ROS signaling in the hypersensitive response When, where and what for?

被引:129
作者
Zurbriggen, Matias D. [1 ]
Carrillo, Nestor [1 ]
Hajirezaei, Mohammad-Reza [2 ]
机构
[1] Univ Nacl Rosario, CONICET, Inst Biol Mol & Celular Rosario IBR, Rosario, Santa Fe, Argentina
[2] Leibniz Inst Plant Genet & Crop Plant Res Leibniz, Gatersleben, Germany
关键词
biotic stress; chloroplasts; flavodoxin; hypersensitive response (HR); reactive oxygen species (ROS); ROS signaling;
D O I
10.4161/psb.5.4.10793
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Plants generally react to the attack of non-host and incompatible host microorganisms by inducing pathogenesis-related (PR) genes and localised cell death (LCD) at the site of infection, a process collectively known as the hypersensitive response (HR). Reactive oxygen species (ROS) are generated in various sub-cellular compartments shortly after pathogen recognition, and proposed to cue subsequent orchestration of the HR. Although apoplast-associated ROS production by plasma membrane NADPH oxidases have been most thoroughly studied, recent observations suggest that ROS are generated in chloroplasts earlier in the response and play a key role in execution of LCD. A model is presented in which the initial outcome of successful pathogen detection is ROS accumulation in plastids, likely mediated by mitogen-activated protein kinases and caused by dysfunction of the photosynthetic electron transport chain. ROS signaling is proposed to spread from plastids to the apoplast, through the activation of NADPH oxidases, and from there to adjacent cells, leading to suicidal death in the region of attempted infection.
引用
收藏
页码:393 / 396
页数:4
相关论文
共 29 条
[1]   Changes in plant mitochondrial electron transport alter cellular levels of reactive oxygen species and susceptibility to cell death signaling molecules [J].
Amirsadeghi, Sasan ;
Robson, Christine A. ;
McDonald, Allison E. ;
Vanlerberghe, Greg C. .
PLANT AND CELL PHYSIOLOGY, 2006, 47 (11) :1509-1519
[2]   Production and scavenging of reactive oxygen species in chloroplasts and their functions [J].
Asada, Kozi .
PLANT PHYSIOLOGY, 2006, 141 (02) :391-396
[3]   The role of radical burst via MAPK signaling in plant immunity [J].
Asai, Shuta ;
Yoshioka, Hirofumi .
PLANT SIGNALING & BEHAVIOR, 2008, 3 (11) :920-922
[4]   MAPKKKα is a positive regulator of cell death associated with both plant immunity and disease [J].
del Pozo, O ;
Pedley, KF ;
Martin, GB .
EMBO JOURNAL, 2004, 23 (15) :3072-3082
[6]   Redox control of systemic acquired resistance [J].
Fobert, PR ;
Després, C .
CURRENT OPINION IN PLANT BIOLOGY, 2005, 8 (04) :378-382
[7]   Different signaling and cell death roles of heterotrimeric G protein α and β subunits in the arabidopsis oxidative stress response to ozone [J].
Joo, JH ;
Wang, SY ;
Chen, JG ;
Jones, AM ;
Fedoroff, NV .
PLANT CELL, 2005, 17 (03) :957-970
[8]   Light perception in plant disease defence signalling [J].
Karpinski, S ;
Gabrys, H ;
Mateo, A ;
Karpinska, B ;
Mullineaux, PM .
CURRENT OPINION IN PLANT BIOLOGY, 2003, 6 (04) :390-396
[9]   Chloroplast-generated reactive oxygen species are involved in hypersensitive response-like cell death mediated by a mitogen-activated protein kinase cascade [J].
Liu, Yidong ;
Ren, Dongtao ;
Pike, Sharon ;
Pallardy, Stephen ;
Gassmann, Walter ;
Zhang, Shuqun .
PLANT JOURNAL, 2007, 51 (06) :941-954
[10]   Timing is everything: regulatory overlap in plant cell death [J].
Love, Andrew J. ;
Milner, Joel J. ;
Sadanandom, Ari .
TRENDS IN PLANT SCIENCE, 2008, 13 (11) :589-595