Comprehensive identification of Arabidopsis thaliana MYB transcription factors interacting with R/B-like BHLH proteins.

By Ilona Zimmermann, Marc A Heim, Bernd Weisshaar, Joachim F. Uhrig. The Plant Journal, 2004

788 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/068d1f6b7db82789d5dc2ec35b56e2d31f12c1a5

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Citations in the corpus

The Jasmonate-ZIM-Domain Proteins Interact with the WD-Repeat/bHLH/MYB Complexes to Regulate Jasmonate-Mediated Anthocyanin Accumulation and Trichome Initiation in Arabidopsis thaliana[C][W] (2011, methodology): “We further found that JA-induced expression of the bHLH factors TT8 and GL3 and all the MYB members (MYB113, MYB75, MYB114, MYB90, and GL1) was severely attenuated in coi1-2 (Figure 9), suggesting that expression of these WD-repeat/bHLH/MYB components is regulated by JA in a COI1-dependent manner.”
Differential regulation of closely related R2R3-MYB transcription factors controls flavonol accumulation in different parts of the Arabidopsis thaliana seedling (2007, background): “Both factors depend on a BHLH partner that might be present constitu- tively (Borevitz et al., 2000; Zimmermann et al., 2004).”
Flavonoids: a colorful model for the regulation and evolution of biochemical pathways. (2005, background): “In functional assays MYBs and HLHs of distinct clades are often exchangeable (Spelt et al., 2000; Quattrocchio et al., 1998; Zimmermann et al., 2004), but it should be noted that the high expression levels that are generally used can hide R2R3-MYB”
Light-regulated transcriptional networks in higher plants (2007, background): “In addition, interactions between different families further extend the complexity of regulatio”
Plant phenolics: recent advances on their biosynthesis, genetics, and ecophysiology. (2013, background): “The R3MYBs are much smaller than the R2R3MYBs, containing the R3-region of the MYB DNA-binding domain and the amino acid motif necessary to bind bHLH partners but lacking active repression domains [101].”
A Conserved Network of Transcriptional Activators and Repressors Regulates Anthocyanin Pigmentation in Eudicots[C][W][OPEN] (2014, background): “, 2010) and contains the amino acid motif [D/E]Lx2[R/K]x3Lx6Lx3R, which is required for interaction with bHLH partners (Zimmermann et al., 2004).”
Negative Regulation of Anthocyanin Biosynthesis in Arabidopsis by a miR156-Targeted SPL Transcription Factor[W][OA] (2011, background): “In addition, both SPL9 and TT8 bound to the same domain, R2R3 domain, of PAP1 (Figure 6B) (Zimmermann et al., 2004).”
Sucrose-Specific Induction of Anthocyanin Biosynthesis in Arabidopsis Requires the MYB75/PAP1 Gene1 (2005, background): “Anthocyanin synthesis is regulated by a heterotrimeric MYB-basic helix-loop-helix (bHLH)-WD40 protein complex (Zhang et al., 2003; Baudry et al., 2004; Zimmermann et al., 2004).”
Evolutionary and comparative analysis of MYB and bHLH plant transcription factors. (2011, background): “It is possible that members of sub-group IIId and IIIe interact with as yet unidentified MYB factors.”
Recent advances on the regulation of anthocyanin synthesis in reproductive organs. (2011, background): “1) through the bHLH interaction domain located in the R3 repeat of the MYB domain, identified as a motif highly conserved in anthocyanin-related MYB regulators [27].”
Overexpression of AtMYB44 Enhances Stomatal Closure to Confer Abiotic Stress Tolerance in Transgenic Arabidopsis1[C][W][OA] (2007, background): “In many cases, MYB transcription factors interact with basic helix-loop-helix (bHLH) transcription factors to exert their specific roles (Grotewold et al., 2000; Zimmermann et al., 2004; Quattrocchio et al., 2006).”
The Arabidopsis Transcription Factor MYB12 Is a Flavonol-Specific Regulator of Phenylpropanoid Biosynthesis1 (2005, background): “Vol. 138, 2005 1091 R2R3-MYB and a BHLH-type transcription factor is a conserved feature in both species (Baudry et al., 2004 and refs. therein; Zimmermann et al., 2004), while phlobaphene synthesis in maize is controlled by ZmP and flavonol synthesis in Arabidopsis by the R2R3MYB factor MYB12.”
Light-Induced Expression of a MYB Gene Regulates Anthocyanin Biosynthesis in Red Apples1 (2006, background): “The bHLH (also called MYC) proteins may have overlapping regulatory targets (Zhang et al., 2003; Zimmermann et al., 2004), but the MYB proteins are the key components providing specificity for the subsets of genes activated.”
The JAZ Proteins: A Crucial Interface in the Jasmonate Signaling Cascade (2011, background): “…of flavonoids (anthocyanins and proanthocyanidins), stomata patterning on hypocotyls, and seed coat mucilage production (Zhang et al., 2003; Zimmermann et al., 2004; Broun, 2005; Serna and Martin, 2006; Gonzalez et al., 2008; Ishida et al., 2008; Balkunde et al., 2010; Dubos et al., 2010).”
Recent advances in the transcriptional regulation of the flavonoid biosynthetic pathway. (2011, background): “Regulators of the PA and anthocyanin pathways display the [D/E]Lx2[R/K]x3Lx6Lx3R motif necessary for interaction with bHLH transcription factors in their R3 repeat (Grotewold et al., 2000; Zimmermann et al., 2004), while MYB transcription factors governing flavonol biosynthesis exhibit the SG7 [K/R]”
Retrotransposons Control Fruit-Specific, Cold-Dependent Accumulation of Anthocyanins in Blood Oranges[W][OA] (2012, background): “The Ruby cDNA encodes a 262–amino acid protein containing an R2R3 Myb domain with a signature motif for interaction with bHLH proteins from the clade 3f (DLX2RX3LX6LX3R; Heim et al., 2003; Zimmermann et al., 2004; Lin-Wang et al., 2010; Figure 2A).”