Cotton (Gossypium spp.) is a member of the Malvaceae family's Gossypium genus, which includes over 50 species, only four of which are farmed (Gossypium arboreum, Gossypium herbaceum, Gossypium hirsutum, and Gossypium barbadense) [1]. The first two species are diploid (2n = 2x = 26) and are thought to have shared an ancestor. After that, the diploid cotton species were divided into eight groups, A-G and K. Both of the latter two species are tetraploid (2n = 4x = 52). Polyploidization between A-genome and D-genome cotton species produces all tetraploid cotton species [2]. The A-genome species have undergone a long period of artificial selection for their high-quality staple fibers, while the D-genome species, under natural selection, have retained great genetic diversity and a variety of desirable traits such as fiber quality and salt resistance [2,3].

Cotton is a globally important cash crop that produces raw cotton lint for the textile industry, cottonseed oil for culinary use, and edible and protein-rich oil cake wastes for livestock, as well as benefiting humans through its sticks, fiber, seeds, and oil as a key product [4].

Cotton production is influenced by weather conditions. High humidity from rain or irrigation, as well as dry and warm harvest seasons produce the highest yield [5]. Cotton is farmed as a principal crop in more than 100 countries, with large proportions in China (6,423,000 tons), India (6,162,000 tons), the United States (3,181,000 tons), and Brazil (2,341,000 tons), and Pakistan (980,000 tons) due to its monetary importance. Cotton is usually grown in moderately hot climates [6].

Cotton production, on the other hand, is hampered by several reasons, including inadequate environmental conditions (abiotic stresses) and biotic stresses, both of which have been linked to yield declines [7]. Drought is the most significant abiotic limitation, limiting photosynthesis, glucose metabolism, and the activity of key enzymes involved in fiber production [8]. Salinity, on the other hand, is a severe concern for agriculture since it depletes farmland. More than 6% of the world's land (830 million hectares impacted by salinity, 403 million hectares) is affected by salt water, with the rest affected by linked factors like sodicity [9]. Even though cotton is a salt-tolerant plant, its salt level can have a major negative influence on its development and productivity [10]. Cotton types and hybrids are more susceptible to insect pests such as jassids (leafhoppers), whiteflies, and bollworms, as well as diseases such as bacterial blight, and verticillium wilt, and leaf curl virus [2].

Plants deploy several internal mechanisms to deal with pathogens during the growth and development process to battle such situations, and it is vital to understand the mechanisms that plants use to deal with varied stresses at the genetic level. Abiotic and biotic stress activates a network of plant gene expression mechanisms, which causes the stress response to reprogramme several physiological and metabolic processes [7,11]. Changes in the expression of stress genes govern these defensive systems, according to the findings of numerous studies. Many of these stress genes are known to be transcriptionally controlled [12].

Transcriptome profiling identified some stress-responsive genes that were successfully transferred to other plants and were up-or down-regulated in cotton. Single or multiple pressures substantially activate transcription factors, and transcription factors play a key role in the response to biotic and abiotic stresses [9]. MYB (myeloblastosis), MADS (minichromosome maintenance agamous deficiens serum response factor), ARF (auxin response factors), EREBP (ethylene-responsive element-binding protein), DRE (drought-responsive element), HB (Homeobox), SBP (squamosa promoter binding protein), bZIP (basic region leucine zipper), GRAS (gibberellic-acid insensitive, repressor [13,14].

The WRKY transcription factors are rated ninth in the plant transcription factor families and have received a lot of attention [15,16]. WRKY[(Trp(W)-Arg(R)-Lys(K)-Try(Y), tryptophan arginine lysine-Tyrosine] proteins are newly discovered transcription factors with either one or two highly conserved amino acid sequence WRKYGQK motif at their N-terminus and a 60 amino acid zinc finger motif at their C-terminus [17,18]. These plant-specific WRKY transcription factors work in tandem with other proteins or DNA sequences to promote or inhibit gene transcription. It also regulates a variety of physiological processes in plants by acting as a component of signaling networks [19-21,11]. It also controls biotic and abiotic stressors, as well as germination, seed growth, metabolism, phosphate limitation, and senescence [22]. As a result, the role of the WRKY TF in Gossypium spp. was briefly reviewed in this paper.

Depending on their biological and physiological function, genes show distinct expression patterns in a variety of adverse environmental conditions such as drought, cold, excessive salinity, and pathogen incursion [23]. Gene expression is required for a range of key plant functions, including growth, development, differentiation, metabolism, and environmental adaptability. The transcription of genes, which plays a key role in regulating the process, is the initial stage in gene expression. Numerous transcription factors that mediate the impact of intercellular and extracellular signals appear to govern transcription [24,25].

Each DNA promoter contains particular groups of short conserved sequences that TFs can bind to. Some of these components and variables are ubiquitous, and can be discovered and utilized in a wide range of promoters; others are unique, and their usage is controlled [26]. Transcription factors are classified into three groups based on their mode of activity. There are three types of factors: general factors, upstream factors, and inducible factors, all of which play various regulatory functions in gene transcription [27].

TFs are also divided into groups according to the structure of their DNA-binding domains [28]. Some TF families are found in all eukaryotes, while others are only found in certain lineages [29]. TFs have additional domains that are important in gene activation or repression, dimerization, and the development of protein-protein interactions in addition to the DNA-binding domain [30]. TFs are encoded by around 10% of genes in plants at various stages to regulate distinct signaling functions [28]. TFs are frequently found in several copies or isoforms, which allow them to carry out their regulatory functions [31]. According to the Plant Transcription Factor Database, there are now 58 transcription factor families engaged in various plant biological functions [15].

WRKY TFs are one of the largest groups of transcriptional regulators that are only found in plants [32]. Numerous studies, ranging from model plants to crops and other species, have looked at the role and mechanism of members of the WRKY family in recent years [33]. WRKY-TFs are involved in plant disease resistance [34,35]. Abiotic stress responses (drought, saline, alkali, temperature, and ultraviolet radiation) [36,37]. Nutrient deficiency, senescence, seed and trichome development embryogenesis and development [18].WRKYs can act as transcription activators or repressors in various homo- and heterodimer combinations [32].

Origin, Structure and Domains of WRKY Tfs

WRKY genes are prevalent in plants and have recently been recognized as important family regulators of genes. They appear to have originated in early eukaryotes and have recently been identified as major family regulators of genes [38]. SPF1, the first cDNA encoding a WRKY protein, was discovered in sweet potato (Ipomoea batatas) and binds to the SP8a (ACTGTGTA) and SP8b (TACTATT) sequences in the 5 upstream regions of three distinct genes expressing sporamine and tuber root amylase (Ishiguro and Nakamura).

WRKY protein genes have since been found in a variety of plant species, including wild oats (Avena fatua) parsley (Petroselinum crispum) (Rushton et al. 1996), Arabidopsis thaliana, barley (Hordeum vulgare), cotton (Gossypium arboreum) etc [40-43]. Plants have WRKY-TF gene families, and the number of WRKY-TFs varies by species. For example, Solanum lycopersicum (81), Arabidopsis thaliana (90), Gossypium arboretum (111), Oryza sativa (128), Sorghum bicolor (134), Zea mays (161), Triticum aestivum (171), Gossypium raimondi [15].

The WRKY TFs' structures are highly diverse in general; the structure is divided into two parts: the N-terminal DNA binding domain (DBD), which contains the WRKYGQR amino acid sequence, and the C-terminal zinc finger motif [16]. The DBD sequence of WRKY is based on the heptapeptide WRKYGQK; however other WRKY proteins feature W-R-R-Y, W-S-K-Y, and W-K-R-Y, W-V-K-Y, or W-K-K-Y motifs in place of the WRKY amino acid sequences. This domain is a four-stranded beta-sheet with a zinc-binding pocket, forming a unique zinc and DNA binding structure, according to structural investigations. The WRKYGQK residues are found in the N-terminal beta-strand, which provides for a wide range of hydrophobic contacts and adds to the beta-structural sheet's stability [44].

WRKY-TFs from the Arabidopsis genome can be classified into three groups and types of WRKY domains based on the number of WRKY domains and the layout of the zinc finger motif, which may reflect their various activities [45]. The varied binding ability of the WRKY-TFs could be related to a different amount of DBDs and zinc finger-like motifs, despite a substantially conserved W-box. WRKY proteins are divided into four classes based on these characteristics: I (two WRKY DBDs), II (single DBD with various C2H2 zinc fingers), III (single DBD with C2HC zinc fingers), and IV (incomplete WRKY domain/without zinc fingers) (Finatto et al. 2018). Most proteins with two WRKY domains belong to group I, while most proteins with one WRKY domain belong to group II. Although Group III proteins contain a single WRKY domain, the zinc finger motif layout is distinct or varied. According to the phylogenetic study of WRKY domains, Group II was further separated into five subgroups [17,33]. GhWRKY19, contrary to popular belief, has two WRKY domains and an inserted zinc finger motif, but it lacks the zinc-finger structure at the C-terminus.

A glutamate accumulation domain, a proline accumulation domain, and a leucine zipper structure are also seen in several WRKY proteins. Gu et al. [46] also discovered 34 genes for group IId WRKY-TFs and divided them into four groups (clade I-IV). Other studies on the WRKY subfamily of group IId in cotton have also been published. In Gossypium raimondii, Cai et al. [47] found 15 WRKY members of group IId, while Fan et al. [48] found 15 in Gossypium iridium. Due to the presence of two WRKY domains, evolutionary study implies that group I is the oldest, and groups II and III evolved from group I. [49]. In general, the WRKY domains of Group I and Group II members have the same type of C2-H2 zinc finger motif, which has a unique pattern of possible zinc ligands (CX4-5CX22-23-HXH) [48].

WRKY Transcription Factors in Gossypium spp

The plant TF database was used to construct transcription factors for three Gossypium species. More TFs (5022) is found in Gossypium hirsutum, followed by Gossypium raimondii (4894) and Gossypium arboretum (2532). WRKY is responsible for 4.7 percent (238), 4.5 percent (219), and 4.4 percent (111) of the identified TFs, respectively [15]. In total, 58 WRKY TFs have been identified in the three species, accounting for 4.8 percent of all documented TF families. Similarly, 116 WRKY TFs in Gossypium raimondii had the entire genome sequence and roughly 239 GhWRKY TFs in Gossypium hirsutum and three genes with partial WRKY domain structures (GhWRKY27, GhWRKY238, and GhWRKY239) were classed as group IV in Gossypium hirsutum [15]. A total of 15 GhWRKY group IIa members were discovered, mostly on chromosomes 5, 6, and 7 [46].

The process of plant adaptation to environmental stress is controlled through the orchestration of complex molecular networks regulated by TF proteins. WRKY proteins represent a large family of these TFs along with bHLH, MYB, ERF, NAC, C2H2,  bZIP, and MYB are related, and many reports have shown that the WRKY protein family has multiple developmental and physiological functions that are in response to external stimuli [17,18]. TF expression patterns are generally divided into constitutive and inducible expression, and therefore WRKYs-TFs protein expression is inducible in response to various stresses. WRKY-TFs regulate the expression of pathogen-initiated, senescence-initiated, abscisic acid-induced, gibberellic acid-induced, and salicylic acid-induced genes and play important roles in the regulation of plant growth and development, and their response to numerous types of abiotic stress [51]. Furthermore, its expression is rapid, immediate, tissue-specific (roots, stems, leaves, and embryos) and involved in various physiological processes in plants [53]. GhWRKY17 expression in cotton can be induced by drought, salt and H2O2 [54]. Ultraviolet irradiation induces the expression of three AtWRKYs in Arabidopsis and OsWRKY89 in rice, resulting in the production of a thick waxy substance on the leaf surface and improving high-temperature tolerance [52]. Expression analysis showed that most group II and III GhWRKY genes are highly expressed under different strains.

However, WRKY can also act as a negative regulator of gene expression. Heterologous expression of Gossypium hirsutum GhWRKY33 gene reduced drought tolerance of transgenic Arabidopsis plants. Several WRKY33-interacting proteins containing the VQ motif have been discovered that affect the expression of defense genes. VQ proteins appear to act as suppressors of defense genes through their interaction with WRKY-TFs. Indeed, WRKY33, SIB1, and SIB2 were significantly induced by Botrytis cinerea infection and showed similar expression patterns [55].

Overall, WRKY TF is thought to act as transcriptional regulator by binding to the W box, a promoter element common to numerous defense-associated genes [56]. These include resistance to plant diseases (bacteria, fungi, and viruses). For example, GhWRKY11, GhWRKY15, and GhWRKY39, which are three structurally related groups IId WRKY members, interact physically and functionally in a complex to confer resistance to the various pathogens in plants [5734].Aabiotic stress responses (drought, cold, wounding, nutrient deprivation from high salinity and UV exposure, and aging) [45,53]. Microarray, expression profiling, and qRT-PCR data showed that WRKY genes in Gossypium hirsutum regulate the development of fibers, anthers, tissues (roots, stems, leaves, and embryos) and are involved in stress response. In addition, some members of the WRKY family play a role in hormone signaling [45]. For example, GhWRKY3 expression upregulates SA, MeJA, GA, ABA, and ET biosynthesis in response to pathogen infection, drought, salt, and cold stress [58]. WRKY TFs families directly or indirectly control the plant defense response by altering the biosynthesis of the secondary metabolite [59]. All of these benefits have been considered by growers in crops because of the intrinsic role TF plays in these bio-molecular processes.

The Roles of WRKY Tfs in Abiotic Stress Responses

Abiotic factors in the environment are non-living chemical and physical elements that have an impact on both individual organisms and ecosystems. Low or high temperatures, insufficient or excessive water, high salt, heavy metals, and UV radiation are all abiotic stressors that affect plant growth and development, resulting in large crop losses around the world. Plants have developed a more general defense against abiotic stress through a complex regulatory network that includes upstream signaling molecules like stress hormones, reactive oxygen species, polyamines, phytochromes, and calcium, as well as downstream gene regulation elements, particularly transcription factors (TFs) [36, 60].

Drought Response: Drought is a continuous water scarcity that plants must adjust to as one of the principal abiotic environmental stresses, and it can cause significant economic losses in agriculture [61,60]. Water for irrigating crops is becoming increasingly scarce as a result of global warming and water shortages; hence the creation of drought-resistant agricultural species is critical [62]. Drought is a major limiting factor in cotton production, as more than half of the world's cotton is farmed in areas with high water stress [63].  Drought stress has a significant impact on cotton output. Drought stress has been shown to cause a 42 percent drop in seed production and a 55 percent drop in cotton biological yield [64]. Drought tolerance is a complicated feature mediated by a variety of genes, transcription factors, microRNAs, hormones, proteins, cofactors, ions, and metabolites. Cotton stomata, root development, cellular adaptations, photosynthesis, generation of abscisic acid (ABA) and jasmonic acid (JA), and scavenging of reactive oxygen species (ROS) have all been recognized as significant physiological responses to drought stress [62]. Several stress-responsive genes and transcription factors (TFs) responsible for establishing stress tolerance in crop plants have been found through molecular and biochemical research during the last decade. Drought resistance in plants is a complicated process that is generally controlled by several genes, including those encoding WRKY-TFs [60].

This protein is involved in several processes, including organogenesis and development, as well as stress and defense pathways and other abiotic stressors. Drought stress activates several drought-related signaling pathways by inducing the production of stress-related transcription factors and genes such as ROS scavenging, ABA, or mitogen-activated protein kinase (MAPK) signaling genes [62]. WRKY family members play a significant role in various stress responses among numerous stress-related TFs [33].

Plants have WRKY-TF gene families, and the number of WRKY-TFs varies by species. Overexpression of AtWRKY57 in Arabidopsis plants has been demonstrated to improve drought tolerance [36]. GhWRKY17 was discovered to be triggered by dryness, salt, H2O2, and ABA [54]. Physiological analyses of germination rate, root growth, survival rate, leaf water loss, and chlorophyll content revealed that constitutive expression of GhWRKY17 in Nicotiana benthamiana significantly lowered plant tolerance to drought and salt stress. GhWRKY17 transgenic plants are more responsive to ABA-mediated seed germination and root development. Overexpression of GhWRKY17 in Nicotiana benthamiana, on the other hand, prevented ABA-induced stomata blockage. Furthermore, GhWRKY17 reduced ABA levels, which reduced plant susceptibility to drought, and transcript levels of ABA-inducible genes such as AREB, DREB, NCED, ERD, and LEA were significantly decreased under drought and salt stress conditions [54]. Drought, salt, ABA, and H2O2 treatment increased glucuronidase activity mediated by the GhWRKY68 promoter [55]. By altering ABA concentration and boosting transcript levels of ABA-responsive genes, GhWRKY68 can influence salt and drought responses [55]. GhWRKY33 is a leaf-specific gene that is activated by drought. The transgenic Arabidopsis plant's drought sensitivity is increased by overexpression of GhWRKY33, and the transcription levels of certain genes implicated in drought stress are also altered during drought stress [20]. However, when subjected to drought, the GhWRKY33 transgenic plants maintained larger stomata opening than the wild-type, resulting in a higher rate of water loss. In the transgenic plants' leaves, both chlorophyll content and proline accumulation were significantly reduced.

This circumstance suggested that GhWRKY33 may have a role in drought responses by modulating stomatal mobility [20]. Furthermore, according to Li et al. [63] GhWRKY59, a WRKY TF, is phosphorylated by a MAPK cascade composed of GhMAP3K15-GhMKK4-GhMPK6 and plays a significant role in the drought stress response in cotton. GhWRKY59 regulates MAPK activation via feedback regulation of GhMAP3K expression, which is interesting. GhWRKY59 controls drought-responsive gene expression by binding directly to the promoter of GhDREB2.

Hu et al [65] found and reported that WRKY has a positive regulatory role in drought intolerance, which directly manipulates ABA biosynthesis, using the GhWRKY1-like from highland cotton. GhWRKY1-like overexpression in Arabidopsis activated ABA biosynthetic genes, signaling genes, responsive genes, and drought-related maker genes, resulting in improved drought tolerance [65]. Group IId WRKY gene families were highly expressed during drought treatment circumstances, according to Gu et al. [10] Drought tolerance was greatly boosted when GhWRKY21 was silenced, whereas ectopic GhWRKY21 overexpression in Nicotiana benthamiana lowered drought tolerance [52]. GhWRKY91 may inhibit natural and stress-induced leaf senescence, laying the groundwork for more functional research into leaf senescence and stress response in cotton, as well as improving drought tolerance in transgenic Arabidopsis plants. Furthermore, in cotton plants, virus-induced gene silencing (VIGS) of Gh A11G1801 could lower drought tolerance [10, 52]. GhWRKY91, on the other hand, stimulates the expression of its target gene, GhWRKY17 [20].

Salt Stress Response: Salt is an environmental component that limits crop development and yields, and it is becoming a major concern around the world. Plants are affected by salt stress in a variety of ways, including osmotic stress, ionic stress, and, most importantly, oxidative damage [9]. Salt stress has a major impact on the expression levels of genes involved in a variety of biological processes and signaling pathways.

It's critical to find salt resistance genes to boost cotton production in salt-stressed areas. Cotton has a low diversity of salt tolerance genes when compared to other model plants [66].

Activation of numerous transcription factors such as MYB, WRKY, AP2, and cell wall modification are complex molecular mechanisms of salt stress response in cotton and are very active in response to salt stress [66]. Understanding the expression patterns of these important genes implicated in the response to salinity could provide insight into the molecular mechanisms behind salt stress. In recent decades, a substantial number of salt-sensitive WRKY genes in cotton have been found and described [34, 54, 67].

Wild-type (WT) and overexpressing (OE) plants were irrigated with saline water (200 mM) for one month to assess the effect of salinity on seed germination and if GhWRKY68 affects the salt tolerance of transgenic plants in the vegetative stage. In comparison to the WT plants, the OE plants showed substantial growth retardation, leaf curling, and chlorosis after NaCl treatment. Only around 40% of the OE plants survived the high salinity conditions, and their survival rate was lower than the WT plants. These findings imply that overexpression of GhWRKY68 in transgenic plants during seed germination and vegetative state may result in decreased salt tolerance [55]. Yan et al. published a paper that was similar to this one in 2014.

Based on overexpression of GarWRKY5 in Arabidopsis and virus-induced gene silencing of GarWRKY5 in cotton, Guo et al. [37] investigated the role of the GarWRKY5 gene family in the response to salt stress in Gossypium aridum and found that GarWRKY5 is involved in the response to salt stress through the JA or SA signaling pathway. Under salt stress, GarWRKY5 overexpressors had greater superoxide dismutase and peroxidase activity. As a result, GarWRKY5 may operate as a positive transcriptional regulator in response to excessive salt stress by stimulating the expression of glutathione-S-transferase genes via the ROS scavenging mechanism. Similarly, virus-induced GhWRKY6 gene silencing increases salt tolerance in salt-sensitive cotton cultivars. At different developmental stages, the transgenic Arabidopsis lines GarWRKY17 and GarWRKY104 can improve salt tolerance [48].

GhWRKY6 downregulation promotes salt tolerance in cotton, presumably due to GhWRKY6 binding to the promoter region of the RAV1 gene, which has three W boxes within a 1 kb region upstream of the gene [68]. Overexpression of WRKY proteins in the upland cotton cultivars LMY37 and ZM12 resulted in robust responses to salt stress. At the transcriptional level, this protein alters the downstream expression patterns of targeted functional genes involved in ROS production and scavenging. At the transcriptional level, this protein alters the downstream expression patterns of targeted functional genes involved in ROS production and scavenging. Differential expression of signaling elements and downstream functional genes can change salinity tolerances directly or indirectly [65]. In general, GhWRKY TFs help researchers better understand how cotton copes with salt and osmotic stress [9].

Temperature Stress Response: Significant abiotic stress is defined as temperatures that are outside of an organism's optimal tolerance range. Extremely hot or low temperatures result in significant crop losses. As a result, to enhance agricultural production, techniques to protect plant cells from harm caused by severe temperature swings must be developed. When plants are exposed to high-temperature stress, the WRKY family is known to be implicated in the high-temperature response, controlling gene expression through many pathways and at different levels, and therefore influencing plant stress response signaling [22].

WRKY TFs have been found to respond positively to plant tolerance to high temperatures in a growing number of studies. CaWRKY40, for example, is implicated in the response of plants to high-temperature stress in pepper, and overexpression of this TF reduces tobacco's susceptibility to high-temperature treatment, whereas deletion of this TF reduces tolerance to high-temperature treatment [56]. GhWRKY39 expressed in upland cotton had a similar outcome [34].

In Arabidopsis, high-temperature treatment inhibited AtWRKY33 expression while inducing AtWRKY25 and AtWRKY26 expression, and constitutive overexpression of AtWRKY25 and AtWRKY26 increased resistance to high-temperature stress, while inhibition of AtWRKY41 expression reduced inhibition of dormant and dormant seed high-temperature inhibition [69]. Overexpression of TaWRKY30 in wheat resulted in a boost in high-temperature tolerance [70]. However, some WRKYs in plants hurt high-temperature tolerance; for example, heterologous expression of sunflower HaWRKY6 in Arabidopsis could drastically impair the plant's tolerance to high temperatures [71].

In conclusion, it can be concluded that WRKY-TFs can improve plant tolerance to high temperatures via regulating transcription. Furthermore, these findings suggest that WRKY25, WRKY26, and WRKY33 functionally interact and play overlapping and synergistic roles in plant thermo-tolerance by positively regulating the collaboration between the ethylene-activated and heat shock protein-related signaling pathways that mediate responses to heat stress; and that these three proteins functionally interact and play overlapping and synergistic roles in plant thermo-tolerance [33].

Oxidative Stress Response: Oxidative stress is a complicated chemical and physiological phenomenon that occurs in higher plants in response to the overproduction and buildup of reactive oxygen species (ROS) as a result of the disruption of multiple metabolic pathways (i.e., respiration and photosynthesis) [72]. ROS regulates a variety of biological processes, including cell death, biotic and abiotic stress responses, and plant growth and development [37]. ROS, which was once thought to be a poisonous and unwanted chemical, is now widely acknowledged as an essential component for plants [72, 60].

Plant stress reactions are frequently linked to the production of reactive oxygen species (ROS). As a result, plants protect themselves by activating numerous stress-related genes linked to the antioxidant defense system [73]. To preserve ROS scavenging capabilities and maintain intracellular ROS homeostasis [74]. These are regulated by a variety of genres, including:

• Genes involved in the direct defense of cell membranes and proteins, such as osmotic protectants, radical scavengers, and detoxification enzymes.
• Genes involved in signaling cascades and transcription control, such as Mitogen-activated protein kinase (MAPK), phospholipases, calcium-dependent protein kinase (CDPK), SOS kinase, phospholipases [75]. In Arabidopsis, a complicated network containing at least 152 genes regulates ROS levels.

Recent cotton research revealed that Gossypium hirsutum has 515 ROS genes, Gossypium raimondii has 261 ROS genes, and Gossypium arboreum has 260 ROS genes. Gossypium's high number of ROS genes suggested a more complicated ROS network for fiber formation and abiotic stress tolerance [37].

WRKY-TFs have been demonstrated to inhibit ROS generation in cells, and they are involved in several ROS signaling-dependent responses, including senescence progression [76]. ROS such as superoxide, hydroxyl radicals, and hydrogen peroxide have a significant detrimental impact on the cell wall of the affected cell, resulting in lipid peroxidation, cell damage, and oxidative stress [77]. As a result, WRKY proteins indirectly help to reduce oxidative stress by scavenging ROS. Transgenic tobacco plants overexpressing GhWRKY17 demonstrated increased oxidative stress sensitivity. In the transgenic lines, the expression of genes for ROS scavenging enzymes such as APX, catalase, and SOD was decreased [54].

Yan et al. [54] described the effect of H2O2 on GhWRKY17 transcription, stating that the expression of GhWRKY17 transcript was down-regulated at 2 hours and up-regulated by H2O2 from 4 to 6 hours, with a substantial reduction (1.5-fold induction) 8 hours after treatment. Drought and salt stress both raised leaf proline levels in WT and OE plants, but the OE lines accumulated 11% and 15% less proline during drought and salt stress, respectively. These findings suggest that GhWRKY17 is important for controlling cellular ROS levels.

GhWRKY6-like were also examined in transgenic and WT plants in the presence of oxidative stressors such as malondialdehyde and H2O2, with WT plants accumulating more malondialdehyde and H2O2 than transgenic lines. As a result of the findings, it was shown that WT plants were badly harmed by ROS, whereas the overexpressing GhWRKY6-like transgenic lines were protected in comparison to WT plants [9].

In cotton, however, GhWRKY68 transcripts influenced drought stress response by modulating the expression of ABA-responsive genes and ROS detoxification [55]. Increased activity of antioxidant enzymes to scavenge ROS was observed in Arabidopsis plants overexpressing the GarWRKY5 TF [37]. Pathogen invasion frequently results in the generation of reactive oxygen species (ROS), which are important in defense responses. GhWRKY39-1 and GhWRKY44 overexpression improved resistance by preventing the buildup of pathogen-induced ROS in cotton [34].

Biotic Stress Response

All phonological phases of plant development are affected by biotic stress. Pathogenic bacteria, fungi, and viruses’ all-cause biotic stress [36]. Plants have evolved a variety of defense systems to combat microbial infestations. In this process, transcription factors play a crucial function. During the response to pathogen infection, the transcriptional expression of several defense-related plant genes is controlled [78,36]. The most significant proteins in the WRKY family interact with other transcription factors to govern plant defensive responses [78,36].

Multiple WRKYs can confer resistance to multiple bacterial or fungal pathogens. AtWRKY52, which contains a TIRNBSLRR domain (Toll/interleukin-1 receptor nucleotide-binding site leucine-rich repeat), works in combination with RPS4 to confer resistance to the fungal pathogen Colletotrichum higginsianum and the bacterial pathogen Pseudomonas syringae [79]. It also displays a nuclear interaction with the bacterial effector PopP2 and confers immunity to the bacterial pathogen Ralstonia solanacearum [80]. Others like AtWRKY16 and AtWRKY19 also share a similar TIRNBSLRR domain, suggesting that these proteins are involved in defense-related ETI signaling [81].

WRKY70 and WRKY33 mutations increased Arabidopsis susceptibility to Botrytis cinerea necrotrophic fungal infection [82]. In Arabidopsis, wounding causes the expression of WRKY11, WRKY15, WRKY22, WRKY33, WRKY40, WRKY53, and WRKY60 [83]. During fungal infections, about 28 WRKY-related transcripts were differently expressed in pericarp and cottonseed. In response to Aspergillus flavus infection, WRKY75 and WRKY72 were induced in the pericarp and seed, respectively.

Under toxigenic strain infection, WRKY75 and WRKY40 were specifically up-regulated in both pericarp and seed. In the pericarp, WRKY6, WRKY41, WRKY53, and WRKY50 were down-regulated [84].

Wang et al [54] found that wounding, infection with a bacterial pathogen, stress hormones (SA, MJ, and ET), and contact with the MAPK kinase GhMPK20 raised the expression of GhWRKY40 transcript. GhWRKY40 overexpression decreased defense gene expression and enhanced vulnerability to Ralstonia solanacearum. In Nicotiana benthamiana, however, constitutive overexpression of GhWRKY39 conferred higher resistance to bacterial and fungal pathogen infections, as well as enhanced expression of numerous pathogen-related genes [85]. GhWRKY70 expression was induced by Verticillium dahlia infection, SA, and MJ therapy, according to Xion et al [86]. In GhWRKY70 virus-silenced cotton plants, genes linked with the JA response were increased, while genes related to the SA response were downregulated. GbWRKY1 is also controlled by the SA, JA, and ET pathways [87]. In Arabidopsis thaliana, overexpression of GhWRKY70 lowered resistance to Verticillium dahliae. SA-associated genes were expressed more frequently in transgenic Arabidopsis plants, while JA response-associated genes were expressed less frequently. This could be because the promoters of GhWRKY70 genes contain at least one hormone-responsive region.

Downregulating GhWRKY70D13 enhanced cotton resistance to Verticillium dahliae, which promoted the accumulation of 1-aminocyclopropane-1-carboxylic acid, JA, and JA-Ile and impeded SA biosynthesis. Cotton's response to Verticillium dahliae infection is inhibited by GhWRKY70D13, which blocks the ET and JA signaling pathways [16]. Biological activities mediated by SA and JA are involved in many AtWRKY genes. In basal plant defenses, however, AtWRKY46, WRKY70, and WRKY53 all have overlapping and synergistic roles, favorably influencing basal resistance to Pseudomonas syringae and SA stress.

GhWRKY7, GhWRKY27, GhWRKY31, GhWRKY50, GhWRKY56, GhWRKY59, GhWRKY60, and GhWRKY102 were all significantly elevated in response to SA and JA, and these genes were linked to probable roles in the SA and JA signaling pathways [50]. Overexpression of Group I, GhWRKY44, in Nicotiana benthamiana improved its resistance to bacterial and fungal diseases. Increased resistance may be linked to defense processes mediated by SA, JA, and ROS. This suggests that GhWRKY resistance to pathogenic pathogens has positive regulatory roles [35].

To protect future generations from potential crises, it is critical to strengthen cotton's biotic and abiotic tolerance capabilities. This enables the development of biotic and abiotic resistant transgenic lines using a variety of technologies utilizing transgenic procedures. WRKY TFs are thought to play a role in a variety of stress signaling pathways. Every day, no fewer than 58 TF families implicated in plant stress responses are discovered. The WRKY TFs have been found as molecular stress regulators in Gossypium spp. to fight biotic stress (bacteria, fungi, viruses, etc.). Some GhWRKY-TFs, on the other hand, is negatively regulated by pathogen infections, while others are positively regulated by abiotic (drought, salinity, temperature, oxidation, and so on) stresses. In general, WRKY-TFs play a role in both biotic and abiotic processes. However, future research should focus on how these transcription factors interact with other regulatory components to resist environmental stimuli and to better understand their role in metabolic processes. This allows the researchers to better understand how WRKYs regulate metabolism and, as a result, not only improve plant stress tolerance but also increase the synthesis of vital natural plant compounds.

Conflict Of Interest

The authors declare that they have no conflict of interest.

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