Arabidopsis Ethylene-Responsive Element Binding Factors Act as Transcriptional Activators or Repressors of GCC Box–Mediated Gene Expression

By Susan Y. Fujimoto, Masaru Ohta, A. Usui, H. Shinshi, M. Ohme-Takagi. The Plant Cell, 2000

1,104 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/185efafab4fd69922eb87016700bf0b02b5f2124

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Citations in the corpus

The Jasmonate Signal Pathway Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.000679. (2002, background): “Thus the AtERFs respond to extracellular signals to modulate GCC box–mediated gene expression positively or negatively (Fujimoto et al., 2000).”
The NAC Transcription Factors NST1 and NST2 of Arabidopsis Regulate Secondary Wall Thickenings and Are Required for Anther Dehiscencew⃞ (2005, methodology): “Effector, reporter, and reference (Renilla LUC gene) plasmids were transiently introduced into rosette leaves of 2- to 4-week-old plants by particle bombardment, and relative luciferase activity was quantified and normalized as described previously (Fujimoto et al., 2000).”
The use of microarray μPEACH1.0 to investigate transcriptome changes during transition from pre-climacteric to climacteric phase in peach fruit (2006, background): “It has been reported that other EREBPs proteins, named Ethylene Responsive Factors (ERFs) act either as transcriptional activators or repressors in plant [40].”
Arabidopsis Transcriptome Profiling Indicates That Multiple Regulatory Pathways Are Activated during Cold Acclimation in Addition to the CBF Cold Response Pathway Online version contains Web-only data. Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1 (2002, background): “Within the first hour of transfer, transcripts accumulated for 1-aminocyclopropane-1-carboxylic acid synthase ( AtACS-6 ), which catalyzes a limiting step in ethylene synthesis, and two ethylene-responsive transcription factors, AtERF-4 and AtERF-5 (Fujimoto et al., 2000).”
Understanding plant responses to drought - from genes to the whole plant. (2003, background): “In Arabidopsis, the AAO3 mRNAs are upregulated by water stress but the enzyme levels remain unchanged (Seo et al. 2000; Taylor et al. 2000).”
Jasmonic Acid Signaling Pathway in Plants (2019, background): “Moreover, JAs-responsive AtERF3 and AtERF4 act as repressors by not only down regulating their target genes’ expression, but also interfering with the activity of other activators [61].”
Ethylene Role in Plant Growth, Development and Senescence: Interaction with Other Phytohormones (2017, background): “In Arabidopsis, ABA-deficient mutants aba2-1 and aba1-6 have a late flowering phenotype (Riboni et al., 2013) and the level of floral suppressing hormone ethylene have been shown to increase in aba mutant (LeNoble et al., 2004), and this condition may contribute to their late flowering phenotype.”
Tomato stress-responsive factor TSRF1 interacts with ethylene responsive element GCC box and regulates pathogen resistance to Ralstonia solanacearum (2004, background): “For example, the tomato Pti4-6 (Zhou et al., 1997; Gu et al., 2000), LeERF1-4 (Tournier et al., 2003), Arabidopsis ERF1 (Solano et al., 1998), AtERFs (Fujimoto et al., 2000), tobacco ERFs (Ohme-Takagi and Shinshi, 1995), and periwinkle ORCA1-3 (Menke et al., 1999; van der Fits and Memelink, 2000, 20”