Abstract

The pbs3-1 mutant, identified in a screen for Arabidopsis (Arabidopsis thaliana) mutants exhibiting enhanced susceptibility to the avirulent Pseudomonas syringae pathogen DC3000 (avrPphB), also exhibits enhanced susceptibility to virulent P. syringae strains, suggesting it may impact basal disease resistance. Because induced salicylic acid (SA) is a critical mediator of basal resistance responses, free and glucose-conjugated SA levels were measured and expression of the SA-dependent pathogenesis-related (PR) marker, PR1, was assessed. Surprisingly, whereas accumulation of the SA glucoside and expression of PR1 were dramatically reduced in the pbs3-1 mutant in response to P. syringae (avrRpt2) infection, free SA was elevated. However, in response to exogenous SA, the conversion of free SA to SA glucoside and the induced expression of PR1 were similar in pbs3-1 and wild-type plants. Through positional cloning, complementation, and sequencing, we determined that the pbs3-1 mutant contains two point mutations in the C-terminal region of the protein encoded by At5g13320, resulting in nonconserved amino acid changes in highly conserved residues. Additional analyses with Arabidopsis containing T-DNA insertion (pbs3-2) and transposon insertion (pbs3-3) mutations in At5g13320 confirmed our findings with pbs3-1. PBS3 (also referred to as GH3.12) is a member of the GH3 family of acyl-adenylate/thioester-forming enzymes. Characterized GH3 family members, such as JAR1, act as phytohormone-amino acid synthetases. Thus, our results suggest that amino acid conjugation plays a critical role in SA metabolism and induced defense responses, with PBS3 acting upstream of SA, directly on SA, or on a competitive inhibitor of SA.

Highlights

  • The pbs3-1 mutant, identified in a screen for Arabidopsis (Arabidopsis thaliana) mutants exhibiting enhanced susceptibility to the avirulent Pseudomonas syringae pathogen DC3000, exhibits enhanced susceptibility to virulent P. syringae strains, suggesting it may impact basal disease resistance

  • An F2 mapping population was inoculated with Pst DC3000, and plants displaying disease symptoms were identified and scored for PCR-based markers adjacent to nga249

  • These 70 lines were scored for resistance to Pst DC3000 and for additional markers located between nga249 and nga151

Read more

Summary

Introduction

The pbs mutant, identified in a screen for Arabidopsis (Arabidopsis thaliana) mutants exhibiting enhanced susceptibility to the avirulent Pseudomonas syringae pathogen DC3000 (avrPphB), exhibits enhanced susceptibility to virulent P. syringae strains, suggesting it may impact basal disease resistance. To identify additional components of the R-protein signal transduction pathway, Warren et al (1999) screened for Arabidopsis mutants that displayed enhanced susceptibility after inoculation with an avirulent strain of Pseudomonas syringae pv tomato (Pst DC3000 [avrPphB]). Resistance to this strain by Arabidopsis var. Columbia-0 (Col-0) is mediated by the RPS5 gene (Simonich and Innes, 1995), which encodes a member of the nucleotide-binding site Leu-rich repeat family of R proteins (Warren et al, 1998) This mutant screen led to the identification of several susceptible alleles of RPS5 plus mutations in three additional genes, which were named PBS1, PBS2, and PBS3 for avrPphB susceptible (Warren et al, 1999). We present the above findings and discuss possible biochemical functions for PBS3 consistent with its observed functional impact and its putative biochemical activity as a GH3 family member

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.