Down-regulation of free riboflavin content induces hydrogen peroxide and a pathogen defense in Arabidopsis
Riboflavin mediates many bioprocesses associated with the generation of hydrogen peroxide (H 2 O 2 ), a cellular signal that regulates defense responses in plants. Although plants can synthesize riboflavin, the levels vary widely in different organs and during different stages of development, indica...
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Veröffentlicht in: | Plant molecular biology 2011-09, Vol.77 (1-2), p.185-201 |
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Sprache: | eng |
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Zusammenfassung: | Riboflavin mediates many bioprocesses associated with the generation of hydrogen peroxide (H
2
O
2
), a cellular signal that regulates defense responses in plants. Although plants can synthesize riboflavin, the levels vary widely in different organs and during different stages of development, indicating that changes in riboflavin levels may have physiological effects. Here, we show that changing riboflavin content affects H
2
O
2
accumulation and a pathogen defense in
Arabidopsis thaliana
. Leaf content of free riboflavin was modulated by ectopic expression of the turtle gene encoding riboflavin-binding protein (RfBP). The
RfBP
-expressing
Arabidopsis thaliana
(REAT) plants produced the RfBP protein that possessed riboflavin-binding activity. Compared with the wild-type plant, several tested REAT lines had >70% less flavins of free form. This change accompanied an elevation in the level of H
2
O
2
and an enhancement of plant resistance to a bacterial pathogen. All the observed REAT characters were eliminated due to
RfBP
silencing (RfBPi) under REAT background. When an H
2
O
2
scavenger was applied, H
2
O
2
level declined in all the plants, and REAT no longer exhibited the phenotype of resistance enhancement. However, treatment with an NADPH oxidase inhibitor diminished H
2
O
2
content and pathogen defense in wild-type and RfBPi but not in REAT. Our results suggest that the intrinsic down-regulation of free flavins is responsible for NADPH oxidase-independent H
2
O
2
accumulation and the pathogen defense. |
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ISSN: | 0167-4412 1573-5028 |
DOI: | 10.1007/s11103-011-9802-0 |