Dingyue Duan,Ran Yi,Mingrui Shi,Jiwei Zhou,Qinglong Dong,Ke Mao,Jie Yang,Fengwang Ma
{"title":"The MdVQ17/MdVQ37-MdWRKY100 module coordinates apple salt tolerance by modulating Na+/K+ homeostasis and ROS scavenging.","authors":"Dingyue Duan,Ran Yi,Mingrui Shi,Jiwei Zhou,Qinglong Dong,Ke Mao,Jie Yang,Fengwang Ma","doi":"10.1093/plphys/kiaf434","DOIUrl":null,"url":null,"abstract":"Salt stress greatly affects the yield and quality of agricultural crops, limiting their geographic distribution. Valine-glutamine (VQ) motif-containing proteins function as transcriptional regulators of plant growth and stress responses. However, the role and underlying molecular mechanisms of VQ proteins in apple (Malus domestica) salt stress responses remain largely unknown. Here, MdVQ17 was identified as a salt-responsive gene that negatively regulates salt tolerance in apple plants by increasing the Na+/K+ ratio and suppressing reactive oxygen species (ROS) scavenging under salt stress. MdWRKY100, a WRKY transcription factor that enhances apple salt tolerance, was identified as an MdVQ17-interacting protein. MdWRKY100 directly bound to the Arabidopsis K⁺ TRANSPORTER 1-LIKe (MdAKT1-like) and PEROXIDASE 57 (MdPER57) promoters, activating their transcription. MdVQ17 inhibited the binding and transcriptional activation activity of MdWRKY100 at these promoters, thereby suppressing MdWRKY100-mediated regulation of Na+/K+ homeostasis and antioxidant enzyme activity. MdVQ37, another MdWRKY100-interacting VQ protein, modulated the MdWRKY100-mediated salt response through a similar mechanism. Overall, these findings reveal that the MdVQ17/MdVQ37-MdWRKY100 module co-regulates Na+/K+ homeostasis and ROS scavenging by modulating MdAKT1-like and MdPER57 expression, providing insights into how the VQ-WRKY complex influences salt tolerance in apple.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"17 1","pages":""},"PeriodicalIF":6.9000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiaf434","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Salt stress greatly affects the yield and quality of agricultural crops, limiting their geographic distribution. Valine-glutamine (VQ) motif-containing proteins function as transcriptional regulators of plant growth and stress responses. However, the role and underlying molecular mechanisms of VQ proteins in apple (Malus domestica) salt stress responses remain largely unknown. Here, MdVQ17 was identified as a salt-responsive gene that negatively regulates salt tolerance in apple plants by increasing the Na+/K+ ratio and suppressing reactive oxygen species (ROS) scavenging under salt stress. MdWRKY100, a WRKY transcription factor that enhances apple salt tolerance, was identified as an MdVQ17-interacting protein. MdWRKY100 directly bound to the Arabidopsis K⁺ TRANSPORTER 1-LIKe (MdAKT1-like) and PEROXIDASE 57 (MdPER57) promoters, activating their transcription. MdVQ17 inhibited the binding and transcriptional activation activity of MdWRKY100 at these promoters, thereby suppressing MdWRKY100-mediated regulation of Na+/K+ homeostasis and antioxidant enzyme activity. MdVQ37, another MdWRKY100-interacting VQ protein, modulated the MdWRKY100-mediated salt response through a similar mechanism. Overall, these findings reveal that the MdVQ17/MdVQ37-MdWRKY100 module co-regulates Na+/K+ homeostasis and ROS scavenging by modulating MdAKT1-like and MdPER57 expression, providing insights into how the VQ-WRKY complex influences salt tolerance in apple.
期刊介绍:
Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research.
As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.