Jul 2026· Journal of Experimental Botany· 0 citations
Medicine
TL;DR
It is demonstrated that PIF3 negatively regulates plant salt tolerance in Arabidopsis, and salt stress significantly enhances the interaction between PIF3 and light-activated PHYTOCHROME B (PHYB), leading to accelerated degradation of PIF3 in light, thus alleviating its negative regulation on plant salt tolerance.
Abstract
Salt stress poses a threat to plant water and nutrient uptake and leads to multiple forms of damages in plants, making it a major challenge to global crop production. PHYTOCHROME-INTERACTING FACTOR 3 (PIF3) is a key transcription factor in light signaling and it has been reported to play a critical role in plant responses to salt stress. Here, we demonstrated that PIF3 negatively regulates plant salt tolerance in Arabidopsis, and salt stress significantly enhances the interaction between PIF3 and light-activated PHYTOCHROME B (PHYB), leading to accelerated degradation of PIF3 in light, thus alleviating its negative regulation on plant salt tolerance. Additionally, we identified AGAMOUS-LIKE 21 (AGL21) as a downstream target gene of PIF3. PIF3 directly binds to the promoter of the AGL21 gene to promote its expression. The PIF3-AGL21 module transcriptionally modulates the expression a battery of downstream genes, including those involved in redox homeostasis regulation, thereby leading to accumulation of reactive oxygen species (ROS) and disruption of redox homeostasis within plants in response to salt stress. PHYB-mediated degradation of PIF3 attenuates the PIF3-AGL21 module to restore redox homeostasis and enhance plant tolerance to salt stress.
Salt stress severely limits plant growth and productivity. GDP-mannose-3',5'-epimerase (GME), a key enzyme in ascorbic acid (AsA) biosynthesis, has been implicated in plant stress responses, but its role in pear salt tolerance remains unclear. Here, we identified PbGME1 as a positive regulator of salt tolerance in pear. The basic helix-loop-helix transcription factor PbbHLH67 directly binds to the PbGME1 promoter and activates its transcription, as shown by yeast one-hybrid, electrophoretic mobility shift, and dual-luciferase assays. Overexpression of PbbHLH67 enhanced salt tolerance in pear seedlings, pear calli, and Arabidopsis, whereas silencing of PbbHLH67 increased salt sensitivity in Pyrus betulifolia, accompanied by corresponding changes in AsA accumulation. We further identified PbbHLH53 as a PbbHLH67-interacting protein, which also binds the PbGME1 promoter and activates its transcription. Similar to PbbHLH67, overexpression of PbbHLH53 enhanced salt tolerance, whereas its silencing increased salt sensitivity. Notably, heterodimerization of PbbHLH67 and PbbHLH53 further strengthened PbGME1 transcriptional activation. Moreover, the AsA biosynthesis inhibitor lycorine largely abolished the enhanced salt tolerance conferred by PbbHLH67 or PbbHLH53 overexpression. Together, these findings demonstrate that the PbbHLH67-PbbHLH53 module promotes pear salt tolerance by activating PbGME1 expression and increasing AsA accumulation.
Hui-Zhen Dong, Min Ma, Can Liu et al.· Plant Physiology· 0 citations
It is shown that salt stress–induced ABA accumulation up-regulates Heat Shock Factor 4 (CmHSFA4), a gene that is known to enhance chrysanthemum salt tolerance, and an ABA-SnRK2.2-ABF1/BRM signaling module that integrates phosphorylation-dependent protein stabilization and degradation with histone methylation dynamics to fine-tune salt stress–responsive gene expression in chrysanthemum is revealed.
Xinhui Wang, Han Wang, Hong-Yu Wei et al.· Science Advances· 0 citations
Soil salinization severely impacts cotton yield and quality. Excess salt stimulates excessive accumulation of reactive oxygen species (ROS), resulting in oxidative damage and impairment of cell membrane integrity. Therefore, enhancing the antioxidant capacity of cotton is a key strategy to improve salt tolerance. In this study, we systematically characterized the salt tolerance function of GhVIP1, a bZIP family transcription factor. Overexpression (OE) of GhVIP1 enhanced tolerance to salt stress in Arabidopsis, as evidenced by higher germination rates, root length, chlorophyll content, and total antioxidant capacity (T-AOC), along with lower malondialdehyde (MDA) and ROS contents compared to the wild-type (WT). Conversely, virus-induced gene silencing (VIGS) of GhVIP1 resulted in salt-sensitive phenotypes in cotton. Yeast one-hybrid (Y1H) and dual-luciferase (LUC) reporter assays further confirmed that GhVIP1 directly binds to the promoter of GhMYB44 and activated its transcription in vitro. However, genetic analysis revealed that GhMYB44 functions as a negative regulator of salt tolerance, as its silencing significantly enhanced ROS-scavenging capacity and upregulated the expression of ROS-related genes. Notably, silencing GhVIP1 unexpectedly led to elevated GhMYB44 transcript levels in cotton, suggesting the existence of a complex in vivo regulatory network involving additional intermediate factors. Collectively, our results demonstrate that GhVIP1 positively regulates salt tolerance by enhancing ROS detoxification, partially through its interplay with the antagonistic GhMYB44 pathway. This study provides new genetic resources and a theoretical basis for molecular breeding of salt-tolerant cotton.
Huiyun Shan, Ze-Xu Li, Chan Liu et al.· Plant physiology and biochem...· 0 citations
It is demonstrated that PlPAT1 functions as a positive regulator of salt stress tolerance, likely through modulating osmotic balance and enhancing reactive oxygen species scavenging capacity.
Jian Cai, Xuemei Zhang, Cong Yan et al.· BMC Genomics· 0 citations
This AGL103-TCPs module integrates developmental and stress signaling, offering mechanistic insight into how plants balance growth and resilience and highlighting potential targets for engineering stress-tolerant crops.
Lan Yang, Die Liu, Jing Zhang et al.· Plant Communications· 0 citations
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