Different mechanisms for phytoalexin induction by pathogen and wound signals in Medicago truncatula

被引:145
作者
Naoumkina, Marina
Farag, Mohamed A.
Sumner, Lloyd W.
Tang, Yuhong
Liu, Chang-Jun
Dixon, Richard A.
机构
[1] Samuel Roberts Noble Fdn Inc, Div Plant Biol, Ardmore, OK 73401 USA
[2] Cairo Univ, Fac Pharm, Dept Pharmacognosy, Cairo, Egypt
[3] Brookhaven Natl Lab, Dept Biol, Upton, NY 11973 USA
关键词
glucosidase; methyl jasmonate; phytoanticipin; cell culture; elicitation;
D O I
10.1073/pnas.0708697104
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 suspensions of the model legume Medicago truncatula accumulated the isoflavonoid phytoalexin medicarpin in response to yeast elicitor or methyl jasmonate (MJ), accompanied by decreased levels of isoflavone glycosides in W-treated cells. DNA microarray analysis revealed rapid, massive induction of early (iso)flavonoid pathway gene transcripts in response to yeast elicitor, but not MJ, and differential induction by the two elicitors of sets of genes encoding transcription factors, ABC transporters, and beta-glucosidases. In contrast, both elicitors induced genes encoding enzymes for conversion of the isoflavone formononetin to medicarpin. Four MJ-induced beta-glucosidases were expressed as recombinant enzymes in yeast, and three were active with isoflavone glucosides. The most highly induced beta-glucosidase was nuclear localized and preferred flavones to isoflavones. The results indicate that the genetic and biochemical mechanisms underlying accumulation of medicarpin differ depending on the nature of the stimulus and suggest a role for MJ as a signal for rapid hydrolysis of preformed, conjugated intermediates for antimicrobial biosynthesis during wound responses.
引用
收藏
页码:17909 / 17915
页数:7
相关论文
共 49 条
[1]   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
[2]   Molecular and biochemical characterization of 2-hydroxyisoflavanone dehydratase. Involvement of carboxylesterase-like proteins in leguminous isoflavone biosynthesis [J].
Akashi, T ;
Aoki, T ;
Ayabe, S .
PLANT PHYSIOLOGY, 2005, 137 (03) :882-891
[3]   cDNA cloning and biochemical characterization of S-adenosyl-L-methionine:: 2,7,4′-trihydroxyisoflavanone 4′-O-methyltransferase, a critical enzyme of the legume isoflavonoid phytoalexin pathway [J].
Akashi, T ;
Sawada, Y ;
Shimada, N ;
Sakurai, N ;
Aoki, T ;
Ayabe, S .
PLANT AND CELL PHYSIOLOGY, 2003, 44 (02) :103-112
[4]   Transcriptome analysis of alfalfa glandular trichomes [J].
Aziz, N ;
Paiva, NL ;
May, GD ;
Dixon, RA .
PLANTA, 2005, 221 (01) :28-38
[5]   THE CRYSTAL-STRUCTURE OF A CYANOGENIC BETA-GLUCOSIDASE FROM WHITE CLOVER, A FAMILY-1 GLYCOSYL HYDROLASE [J].
BARRETT, T ;
SURESH, CG ;
TOLLEY, SP ;
DODSON, EJ ;
HUGHES, MA .
STRUCTURE, 1995, 3 (09) :951-960
[6]   Metabolic profiling of Medicago truncatula cell cultures reveals the effects of biotic and abiotic elicitors on metabolism [J].
Broeckling, CD ;
Huhman, DV ;
Farag, MA ;
Smith, JT ;
May, GD ;
Mendes, P ;
Dixon, RA ;
Sumner, LW .
JOURNAL OF EXPERIMENTAL BOTANY, 2005, 56 (410) :323-336
[7]   ELICITOR-INDUCIBLE 3-HYDROXY-3-METHYLGLUTARYL COENZYME-A REDUCTASE-ACTIVITY IS REQUIRED FOR SESQUITERPENE ACCUMULATION IN TOBACCO CELL-SUSPENSION CULTURES [J].
CHAPPELL, J ;
VONLANKEN, C ;
VOGELI, U .
PLANT PHYSIOLOGY, 1991, 97 (02) :693-698
[8]   Microarray profiling of gene expression patterns in bladder tumor cells treated with genistein [J].
Chen, CC ;
Shieh, B ;
Jin, YT ;
Liau, YE ;
Huang, CH ;
Liou, JT ;
Wu, LW ;
Huang, WY ;
Young, KC ;
Lai, MD ;
Liu, HS ;
Li, C .
JOURNAL OF BIOMEDICAL SCIENCE, 2001, 8 (02) :214-222
[9]   Finding nuclear localization signals [J].
Cokol, M ;
Nair, R ;
Rost, B .
EMBO REPORTS, 2000, 1 (05) :411-415
[10]   Characterization in vitro and in vivo of the putative multigene 4-coumarate:CoA ligase network in Arabidopsis:: syringyl lignin and sinapate/sinapyl alcohol derivative formation [J].
Costa, MA ;
Bedgar, DL ;
Moinuddin, SGA ;
Kim, KW ;
Cardenas, CL ;
Cochrane, FC ;
Shockey, JM ;
Helms, GL ;
Amakura, Y ;
Takahashi, H ;
Milhollan, JK ;
Davin, LB ;
Browse, J ;
Lewis, NG .
PHYTOCHEMISTRY, 2005, 66 (17) :2072-2091