PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
April 22, 2026The Plant Journal2 citations

Phosphorylation of a zinc finger‐homeodomain transcription factor SlZHD7 by a pathogen‐responsive SlMAPK4 activates tomato resistance to Phytophthora

View Full Paper
TLTingting LiYLYingying Liu康梶康雄 梶

Key Points

  • The study aims to explore the role of the SlZHD7 transcription factor in tomato resistance to Phytophthora infestans and the involvement of SlMAPK4.
  • Functional analyses of SlZHD7 in the context of Phytophthora infestans
  • Investigation of the interaction between SlZHD7 and SlMAPK4
  • Assessment of resistance in plants with SlZHD7 overexpression and knockout
  • Overexpression of SlZHD7 enhances tomato resistance to P. infestans, while knockout decreases resistance.
  • SlMAPK4 phosphorylates SlZHD7, stabilizing it and promoting cell death required for immunity.
  • Phosphorylation-deficient mutants of SlZHD7 fail to confer disease resistance.

Abstract

SUMMARY Tomato production is severely threatened by late blight disease caused by Phytophthora infestans , yet durable control strategies remain limited. Identifying molecular resistance components is critical for sustainable disease management. Transcriptional reprogramming mediated by MAPK‐regulated transcription factors (TFs) plays a pivotal role in plant immunity to Phytophthora and remains to be explored. Here, we identify the zinc finger‐homeodomain transcription factor SlZHD7 as a positive regulator of tomato resistance to P. infestans . Functional analyses reveal that SlZHD7 induces salicylic acid‐dependent plant cell death and enhances pathogen‐associated molecular pattern (PAMP)‐triggered immunity (PTI). Overexpression of SlZHD7 significantly enhances resistance, whereas its knockout compromises resistance. Furthermore, SlMPK4 interacts with and phosphorylates SlZHD7 at three threonine residues to stabilize it. Importantly, phosphorylation‐deficient mutants fail to confer disease resistance, and MPK4 silencing abolishes SlZHD7‐induced cell death, thereby establishing that MPK4‐mediated phosphorylation is essential for the immune function of SlZHD7. Collectively, our study elucidates the function of the SlMPK4‐SlZHD7 signaling module, demonstrating that MPK4‐dependent phosphorylation stabilizes SlZHD7 to activate tomato resistance to P. infestans . These findings reveal mechanistic insights into late blight regulatory networks and highlight molecular targets for engineering crop resistance.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Li et al. (2026) studied this question.

synapsesocial.com/papers/69e866616e0dea528ddead76https://doi.org/10.1111/tpj.70873
Ask AI
Helpful
Bookmark
Share
View Full Paper