Biotechnology Bulletin ›› 2026, Vol. 42 ›› Issue (2): 278-292.doi: 10.13560/j.cnki.biotech.bull.1985.2025-0585

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Identification and Expression Analysis of the RALF Gene Family in Panax notoginseng

YANG Zi-han1,2,3(), LI Kui-xiu1,2,3, LI Jun-liang1,2,3, LYU Wen-hui1,2,3, HE Wen-ting4, LIU Xu-yan5, LIU Guan-ze1,2()   

  1. 1.National & Local Joint Engineering Research Center of Germplasm Innovation and Utilization of Southwest Chinese Medicinal Materials, Yunnan Agricultural University, Kunming 650201
    2.Yunnan Key Laboratory for Medicinal Plant Biology, Yunnan Agricultural University, Kunming 650201
    3.College of Agronomy and Biotechnology, Yunnan Agricultural University, Kunming 650201
    4.College of Tobacco, Yunnan Agricultural University, Kunming 650201
    5.College of Plant Protection, Yunnan Agricultural University, Kunming 650201
  • Received:2025-06-06 Online:2026-02-26 Published:2026-03-17
  • Contact: LIU Guan-ze E-mail:1439104670@qq.com;guanzeliu@ynau.edu.cn

Abstract:

Objective Rapid alkalinization factors (RALFs) are plant peptide hormones that participate in immune responses. This study is aimed to identify the RALF gene family members in Panax notoginseng and to investigate the roles of PnoRALFs in P. notoginseng immune responses. Method The RALF gene family in P. notoginseng was identified using bioinformatics tools. Chromosomal localization, protein physicochemical properties, phylogenetic relationships, conserved motifs, gene structures, promoter cis-acting elements, and tissue-specific expression patterns were analyzed. Expression profiles were assessed under four hormone treatments-salicylic acid (SA), methyl jasmonate (MeJA), abscisic acid (ABA), and ethylene (ETH) and after infection with C. destructans. The function of a key gene was further validated through transient expression in Nicotiana benthamiana. Result Thirteen PnoRALFs genes were identified and mapped to eight chromosomes. These genes were classified into two subgroups. Conserved motif analysis showed the presence of RRXL and YISY motifs. Promoter regions contained multiple hormone-responsive cis-elements, including those responsive to ABA, MeJA, SA, and gibberellins (GA). Tissue-specific expression analysis revealed considerable variation in gene expressions among different tissues. The expressions of PnoRALF2, PnoRALF5, PnoRALF6, and PnoRALF9 were upregulated by hormone treatments. Transcriptome and RT-qPCR analyses indicated that nine PnoRALFs genes responded to C. destructans infection, with PnoRALF9 showing a marked increase in expression. Transient overexpression of PnoRALF9 in N. benthamiana increased the expressions of immunity-related genes such as NbFPK1 and NbWRKY29 in the pattern-triggered immunity (PTI) pathway and NbMPK6 and NbGAPDH in the reactive oxygen species (ROS) signaling pathway. Conclusion Thirteen PnoRALFs genes are identified in the P. notoginseng genome. Among them, PnoRALF9 responds to multiple hormone treatments and C. destructans infection. Transient overexpression of PnoRALF9 induces plant immunity-related gene expression, suggesting that PnoRALF9 plays a critical role in the immune response in P. notoginseng to disease.

Key words: Panax notoginseng, RALF gene family, hormone treatment, Cylindrocarpon destructans, expression analysis