Calcium signalling mediates self-incompatibility response in the Brassicaceae

被引:0
|
作者
Iwano, Megumi [1 ]
Ito, Kanae [1 ]
Fujii, Sota [1 ]
Kakita, Mitsuru [1 ]
Asano-Shimosato, Hiroko [1 ]
Igarashi, Motoko [1 ]
Kaothien-Nakayama, Pulla [1 ]
Entani, Tetsuyuki [1 ]
Kanatani, Asaka [1 ]
Takehisa, Masashi [1 ]
Tanaka, Masaki [1 ]
Komatsu, Kunihiko [1 ]
Shiba, Hiroshi [1 ]
Nagai, Takeharu [2 ]
Miyawaki, Atsushi [3 ]
Isogai, Akira [1 ]
Takayama, Seiji [1 ]
机构
[1] Nara Inst Sci & Technol, Grad Sch Biol Sci, Ikoma 6300192, Japan
[2] Osaka Univ, Inst Sci & Ind Res, Osaka 5670047, Japan
[3] RIKEN, Inst Phys & Chem Res, Brain Sci Inst, Wako, Saitama 3510198, Japan
关键词
LOCUS RECEPTOR KINASE; E3 LIGASE PROMOTES; ARABIDOPSIS-THALIANA; PLASMA-MEMBRANE; POLLEN HYDRATION; PAPILLA CELLS; ARC1; CA2+; PROTEIN; EVOLUTION;
D O I
10.1038/NPLANTS.2015.128
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Self-incompatibility in the Brassicaceae is controlled by multiple haplotypes encoding the pollen ligand (S-locus protein 11, SP11, also known as S-locus cysteine-rich protein, SCR) and its stigmatic receptor (S-receptor kinase, SRK). A haplotype-specific interaction between SP11/SCR and SRK triggers the self-incompatibility response that leads to self-pollen rejection, but the signalling pathway remains largely unknown. Here we show that Ca2+ influx into stigma papilla cells mediates self-incompatibility signalling. Using self-incompatible Arabidopsis thaliana expressing SP11/SCR and SRK, we found that self-pollination specifically induced an increase in cytoplasmic Ca2+ ([Ca2+](cyt)) in papilla cells. Direct application of SP11/SCR to the papilla cell protoplasts induced Ca2+ increase, which was inhibited by D-(-)-2-amino-5-phosphonopentanoic acid (AP-5), a glutamate receptor channel blocker. An artificial increase in [Ca2+](cyt) in papilla cells arrested wild-type (WT) pollen hydration. Treatment of papilla cells with AP-5 interfered with self-incompatibility, and Ca2+ increase on the self-incompatibility response was reduced in the glutamate receptor-like channel (GLR) gene mutants. These results suggest that Ca2+ influx mediated by GLR is the essential self-incompatibility response leading to self-pollen rejection.
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页数:8
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