Co-option of a default secretory pathway for plant immune responses

被引:361
作者
Kwon, Chian [1 ]
Neu, Christina [1 ]
Pajonk, Simone [1 ]
Yun, Hye Sup [1 ]
Lipka, Ulrike [1 ,2 ]
Humphry, Matt [1 ]
Bau, Stefan [1 ]
Straus, Marco [1 ]
Kwaaitaal, Mark [1 ]
Rampelt, Heike [2 ]
El Kasmi, Farid
Juergens, Gerd
Parker, Jane [1 ]
Panstruga, Ralph [1 ]
Lipka, Volker [1 ,2 ]
Schulze-Lefert, Paul [1 ]
机构
[1] Max Planck Inst Zuchtungsforsch, Dept Plant Microbe Interact, D-50829 Cologne, Germany
[2] Univ Tubingen, ZMBP, D-72076 Tubingen, Germany
基金
新加坡国家研究基金会;
关键词
D O I
10.1038/nature06545
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cell- autonomous immunity is widespread in plant - fungus interactions and terminates fungal pathogenesis either at the cell surface or after pathogen entry. Although post- invasive resistance responses typically coincide with a self- contained cell death of plant cells undergoing attack by parasites, these cells survive pre- invasive defence. Mutational analysis in Arabidopsis identified PEN1 syntaxin as one component of two pre- invasive resistance pathways against ascomycete powdery mildew fungi(1-3). Here we show that plasma- membrane- resident PEN1 promiscuously forms SDS- resistant soluble N- ethylmaleimide sensitive factor attachment protein receptor ( SNARE) complexes together with the SNAP33 adaptor and a subset of vesicle- associated membrane proteins ( VAMPs). PEN1- dependent disease resistance acts in vivo mainly through two functionally redundant VAMP72 subfamily members, VAMP721 and VAMP722. Unexpectedly, the same two VAMP proteins also operate redundantly in a default secretory pathway, suggesting dual functions in separate biological processes owing to evolutionary co- option of the default pathway for plant immunity. The disease resistance function of the secretory PEN1 - SNAP33 - VAMP721/ 722 complex and the pathogen- induced subcellular dynamics of its components are mechanistically reminiscent of immunological synapse formation in vertebrates, enabling execution of immune responses through focal secretion.
引用
收藏
页码:835 / U10
页数:7
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