Abstract
In this study, we showed that overexpression of ethylene-responsive transcription factor (ERF) 2 activated the expression of endogenous genes that have the GCC box in their promoter region, in tobacco plants. These include not only a defense-related gene, CHN50, encoding class I basic chitinase, but also a transcriptional repressor gene, ERF3. In tobacco plants constitutively expressing ERF2:glucocorticoid receptor fusion protein, treatment with dexamethazone induced a rapid increase of ERF3 mRNA and a slow increase of CHN50 mRNA. These results suggest that an antagonistic interplay of ERF2 and ERF3 is involved in the transcriptional regulation of the class I basic chitinase genes in tobacco.
MeSH terms
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Chitinases / genetics
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DNA, Plant / analysis
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DNA, Plant / genetics
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Dexamethasone / pharmacology
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G-Box Binding Factors / genetics
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G-Box Binding Factors / physiology
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Gene Expression Regulation, Plant* / drug effects
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Genes, Plant*
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Nicotiana / genetics*
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Promoter Regions, Genetic
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RNA, Messenger / analysis
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Receptors, Glucocorticoid / genetics
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Receptors, Glucocorticoid / physiology
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Regulatory Sequences, Nucleic Acid / genetics
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Regulatory Sequences, Nucleic Acid / physiology
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Repressor Proteins / genetics
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Repressor Proteins / physiology
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Transcription Factors / physiology*
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Transcription, Genetic*
Substances
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DNA, Plant
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G-Box Binding Factors
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RNA, Messenger
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Receptors, Glucocorticoid
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Repressor Proteins
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Transcription Factors
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Dexamethasone
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Chitinases