Plant and animal PR1 family members inhibit programmed cell death and suppress bacterial pathogens in plant tissues. (7th May 2018)

• Record Type: Journal Article
• Authors: Lincoln, James E.; Sanchez, Juan P.; Zumstein, Kristina; Gilchrist, David G.
• Is Part Of: Molecular plant pathology. Volume 19:Number 9(2018)
• Page Start: 2111
• Page End: 2123
• Publication Date: 2018-05-07
• Subjects: GLIPR -- pathogenesis‐related -- PCD -- Pierce's disease -- plant disease -- PR1 -- Xyllela; Plant diseases -- Molecular aspects -- Periodicals; Plant-pathogen relationships -- Molecular aspects -- Periodicals; 571.936
• DOI: 10.1111/mpp.12685
• Languages: English
• ISSNs: 1464-6722

Abstract

Summary: A role for programmed cell death (PCD) has been established as the basis for plant–microbe interactions. A functional plant‐based cDNA library screen identified possible anti‐PCD genes, including one member of the PR1 family, designated P14a, from tomato. Members of the PR1 family have been subject to extensive research in view of their possible role in resistance against pathogens. The PR1 family is represented in every plant species studied to date and homologues have been found in animals, fungi and insects. However, the biological function of the PR1 protein from plants has remained elusive in spite of extensive research regarding a role in the response of plants to disease. Constitutive expression of P14a in transgenic tomato roots protected the roots against PCD triggered by Fumonisin B1, as did the human orthologue GLIPR1, indicating a kingdom crossing function for PR1. Tobacco plants transformed with a P14a‐GFP fusion construct and inoculated with Pseudomonas syringae pv. tabaci revealed that the mRNA was abundant throughout the leaves, but the fusion protein was restricted to the lesion margins, where cell death and bacterial spread were arrested. Vitus vinifera grapes expressing the PR1 homologue P14a as a transgene were protected against the cell death symptoms of Pierce's disease. A pull‐down assay identified putative PR1‐interacting proteins, including members of the Rac1 immune complex, known to function in innate immunity in rice and animal systems. The findings herein are consistent with a role of PR1 in the suppression of cell death‐dependent disease symptoms and a possible mode of action.