Binding of brassinosteroids to the extracellular domain of plant receptor kinase BRI1
By T. Kinoshita, Ana I. Caño-Delgado, H. Seto, S. Hiranuma, S. Fujioka, S. Yoshida, Joanne Chory. Nature, 2005
644 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/827cedeb34ebd81cb702c05a2ba1aa7a2fab8b86
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In Molecular Biology
In Plant Science
- Cyril Zipfel
- T. Boller
- Jonathan D. G. Jones
- Ping He
- Libo Shan
- T. Nürnberger
- Altaf Ahmad
- D. Chinchilla
Citations in the corpus
- Hormone crosstalk in plant disease and defense: more than just jasmonate-salicylate antagonism. (2011, background): “However, in Arabidopsis three close homologs of BRI1—BRL1, BRL2, and BRL3—can also bind BL (91), and any of these homologs in a bri1 mutant background under the bri1 promoter rescues the bri1 phenotype (91).”
- The Arabidopsis Receptor Kinase FLS2 Binds flg22 and Determines the Specificity of Flagellin Perception[W] (2005, background): “Demonstration of functional binding sites for plant receptors expressed in cells of other kingdoms has been reported only for the tomato xylanase receptor expressed in mammalian COS-7 cells (Ron and Avni, 2004) and the brassinolide binding epitope of BRI1 in E. coli (Kinoshita et al., 2005).”
- The Arabidopsis CORONATINE INSENSITIVE1 Protein Is a Jasmonate Receptor[C][W] (2009, methodology): “The photoaffinity labeling technology has been used to successfully demonstrate the direct binding of brassinosteroids to the receptor BRI1 (Kinoshita et al., 2005).”
- Brassinosteroids and their role in response of plants to abiotic stresses (2014, background): “BRI1 has also a unique feature that is required for BR binding, a stretch of amino acids called an island domain that interrupts the LRRs between LRRs 21 and 22 (Kinoshita et al. 2005).”
- Vacuolar H+-ATPase Activity Is Required for Endocytic and Secretory Trafficking in Arabidopsis[W] (2006, background): “Root cells of seedlings expressing the plasma membrane steroid receptor BRI1 (Friedrichsen et al., 2000; Kinoshita et al., 2005) fused to GFP show detectable intracellular fluorescence (Russinova et al.”
- Bacterial effectors target the common signaling partner BAK1 to disrupt multiple MAMP receptor-signaling complexes and impede plant immunity. (2008, background): “However, bak1 mutants have been shown to have normal binding capacity for BR to BRI1 and flagellin to FLS2, respectively (Chinchilla et al., 2007; Kinoshita et al., 2005).”
- A receptor-like cytoplasmic kinase, BIK1, associates with a flagellin receptor complex to initiate plant innate immunity (2009, background): “Rather than being involved in direct binding of BR to BRI1 and flagellin to FLS2 (7, 12), BAK1more likely functions as an adaptor or signaling partner for the regulationofFLS2andBRI1.”
- Role of phytohormones in insect-specific plant reactions (2012, background): “BR are perceived by BR insensitive 1 (BRI1), a leucine-rich repeat receptorlike kinase [103, 104].”
- Plant hormone interactions during seed dormancy release and germination (2005, background): “They are perceived by the plasma membrane-localized leucinerich repeat receptor kinase, BRI1 (BR insensitive 1) in Arabidopsis, and several homologues have been identified utilizing BR-insensitive mutants of other species (Szekeres, 2003; Kinoshita et al., 2005).”
- Brassinosteroid signal transduction from receptor kinases to transcription factors. (2010, background): “These include a chimeric receptor of BRI1-XA21 conferring BR-induced defense responses (29), binding of BRI1 immunoprecipitated from Arabidopsis plants (94) or expressed and purified in Escherichia coli (43) to tritium-labeled BL (3H-BL), and BRinduced BRI1 auto-phosphorylation (90, 91, 94).”