Plant and animal PR1 family members inhibit programmed cell death and suppress bacterial pathogens in plant tissues

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...

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Published inMolecular plant pathology Vol. 19; no. 9; pp. 2111 - 2123
Main Authors Lincoln, James E., Sanchez, Juan P., Zumstein, Kristina, Gilchrist, David G.
Format Journal Article
LanguageEnglish
Published England John Wiley & Sons, Inc 01.09.2018
John Wiley and Sons Inc
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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.
AbstractList 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.
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.
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.
Author Lincoln, James E.
Gilchrist, David G.
Sanchez, Juan P.
Zumstein, Kristina
AuthorAffiliation 1 Department of Plant Pathology University of California Davis CA 95616 USA
3 Present address: Department of Plant Science University of California Davis CA 95616 USA
2 Present address: Monsanto Company Woodland CA 95695 USA
AuthorAffiliation_xml – name: 2 Present address: Monsanto Company Woodland CA 95695 USA
– name: 3 Present address: Department of Plant Science University of California Davis CA 95616 USA
– name: 1 Department of Plant Pathology University of California Davis CA 95616 USA
Author_xml – sequence: 1
  givenname: James E.
  orcidid: 0000-0002-2420-8653
  surname: Lincoln
  fullname: Lincoln, James E.
  organization: University of California
– sequence: 2
  givenname: Juan P.
  surname: Sanchez
  fullname: Sanchez, Juan P.
  organization: University of California
– sequence: 3
  givenname: Kristina
  surname: Zumstein
  fullname: Zumstein, Kristina
  organization: University of California
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  givenname: David G.
  orcidid: 0000-0003-0187-4546
  surname: Gilchrist
  fullname: Gilchrist, David G.
  email: dggilchrist@ucdavis.edu
  organization: University of California
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29603552$$D View this record in MEDLINE/PubMed
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plant disease
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SSID ssj0017925
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Snippet 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...
A role for programmed cell death (PCD) has been established as the basis for plant–microbe interactions. A functional plant‐based cDNA library screen...
A role for programmed cell death (PCD) has been established as the basis for plant-microbe interactions. A functional plant-based cDNA library screen...
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pubmed
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wiley
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Publisher
StartPage 2111
SubjectTerms Animals
antigen-antibody complex
Apoptosis
cDNA libraries
Cell death
complementary DNA
Fumonisin B1
Fungi
Fusion protein
gene expression
Gene Expression Regulation, Plant
GLIPR
grapes
Homology
Humans
Immunity
Innate immunity
Insects
leaves
mechanism of action
messenger RNA
Mode of action
Mortality
mRNA
Nicotiana - microbiology
Original
pathogenesis‐related
Pathogens
PCD
Pierce's disease
plant disease
Plant diseases
Plant Diseases - microbiology
Plant Proteins - genetics
Plant Proteins - metabolism
Plant species
Plant tissues
Plants (botany)
PR1
programmed cell death
Proteins
Pseudomonas syringae - pathogenicity
Pseudomonas syringae pv. tabaci
Rac1 protein
rice
Roots
Solanum lycopersicum - microbiology
Tobacco
Tomatoes
transgenes
Transgenic plants
Xyllela
Title Plant and animal PR1 family members inhibit programmed cell death and suppress bacterial pathogens in plant tissues
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fmpp.12685
https://www.ncbi.nlm.nih.gov/pubmed/29603552
https://www.proquest.com/docview/2088063865
https://www.proquest.com/docview/2153618018
https://pubmed.ncbi.nlm.nih.gov/PMC6638019
Volume 19
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