Safeners recruit multiple signalling pathways for the orchestrated induction of the cellular xenobiotic detoxification machinery in Arabidopsis

被引:61
作者
Behringer, Carina [1 ,2 ]
Bartsch, Klaus [2 ]
Schaller, Andreas [1 ]
机构
[1] Univ Hohenheim, Inst Plant Physiol & Biotechnol, D-70599 Stuttgart, Germany
[2] Bayer CropSci AG, D-65926 Frankfurt, Germany
关键词
Arabidopsis; as1; element; isoxadifen; mefenpyr; oxidative stress; TGA factor; safener; salicylic acid; xenobiotics; GLUTATHIONE S-TRANSFERASES; TGA TRANSCRIPTION FACTORS; SALICYLIC-ACID INDUCTION; HERBICIDE RESISTANCE; GENE-EXPRESSION; PLANT DEFENSE; PROTEOMIC ANALYSIS; STRESS; THALIANA; IDENTIFICATION;
D O I
10.1111/j.1365-3040.2011.02392.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Safeners enhance herbicide tolerance in crop plants but not in target weeds, thus improving herbicide selectivity. The safeners isoxadifen-ethyl and mefenpyr-diethyl protect cereal crops from sulfonyl urea herbicides in postemergence application. The two safeners were shown here to induce the cellular xenobiotic detoxification machinery in Arabidopsis thaliana when applied to leaves in a way mimicking field application. Gene expression profiling revealed the induction of 446 genes potentially involved in the detoxification process. Transgenic Arabidopsis plants expressing a reporter gene under control of a safener-responsive maize promoter were used as a model system to study the safener signalling pathway. Reporter gene analysis in the tga2/3/5/6, sid2-2 and npr1 mutants as compared with the wild-type background showed that safener inducibility required TGA transcription factors and salicylic acid (SA) in a NON-EXPRESSOR of PR-1 (NPR1)-independent pathway converging on two as-1 promoter elements. For the majority of the safener-responsive Arabidopsis genes, a similar dependence on TGA transcription factors and/or SA was shown by gene expression profiling in wild-type plants as compared with the tga2/3/5/6 and sid2-2 mutants. Thirty-eight percent of the genes, however, were induced by safeners in a TGA/SA-independent manner. These genes are likely to be controlled by WRKY transcription factors and cognate W-boxes in their promoters.
引用
收藏
页码:1970 / 1985
页数:16
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