GL3 encodes a bHLH protein that regulates trichome development in arabidopsis through interaction with GL1 and TTG1.

By C. Payne, Fan Zhang, A. Lloyd. Genetics, 2000

738 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/d34aaaf0ccab711e755fb652c59fb3ee0ae30f92

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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): “The mutants tt8 (Salk_082999 with T-DNA insertion in the second intron), gl3 (gl3-1) (Payne et al., 2000), egl3 (Salk_077439), ttg1 (ttg1-1) (Walker et al., 1999), pap1-D (Borevitz et al., 2000), and gl1 (Herman and Marks, 1989) were all obtained from the ABRC.”
A Conserved Network of Transcriptional Activators and Repressors Regulates Anthocyanin Pigmentation in Eudicots[C][W][OPEN] (2014, background): “An alternative interpretation of the biolistic data is that MYBx prevented AN11 from moving; however, this is unlikely given that the MYBs are not effective binders of WDR proteins (Figure 1; Payne et al., 2000; Baudry et al., 2004, 2006; Chiu et al., 2010; An et al., 2012).”
Recent advances on the regulation of anthocyanin synthesis in reproductive organs. (2011, background): “Once in the nucleus, TTG1 could stabilize the bHLH-MYB transcriptional complexes, as suggested by interaction studies in yeast [33,45], thus allowing the binding of the resulting MBW complex to promoters of anthocyanin biosynthesis genes.”
JASMONATE-INSENSITIVE1 Encodes a MYC Transcription Factor Essential to Discriminate between Different Jasmonate-Regulated Defense Responses in Arabidopsis (2004, background): “In several instances, MYC proteins have been shown to homodimerize and heterodimerize through the HLH domain and also to interact with proteins of the MYB family (Martin and Paz-Ares, 1997; Grotewold et al., 2000; Payne et al., 2000).”
The basic helix-loop-helix transcription factor family in plants: a genome-wide study of protein structure and functional diversity. (2003, background): “The bHLH/MYB partnership has been shown to be important in the differentiation of A. thaliana trichomes through the interaction of a bHLH protein encoded by GLABRA3 (GL3) and the R2R3-MYB protein GLA-BROUS1 (GL1; Payne, Zhang, and Lloyd 2000 ).”
Proanthocyanidins--a final frontier in flavonoid research? (2005, background): “TTG1, a WD domain protein, is known to interact physically with MYB (PAP1 and PAP2) and MYC (GL3 and EGL3) transcription factors in the yeast two-hybrid system (Payne et al., 2000; Zhang et al., 2003).”
Flavonoids: a colorful model for the regulation and evolution of biochemical pathways. (2005, background): “19 resembles the activation of pigmentation genes (Payne et al., 2000; Bernhardt et al., 2003; Zhang et al., 2003; Pesch et al., 2004).”
Conserved MYC transcription factors play a key role in jasmonate signaling both in tomato and Arabidopsis. (2004, background): “Consistent with this latter hypothesis, animal and plant MYC-like proteins were often found to require interaction with partner proteins to activate target gene expression (Roth et al. 1991; Kretzner et al. 1992; Payne et al. 2000).”
Light-induced expression of basic helix-loop-helix genes involved in anthocyanin biosynthesis in flowers and leaves of Asiatic hybrid lily. (2009, background): “, 2000), AtGL3 (Payne et al., 2000) and AtEGL3 (Zhang et al.”
TRANSPARENT TESTA GLABRA2, a Trichome and Seed Coat Development Gene of Arabidopsis, Encodes a WRKY Transcription Factor Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.001404. (2002, background): “Recently, evidence for a direct link between GL1 and TTG1 function has come from characterization of the GL3 gene and its function (Koornneef et al., 1982; Payne et al., 2000).”
Comprehensive identification of Arabidopsis thaliana MYB transcription factors interacting with R/B-like BHLH proteins. (2004, background): “Direct physical interactions have been shown for GL1/ AtMYB0 and the one-repeat MYB protein AtMYBL2, respectively, which both interact with GL3 (Payne et al., 2000; Sawa, 2002).”
A network of redundant bHLH proteins functions in all TTG1-dependent pathways of Arabidopsis (2003, methodology): “EGL3 interacts with GL1 and PAP1 in plants GL3 and R interact with GL1 when co-overexpressed in Arabidopsisto produce more trichomes (Larkin et al., 1994; Payne et al., 2000) and R and C1 interact to produce more anthocyanin pigment (Lloyd et al., 1992).”
Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) Function as Transcriptional Activators in Abscisic Acid Signaling Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.006130. (2003, background): “Recently, some bHLH-type transcription factors (SPATULA, TT8, and GL3) were reported in Arabidopsis (Nesi et al., 2000; Payne et al., 2000; Heisler et al., 2001).”
TT2, TT8, and TTG1 synergistically specify the expression of BANYULS and proanthocyanidin biosynthesis in Arabidopsis thaliana. (2004, background): “However, analysis of the TTG1 sequence reveals no other known specific domain than the WDR and its precise regulatory function remains poorly understood (Payne et al., 2000; Walker et al., 1999).”
Through the genetic bottleneck: O. rufipogon as a source of trait-enhancing alleles for O. sativa (2007, unknown): “tion (Payne et al. 2000; Spelt et al. 2002).”