GATA factors are evolutionarily conserved transcription regulators that are implicated in the regulation of physiological changes under abiotic stress. Unfortunately, there are few studies investigating the potential role of GATA genes in potato plants responding to salt and osmotic stresses. The physicochemical properties, chromosomal distribution, gene duplication, evolutionary relationships and classification, conserved motifs, gene structure, interspecific collinearity relationship, and cis-regulatory elements were analyzed. Potato plants were treated with NaCl and PEG to induce salinity and osmotic stress responses. qRT-PCR was carried out to characterize the expression pattern of StGATA family genes in potato plants subjected to salinity and osmotic stress. StGATA12 loss-of-function and gain-of-function plants were established. Morphological phenotypes and growth were indicated. Photosynthetic gas exchange was suggested by the net photosynthetic rate, transpiration rate, and stomatal conductance. Physiological indicators and the corresponding genes were indicated by enzyme activity and mRNA expression of genes encoding CAT, SOD, POD, and P5CS, and contents of H₂O₂, MDA, and proline. The expression patterns of StGATA family genes were altered in response to salinity and osmotic stress. StGATA12 protein is located in the nucleus. StGATA12 is involved in the regulation of potato plant growth in response to salinity and osmotic stress. Overexpression of StGATA12 promoted photosynthesis, transpiration, and stomatal conductance under salinity and osmotic stress. StGATA12 overexpression induced biochemical responses of potato plants to salinity and osmotic stress by regulating the levels of H₂O₂, MDA, and proline and the activity of CAT, SOD, and POD. StGATA12 overexpression induced the up-regulation of StCAT, StSOD, StPOD, and StP5CS against salinity and osmotic stress. StGATA12 could reinforce the ability of potato plants to resist salinity and osmosis-induced damages, which may provide an effective strategy to engineer potato plants for better adaptability to adverse salinity and osmotic conditions.

Heat stress is one of the most devastating abiotic stresses which causes significant loss of agricultural crop productivity. Thus, it is critical to examine the wheat’s response to the heat stress at seedling stage and adopt an appreciated breeding method to develop heat tolerance and to avoid harmful effects. Therefore, twenty wheat genotypes, including two local landraces, were evaluated in the current study to investigate the genetic diversity for heat tolerance at the seedling stage. Grains of wheat genotypes were placed on filter papers in Petri dishes for germinating at different temperature ranges (i.e., 25 °C as control, 30 °C, 35 °C, and 40 °C). The experiment was laid out in a completely randomized design (CRD) with the factorial arrangement and the number of replications was three. Analysis of variance (ANOVA) for seedling traits and biochemical analysis showed that the genotypes had significant differences for coleoptile length, shoot length (SL), root length (RL), shoot fresh weight (SFW), vigor index (VI), glycine betaine (GB) and proline content. The effect of temperature treatments on different wheat genotypes also exhibited highly significant variation for VI. Principal component analysis (PCA) showed that four factors contributed 82.8% to total variability with the Eigen value greater than 0.7 at 35 °C. Correlation analysis showed that coleoptile length and germination percentage (GP) had a highly significant-positive correlation with SL, VI, and SFW. Results showed that wheat genotypes of ‘Maraj’, ‘Fareed’, ‘Darabi’, ‘Zincol-16’, ‘Barsat’, ‘NARC-2011’, and ‘Mundar’ showed superior performance when grown under different temperatures. ‘NARC-2011’, ‘Inqalab-91’, and ‘Galexy’ wheat genotypes performed well regarding of H2O2 and antioxidant activity. These genotypes had a significant level of variability under heat stress and can be used under high temperatures in future breeding programs for further research purposes.

Drought stress is a significant abiotic factor influencing maize growth and development. Understanding the molecular mechanism of drought tolerance is critical to develop the drought tolerant genotype. The identification of the stress responsive gene is the first step to developing a drought tolerant genotype. The aim of the current research was to pinpoint the genes that are essential for conserved samples in maize drought tolerance. In the current study, inbred lines of maize, 478 and H21, a drought-tolerant and susceptible line, were cultivated in the field and various treatments were applied. The circumstances during the vegetative stage (severe drought, moderate drought and well-watered environments) and RNA sequencing were used to look into their origins. In 478, 68%, 48% and 32% of drought-responsive genes (DRGs) were found, with 63% of DRGs in moderate drought and severe drought conditions in H21, respectively. Gene ontology (GO) keywords were explicitly enriched in the DRGs of H21, which were considerably over-represented in the two lines. According to the results of the GSEA, “phenylpropanoid biosynthesis” was exclusively enriched in H21, but “starch and sucrose metabolism” and “plant hormone signal transduction” were enhanced in both of the two lines. Further investigation found that the various expression patterns of genes linked to the trehalose biosynthesis pathway, reactive oxygen scavenging, and transcription factors, may have a role in maize’s ability to withstand drought. Our findings illuminate the molecular ways that respond to lack and offer gene resources for maize drought resistance. Similarly, SNP and correlation analysis gave us noticeable results that urged us to do the same kind of analysis on other crops. Additionally, we isolated particular transcription factors that could control the expression of genes associated to photosynthesis and leaf senescence. According to our findings, a key factor in tolerance is the equilibrium between the induction of leaf senescence and the preservation of photosynthesis under drought.

Heat stress severely restricts potato tuber growth and development, yet the roles of WRKY transcription factors (TFs) in mediating heat responses remain poorly understood. Using quantitative reverse transcription PCR (qRT-PCR), we identified StWRKY75 in potato cultivars ‘Atlantic’ and ‘Desiree’ as a heat-inducible gene, showing significant upregulation under 30°C and 35°C treatments. Phylogenetic analysis classified StWRKY75 into the WRKY Group II family, with close evolutionary homology to tomato SlWRKY75, and subcellular localization confirmed its nuclear targeting. To characterize its function, we generated transgenic lines overexpressing StWRKY75 (OE) or knockdown by RNA interference (RNAi). Under heat stress conditions, OE plants demonstrated superior thermotolerance compared to non-transgenic (NT) controls, manifested by improved growth parameters (plant height, tuber weight per plant, fresh weight, dry weight, root fresh weight, and root dry weight), enhanced activities of antioxidant enzymes (ascorbate peroxidase [APX], catalase [CAT], peroxidase [POD], and superoxide dismutase [SOD]), increased proline accumulation, elevated photosynthetic efficiency, and reduced malondialdehyde (MDA) content. Conversely, RNAi lines exhibited compromised thermotolerance with reversed growth parameters and biochemical characteristics. qRT-PCR analysis revealed that StWRKY75 positively regulated key heat-stress responsive genes, including those encoding antioxidant enzymes (StAPX, StCAT, StSOD, StPOD), proline biosynthesis Pyrroline-5-carboxylate synthase (StP5CS), and heat shock proteins (StHSP20, StHSP70, StHSP90). These findings demonstrate that StWRKY75 acts as a positive regulator of potato thermotolerance by enhancing growth, antioxidant capacity, proline metabolism, photosynthesis, and heat-responsive gene expression, providing a valuable target for improving crop heat resilience in breeding programs.

Heat stress severely impacts the growth and development of potato plants. However, the molecular mechanisms underlying thermotolerance, particularly the role of WRKY transcription factors (TFs), remain poorly understood. Here, we identified StWRKY65 as a heat-responsive gene in potato, demonstrating significant transcriptional upregulation under 30°C and 35°C heat stress conditions. Phylogenetic analysis classified StWRKY65 into the WRKY Group II family, revealing high evolutionary conservation with its tomato ortholog SlWRKY65. Subcellular localization confirmed its nuclear targeting. Additionally, we generated transgenic potato lines with overexpression (OE) or RNA interference (RNAi)-mediated suppression of the target gene. Under heat stress, OE lines exhibited enhanced thermotolerance, manifested through improvements in plant height, fresh/dry weights of plants and roots, tuber yield, photosynthetic efficiency, transpiration rate, and stomatal conductance. Concurrently, compared to non-transgenic (NT) controls, StWRKY65 overexpression significantly elevated the activities of antioxidant enzymes (ascorbate peroxidase [APX], catalase [CAT], peroxidase [POD], superoxide dismutase [SOD]), proline accumulation, and total chlorophyll content, while reducing malondialdehyde (MDA) and hydrogen peroxide (H₂O₂) levels. Conversely, RNAi lines displayed heightened heat sensitivity, impaired growth parameters, diminished antioxidant capacity, and elevated oxidative stress markers. Furthermore, StWRKY65 overexpression transcriptionally activated key antioxidant enzyme-related genes (StAPX, StCAT1/2, StPOD12/47, StFeSOD2/3, StMnSOD, StCuZnSOD1/2), whereas its knockdown produced opposing effects. This study demonstrates the pivotal role of StWRKY65 in enhancing potato thermotolerance by simultaneously boosting antioxidant defenses and maintaining photosynthetic efficiency under heat stress. As climate change intensifies thermal extremes, these findings position StWRKY65 as a valuable genetic target for developing heat-resistant potato varieties, offering a timely strategy to protect this vital crop and global food security.