植物学报

• 研究论文 • 上一篇    下一篇

外源磺肽素调控茭白分蘖的内源激素和转录组分析

谭驭宇1, 邱红静1, 张峻浩1, 钟一帆1, 肖羽含1, 金昱何1, 王雪菲1, 朱静仪1, 缪德麟1, 黄加琦1, 吴馨婷1, 郑寨生2, 杨梦飞2, 查笑君1*   

  1. 1浙江师范大学生命科学学院, 金华 321004; 2金华市农业科学研究院, 浙江省特色水生蔬菜育种与栽培重点实验室, 金华 321000
  • 收稿日期:2025-10-17 修回日期:2025-12-09 出版日期:2026-01-12 发布日期:2026-01-12
  • 通讯作者: 查笑君
  • 基金资助:
    国家自然科学基金(No.31000741)、金华市科技局项目(No.2020-2-016)、浙江省农业(蔬菜)新品种选育重大科技专项(No.2021C02065)和金华市科技计划主动设计项目(No.2023-2-001a)

Exogenous Phytosulfokine Regulates Endogenous Hormones and Transcriptomic Analysis in the Tillering of Zizania latifolia

Yuyu Tan1, Hongjing Qiu1, Junhao Zhang1, Yifan Zhong1, Yuhan Xiao1, Yuhe Jin1, Xuefei Wang1, Jingyi Zhu1, Delin Miao1, Jiaqi Huang1, Xinting Wu1, Saisheng Zheng2, Mengfei Yang2, Xiaojun Zha1*   

  1. 1College of Chemistry and Life Sciences, Zhejiang Normal University, Jinhua 321004, China; 2Jinhua Academy of Agricultural Sciences, Zhejiang Provincial Key Laboratory of Aquatic Vegetable Breeding and Cultivation, Jinhua 321000, China
  • Received:2025-10-17 Revised:2025-12-09 Online:2026-01-12 Published:2026-01-12
  • Contact: Xiaojun Zha

摘要: 为实现茭白(Zizania latifolia)高产优质栽培, 探究外源磺肽素(PSK)对茭白生长发育的影响。用磺肽素(PSK)处理茭白, 通过转录组测序(登录号PRJNA1377146)探讨其叶片基因表达, 以挖掘关键代谢途径及调控基因, 并测定其对内源激素水平、茭白分蘖数的影响。结果表明, 外源PSK能显著促进茭白分蘖, 改变内源激素, 如生长素、赤霉素、细胞分裂素的水平, 从而正向调控茭白的生长和发育。KEGG通路分析显示, PSK处理显著影响苯丙烷生物合成和脂肪酸降解途径, 主要通过影响木质素类的生物合成与过氧化物酶体反应来调控茭白的代谢发育。此外, 通过荧光定量PCR检测了部分差异表达基因的表达水平, 与转录组结果一致, 进一步证实了PSK对茭白的调控作用。研究为理解PSK在茭白生长发育中的作用提供了分子层面的见解, 并为茭白高产优质栽培提供了新策略。

关键词: 磺肽素,   茭白,   分蘖,   内源激素,   转录组

Abstract: INTRODUCTION: Zizania latifolia is an important aquatic vegetable in China with both economic and nutritional values, but it is currently facing industrial challenges such as lack of crop rotation, declining quality, and insufficient supply, and is in urgent need of efficient means to increase production. As a novel small peptide hormone, phytosulfokine (PSK) has significant potential in plant growth regulation and agricultural applications, but its mechanism of regulating tillering in Z. latifolia has not yet been clarified. In this study, we used PSK-treated Z. latifolia as the material, combined with transcriptome sequencing (accession No.PRJNA1377146), fluorescence quantitative PCR validation and endogenous hormone determination, to investigate the molecular and physiological mechanisms of PSK in regulating the tillering of Z. latifolia, and to provide a theoretical basis and technological support for the high-yield and high-quality cultivation of Z. latifolia.  RATIONALE: Z. latifolia is the second largest aquatic vegetable after lotus root in China, with remarkable economic and nutritional value, but the current cultivation is facing problems such as lack of crop rotation, strong seasonality, and declining soil fertility, which leads to quality degradation and insufficient supply, and there is an urgent need for efficient means of yield increase; PSK, as a small peptide hormone in plants, can regulate the physiological processes such as cell elongation and development of meristematic tissues, and it has demonstrated its value of promoting crop growth and delaying senescence in agriculture, but the molecular mechanism of PSK regulation has not been clearly defined. In agriculture, PSK has demonstrated its value in promoting crop growth, delaying aging and other applications. However, there are fewer studies on the regulation of plant growth and development, and the molecular mechanism has not yet been clarified. Therefore, it is of great significance to systematically analyze the changes in gene expression of Z. latifolia after PSK treatment by means of RNA-seq sequencing, combined with the determination of endogenous hormones and observation of the tillering phenotypes, to excavate key metabolic pathways and regulatory genes, and to elucidate the molecular and physiological mechanisms of its regulation of water bamboo tillering.  RESULTS: After transcriptome sequencing, a total of 806 differentially expressed genes (365 up-regulated and 441 down-regulated) were screened out, and GO enrichment analysis showed that the differentially expressed genes were mainly involved in biological processes such as response to water deficit, cell wall organization, etc., and KEGG analysis showed that the differentially expressed genes were significantly enriched in the pathways of phenylpropane biosynthesis and tryptophan metabolism, etc. The results of fluorescence quantitative PCR of four differentially expressed genes were in line with the trend of expression of transcriptome, PSK treatment significantly promoted tillering in Z. latifolia, and the number of tillers at 14 days of treatment was 122.22% higher than that of the control group, which was the most significant effect. Two-way ANOVA confirmed that the treatment, time and the interaction effect were all highly significant, and there was a time-dependent “window period”. As for endogenous hormones, the content of growth hormone, gibberellin and jasmonic acid increased significantly after PSK treatment (GA3 increased by 188.59%), and the content of abscisic acid and cytokinin decreased significantly, and the hormone ratio was significantly reconfigured.  CONCLUSION: Exogenous PSK regulates the tillering and growth of Z. latifolia through multiple pathways: it significantly alters the endogenous hormone levels, promotes the increase of growth-related hormones and inhibits the decrease of hormone-like hormones; it regulates the key metabolic pathways such as phenylpropane biosynthesis and fatty acid degradation, and influences the synthesis of the cell wall and energy metabolism; and it promotes the synthesis of indoleacetic acid through the expression of the key genes in the tryptophan metabolic pathway, which provides the material and signal basis for tillering. The optimal concentration of PSK treatment is 1 μmol·L–1, and the optimal application “window” is about 14 days after treatment. This study reveals the molecular mechanism of PSK regulation tillering of Z. latifolia, and provides feasible technical solutions and theoretical support for large-scale high-yield and high-quality cultivation of Z. latifolia.

Key words: Phytosulfokine,   Zizania latifolia,   tillering,   endogenous hormone,   transcriptome