TY - JOUR
T1 - Gene Expression Profiling Soybean Stem Tissue Early Response to Sclerotinia sclerotiorum and In Silico Mapping in Relation to Resistance Markers
AU - Calla, Bernarda
AU - Vuong, Tri
AU - Radwan, Osman
AU - Hartman, Glen L.
AU - Clough, Steven J.
N1 - The authors would like to thank Dr. Matthew Hudson and Dr. Min Li of the University of Illinois for their assistance with various aspects of the bioinformatics work, Dr. Brian Diers of the University of Illinois for assistance with marker selection, David Neece of the USDA-ARS, Urbana, IL for wet-lab assistance, and Dr. Perry Cregan of the USDA-ARS, Beltsville, MD for marker sequences. The authors would also like to thank Dr. Daina Simmonds of AgCanada for critical review of the manuscript.
Work supported by the USDA‐CREES National Sclerotinia Initiative and USDA‐ARS CRIS project 3611‐21000‐018‐00D. Mention of trade names or commercial products in this publication is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the United States Department of Agriculture. Normalized microarray data has been deposited in NCBI GEO as accession # GSE15369 .
PY - 2009/7
Y1 - 2009/7
N2 - White mold, caused by Sclerotinia sclerotiorum (Lib.) de Bary, can be a serious disease of crops grown under cool, moist environments. In many plants, such as soybean [Glycine max (L.) Merr.], complete genetic resistance does not exist. To identify possible genes involved in defense against this pathogen, and to determine possible physiological changes that occur during infection, a microarray screen was conducted using stem tissue to evaluate changes in gene expression between partially resistant and susceptible soybean genotypes at 8 and 14 hours post inoculation. RNA from 15 day-old inoculated plants was labeled and hybridized to soybean cDNA microarrays. ANOVA identified 1270 significant genes from the comparison between time points and 105 genes from the comparison between genotypes. Selected genes were classified into functional categories. The analyses identified changes in cell-wall composition and signaling pathways, as well as suggesting a role for anthocyanin and anthocyanidin synthesis in the defense against S. sclerotiorum. In-silico mapping of both the differentially expressed transcripts and of public markers associated with partial resistance to white mold, provided evidence of several differentially expressed genes being closely positioned to white mold resistance markers, with the two most promising genes encoding a PR-5 and anthocyanidin synthase.
AB - White mold, caused by Sclerotinia sclerotiorum (Lib.) de Bary, can be a serious disease of crops grown under cool, moist environments. In many plants, such as soybean [Glycine max (L.) Merr.], complete genetic resistance does not exist. To identify possible genes involved in defense against this pathogen, and to determine possible physiological changes that occur during infection, a microarray screen was conducted using stem tissue to evaluate changes in gene expression between partially resistant and susceptible soybean genotypes at 8 and 14 hours post inoculation. RNA from 15 day-old inoculated plants was labeled and hybridized to soybean cDNA microarrays. ANOVA identified 1270 significant genes from the comparison between time points and 105 genes from the comparison between genotypes. Selected genes were classified into functional categories. The analyses identified changes in cell-wall composition and signaling pathways, as well as suggesting a role for anthocyanin and anthocyanidin synthesis in the defense against S. sclerotiorum. In-silico mapping of both the differentially expressed transcripts and of public markers associated with partial resistance to white mold, provided evidence of several differentially expressed genes being closely positioned to white mold resistance markers, with the two most promising genes encoding a PR-5 and anthocyanidin synthase.
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U2 - 10.3835/plantgenome2008.02.0008
DO - 10.3835/plantgenome2008.02.0008
M3 - Article
AN - SCOPUS:85169097653
SN - 1940-3372
VL - 2
JO - Plant Genome
JF - Plant Genome
IS - 2
M1 - TPG2PLANTGENOME2008020008
ER -