4.5 Article

GmEREBP1 is a transcription factor activating defense genes in soybean and Arabidopsis

Journal

MOLECULAR PLANT-MICROBE INTERACTIONS
Volume 20, Issue 2, Pages 107-119

Publisher

AMER PHYTOPATHOLOGICAL SOC
DOI: 10.1094/MPMI-20-2-0107

Keywords

cis elements; ethylene-insensitive soybean mutant etr1-1; GFP; GUS; protoplasts; quantitative real-time reverse-transcription PCR

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Ethylene-responsive element-binding proteins (EREBPs) are plant-specific transcription factors, many of which have been linked to plant defense responses. Conserved EREBP domains bind to the GCC box, a promoter element found in pathogenesis-related (PR) genes. We previously identified an EREBP gene from soybean (GmEREBP1) whose transcript abundance decreased in soybean cyst-nematode-infected roots of a susceptible cultivar, whereas it increased in abundance in infected roots of a resistant cultivar. Here, we report further characterization of this gene. Transient expression analyses showed that GmEREBP1 is localized to the plant nucleus and functions as a transcriptional activator in soybean leaves. Transgenic soybean plants expressing GmEREBP1 activated the expression of the ethylene (ET)responsive gene PR2 and the ET- and jasmonic acid (JA)-responsive gene PR3, and the salicyllic acid (SA)-responsive gene PR1 but not the SA-responsive PR5. Similarly, transgenic Arabidopsis plants expressing GinEREBP1 showed elevated mRNA abundance of the ET-regulated gene PR3 and the ET- and JA-regulated defense-related gene PDF1.2 but not the ET-regulated GST2, and the SA-regulated gene PR1 but not the SA-regulated PR2 and PR5. Transgenic soybean and Arabidopsis plants inoculated with cyst nematodes did not display a significantly altered susceptibility to nematode infection. These results collectively show that GmEREBP1 functions as a transacting inducer of defense gene expression in both soybean and Arabidopsis and mediates the expression of both ET-and JA- and SA-regulated defense-related genes in these plant species.

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