生物技术通报 ›› 2025, Vol. 41 ›› Issue (1): 85-94.doi: 10.13560/j.cnki.biotech.bull.1985.2024-0535

• 技术与方法 • 上一篇    下一篇

基于软腐病菌诱导的魔芋酵母双杂交文库筛选WRKY72互作蛋白

沈川1(), 李夏1, 覃剑锋2, 段龙飞2, 刘佳3   

  1. 1.安康学院陕南生态经济研究中心,安康 725000
    2.安康市农业科学研究院,安康 725000
    3.安康学院现代农业与生物技术学院,安康 725000
  • 收稿日期:2024-06-03 出版日期:2025-01-26 发布日期:2025-01-22
  • 通讯作者: 沈川
  • 作者简介:沈川,男,博士,副教授,研究方向:植物与病原菌互作;E-mail: chuan_shen@aku.edu.cn
  • 基金资助:
    陕西省科技厅创新人才推进计划项目(2024ZC-KJXX-056);陕西省科协青年人才托举计划项目(20240629);陕西省教育厅青年创新团队科研计划项目(23JP001);安康市科学计划项目(AK2023PD-KJXX-07)

Screening for WRKY72-interacting Proteins Using a Yeast Two-hybrid Library Derived from Soft Rot Pathogen-induced Amorphophallus konjac

SHEN Chuan1(), LI Xia1, QIN Jian-feng2, DUAN Long-fei2, LIU Jia3   

  1. 1. Shaannan Eco-economy Research Center, Ankang University, Ankang 725000
    2. Ankang Academy of Agricultural Sciences, Ankang 725000
    3. School of Modern Agriculture & Biotechnology, Ankang University, Ankang 725000
  • Received:2024-06-03 Published:2025-01-26 Online:2025-01-22

摘要:

【目的】通过构建魔芋cDNA文库,筛选转录因子WRKY72的互作蛋白,为解析WRKY72调控魔芋抗病的分子机制提供帮助。【方法】以胡萝卜软腐果胶杆菌侵染不同阶段的魔芋为实验材料,提取总RNA等量混匀后构建魔芋cDNA文库,使用同源重组的方法构建转录因子WRKY72的诱饵载体,采用酵母双杂交技术筛选候选靶标蛋白,并进行一对一验证。【结果】酵母文库滴度为1.6×107 CFU/mL,插入片段的平均长度在1 000 bp左右,诱饵载体在酵母中经验证无自激活。诱饵载体pGBKT7-WRKY72筛库获得了41个阳性互作蛋白,包括转运蛋白、通道蛋白、热休克蛋白、叶绿素结合蛋白和过氧化物酶等。对这些互作蛋白进行GO和KEGG功能富集分析,最后选取12个互作蛋白进行一对一酵母双杂交验证。【结论】成功构建了高质量的魔芋文库并筛选到了转录因子WRKY72的互作蛋白,为解析魔芋抗软腐病机制提供了理论基础。

关键词: 魔芋软腐病, 酵母双杂交, cDNA文库, WRKY转录因子, 互作蛋白

Abstract:

【Objective】This study is aimed to construct a konjac cDNA library and screen for interacting proteins of the transcription factor WRKY72 in order to elucidate the molecular mechanism underlying WRKY72-mediated konjac resistance against diseases.【Method】Konjac plants at different stages of bacterial soft rot infection were used as experimental materials. Total RNA was extracted, pooled in equal amounts, and used to construct a konjac cDNA library. The bait vector containing the transcription factor WRKY72 was constructed using the homologous recombination method, and a yeast two-hybrid screen was performed to identify candidate target proteins, which were further verified individually.【Result】The yeast library titer was 1.6×107 CFU/mL, and the average length of the inserted fragments was around 1 000 bp. The bait vector was verified to have no self-activation in yeast. The bait vector pGBKT7-WRKY72 was used to screen library and 41 positive interacting proteins were obtained, including transport proteins, channel proteins, heat shock proteins, chlorophyll-binding proteins, and peroxidases. Gene Ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)functional enrichment analyses were performed on these interacting proteins, and 12 of them were further verified by one-on-one yeast two-hybrid assays.【Conclusion】A high-quality konjac cDNA library was successfully constructed, and the interacting proteins of the transcription factor WRKY72 were screened, providing a theoretical basis for elucidating the mechanism of resistance against soft rot disease in konjac.

Key words: konjac soft rot, yeast two-hybrid, cDNA library, WRKY transcription factor, interacting proteins