Pathogen-responsive expression of glycosyltransferase genes UGT73B3 and UGT73B5 is necessary for resistance to Pseudomonas syringae pv tomato in Arabidopsis

被引:147
作者
Langlois-Meurinne, M [1 ]
Gachon, CMM [1 ]
Saindrenan, P [1 ]
机构
[1] Univ Paris 11, CNRS, Inst Biotechnol Plantes, UMR 8618, F-91405 Orsay, France
关键词
D O I
10.1104/pp.105.067223
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The genome sequencing of Arabidopsis (Arabidopsis thaliana) has revealed that secondary metabolism plant glycosyltransferases (UGTs) are encoded by an unexpectedly large multigenic family of 120 members. Very little is known about their actual function in planta, in particular during plant pathogen interactions. Among them, members of the group D are of particular interest since they are related to UGTs involved in stress-inducible responses in other plant species. We provide here a detailed analysis of the expression profiles of this group of Arabidopsis UGTs following infection with Pseudomonas syringae pv tomato or after treatment with salicylic acid, methyljasmonate, and hydrogen peroxide. Members of the group D displayed distinct induction profiles, indicating potential roles in stress or defense responses notably for UGT73B3 and UGT73B5. Analysis of UGT expression in Arabidopsis defense-signaling mutants further revealed that their induction is methyljasmonate independent, but partially salicylic acid dependent. T-DNA tagged mutants (ugt73b3 and ugt73b5) exhibited decreased resistance to P. syringae pv tomato-AvrRpm1, indicating that expression of the corresponding UGT genes is necessary during the hypersensitive response. These results emphasize the importance of plant secondary metabolite UGTs in plant-pathogen interactions and provide foundation for future understanding of the exact role of UGTs during the hypersensitive response.
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页码:1890 / 1901
页数:12
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共 67 条
[1]   Early genes and auxin action [J].
Abel, S ;
Theologis, A .
PLANT PHYSIOLOGY, 1996, 111 (01) :9-17
[2]   Genomics-based selection and functional characterization of triterpene glycosyltransferases from the model legume Medicago truncatula [J].
Achnine, L ;
Huhman, DV ;
Farag, MA ;
Sumner, LW ;
Blount, JW ;
Dixon, RA .
PLANT JOURNAL, 2005, 41 (06) :875-887
[3]   Genome-wide Insertional mutagenesis of Arabidopsis thaliana [J].
Alonso, JM ;
Stepanova, AN ;
Leisse, TJ ;
Kim, CJ ;
Chen, HM ;
Shinn, P ;
Stevenson, DK ;
Zimmerman, J ;
Barajas, P ;
Cheuk, R ;
Gadrinab, C ;
Heller, C ;
Jeske, A ;
Koesema, E ;
Meyers, CC ;
Parker, H ;
Prednis, L ;
Ansari, Y ;
Choy, N ;
Deen, H ;
Geralt, M ;
Hazari, N ;
Hom, E ;
Karnes, M ;
Mulholland, C ;
Ndubaku, R ;
Schmidt, I ;
Guzman, P ;
Aguilar-Henonin, L ;
Schmid, M ;
Weigel, D ;
Carter, DE ;
Marchand, T ;
Risseeuw, E ;
Brogden, D ;
Zeko, A ;
Crosby, WL ;
Berry, CC ;
Ecker, JR .
SCIENCE, 2003, 301 (5633) :653-657
[4]   Trends in lignin modification: a comprehensive analysis of the effects of genetic manipulations/mutations on lignification and vascular integrity [J].
Anterola, AM ;
Lewis, NG .
PHYTOCHEMISTRY, 2002, 61 (03) :221-294
[5]   Reactive oxygen species: Metabolism, oxidative stress, and signal transduction [J].
Apel, K ;
Hirt, H .
ANNUAL REVIEW OF PLANT BIOLOGY, 2004, 55 :373-399
[6]   Fumonisin B1-induced cell death in Arabidopsis protoplasts requires jasmonate-, ethylene-, and salicylate-dependent signaling pathways [J].
Asai, T ;
Stone, JM ;
Heard, JE ;
Kovtun, Y ;
Yorgey, P ;
Sheen, J ;
Ausubel, FM .
PLANT CELL, 2000, 12 (10) :1823-1835
[7]  
CAO H, 1994, PLANT CELL, V6, P1583, DOI 10.1105/tpc.6.11.1583
[8]   SEMI-CONSTITUTIVE EXPRESSION OF AN ARABIDOPSIS-THALIANA ALPHA-TUBULIN GENE [J].
CARPENTER, JL ;
KOPCZAK, SD ;
SNUSTAD, DP ;
SILFLOW, CD .
PLANT MOLECULAR BIOLOGY, 1993, 21 (05) :937-942
[9]   Expression profiling of the whole Arabidopsis Shaggy-like kinase multigene family by real-time reverse transcriptase-polymerase chain reaction [J].
Charrier, B ;
Champion, A ;
Henry, Y ;
Kreis, M .
PLANT PHYSIOLOGY, 2002, 130 (02) :577-590
[10]   Downregulation of a pathogen-responsive tobacco UDP-Glc:phenylpropanoid glucosyltransferase reduces scopoletin glucoside accumulation, enhances oxidative stress, and weakens virus resistance [J].
Chong, J ;
Baltz, R ;
Schmitt, C ;
Beffa, R ;
Fritig, B ;
Saindrenan, P .
PLANT CELL, 2002, 14 (05) :1093-1107