Immune signaling and drought tolerance mediated by NDR1-AHA5 regulation of H⁺–ATPase, guard cells, and homeostasis


Lu Y., Chen H., Corrion A., Li P., Samaradivakara S., Wai C. M., ...Daha Fazla

Plant Cell Reports, cilt.44, sa.11, 2025 (SCI-Expanded, Scopus) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 44 Sayı: 11
  • Basım Tarihi: 2025
  • Doi Numarası: 10.1007/s00299-025-03637-0
  • Dergi Adı: Plant Cell Reports
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Agricultural & Environmental Science Database, BIOSIS, Biotechnology Research Abstracts, CAB Abstracts, Chemical Abstracts Core, Food Science & Technology Abstracts, Veterinary Science Database
  • Anahtar Kelimeler: Arabidopsis immunity, Drought stress, NDR1, Plasma membrane H+–ATPase (AHA5), Stomatal regulation
  • Ankara Üniversitesi Adresli: Evet

Özet

Key message: NDR1 and AHA5 coordinate drought stress and immune responses via stomatal regulation, uncovering a molecular link between abiotic and biotic stress adaptation in Arabidopsis. Abstract: Plant stress responses have overlapping molecular and physiological signatures. Not surprisingly, many of these are also shared with numerous other processes, including growth and development, as well as abiotic and biotic signaling. NON-RACE-SPECIFIC DISEASE RESISTANCE1 (NDR1) is a key component of plant immune signaling, required for defense against the bacterial pathogen Pseudomonas syringae. In this study, we have identified that NDR1 contributes to stomatal-based processes following exposure to biotic (flg22 (flagellin peptide) and elf26 (EF-Tu-related elicitor)) and abiotic (ABA, drought, etc.) elicitors. Interestingly, we found that NDR1 is part of a signaling cascade that confers tolerance to water loss—a required component of drought stress responses in plants, a role that couples stress signaling in an abscisic acid-dependent manner. As a definition of its broader connectivity to this response, we identified that NDR1 physically associates with the PM-localized H+–ATPases AHA1, AHA2, and AHA5, an association that is required for proper regulation of H+–ATPase activity and stomatal guard cell dynamics. Using a comprehensive whole-transcriptome analysis, we further show that NDR1 is required for multiple, genetically overlapping physiological processes, including response to water withholding. In total, we demonstrate that NDR1 functions in signaling processes associated with both biotic and abiotic stress response pathways, a function we hypothesize illustrates NDR1’s role in the maintenance of cellular homeostasis during stress response activation.