ORIGINAL RESEARCH article

Front. Plant Sci.

Sec. Functional and Applied Plant Genomics

Volume 16 - 2025 | doi: 10.3389/fpls.2025.1614011

This article is part of the Research TopicAI-Assisted Bioinformatics and Functional Genomics Technologies in Medicinal PlantsView all articles

Genome-wide identification, characterization, and expression analysis of the SOS1 gene family in the medicinal plant Paeonia ostii under salt stress

Provisionally accepted
Yahong  ChenYahong Chen1Huabing  LiangHuabing Liang2Zhanchang  WangZhanchang Wang2Quaid  HussainQuaid Hussain3Xuexiong  ZhangXuexiong Zhang4Fazhi  ChenFazhi Chen2*Xiaohua  WangXiaohua Wang1*
  • 1College of Life Sciences, Wuchang University of Technology, Wuhan, Hubei Province, 430223, China, Wuhan, China
  • 2Wuhan Academy of Agricultural Sciences, Wuhan, Hubei Province, 430070, China, Wuhan, China
  • 3Shenzhen Key Laboratory of Marine Bioresource and Eco-environmental Science, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, PR China, Shenzhen, China
  • 4Baokang County Forestry Bureau, Xiangyang, Hubei Province, 441600, China, wuhan, China

The final, formatted version of the article will be published soon.

Paeonia ostii is a commercially important ornamental and traditional medicinal plant that is esteemed in China. Salt stress is a widespread abiotic stress that significantly affects plant growth and development, and moderate stress can significantly promote the synthesis of plant secondary metabolites, requiring clarification of its underlying molecular mechanisms. The Salt Overly Sensitive 1 (SOS1) gene family is essential for salt stress tolerance, encoding Na + /H + antiporters that preserve ion homeostasis and reduce cellular damage. This study conducted an extensive genome-wide analysis of the SOS1 gene family in Paeonia ostii, encompassing gene identification, characterization, three-dimensional and secondary structure prediction, gene structure and motif analysis, multiple alignments, phylogenetic tree construction, chromosomal localization, cis-regulatory element analysis, synteny analysis, Ka/Ks calculation, and gene expression analysis under salt stress treatments in three cultivars. Our findings identified 19 SOS1 genes within the P. ostii genome, demonstrating unique structural and functional attributes.All SOS1 genes were located on the plasma membrane and distributed across five chromosomes and two scaffolds. The conserved motif analysis results indicated that the SOS1 homologs had 2 comparable protein structures. The coding sections of 19 PoSOS1 genes comprise amino acid sequences varying from 455 to 859, whereas the exons encompass amino acids ranging from 3 to 20. Furthermore, we discovered that the 2.5 kb upstream promoter region of the PoSOS1s gene has many cis-elements linked to phytohormones and stress responses. The phylogenetic study categorized the PoSOS1 genes into three subfamilies. In total, 38 miRNAs that target 19 PoSOS1 genes from 18 distinct families were identified. Conversely, gene expression analysis revealed six differentially expressed SOS1 genes in three distinct cultivars subjected to salt stress, with all six genes down-regulated and only one gene up-regulated in the QF230 cultivar after six days of salt stress. This study offers new insights into the SOS1 gene family in P. ostii, elucidating its function in salt stress tolerance and establishing a foundation for future research on the functional characterization of SOS1 genes in P. ostii.

Keywords: Paeonia ostii, SOS1 gene family, salinity stress, miRNAs, expression analysis

Received: 18 Apr 2025; Accepted: 19 Jun 2025.

Copyright: © 2025 Chen, Liang, Wang, Hussain, Zhang, Chen and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Fazhi Chen, Wuhan Academy of Agricultural Sciences, Wuhan, Hubei Province, 430070, China, Wuhan, China
Xiaohua Wang, College of Life Sciences, Wuchang University of Technology, Wuhan, Hubei Province, 430223, China, Wuhan, China

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