BES1 accumulates in the nucleus in response to brassinosteroids to regulate gene expression and promote stem elongation.

By Yanhai Yin, Zhi-Yong Wang, S. Mora-García, Jianming Li, S. Yoshida, T. Asami, Joanne Chory. Cell, 2002

1,165 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/b8546686a66e90dff82eb365eba309bd90fefef9

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Citations in the corpus

Interdependency of Brassinosteroid and Auxin Signaling in Arabidopsis (2004, background): “…September 2004 | Volume 2 | Issue 9 | e2581460 Open access, freely available online PLoS BIOLOGY auxin and BRs, as it was found that a significant percentage of the BR genomic response comprised genes annotated as auxin responsive (Goda et al. 2002; Mussig et al. 2002; Yin et al. 2002a).”
Brassinosteroid signal transduction from receptor kinases to transcription factors. (2010, background): “First, the bzr1-1D and bes1-D mutations fully suppress the bin2-1 mutant phenotype, supporting the idea that BZR1 and BZR2/BES1 are downstream of BIN2 in the BR signaling pathway (93, 97).”
Integration of Brassinosteroid Signal Transduction with the Transcription Network for Plant Growth Regulation in Arabidopsis (2010, positive): “Genetic studies have revealed a central role for BZR1 and BZR2 (also named BES1) in BR regulation of plant growth (Wang et al., 2002; Yin et al., 2002).”
Growth-defense tradeoffs in plants: a balancing act to optimize fitness. (2014, neutral): “In the absence of BR, the glycogen-synthase-kinase-3-like kinase BRASSINOSTEROID INSENSITIVE 2 (BIN2) phosphorylates two nuclear-localized transcription factors, BRI1-EMS-SUPPRESSOR 1 (BES1) and BRASSINAZOLE-RESISTANT 1 (BZR1), to block activation of BR-responsive genes (He et al., 2002; Wang et al.”
A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana. (2011, background): “The result may also explain, at least in part, the fact that BRs usually induce gene expression by about two to four-fold (Yin et al., 2002).”
The β-Subunit of the Arabidopsis G Protein Negatively Regulates Auxin-Induced Cell Division and Affects Multiple Developmental Processes Online version contains Web-only data. Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.006148. (2003, neutral): “…evidence based on pharmacological experiments suggests a role for a heterotrimeric G protein in various signal transductions, such as for auxin (Zaina et al., 1990, 1991, 1994), abscisic acid (Fairley-Grenot and Assmann, 1991), gibberellin (Jones et al., 1998; Ueguchi-Tanaka et al., 2000),…”
Binding of brassinosteroids to the extracellular domain of plant receptor kinase BRI1 (2005, background): “To test whether BPCS is a biologically active BR, we investigated the phosphorylation status and accumulation of BES1, a downstream component in the BR signalling pathway that accumulates in its dephosphorylated state in the presence of B”
Plant responses to ethylene gas are mediated by SCF(EBF1/EBF2)-dependent proteolysis of EIN3 transcription factor. (2003, background): “Thus, the down- stream positive regulators in the pathway are dere- two nuclear proteins BES1/BZR1 (He et al., 2002; Yin et al., 2002).”
Microalgal Biostimulants and Biofertilisers in Crop Productions (2019, background): “These compounds seem to interact with leucine-rich repeat membrane receptors that can activate mechanisms [110,111] leading to the regulation of several genes involved in the cell expansion [112].”
Nuclear-localized BZR1 mediates brassinosteroid-induced growth and feedback suppression of brassinosteroid biosynthesis. (2002, background): “While the synthesis in this tissue, which would establish a gradient bzr1-1D mutant has reduced BR levels and CPD gene of BRs along the hypocotyl with the highest BR level in expression, the bes1 mutation has only a small effect on CPD gene expression (Yin et al., 2002).”
Brassinosteroids: Multidimensional Regulators of Plant Growth, Development, and Stress Responses[OPEN] (2019, background): “The bes1-D and bzr1-D mutants were originally identified as harboring gain-of-function mutations leading to aPro to Leu substitution in thePESTdomain of BES1or BZR1 (Wang et al., 2002; Yin et al., 2002).”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “, 1996), bes1-D (Yin et al., 2002), and phyB-1 (Bo64) (Reed et al.”