{"title":"Genome-wide identification and expression analysis Pvrboh genes reveal their potential roles in salt tolerance and calcium signaling.","authors":"Ling Pan, Lirong Cai, Yang Lu, Di Peng","doi":"10.1093/pcp/pcaf115","DOIUrl":null,"url":null,"abstract":"<p><p>Salinity stress is a major environmental factor that limits plant growth and productivity. Understanding the mechanisms of plant salt tolerance is crucial for improving crop yields in saline soils. The Respiratory Burst Oxidases (Rboh) gene family triggers the production of reactive oxygen species (ROS), which act as a signaling molecule to regulate plant tolerance and development under saline conditions. However, a comprehensive analysis of the Rboh gene family in halophytic plants is largely unexplored. In this study, we characterized members of the Rboh gene family in Paspalum vaginatum, a typical halophyte. Evolutionary analysis revealed numerical differences in Pvrboh genes compared to those related species. Additionally, cis-acting elements related to plant hormones, light response, and plant development were identified in Pvrboh promoters. All Pvrboh genes were found to be membrane-localized and upregulated under high salinity, contributing to either root-sourced or leaf-sourced H2O2 production. Gene structural analysis and Ca2+ inhibitor experiments further indicated that Pvrboh4 and Pvrboh5 were closely associated with Ca2+ signaling, whereas Pvrboh6 did not exhibit such an association. Split-luciferase assay in N. benthamiana showed that PvRBOH5 strongly interacted with AtCPK5. Furthermore, a gene regulatory network analysis revealed multiple transcription factors from 32 distinct families that may regulate Pvrboh5 expression. These findings provide new insights into the role of Pvrboh genes in enhancing plant salt tolerance, offering potential targets for improving stress resilience in crops.</p>","PeriodicalId":20575,"journal":{"name":"Plant and Cell Physiology","volume":" ","pages":""},"PeriodicalIF":4.0000,"publicationDate":"2025-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant and Cell Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/pcp/pcaf115","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Salinity stress is a major environmental factor that limits plant growth and productivity. Understanding the mechanisms of plant salt tolerance is crucial for improving crop yields in saline soils. The Respiratory Burst Oxidases (Rboh) gene family triggers the production of reactive oxygen species (ROS), which act as a signaling molecule to regulate plant tolerance and development under saline conditions. However, a comprehensive analysis of the Rboh gene family in halophytic plants is largely unexplored. In this study, we characterized members of the Rboh gene family in Paspalum vaginatum, a typical halophyte. Evolutionary analysis revealed numerical differences in Pvrboh genes compared to those related species. Additionally, cis-acting elements related to plant hormones, light response, and plant development were identified in Pvrboh promoters. All Pvrboh genes were found to be membrane-localized and upregulated under high salinity, contributing to either root-sourced or leaf-sourced H2O2 production. Gene structural analysis and Ca2+ inhibitor experiments further indicated that Pvrboh4 and Pvrboh5 were closely associated with Ca2+ signaling, whereas Pvrboh6 did not exhibit such an association. Split-luciferase assay in N. benthamiana showed that PvRBOH5 strongly interacted with AtCPK5. Furthermore, a gene regulatory network analysis revealed multiple transcription factors from 32 distinct families that may regulate Pvrboh5 expression. These findings provide new insights into the role of Pvrboh genes in enhancing plant salt tolerance, offering potential targets for improving stress resilience in crops.
期刊介绍:
Plant & Cell Physiology (PCP) was established in 1959 and is the official journal of the Japanese Society of Plant Physiologists (JSPP). The title reflects the journal''s original interest and scope to encompass research not just at the whole-organism level but also at the cellular and subcellular levels.
Amongst the broad range of topics covered by this international journal, readers will find the very best original research on plant physiology, biochemistry, cell biology, molecular genetics, epigenetics, biotechnology, bioinformatics and –omics; as well as how plants respond to and interact with their environment (abiotic and biotic factors), and the biology of photosynthetic microorganisms.