Molecular Plant-Microbe Interactions (Nov 2011)

Medicago truncatula IPD3 Is a Member of the Common Symbiotic Signaling Pathway Required for Rhizobial and Mycorrhizal Symbioses

  • Beatrix Horváth,
  • Li Huey Yeun,
  • Ágota Domonkos,
  • Gábor Halász,
  • Enrico Gobbato,
  • Ferhan Ayaydin,
  • Krisztina Miró,
  • Sibylle Hirsch,
  • Jongho Sun,
  • Million Tadege,
  • Pascal Ratet,
  • Kirankumar S. Mysore,
  • Jean-Michel Ané,
  • Giles E. D. Oldroyd,
  • Péter Kaló

DOI
https://doi.org/10.1094/MPMI-01-11-0015
Journal volume & issue
Vol. 24, no. 11
pp. 1345 – 1358

Abstract

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Legumes form endosymbiotic associations with nitrogen-fixing bacteria and arbuscular mycorrhizal (AM) fungi which facilitate nutrient uptake. Both symbiotic interactions require a molecular signal exchange between the plant and the symbiont, and this involves a conserved symbiosis (Sym) signaling pathway. In order to identify plant genes required for intracellular accommodation of nitrogen-fixing bacteria and AM fungi, we characterized Medicago truncatula symbiotic mutants defective for rhizobial infection of nodule cells and colonization of root cells by AM hyphae. Here, we describe mutants impaired in the interacting protein of DMI3 (IPD3) gene, which has been identified earlier as an interacting partner of the calcium/calmodulin-dependent protein, a member of the Sym pathway. The ipd3 mutants are impaired in both rhizobial and mycorrhizal colonization and we show that IPD3 is necessary for appropriate Nod-factor-induced gene expression. This indicates that IPD3 is a member of the common Sym pathway. We observed differences in the severity of ipd3 mutants that appear to be the result of the genetic background. This supports the hypothesis that IPD3 function is partially redundant and, thus, additional genetic components must exist that have analogous functions to IPD3. This explains why mutations in an essential component of the Sym pathway have defects at late stages of the symbiotic interactions.