Hyperphosphorylation of a mitochondrial protein, prohibitin, is induced by calyculin A in a rice lesion-mimic mutant cdr1

被引:55
作者
Takahashi, A
Kawasaki, T
Wong, HL
Suharsono, U
Hirano, H
Shimamoto, K
机构
[1] Nara Inst Sci & Technol, Plant Mol Genet Lab, Ikoma 6300101, Japan
[2] Yokohama City Univ, Kihara Inst Biol Res, Yokohama, Kanagawa 2440813, Japan
关键词
D O I
10.1104/pp.103.021733
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The rice (Oryza saliva) lesion-mimic mutants, cell death and resistance (cdr), show spontaneous cell death on the entire leaf and exhibited significant resistance to the rice blast fungus. Our previous studies showed that CDR1 and CDR2 genes negatively regulated the phosphorylation steps leading to the activation of NADPH oxidase, which is associated with oxidative burst. To identify novel factors involved in the phosphorylation steps, the phosphorylation level of total proteins was compared between cdr mutants and wild type using two-dimensional gel electrophoresis. Here, we show that the phosphorylation level of four proteins in cdr1 was increased as compared with the wild type after calyculin A treatment. Partial amino acid sequences revealed that one of the four proteins is homologous to prohibitin (PHB), which has been shown to be associated with senescence and cell death and to function as a chaperone in the assembly of mitochondrial respiratory chain complex in yeast and mammals. Analysis of green fluorescent protein fusions indicated that rice PHB (OsPHB1) was targeted to mitochondria as found in yeast and mammals, suggesting a possibility that PHB is involved in defense response and/or programmed cell death through the mitochondrial function.
引用
收藏
页码:1861 / 1869
页数:9
相关论文
共 48 条
[1]   Chloroplast and mitochondrial proteases in Arabidopsis. A proposed nomenclature [J].
Adam, Z ;
Adamska, I ;
Nakabayashi, K ;
Ostersetzer, O ;
Haussuhl, K ;
Manuell, A ;
Zheng, B ;
Vallon, O ;
Rodermel, SR ;
Shinozaki, K ;
Clarke, AK .
PLANT PHYSIOLOGY, 2001, 125 (04) :1912-1918
[2]   Prohibitin family members interact genetically with mitochondrial inheritance components in Saccharomyces cerevisiae [J].
Berger, KH ;
Yaffe, MP .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (07) :4043-4052
[3]   Biochemical pathways of caspase activation during apoptosis [J].
Budihardjo, I ;
Oliver, H ;
Lutter, M ;
Luo, X ;
Wang, XD .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1999, 15 :269-290
[4]   The prohibitin family of mitochondrial proteins regulate replicative lifespan [J].
Coates, PJ ;
Jamieson, DJ ;
Smart, K ;
Prescott, AR ;
Hall, PA .
CURRENT BIOLOGY, 1997, 7 (08) :607-610
[5]   The oat mitochondrial permeability transition and its implication in victorin binding and induced cell death [J].
Curtis, MJ ;
Wolpert, TJ .
PLANT JOURNAL, 2002, 29 (03) :295-312
[6]   Plant pathogens and integrated defence responses to infection [J].
Dangl, JL ;
Jones, JDG .
NATURE, 2001, 411 (6839) :826-833
[7]   Prohibitin and the senescent phenotype [J].
DellOrco, RT ;
McClung, JK ;
Jupe, ER ;
Liu, XT .
EXPERIMENTAL GERONTOLOGY, 1996, 31 (1-2) :245-252
[8]   EARLY EVENTS IN THE ACTIVATION OF PLANT DEFENSE RESPONSES [J].
DIXON, RA ;
HARRISON, MJ ;
LAMB, CJ .
ANNUAL REVIEW OF PHYTOPATHOLOGY, 1994, 32 :479-501
[9]   THE PROTEIN PHOSPHATASE INHIBITOR CALYCULIN-A MIMICS ELICITOR ACTION IN PLANT-CELLS AND INDUCES RAPID HYPERPHOSPHORYLATION OF SPECIFIC PROTEINS AS REVEALED BY PULSE LABELING WITH [P-33] PHOSPHATE [J].
FELIX, G ;
REGENASS, M ;
SPANU, P ;
BOLLER, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (03) :952-956
[10]   PERCEPTION AND RESPONSE IN PLANT-DISEASE RESISTANCE [J].
GODIARD, L ;
GRANT, MR ;
DIETRICH, RA ;
KIEDROWSKI, S ;
DANGL, JL .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1994, 4 (05) :662-671