABAindependent pathway controlling drought resistance by regulating cell wall modifications. After OsERF71 overexpression, roots are sufficient for drought resistance phenotypes and increase yield under drought stress [47]. The Arabidopsis shine (SHN) clade of the AP2 domain TFs activates wax biosynthesis and lipid biosynthetic pathways. Overexpression of each of the three SHN-1, -2, and -3 genes produced a phenotype similar to that of the first SHN mutant. SHN gene overexpression changed leaf and petal epidermal cell structure, trichome number and branching, and stomatal index. The SHN clade plays a role in plant protective layers; for example, those shaped during abscission, dehiscence, wounding, and diverse functions are mediated by regulating lipid or cell wall components [48] (Figure 2, Table 1). The OsERF922 gene was strongly induced in an ABA-signaling pathway after salt treatment and has been targeted successfully in rice. After overexpressing this gene, the ratio of Na + /K + in the shoots increased, and consequently, the tolerance to salt stress decreased. The cis-regulatory sequences of the OsERF922 gene's GCC box (AGCCGCC) function as negative regulators of salinity tolerance by providing binding sites for particular TFs. These cis-regulatory sequences could serve as a suitable target for creating nucleotide level mutations using recent genome editing tools that improve the tolerance to salinity stress in crops [49]. AP2/ERFs stand out among the essential TFs that regulate reactions, such as metabolism, stress, and improvement in plants. PsAP2 was isolated from a different AP2/ERF in Papaver somniferum, upregulated in response to methyl jasmonate, wounding by ethylene, and activation of ABA [43]. PsAP2 overexpression in transgenic tobacco plants showed increased tolerance to both abiotic and biotic stress [43]. ERF TFs are involved in regulating gene expression under biotic and abiotic stress. Transcription of the T. aestivum ethylene-responsive factor 1 (TaERF1) gene was induced not only by salinity, exogenous ABA, drought and low-temperature stress, salicylic acid, and ethylene, but also by infection with Blumeria graminis f. sp. tritici. Moreover, TaERF1 overexpression activated stress-related genes, including PR and COR/RD genes, under normal growth conditions and enhanced pathogen and abiotic stress resistance in transgenic plants [50] (Table 1). Furthermore, its overexpression in Arabidopsis caused more leaves and a greater leaf area and increased the primary root length [53]. The wheat TabHLH49 gene is drought stress-related bHLH TF that positively regulates the dehydrin WZY2 gene and improves drought tolerance in wheat [54]. The rice OsbHLH068 gene is a member of the bHLH TFs, Figure 2. Genes and signaling pathways that regulate drought stress tolerance. These pathways include the AP2/ERF, bHLH, bZIP, HD-Zip, MADS-box, MYB, NAC, WHIRLY, WRKY, and zinc finger. These regulators control drought stress tolerance through ABA-independent and -induced pathways, which play an essential role in ROS-scavenging pathways. They are positive regulators in the BR pathway, enable wax biosynthesis and stomatal development, and alter chlorophyll, MDA, POD, SOD, and CAT content. Different text colors represent different transcription factors.

bHLH
Basic helix-loop-helix (bHLH) TFs are involved in various developmental processes and respond to biotic and abiotic stress. Arabidopsis AtbHLH68 encodes a bHLH through ABA-dependent or -independent pathways and is highly expressed in the lateral root, during LR elongation, and in drought stress knock-out mutants, which have development phenotypes compared to the wild type. After overexpressing AtbHLH68, lateral root formation was defective, and the plant had a significantly increased tolerance to drought stress, which was likely related to its enhanced sensitivity to ABA and increased ABA content. AtbHLH68 functions to directly or indirectly regulate ABA signaling and metabolism components, likely through an ABA-dependent pathway [51]. Overexpression of the Tartary buckwheat (Fagopyrum tataricum) FtbHLH3 gene in Arabidopsis increased drought tolerance, which was attributed to lower MDA, ROS leakage, higher proline content, and photosynthetic efficiency. FtbHLH3 is an ABA-dependent pathway and is a positive regulator of drought stress tolerance in transgenic Arabidopsis [52]. The Populus euphratica PebHLH35 gene was induced by drought and ABA treatment. PebHLH35 is a positive regulator of drought stress responses, influencing growth, photosynthesis, stomatal aperture, and stomatal density.
Furthermore, its overexpression in Arabidopsis caused more leaves and a greater leaf area and increased the primary root length [53]. The wheat TabHLH49 gene is drought stress-related bHLH TF that positively regulates the dehydrin WZY2 gene and improves drought tolerance in wheat [54]. The rice OsbHLH068 gene is a member of the bHLH TFs, part of the ABA-dependent pathway, and delayed seed germination and late flowering. OsbHLH068 overexpression in Arabidopsis resulted in late flowering, delayed seed germination, decreased salt-induced H 2 O 2 accumulation, increased MDA, and promoted root elongation [55]. The rice OsbHLH035 bHLH TF is involved in germinating seeds and enabling the recovery of seedlings from salt stress through the ABA-dependent and ABA-independent pathways. After overexpression of the OsbHLH035 gene, seed germination was delayed, and the average growth of Arabidopsis seedlings recovered after salt stress [56] (Figure 3, Table 1). It is well reported that bHLH TFs play essential roles in gene regulation in many plant species under various abiotic stressors [57]. Arabidopsis AabHLH35, a bHLH gene, conferred cold and drought tolerance to A. andraeanum and might also help bring tolerance to various abiotic stressors in other ornamental species. AabHLH35 transgenic Arabidopsis plants better tolerated both cold and drought stress [57]. AtbHLH112 is a bHLH TF induced by abscisic acid, drought, and salt stress. Arabidopsis plants overexpressing AtbHLH112 had enhanced salt and drought tolerance, caused by various physiological modulations, including higher proline accumulation and enhanced antioxidant enzyme activities to curb ROS damage [58].
Similarly, in another study, salt and drought stress upregulated the AtbHLH112 gene, and their knockout mutant phenotype showed late flowering [55]. EcbHLH57 overexpressing tobacco plants exhibited improved tolerance levels to drought and salt stress. In response to drought stress, transgenic tobacco plants had improved photosynthesis capabilities and higher biomass accumulation. Similarly, EcbHLH57 overexpressing tobacco plants showed minor oxidative damage under salt stress, as lower MDA and H 2 O 2 levels were observed [59]. The apple (Malus Domestica) MdPIF3 gene is a bHLH TF that plays a critical role in plant growth and development during drought and cold stress. MdPIF3 overexpression reduced cold tolerance but enhanced drought resistance in apple callus and Arabidopsis [60]. MfbHLH38 is a bHLH gene and has shown a prominent role in improving drought and salt stress tolerance. MfbHLH38 transgenic Arabidopsis plants have a better water retention ability, osmotic balance, and less oxidative damage. The heterologous expression of MfbHLH38 in Arabidopsis exhibited better performance, which was observed as higher chlorophyll content, lower MDA level, improved antioxidant enzyme activity, and higher proline and soluble sugar content, under both salt and drought stress, thus enhancing their tolerance. Moreover, the water retention ability of MfbHLH38 transgenic plants has been greatly improved via stomatal closure due to a higher ABA content and biosynthesis-related gene expression (NCED3) under mannitol and ABA treatment [61].

HD-Zip
The wheat TaHDZipI-5 gene, encoding the HD-Zip I TF, was ABA-dependent and regulated the development of drought tolerance. Overexpression of the wheat TaHDZipI-5 gene improved frost and drought tolerance of transgenic wheat lines. Compared to wildtype (WT) plants, the transgenic wheat lines were short, had delayed flowering, and had decreased grain yield and biomass [77]. The rice OsTF1L gene is a crucial regulator of drought tolerance mechanisms, and after overexpression in plants, the drought-inducible stomatal movement was upregulated. Lignin biosynthetic genes revealed a superior drought tolerance at the reproductive growth phase with a higher grain yield than nontransgenic controls under field-drought conditions [78]. The physic nut JcHDZ07 gene belongs to the HD-Zip family of TFs and is a nuclear-localized protein essential for physiological indices and the necessary regulatory process of plant responses to salinity stress. JcHDZ07 overexpression in Arabidopsis enhanced the sensitivity of transgenic lines to salt stress.
In contrast, transgenic plants had higher relative electrical leakage and malonaldehyde content than wild-type plants under salinity stress conditions but reduced survival rates, proline content, catalase, and superoxide dismutase activity [79]. Homeodomainleucine zipper I (HD-Zip) is an essential family of TFs that play crucial roles in responding to various abiotic stressors. Zmhdz10 overexpression in rice plants caused better performance under drought and salt stress and a better tolerance level to these stressors. Similarly, Zmhdz10-overexpressing Arabidopsis plants also conferred salt and drought stress . Genes and signaling pathways that regulate salinity stress tolerance. These pathways include the bHLH, HD-Zip, MADS-box, MYB, WRKY, YABBY, and zinc finger. These regulators control salinity stress tolerance through ABAindependent, -responsive, and -mediated pathways, among others, playing an essential role in ROS, chlorophyll content, MDA, POD, SOD, CAT, UV radiation, and proline content. Different text colors represent different transcription factors.

bZIP
The Poncirus trifoliata ABF (PtrABF) was localized in the nucleus and revealed transactivation action in yeast cells bound to ABRE, supporting its role as a TF. Significant levels of PtrABF have been stimulated by ABA, low temperature, and dehydration treatments. PtrABF overexpression enhanced drought tolerance and dehydration in tobacco by scavenging ROS and modifying the expression of stress-responsive genes [62]. ABF3, AREB2, and AREB1 are excellent TFs that cooperate to complete ABRE-dependent ABA-signaling pathways for drought stress tolerance [63]. OsbZIP72 plays a decisive role in drought resistance through ABA signaling and may help with drought tolerance in rice. OsbZIP72 is a critical regulator in abiotic stress reactions and ABA signaling transduction pathways [64] ( Figure 2, Table 1). A subcellular limitation investigation showed that TabZIP60 is an atomic restricted protein that initiates TFs. The TabZIP60 gene is strongly encouraged by treatments with exogenous ABA, salt, polyethylene glycol, and cold. In Arabidopsis, TabZIP60 gene overexpression fundamentally enhanced resistance to salt and drought stress and expanded plant affectability to ABA in seedling development [65]. The OsABF2 gene is a constructive controller of ABA signaling and abiotic stress in rice [66]. OsABF2 has been linked to ABREs (Figure 3), and the homozygous T-DNA insertion mutant of OsABF2 was susceptible to drought, salinity, and oxidative stress relative to wild-type plants. OsABF2 functions as a transcription regulator that controls responsive gene expression with abiotic stress through the ABA-dependent pathway [66]. OsbZIP71 encodes a rice bZIP TF; it is an atomic-limited protein linked to the G-box theme but has no transcriptional movement in yeast or rice protoplasts [67]. OsbZIP71, a bZIP translation factor, may play a vital role in rice ABA-independent drought and salt tolerance [48]. TF OsbZIP46 directs ABA signaling-mediated drought tolerance in rice by regulating pressure-related genes [68]. ABA and drought pressure activated the OsbZIP46-interfacing protein MODD (mediator of OsbZIP46 deactivation and stress), also known as the Arabidopsis thaliana ABSCISIC ACID-INSENSITIVE5 restricting protein AFP; however, the induction was much slower.
OsbZIP23 is a member of the bZIP TFs. Expression of the OsbZIP23 gene can cause an adverse effect on stress, including ABA, salt, and drought, while other stress-responsive genes of this family are slightly induced only by one or two of these stressors [69]. OsABI5 is involved in bZIP TFs and was isolated from Oryza sativa L. ( Table 1). Expression of the OsABI5 gene was initiated by high salinity and ABA and downregulated by cold and drought in seedlings. Overexpression of the OsABI5 gene in rice conserved high sensitivity to salt stress, and OsABI5 repression enhanced drought stress tolerance and resulted in low rice fertility [70] (Table 1).

DREB
Dehydration-responsive element binding genes (DREBs) are essential plant TFs that control the expression of numerous stress-inducible genes, usually in an ABA-independent manner, and perform a critical role in improving drought and salinity stress tolerance in plants by interacting with a DRE/CRT cis-element present in the promoter region of various genes [71]. AtDREB1A overexpression in rice, wheat, groundnut, and tobacco improved drought tolerance and increased the expression of late embryogenic abundant (LEA) genes under greenhouse temperatures [72]. Three DREB homologous genes-GmDREBa, GmDREBb, and GmDREBc-were isolated from soybean; transcription of GmDREBa and GmDREBb caused drought, salt, and cold stress in the leaves of soybean seedlings ( Table 1). Expression of the GmDREBc gene was not significantly affected in leaves but prompted by ABA treatment and drought and salt stress [73]. Transgenic Arabidopsis plants with DREB1 or DREB2 had improved tolerance to various abiotic stressors, including drought, salt, and freezing [74]. The dehydration responsive element binding (DREB) TF is involved in the plant stress signal transduction pathway. SbDREB2A improved abiotic stress tolerance in Escherichia coli; this gene is an A-2 type DREB transferred from the halophyte Salicornia brachiate, and its appearance was encouraged by heat stress, NaCl, and drought [75]. CBF/DREB1 TFs regulate cool acclimation reactions, and COR TFs (cold-regulated) control gene expression levels, thereby encouraging tolerance to freezing. Thus, changes in CBF/DREB1 genes have enabled many plants to resist environmental stress, mainly freezing [74].

GATA
The GATA gene family is one of the most conserved families of TFs, playing a significant role in different aspects of cellular processes, and their members vary in their expression with a different response to exogenous ABA, drought, and salinity stress. In rice, the OsGATA23a gene is a multi-stress responsive TF that increased expression levels under salinity and drought stress. ABA also induced the expression of OsGATA23a in different rice varieties [11]. Similarly, the rice OsGATA16 gene expressed in guard cells and all other plant tissues was induced by ABA treatment but suppressed by drought, cytokinin, and jasmonic acid treatments [76].

HD-Zip
The wheat TaHDZipI-5 gene, encoding the HD-Zip I TF, was ABA-dependent and regulated the development of drought tolerance. Overexpression of the wheat TaHDZipI-5 gene improved frost and drought tolerance of transgenic wheat lines. Compared to wild-type (WT) plants, the transgenic wheat lines were short, had delayed flowering, and had decreased grain yield and biomass [77]. The rice OsTF1L gene is a crucial regulator of drought tolerance mechanisms, and after overexpression in plants, the drought-inducible stomatal movement was upregulated. Lignin biosynthetic genes revealed a superior drought tolerance at the reproductive growth phase with a higher grain yield than non-transgenic controls under field-drought conditions [78]. The physic nut JcHDZ07 gene belongs to the HD-Zip family of TFs and is a nuclear-localized protein essential for physiological indices and the necessary regulatory process of plant responses to salinity stress. JcHDZ07 overexpression in Arabidopsis enhanced the sensitivity of transgenic lines to salt stress.
In contrast, transgenic plants had higher relative electrical leakage and malonaldehyde content than wild-type plants under salinity stress conditions but reduced survival rates, proline content, catalase, and superoxide dismutase activity [79]. Homeodomain-leucine zipper I (HD-Zip) is an essential family of TFs that play crucial roles in responding to various abiotic stressors. Zmhdz10 overexpression in rice plants caused better performance under drought and salt stress and a better tolerance level to these stressors. Similarly, Zmhdz10-overexpressing Arabidopsis plants also conferred salt and drought stress tolerance via differential expression of ABA and stress-responsive gene expression, including P5CS1, RD22, RD29B, and ABI1. Zmhdz10, a transcriptional regulator, activated the ABAdependent pathway under drought and salinity stress, thus bringing tolerance to these stressors [10]. Medicago truncatula MtHB2 encodes a novel stress-responsive HD TF that negatively regulates abiotic stress response mechanisms. In Arabidopsis, transgenic plants expressing MtHB2 were more sensitive to drought, salt, and freezing stress, had fewer pro and soluble sugars, and had significantly higher MDA and H 2 O 2 contents than wild-type plants [9]. The rice Oshox4 gene belongs to the HD-Zip I family, and its overexpression in transgenic lines increased tolerance to drought and salinity stress. The Oshox4 gene plays an essential role in rice osmatic tolerance and higher yield [80]. Gshdz4 is an HD-Zip TF in soybean that plays a responsive role in bicarbonate stress and enhances drought and salinity stress tolerance. Gshdz4 overexpression in Arabidopsis improved transgenic plants' tolerance to bicarbonate stress via reduced chlorophyll degradation, while their performance was poor under osmotic stress [81]. The Arabidopsis ATHB17 HD-Zip TF regulated the expression of several photosynthesis-associated nuclear genes involved in the light reaction and ATSIG5 in response to abiotic stress. ATHB17 was responsive to ABA and multiple stress treatments and positively modulated the expression of many plastid-encoded genes through the regulation of ATSIG5. ATHB17-overexpressing plants displayed enhanced stress tolerance, whereas its knockout mutant was more sensitive than the wild-type and played an essential role in protecting plants by adjusting the expression of PhANGs and PEGs in response to abiotic stress [12].

Homeobox
Homeobox TFs are well-known regulators of plant growth and development [82]. Two stress-responsive homeobox candidate genes, OsHOX22 and OsHOX24, were upregulated under different abiotic stress conditions at various rice growth phases [82]. These gene transcription stages improved in the presence of phytohormones (ABA, auxin, salicylic acid, and gibberellin). OsHOX24 overexpression affected ABA, abiotic stress, and stress hormones in transgenic Arabidopsis [82]. Many of these genes are engaged in transcriptional control and metabolic pathways, which play the role of homeobox proteins as adverse regulators in abiotic stress response [82].

MADS-Box
The MADS-box family of TFs are critical regulators of plants and are involved in many biological processes [83]. The Solanum lycopersicum agamous-like MADS-box protein AGL15-like gene, SlMBP11, is a TF that enhances salt stress tolerance, perhaps through an ABA-independent signaling network, and may have applications in the manufacturing of salt-tolerant tomato. SlMBP11 plays an active role as a stress-responsive TF in the positive regulation of salt stress tolerance utilizing an ABA-independent signaling network and may have significant applications in salt-tolerant tomato design [83]. Overexpression of the rice OsMADS25 gene in Arabidopsis enhanced salinity tolerance compared to the wild type. The MADS-box transcription factor OsMADS25 belongs to the ANR1 clade induced by NO 3− and plays a crucial role in rice root development [84]. MADS-box TFs are involved in stress reactions. The SlMBP8 gene containing a MADS-box factor has been cloned from tomato after being expressed in the presence of high salinity, methyl-jasmonic acid, temperature, dehydration, and wounding [85]. SlMBP8 was downregulated by indole-3acidic acid (IAA), 1-aminocyclopropane-1-carboxylic acid (ACC), and ABA. SlMBP8 acts as a negative stress-responsive TF in high-salinity and drought stress signaling pathways and may have important applications in the engineering of salt and drought-tolerant tomato [85] (Figure 4, Table 1).

MYB
Arabidopsis AtMYB60 is an R2R3-MYB gene expressed in guard cells that is negatively modulated during drought and involved in regulating stomatal movements. The mutant with a T-DNA insertion of ATMYB60 showed a reduction in the stomatal opening,

MYB
Arabidopsis AtMYB60 is an R2R3-MYB gene expressed in guard cells that is negatively modulated during drought and involved in regulating stomatal movements. The mutant with a T-DNA insertion of ATMYB60 showed a reduction in the stomatal opening, and the mutation's effects on water loss and transpiration rate during drought stress [86]. Constructive expression of the rice cold-inducible OsMYB4 gene in transgenic Arabidopsis plants increased under drought and cold stress and was likely due to the constitutive activation of several stress-inducible pathways. OsMYB4 gene expression enhanced the stress response in apples [87]. The GmMYB84 TF from soybean, induced by drought, salt, and ABA, plays a crucial role in ROS homeostasis and control of the abiotic stress response in plants [88]. GmMYB84 overexpression in soybean enhanced drought stress resistance by increasing the ROS and antioxidant enzyme content, including SOD, POD, and CAT.
Moreover, overexpression led to improved primary growth, high survival rates, and reduced dehydration under drought stress [88]. OSMYB55 overexpression in maize shows increased plant biomass and reduced leaf damage caused by high-temperature exposure, likely due to increased stress-responsive gene expression [89]. Moreover, it shows reduced initial leaf damage when the chlorophyll content decreases slightly, probably associated with OsMYB55-mediated stress tolerance [89]. Similarly, GaMYB62L expression in Arabidopsis produced improved drought resistance feedback [90]. GaMYB85 also encouraged drought tolerance in transgenic Arabidopsis by increasing chlorophyll and free proline material with relatively higher water content [91].
A fascinating novel TF of Arabidopsis, AtMYBL, had two estimated DNA-binding domains. The physiological role of R-R-type MYB TFs is unknown in plants [92]. The Arabidopsis AtMYBL gene promotes leaf senescence and decreases salt tolerance compared to wild-type and ATMYBL RNA interference lines during subsequent seed growth when subsequent seed growth high-density plants were under stress. ATMBL regulates stress sensitivity in protein development [92]. Campos et al. [93] described a salt-sensitive ars1 mutant phenotype from a single T-DNA insertion in the ARS1 gene, encoding the R1-MYB TF in tomatoes. The T-DNA insertion ars1 mutant accumulated high Na + in the leaves, accompanied by reduced stomatal conductance and limited transpiration rate, confirming the role of the ARS1 gene in stomatal movement under salt stress. The sweet cherry PacMYBA gene is generally localized to the nucleus and might be induced by ABA. After overexpression of this gene, transgenic Arabidopsis decreased osmotic capability and increased the peroxidase and proline content in response to salt stress [94].
Moreover, GmMYB12B2 was not induced by the ABA and drought stress response. However, its expression in Arabidopsis caused tolerance to salt stress [95]. Similarly, the MYB TF isolated from wheat had a role in mediating abiotic stress responses. In addition, more recently, TaSIM gene overexpression in wheat induced significantly longer roots and further increased the expression level of ABA-dependent (RD22) and ABA-independent (RD29A) signaling [96]. This TF is associated with the regulatory system in response to biotic and abiotic stress in plants. The R2R3-MYB factor in L. purpureus has also been recognized [97]. LpMYB1 overexpression in Arabidopsis improved the regeneration of gene transference to drought and salt stress and the capability of genetically modified seedlings in NaCl or ABA. LpMYB1 is a drought-dependent R2R3-MYB factor that builds salt and drought tolerance in Arabidopsis [97]. MYB genes, especially MdoMYB121, are enhanced by many stressors. MdoMYB121 overexpression improved resistance to high salinity, cold stress, and drought in apple plants and transgenic tomatoes. MdoMYB121 can be used as a target gene in genetic engineering to recover plant tolerance to different abiotic stressors [98]. As a stress protein kinase, the surface protein of MPK3, the Arabidopsis TF, is involved in re-programming pre-stressed MYB44. MYB44 is classified as a phosphorylationbased positive controller of salt stress signaling. MYB44 conveys a putative transcriptional repression motif. Overexpression of an MYB44-REP combination traded salt and drought tolerance [99]. MYB-type proteins take part in various stress responses. The TaMYB19 gene encodes an R2R3-type MYB protein activated by multiple abiotic stressors in wheat.
The expression patterns of TaMYB19-A, TaMYB19-B, and TaMYB19-D were comparable under various stress conditions. The TaMYB19 protein has an essential role in plant stress tolerance, and adjusting the outflow of this protein may enhance abiotic resilience in crop plants [100]. Plant MYB interpretation factors control various natural processes, for example, separation, improvement, and abiotic stress response.
BplMYB46, an MYB gene from Betula platyphylla (birch), is associated with abiotic stress and auxiliary divider biosynthesis. BplMYB46 enhances salt and osmotic resilience by influencing gene expression, including SOD, POD, and P5CS, to increase reactive oxygen species scavenging and proline. Additionally, BplMYB46 may help control stomatal openings to diminish water loss [101]. Transgenic BplMYB46-overexpressing birch plants showed enhanced salt and osmotic pressure resistance, higher lignin cellulose content, and lower hemicellulose content than the control their potential application in the forestry industry [101] (Table 1). OsMYB511 is a TF in rice that controls abiotic stress responses and has been activated by exogenous ABA, high temperature, and osmotic pressure. Expression analysis of the OsMYB511 gene showed high expression at an earlier development stage in rice panicles [102]. A co-articulation investigation uncovered an extra two MYB qualities co-communicated with OsMYB511, suggesting that they coordinate direct pressure reactions in rice [102]. OsMYB3R-2 works in both stress and developmental procedures in rice. Transgenic plants overexpressing OsMYB3R-2 showed improved cold resistance. The cold treatment initiated the outflow of OsMYB3R-2, which encodes a functioning translation factor, and was bound to a mitosis-particular activator cis-component [103].
GmMYB118 is a soybean gene located in the nucleus that improves tolerance to drought and salt stress by reducing ROS and MDA content and regulates the expression of several stress-associated genes in transgenic Arabidopsis plants. After CRISPR, the GmMYB118 gene may improve salt stress tolerance in transgenic plants because CRISPR transformed plants displayed reduced drought and salt tolerance compared to control plants [104]. In barley (Hordeum vulgare L.), transcripts of HvMYB1 are upregulated by drought stress in leaves and roots and acting as a mediator of ABA action. Transgenic barley plants that overexpress HvMYB1 enhanced relative water content and reduced water loss rate, stomatal conductance, and ROS accumulation by constitutively higher ROS scavengers as APX and GPX under drought stress [105].

NAC
The rice gene OsNAC006 is located in the nucleus, and the knock-out of this gene using the CRISPR-Cas9 system is essential for drought resistance. It is regulated by H 2 O 2 , ABA, heat, cold, and drought treatment. The knockout of OsNAC006 caused enhanced sensitivity to drought and heat tolerance in rice, which lowered chlorophyll levels, reduced SOD and POD enzyme activities, and increased MDA content [106]. In addition, under the influence of a predominantly root-expressed promoter, TaRNAC1 improved dehydration resistance, yielding higher biomass, grain production, and root length [107]. TaRNAC1 is a constitutively and pre-dominantly root-expressed NAC TF. TaRNAC1 overexpression in wheat roots conferred increased root length and biomass, drought tolerance, and improved grain yield under water limitation [107]. MfNACsa, a Medicago falcata lipid-anchored NAC gene, positively regulates plant drought stress resistance by differential expression of oxidation-related, lipid-transported, and localization-related genes [108]. In transgenic tobacco, SlNAC35 is a protein used to control biotic and abiotic stress resistance. Expression of the SlNAC35 gene is prompted by salt stress, drought stress, signaling molecules, and bacterial pathogens, suggesting its participation in plant responses to biotic and abiotic stimuli [109]. After overexpression of the SlNAC35 gene, advanced root development occurs under drought and salt stress [109]. ABA and osmotic stressors, such as drought and high salt, promoted OsNAC2, an individual from the NAC translation factor family. OsNAC2 overexpression reduced high salt and drought tolerance [110]. A microarray showed that numerous ABA-subordinate pressure-related qualities were downregulated in OsNAC2 overexpression lines. OsNAC2 directs both abiotic stress reactions and ABA-intervened rice reactions and acts at the intersection between ABA and abiotic stress pathways [110]. NAC proteins are the most significant TFs, and NAC proteins contribute to abiotic stress and plant development regulation. Overexpression of TsNAC1, cloned from the halophyte Thellungiella halophila, enhanced abiotic stress resistance, particularly salt stress, in T. halophila and Arabidopsis thaliana and delayed plant development [111]. The TsNAC1 gene is a crucial TF in abiotic stress resistance and growth [111]. GmNAC5 is a member of the NAM subfamily and is involved in controlling the shoot apical meristem, hormone signaling, and stress responses in soybean [94]. In addition, GmNAC5 is stimulated by mechanical wounding and high salt and cold treatments but is not activated by ABA [112]. RsNACs involving layer-bound individuals have been recognized in the radish genome. The RsNAC023 and RsNAC080 genes reacted to all stressors, except ABA; however, RsNAC145 reacted more to heat, salt, and drought. NAC is a strong candidate gene for upcoming studies on improving abiotic stress tolerance in radish [113]. Overexpression of ANAC069 induced a lower proline content and ROS targeting ability, resulting in enhanced salt and osmotic stress tolerance [114]. After binding to C[A/G]CG[T/G] sequences in the ANAC069 gene promoter in Arabidopsis, the improvement of proline biosynthesis (P5CS) and antioxidant (POD, SOD, and GST) genes under salt stress was observed [96]. The rice ONAC022 gene was localized in the nucleus, modulating an ABA-mediated pathway, and a higher survival ratio and less Na + accumulation were observed in roots and shoots in response to drought and salt stress [115].

Trihelix
One of the leading trihelix TF families is the trihelix family TF, also known as the GT factor. Tea (Camellia sinensis) genes CsGT1-3 and CsGT2-1 belong to the trihelix TFs, which are highly expressed under various abiotic stressors. Salt stress increased the expression of CsGT1-3 and CsGT2-1 genes [116]. The soybean GmGT-2A and GmGT-2B genes are ABA-sensitive trihelix TFs; they increased plant tolerance to abiotic stress when expressed in Arabidopsis [117]. The overexpression of GmGT-2A and GmGT-2B enhanced resistance to freezing, drought, and salt stress in transgenic Arabidopsis [117]. The trihelix family genes are involved in light and other developmental processes, but their characteristics are generally unclear. The BnSIP1-1 protein is focused on the nucleus. Overexpression of BnSIP1-1 enhanced seed germination when exposed to osmotic stress, ABA, and salt. BnSIP1-1 is likely involved in ABA signaling and synthesis and osmotic and salt stress responses [118]. A rice OsGTγ family member, OsGTγ-2, directly interacted with the GT-1 element in the OsRAV2 promoter. OsGTγ-2 specifically targeted the nucleus and was mainly expressed in roots, sheaths, stems, and seeds, and it was induced by salinity, osmotic and oxidative stresses, and ABA [119]. Arabidopsis thaliana AtGT2L and rice OsGTγ-1 were induced by salt, drought, cold stress, and ABA treatment [120]. The function of AST1 was characterized in response to salt and osmotic stress and showed transcriptional activation activity; its expression was induced by osmotic and salt stress [121].

WHIRLY
WHIRLY is a TF family involved in biotic and abiotic stress responses, but its biological function remains unclear. SlWHY2, an individual from the WHIRLY family, was isolated from tomatoes [122]. Overexpression of the SlWHY2 gene in tobacco improved drought stress tolerance, controlled mitochondrial gene transcription, and balanced mitochondrial metabolism. The SlWHY2 gene is a positive controller for plants exposed to biotic and abiotic stress [122].

WOX
WOX (WUSCHEL-related homeobox) is a plant TF linked to plant development and stress responses. The paper mulberry BpWUS gene is an ABA-responsive gene associated with the stem, root, and apical bud. BpWOX5 and BpWOX7 controlled the root tip, and three BpWOXs controlled leaf enlargement [123]. BpWOX9 and BpWOX10 were promoted by indole-3-acidic (IAA) or jasmonic (JA), while five phytohormones repressed BpWOX2. Most BpWOX genes were receptive to drought, salt, cold, and cadmium (CdCl 2 ) [123]. The rice WOX13 gene belongs to the WOX subfamily of TFs and is ABA-responsive, essential for flower improvement, contains proteins, and is involved in drought and salinity stress. OsWOX13 was involved in the regulation of vegetative organs, flowers, and seeds. OsWOX13 caused early flowering and stress responses. OsWOX13 overexpression resulted in early flowering and showed an extensive spectrum of effects on biological processes, such as abiotic and biotic stress, after drought and salinity stress [124].
2.14. WRKY WRKY46, WRKY54, and WRKY70 are three WRKY TFs in Arabidopsis that are correlated with drought response and BR-mediated plant development. The mutants of wrky46, wrky54, and wrky70 had altered plant development, controlled drought, and promoted BR-mediating gene expression and drought response genes in RNA sequencing analysis [125]. Sun et al. [126] found that the activated expression of the group III member protein AtWRKY53 modulated stomatal movement, improving starch metabolism and functioning as osmoregulation by decreasing H 2 O 2 content, contributing negatively to controlling dehydration tolerance. Likewise, in rice, OsWRKY47 imparted drought stress tolerance [127]. OsWRKY47 expression was caused by drought stress in plants, and their mutants showed higher susceptibility to drought and decreased yield, whereas OsWRKY47 plants were more tolerant [127]. Expression of the Glycine soja GsWRKY20 gene improved drought tolerance and modified ABA signaling. After GsWRKY20 overexpression in Arabidopsis, plants had reduced sensitivity to ABA, stomatal closure during seed germination, and early seedling growth, exhibiting a greater tolerance to drought stress [128]. Past microarray investigations of Arabidopsis roots recognized two WRKY TFs (WRKY25 and WRKY33) among the transcripts that expanded NaCl treatment. WRKY33 is not flexible in any situation affecting WRKY25 null mutants' stress, indicating functional redundancy with null mutants and two-fold mutants and promoting NaCl sensitivity. When WRKY25 or WRKY33 were overexpressed in Arabidopsis, plants had NaCl tolerance [129]. Likewise, in cotton, the GhWRKY6 gene was observed to target ROS and stimulate the ABA signaling pathways, consequently improving salt tolerance in Arabidopsis.
In contrast, GhWRKY6 gene silencing by virus-induced gene silencing (VIGS) in cotton improved susceptibility to abiotic stress [130]. In addition, a recent study found that SlWRKY3 protein overexpression encouraged physiological indices correlated with photosynthesis, increased leaf aggregation of K + and Ca 2+ , and decreased sodium and proline content [131]. WRKY TFs are linked with biotic and abiotic stress in plant reactions. Arabidopsis TFs WRKY18, WRKY40, and WRKY60 cooperate functionally and physically in plant resistance responses [132]. The three WRKY genes are associated with plant reactions to ABA and abiotic stress. Overexpression of distinctive mutants for WRKY genes showed that WRKY18 and WRKY60 positively affected plant ABA to restrict seed germination and root development [132]. WRKY18 and WRKY60 genes were affected by abiotic stress in germination, plant sensitivity to ABA, and growth assays. WRKY18 and WRKY40 were quickly induced after ABA treatment, whereas WRKY60 was not rapidly induced [113].
Furthermore, the maize ZmWRKY17 gene in Arabidopsis decreased ABA sensitivity, as shown by healthy green cotyledons and longer roots in response to exogenous ABA application, and increased plant sensitivity to salinity stress [133]. GhWRKY41 [134] and GhWRKY68 are two other cotton WRKY genes that positively regulate salt and drought stress resistance by affecting physiological indices, including stomatal closer and ROS accumulation in transgenic Nicotiana benthamiana [135]. MtWRKY76 induced abiotic stressresponsive genes associated with the ASR protein in M. truncatula, resulting in increased drought and salt tolerance [136]. Genetic research in soybean revealed that GmWRKY27 improves salt and drought tolerance, which was confirmed by the proline and ROS content [137]. The sweet potato IbWRKY2 gene was found in the nucleus, and NaCl and ABA induced its expression. In addition, Arabidopsis overexpressing IbWRKY2 demonstrated improved drought and salt tolerance. The content of ABA and proline and the activity of SOD were higher in transgenic plants after drought and salt treatments, while the contents of MDA and H 2 O 2 were lower [138]. Similarly, ZmWRKY58 also played an essential role in response to drought and salt stress in rice. Overexpression of ZmWRKY58 in rice resulted in delayed germination and inhibited post-germination development [139]. In tomato (Solanum lycopersicum), SlWRKY8 protein was localized to the nucleus, and a positive regulator in plant immunity against pathogen infection and plant response to drought and salt stresses through ABA-dependent and ABA-independent pathways. Overexpression of SlWRKY8 promoted the activities of ROS-scavenging enzymes and proline contents [140]. In tomatoes, the transcript of SlWRKY81 is involved in the regulation of ABA-mediated and acts as a negative regulator for drought tolerance by modulating stomatal movement. Overexpression of SlWRKY81 enhances tomato tolerance to drought and promotes ABA content, stomatal closure, and accumulation of H 2 O 2 in the guard cells [141]. Similarly, Ahammed et al. [142,143] reported that the SlWRKY81 TF inhibits stomatal closure by reducing nitric oxide accumulation in the guard cells and is closely associated with an increased proline content in tomato leaves compared with non-silenced plants of tomatoes under drought.

YABBY
YABBY plays a vital monitoring role in lateral organ development. The pineapple AcYABBY gene, after overexpression in Arabidopsis, displayed a small root under NaCl treatment, representing the adverse effect of AcYABBY4 on plant resistance to salt stress [144]. GmYABBY10 might be a negative regulator of plant tolerance to drought and salt stress. The GmYABBY10 protein was mainly localized in the membranes and cytoplasm, which are more sensitive to drought, salt, and ABA stress. GmYABBY10 played an essential role in drought and salt resistance in Arabidopsis, and wild-type seeds had higher than GmYABBY10 transgenic seeds under both PEG and NaCl treatment. Simultaneously, wild-type seedlings' root length and root surface were more extensive than GmYABBY10 transgenic seedlings [145].

Zinc Finger
The Chrysanthemum morifolium BBX24 gene encoding a zinc finger TF was mainly associated with flowering time and stress tolerance. Transgenic lines with suppressed expression of Cm-BBX24 (Cm-BBX24-RNAi) showed early flowering compared to wild-type plants and exhibited decreased tolerance to drought and freezing stress in chrysanthemum, in part, by influencing GA biosynthesis [146]. The gene from the CCCHZF rice family, OsC3H10, primarily expressed in plants, consequently causes a rapid decline during seed imbibition; moreover, the expression of OsC3H10 was induced by drought high salinity and ABA [147]. OsC3H10 regulated drought resistance by modulating stress-related gene expression involving various drought-tolerant pathways. However, root-specific overexpression of OsC3H10 was inadequate to cause drought tolerance, whereas the plant overall had increased drought tolerance [147]. Overexpression of the zinc finger protein ZAT18, expressed in the roots, silica, and rosette plants, resulted in drought tolerance in Arabidopsis, with more minor leaf water losses, lower ROS quality, higher leaf water content, and higher antioxidant enzyme activity after drought treatment relative to the wild-type [148] (Figure 2, Table 1). Several genes of zinc finger proteins are involved in playing essential roles in salt stress. The Zoysia japonica ZjZFN1 gene is a zinc finger TF that plays a critical role in improved seed germination and enhanced plant salt tolerance in Arabidopsis. Plant variation also improved with salinity stress with improved green cotyledons and growth status under salinity stress. ZjZFN1-overexpressing plants revealed that ZjZFN1 might be a transcriptional activator of changeable stress-responsive pathways, including α-linolenic acid metabolism, phenylalanine metabolism, and phenylpropanoid biosynthesis pathways [149]. The bread wheat TaCHP gene belongs to the zinc finger family, which is essentially expressed in the roots of seedlings at the three-leaf stage. CHP was reduced by the imposition of salinity or drought stress and the exogenous supply of ABA [150] (Figure 3, Table 1). Using CRISPR-Cas9 mediated genome editing in rice (OsDST), the DST gene increased drought and salinity stress tolerance and improved crop production. The DST mutant was first produced in rice, and stomatal density was associated with reducing stomatal development genes in the DST mutant [151] (Figure 4, Table 1).

Other
AITRs, as a family of novel TFs, play a role in regulating plant responses to ABA, drought, and salinity stress. Using CRISPR/Cas9 to target six AITR genes (aitr123456) reduced sensitivity to ABA and enhanced tolerance to drought and salinity in the Arabidopsis mutant, but plant growth, development, and response to pathogen infection remained unaffected in the mutants [152].

Conclusions and Future Research Priorities
Plants cannot escape environmental pressures due to their sessile existence, but they have developed strategies to counteract the adverse effects of stress. Plant endogenous development programs, for example, use physiological and metabolic modifications to help plants cope with unfavorable environmental factors, including salinity and drought. Plant production and productivity may be negatively impacted by the failure to respond to adverse environmental factors, resulting in a substantial reduction in yield. This review covered the current knowledge on drought and salt stress genes and focused on the various TFs involved in drought and salt stress, showing the apparent link with ABAdependent and -independent pathways. Tremendous improvements have been made to understand the molecular mechanisms controlling drought and salinity stress tolerance in recent years. Several regulatory pathways have been identified for drought and salinity tolerance in different plants (apple, Arabidopsis, chrysanthemum, finger millet, maize, pineapple, rapeseed, rice, soybean, tea, tomato, and wheat) using genetic engineering and CRISPR/Cas9 for genome editing.
Similar to Hussain et al. [42], we revealed complex genetic regulatory networks ( Figure 5) based on examining current drought and salinity stress tolerance knowledge in Arabidopsis and other plant species. Several genetic and signaling pathways that determine drought and salinity stress tolerance are well known, including AP2/ERF, bHLH, bZIP, DREB, GATA, HD-Zip, Homeo-box, MADS-box, MYB, NAC, Tri-helix, WHIRLY, WOX, WRKY, YABBY, and zinc finger (Table 1). Interestingly, many of these genes have a conserved function in drought and salinity stress, and their pathways are ABA-dependent, -independent, -induced, -responsive, -mediated, and -sensitive. In addition, many of these genes have similar functions in drought and salinity stress, which belong to ABAdependent, -independent, -inducible, -responsive, and -sensitive pathways that regulate the cell and ROS scavenging. Their TFs are bHLH, bZIP, Homeo-box, DREB, MYB, NAC, HD-Zip, MADS-box, WOX, and WRKY. More importantly, many of the drought and salinity stress-responsive genes have expression activity and additional effects on other organs, such as flowering time (Cm-BBX24) and yield (OsCML16, OsERF71, TaHDZipI-5, OsTF1L, and Oshox4), indicating a cooperative regulation. These results strongly suggest the conserved function of these genes in regulating drought and salinity stress tolerance among different plant species. They can be targeted for the molecular improvement of drought, and salinity stress tolerance through genetic engineering and genome editing approaches, such as CRISPR/Cas.  Figure 5. Genetic regulatory network constructed for drought and salinity tolerance genes. The figure shows different interactions, such as gene neighborhood, fusions, co-occurrence, text mining, co-expression, and protein homology. For example, green represents the gene neighborhood, red represents gene fusion, blue represents gene co-occurrence, yellow represents text mining, and black represents co-expression.

Figure 5.
Genetic regulatory network constructed for drought and salinity tolerance genes. The figure shows different interactions, such as gene neighborhood, fusions, co-occurrence, text mining, co-expression, and protein homology. For example, green represents the gene neighborhood, red represents gene fusion, blue represents gene co-occurrence, yellow represents text mining, and black represents co-expression.
Most importantly, with these approaches to TFs, the future development of droughtand salinity-resistant plants with improved yields and reduced off-target effects will become a reality. In the future, a combination of modern biotechnologies, such as microarray, proteomic genome editing, genomics, genome-wide association, -omics, and bioinformatics, will accelerate the identification of the regulators of drought and salinity stress responses and different genes and signaling pathways. In conclusion, it is necessary to collaborate to convey this science-based benefit to farmers to deliver a food supply adequate to eliminate world hunger. The link between transcription and phytohormones was further identified, as well as their signaling pathways. Candidate genes that regulate and target different phytohormones can consequently mitigate drought and salinity stress. Tolerance to these stressors in crop breeding is mainly unknown.