BZIP transcription factors play key roles in plant growth, development, and stress signaling. A bZIP gene BnbZIP2 (GenBank accession number: KP642148) was cloned from ramie. BnbZIP2 has a 1416 base pair open reading frame, encoding a 471 amino acid protein containing a characteristic bZIP domain and a leucine zipper. BnbZIP2 shares high sequence similarity with bZIP factors from other plants. The BnbZIP2 protein is localized to both nuclei and cytoplasm. Transcripts of BnbZIP2 were found in various tissues in ramie, with significantly higher levels in female and male flowers. Its expression was induced by drought, high salinity, and abscisic acid treatments. Analysis of the cis-elements in promoters of BnbZIP2 identified cis-acting elements involved in growth, developmental processes, and a variety of stress responses. Transgenic Arabidopsis plants’ overexpression of BnbZIP2 exhibited more sensitivity to drought and heavy metal Cd stress during seed germination, whereas more tolerance to high-salinity stress than the wild type during both seed germination and plant development. Thus, BnbZIP2 may act as a positive regulator in plants’ response to high-salinity stress and be an important candidate gene for molecular breeding of salt-tolerant plants.

Ramie (Boehmeria nivea L.) is an important crop that serves as fine fiber material, high protein feedstuff, and valuable herbal medicine in China. However, increasing salinity in soil limits the productivity. We investigated in a greenhouse experiment responses to salinity in two ramie cultivars, Chuanzhu-12 (salt-tolerant cultivar, ST) and Xiangzhu-2 (saltsensitive cultivar, SS), to elucidate the salt tolerance mechanism of this species. Salinity stress substantially reduced both chlorophyll and carotenoid contents. In addition, net photosynthesis, transpiration rate, stomatal conductance, intercellular CO₂ concentration, and the ratio of intercellular CO₂ to ambient CO₂ were affected, less in ST. Nevertheless, salinity stress markedly improved water use efficiency and intrinsic water use efficiency in both species. Moreover, relative water contents, soluble proteins, and catalase activity were substantially impaired, while proline accumulation and superoxide dismutase activity were enhanced substantially, more in ST. Furthermore, noteworthy increase in peroxidase activity and decrease in malondialdehyde content was recorded in ST, whereas, in SS, these attributes changed conversely. Overall, the cultivar ST exhibited salt tolerance due to its higher photosynthetic capacity, chlorophyll content, antioxidative enzyme activity, and nonenzymatic antioxidants, as well as reduced lipid peroxidation and maintenance of the tissue water content. This revealed the salt tolerance mechanism of ramie plants for adaptation to salt affected soil.

Abiotic stresses are one of the significant threats to soybean (Glycine max L.) growth and yields worldwide. Soybean has a crucial role in the global food supply chain and food security and contributes the main protein share compared to other crops. Hence, there is a vast scientific saddle on soybean researchers to develop tolerant genotypes to meet the growing need of food for the huge population. A large portion of cultivated land is damaged by salinity stress, and the situation worsens yearly. In past years, many attempts have increased soybean resilience to salinity stress. Different molecular techniques such as quantitative trait loci mapping (QTL), genetic engineering, transcriptome, transcription factor analysis (TFs), CRISPR/Cas9, as well as other conventional methods are used for the breeding of salt-tolerant cultivars of soybean to safeguard its yield under changing environments. These powerful genetic tools ensure sustainable soybean yields, preserving genetic variability for future use. Only a few reports about a detailed overview of soybean salinity tolerance have been published. Therefore, this review focuses on a detailed overview of several molecular techniques for soybean salinity tolerance and draws a future research direction. Thus, the updated review will provide complete guidelines for researchers working on the genetic mechanism of salinity tolerance in soybean.

Xyloglucan endotransglucosylase/hydrolases (XTH) are cell wall-modifying enzymes important in plant response to abiotic stress. However, the role of XTH in cadmium (Cd) tolerance in ramie remains largely unknown. Here, we identified and cloned BnXTH1, a member of the XTH family, in response to Cd stress in ramie. The BnXTH1 promoter (BnXTH1p) demonstrated that MeJA induces the response of BnXTH1p to Cd stress. Moreover, overexpressing BnXTH1 in Boehmeria nivea increased Cd tolerance by significantly increasing the Cd content in the cell wall and decreasing Cd inside ramie cells. Cadmium stress induced BnXTH1-expression and consequently increased xyloglucan endotransglucosylase (XET) activity, leading to high xyloglucan contents and increased hemicellulose contents in ramie. The elevated hemicellulose content increased Cd chelation onto the cell walls and reduced the level of intracellular Cd. Interestingly, overexpressing BnXTH1 significantly increased the content of Cd in vacuoles of ramie and vacuolar compartmentalization genes. Altogether, these results evidence that Cd stress induced MeJA accumulation in ramie, thus, activating BnXTH1 expression and increasing the content of xyloglucan to enhance the hemicellulose binding capacity and increase Cd chelation onto cell walls. BnXTH1 also enhances the vacuolar Cd compartmentalization and reduces the level of Cd entering the organelles and soluble solution.