Targeted destabilization of HY5 during light-regulated development of Arabidopsis
By M. Osterlund, C. Hardtke, N. Wei, X. Deng. Nature, 2000
1,294 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/040515a51f9337b76d57b7e239d67d16568e057c
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Citations in the corpus
- Phytochrome‐mediated photoperception and signal transduction in higher plants (2002, background): “This suggests that COP1 could negatively regulate photomorphogenesis by mediating the polyubiquitination of HY5, thus marking it for subsequent degradation by the proteasome (Osterlund et al., 2000).”
- Light-dependent regulation of carotenoid biosynthesis in plants (2009, background): “…the UV-damaged DNA binding protein 1 (DDB1) and the de-etiolated-1 (DET1) factor, interact with COP1 and other proteins from the signalosome complex, leading to ubiquitination of transcription factors (Osterlund et al., 2000; Schroeder et al., 2002; Chen et al., 2004; Yanawaga et al., 2004).”
- A QTL for rice grain width and weight encodes a previously unknown RING-type E3 ubiquitin ligase (2007, background): “For example, COP1 has both a RING-type domain in the N terminus and a WD-40 repeat domain in the C terminus that can bind several protein targets, including HY5, thereby recruiting an E2 and targeting HY5 and other substrates for ubiquitination and degradation by the proteasom”
- The Ubiquitin-Proteasome Pathway and Plant Development (2004, background): “Because aMAP kinase cascade has been implicated in ethylene signaling (Novikova et al., 2000; Ouaked et al., 2003), it will be interesting to see if phosphorylation of EIN3 is required for its stabilization.”
- Inducers of plant systemic acquired resistance regulate NPR1 function through redox changes. (2003, neutral): “(Osterlund et al., 2000”
- The ubiquitin–26S proteasome system at the nexus of plant biology (2009, background): “Particularly important to photomorphogenesis is the RING E3 COP1, the dark-dependent translocation of which into the nucleus has been implicated in the turnover of a number of photomorphogenic effectors, including the transcription factor LONG-HYPOCOTYL 5 (HY5”
- Light signal transduction in higher plants. (2004, background): “Similarly, the light-hyposensitive phenotype of hy5 mutants can also be reconciled with this model (77, 142, 161).”
- Photoreceptors and Control of Horticultural Plant Traits (2015, background): “Phytochromes control gene expression, at least in part, by negatively regulating the repression imparted by the COP/DET/FUS proteins, leading to accumulation of transcriptional activators such as HY5, HYH, LAF1, and HFR1 (Duek et al., 2004; Osterlund et al., 2000; Zhu et al., 2008).”
- Analysis of Transcription Factor HY5 Genomic Binding Sites Revealed Its Hierarchical Role in Light Regulation of Development[W] (2007, methodology): “…light-to-dark transition, we first checked the protein levels of HA:HY5 and endogenous HY5 in the transgenic line and the wild type, respectively, grown for 4 d under white light and then trans- ferred to darkness, because HY5 protein is known to be degraded in the dark (Osterlund et al., 2000).”
- Auxin cross-talk: integration of signalling pathways to control plant development. (2002, background): “The C-terminal domain of COP1 has been demonstrated to interact with HY5 (Osterlund et al., 2000) and can repress photomorphogenesis (Oyama et al.”
- Characterization of OsbZIP23 as a Key Player of the Basic Leucine Zipper Transcription Factor Family for Conferring Abscisic Acid Sensitivity and Salinity and Drought Tolerance in Rice1[W][OA] (2008, background): “Among those are HY5, which mediates plant light response (Chattopadhyay et al., 1998; Osterlund et al., 2000), ATB2, which is involved in Suc-specific sugar sensing and signaling (Rook et al., 1998), and AtbZIP60, which regulates the endoplasmic reticulum stress response in amanner unique to plants…”
- HFR1 encodes an atypical bHLH protein that acts in phytochrome A signal transduction (2000, background): “Genetic and molecular approaches have identified a significant number of components that potentially function as signaling intermediates and have provided evidence of both shared and separate pathway branches for individual phytochrome family members (Soh et al. 1998; Bolle et al. 2000; Büche et al.”