Transcriptome changes in the phenylpropanoid pathway of Glycine max in response to Pseudomonas syringae infection

被引:142
作者
Zabala, Gracia
Zou, Jijun
Tuteja, Jigyasa
Gonzalez, Delkin O.
Clough, Steven J.
Vodkin, Lila O. [1 ]
机构
[1] Univ Illinois, Dept Crop Sci, Urbana, IL 61801 USA
[2] USDA ARS, Urbana, IL 61801 USA
关键词
D O I
10.1186/1471-2229-6-26
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Reports of plant molecular responses to pathogenic infections have pinpointed increases in activity of several genes of the phenylpropanoid pathway leading to the synthesis of lignin and flavonoids. The majority of those findings were derived from single gene studies and more recently from several global gene expression analyses. We undertook a global transcriptional analysis focused on the response of genes of the multiple branches of the phenylpropanoid pathway to infection by the Pseudomonas syringae pv. glycinea with or without the avirulence gene avrB to characterize more broadly the contribution of the multiple branches of the pathway to the resistance response in soybean. Transcript abundance in leaves was determined from analysis of soybean cDNA microarray data and hybridizations to RNA blots with specific gene probes. Results: The majority of the genes surveyed presented patterns of increased transcript accumulation. Some increased rapidly, 2 and 4 hours after inoculation, while others started to accumulate slowly by 8-12 hours. In contrast, transcripts of a few genes decreased in abundance 2 hours post inoculation. Most interestingly was the opposite temporal fluctuation in transcript abundance between early responsive genes in defense (CHS and IFS1) and F3H, the gene encoding a pivotal enzyme in the synthesis of anthocyanins, proanthocyanidins and flavonols. F3H transcripts decreased rapidly 2 hours post inoculation and increased during periods when CHS and IFS transcripts decreased. It was also determined that all but one (CHS4) family member genes (CHS1, CHS2, CHS3, CHS5, CHS6 and CHS7/8) accumulated higher transcript levels during the defense response provoked by the avirulent pathogen challenge. Conclusion: Based on the mRNA profiles, these results show the strong bias that soybean has towards increasing the synthesis of isoflavonoid phytoalexins concomitant with the down regulation of genes required for the synthesis of anthocyanins and proanthocyanins. Although proanthocyanins are known to be toxic compounds, the cells in the soybean leaves seem to be programmed to prioritize the synthesis and accumulation of isoflavonoid and pterocarpan phytoalexins during the resistance response. It was known that CHS transcripts accumulate in great abundance rapidly after inoculation of the soybean plants but our results have demonstrated that all but one (CHS4) member of the gene family member genes accumulated higher transcript levels during the defense response.
引用
收藏
页数:18
相关论文
共 63 条
[1]   DIFFERENTIAL ACCUMULATION OF PLANT DEFENSE GENE TRANSCRIPTS IN A COMPATIBLE AND AN INCOMPATIBLE PLANT-PATHOGEN INTERACTION [J].
BELL, JN ;
RYDER, TB ;
WINGATE, VPM ;
BAILEY, JA ;
LAMB, CJ .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (05) :1615-1623
[2]   RACE - CULTIVAR-SPECIFIC INDUCTION OF ENZYMES RELATED TO PHYTOALEXIN BIOSYNTHESIS IN SOYBEAN ROOTS FOLLOWING INFECTION WITH PHYTOPHTHORA-MEGASPERMA F SP GLYCINEA [J].
BONHOFF, A ;
LOYAL, R ;
EBEL, J ;
GRISEBACH, H .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1986, 246 (01) :149-154
[3]   Molecular characterisation and expression of a wound-inducible cDNA encoding a novel cinnamyl-alcohol dehydrogenase enzyme in lucerne (Medicago sativa L.) [J].
Brill, EM ;
Abrahams, S ;
Hayes, CM ;
Jenkins, CLD ;
Watson, JM .
PLANT MOLECULAR BIOLOGY, 1999, 41 (02) :279-291
[4]   EXPRESSION OF DEFENSE-RELATED AND PUTATIVE SIGNALING GENES DURING TOLERANT AND SUSCEPTIBLE INTERACTIONS OF ARABIDOPSIS WITH XANTHOMONAS-CAMPESTRIS PV CAMPESTRIS [J].
BUELL, CR ;
SOMERVILLE, SC .
MOLECULAR PLANT-MICROBE INTERACTIONS, 1995, 8 (03) :435-443
[5]   Gene expression profiling and protection of Medicago truncatula against a fungal infection in response to an elicitor from green algae Ulva spp [J].
Cluzet, S ;
Torregrosa, C ;
Jacquet, C ;
Lafitte, C ;
Fournier, J ;
Mercier, L ;
Salamagne, S ;
Briand, X ;
Esquerré-Tugayé, MT ;
Dumas, B .
PLANT CELL AND ENVIRONMENT, 2004, 27 (07) :917-928
[6]  
CROSS J. E., 1966, PLANT DB REPORT, V50, P557
[7]   CHARACTERIZATION OF ELICITOR-INDUCED DEFENSE RESPONSES IN SUSPENSION-CULTURED CELLS OF ARABIDOPSIS [J].
DAVIS, KR ;
AUSUBEL, FM .
MOLECULAR PLANT-MICROBE INTERACTIONS, 1989, 2 (06) :363-368
[8]   Salicylic acid and disease resistance in plants [J].
Dempsey, DA ;
Shah, J ;
Klessig, DF .
CRITICAL REVIEWS IN PLANT SCIENCES, 1999, 18 (04) :547-575
[9]   Pathogen avirulence and plant resistance: a key role for recognition [J].
DeWit, PJGM .
TRENDS IN PLANT SCIENCE, 1997, 2 (12) :452-458
[10]   Isoflavonoid biosynthesis and accumulation in developing soybean seeds [J].
Dhaubhadel, S ;
McGarvey, BD ;
Williams, R ;
Gijzen, M .
PLANT MOLECULAR BIOLOGY, 2003, 53 (06) :733-743