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The P3 Protein of Turnip mosaic virus Can Alone Induce Hypersensitive Response-Like Cell Death in Arabidopsis thaliana Carrying TuNI
Author(s) -
Bo Min Kim,
Noriko Suehiro,
Tomohide Natsuaki,
Tsuyoshi Inukai,
Chikara Masuta
Publication year - 2010
Publication title -
molecular plant-microbe interactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.565
H-Index - 153
eISSN - 1943-7706
pISSN - 0894-0282
DOI - 10.1094/mpmi-23-2-0144
Subject(s) - turnip mosaic virus , arabidopsis thaliana , arabidopsis , biology , hypersensitive response , programmed cell death , gene , protoplast , necrosis , gene expression , tumor necrosis factor alpha , virology , virus , microbiology and biotechnology , genetics , potyvirus , plant virus , mutant , immunology , plant disease resistance , apoptosis
Strains TuR1 and TuC of Turnip mosaic virus (TuMV) induce different symptoms on Arabidopsis thaliana ecotype Landsberg erecta (Ler); plants infected with TuR1 develop systemic necrosis, while TuC causes mosaics. We previously found that the Ler systemic necrosis was controlled by a single dominant gene, TuNI (TuMV necrosis inducer), and that it was actually a form of host defense response leading to a hypersensitive reaction (HR)-like cell death. To identify the viral factor interacting with TuNI, the domain swapping between the genomic clones of TuR1 and TuC was carried out, and we identified the TuMV symptom determinant interacting with TuNI as the P3 gene. Moreover, it was found that the central 0.5-kb domain of P3, including three different amino acids between the two isolates, was responsible for the systemic HR. To verify that the P3 gene can alone induce necrosis, we analyzed the constitutive P3 expression in Ler transgenic plants and the transient P3 expression in Ler protoplasts. These results indicated that P3 alone caused HR-like cell death. In this study, we successfully demonstrated that the systemic necrosis by TuMV in Arabidopsis was determined by the gene-for-gene interaction between TuNI and P3 using the protoplast system for direct verification.

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