The receptor kinase RiSho1 in Rhizophagus irregularis regulates arbuscule development and drought tolerance during arbuscular mycorrhizal symbiosis

New Phytol. 2024 Jun;242(5):2207-2222. doi: 10.1111/nph.19677. Epub 2024 Mar 14.

Abstract

In terrestrial ecosystems, most plant species can form beneficial associations with arbuscular mycorrhizal (AM) fungi. Arbuscular mycorrhizal fungi benefit plant nutrient acquisition and enhance plant tolerance to drought. The high osmolarity glycerol 1 mitogen-activated protein kinase (HOG1-MAPK) cascade genes have been characterized in Rhizophagus irregularis. However, the upstream receptor of the HOG1-MAPK cascade remains to be investigated. We identify the receptor kinase RiSho1 from R. irregularis, containing four transmembrane domains and one Src homology 3 (SH3) domain, corresponding to the homologue of Saccharomyces cerevisiae. Higher expression levels of RiSho1 were detected during the in planta phase in response to drought. RiSho1 protein was localized in the plasma membrane of yeast, and interacted with the HOG1-MAPK module RiPbs2 directly by protein-protein interaction. RiSho1 complemented the growth defect of the yeast mutant ∆sho1 under sorbitol conditions. Knock-down of RiSho1 led to the decreased expression of downstream HOG1-MAPK cascade (RiSte11, RiPbs2, RiHog1) and drought-resistant genes (RiAQPs, RiTPSs, RiNTH1 and Ri14-3-3), hampered arbuscule development and decreased plants antioxidation ability under drought stress. Our study reveals the role of RiSho1 in regulating arbuscule development and drought-resistant genes via the HOG1-MAPK cascade. These findings provide new perspectives on the mechanisms by which AM fungi respond to drought.

Keywords: Rhizophagus irregularis; AM symbiosis; RiSho1 receptor kinase; arbuscular mycorrhizal fungi; drought stress; host‐induced gene silencing; virus‐induced gene silencing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological / genetics
  • Drought Resistance
  • Droughts*
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism
  • Fungi
  • Gene Expression Regulation, Plant
  • Medicago truncatula / enzymology
  • Medicago truncatula / genetics
  • Medicago truncatula / microbiology
  • Mycorrhizae* / physiology
  • Saccharomyces cerevisiae / genetics
  • Symbiosis* / genetics
  • Symbiosis* / physiology

Substances

  • Fungal Proteins

Supplementary concepts

  • Rhizophagus irregularis

Associated data

  • RefSeq/XP_025173019.1
  • RefSeq/RIB09682.1
  • RefSeq/GBC07197.1
  • RefSeq/KAF0550460.1
  • RefSeq/RIA91777.1
  • RefSeq/NP_011043.1