Abscisic acid-dependent multisite phosphorylation regulates the activity of a transcription activator AREB1.
By T. Furihata, K. Maruyama, Y. Fujita, T. Umezawa, R. Yoshida, Kazuo Shinozaki, Kazuko Yamaguchi-Shinozaki. Proceedings of the National Academy of Sciences of the United States of America, 2006
810 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/810836721d651de029804055ccc108bd0c8ceed4
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Molecular Biology
- Kazuko Yamaguchi-Shinozaki
- Kazuo Shinozaki
- Jian‐Kang Zhu
- K. Nakashima
- M. Prasad
- M. Fujita
- Y. Fujita
- C. Lata
In Plant Science
- Kazuko Yamaguchi-Shinozaki
- Kazuo Shinozaki
- K. Nakashima
- Jian‐Kang Zhu
- M. Prasad
- M. Fujita
- Y. Fujita
- R. Finkelstein
Citations in the corpus
- Regulatory metabolic networks in drought stress responses. (2007, background): “Current Opinion in Plant Biology 2007, 10:296–302 RESPONSIVE ELEMENT (ABRE)-BINDING FACTOR 2 (ABF2) [4,5] and DEHYDRATION-RESPONSIVE ELEMENT (DRE)-BINDING PROTEIN 2A (DREB2A) [6], and protein kinases, such as RECEPTOR-LIKE KINASE 1 (RPK1) [7], SNF1-RELATED PROTEIN KINASE 2C (SRK2C) [8] and the guard”
- Abiotic stress signaling and responses in plants (2016, background): “bZIP transcription factors such as ABI5 and ABFs (ABA-responsive element-binding factors) are phosphorylated by the SnRK2s (Furihata et al., 2006).”
- The transcriptional regulatory network in the drought response and its crosstalk in abiotic stress responses including drought, cold, and heat (2014, background): “ABA is required for full activation of AREB1 (Fujita et al., 2005; Yoshida et al., 2010) and its activity is regulated by the ABA-dependent phosphorylation of multiple sites within conserved domains (Furihata et al., 2006).”
- Role of Plant Transcription Factors in Abiotic Stress Tolerance (2011, background): “AREB1/ABF2, AREB2/ABF4, and ABF3 were mainly expressed in vegetative tissues, whereas ABI5 and EEL were expressed during seed maturation and/or germination (Choi et al., 2000; Uno et al., 2000; Bensmihen et al., 2002; Fujita et al., 2005; Nakashima and Yamaguchi-Shinozaki, 2006).”
- Two Calcium-Dependent Protein Kinases, CPK4 and CPK11, Regulate Abscisic Acid Signal Transduction in Arabidopsis[W] (2007, background): “These 42- and 44- kD phosphorylating activities are consistent with previous reports of SnRK activities on the ABFs (Uno et al., 2000; Furihata et al., 2006; Fujii et al., 2007).”
- ABA signal transduction at the crossroad of biotic and abiotic stress responses. (2012, background): “The OST1 also interacts with and phosphorylates ABF2 and ABF3, which bind to ABA-responsive elements (ABRE) and control ABA-regulated gene expression (Furihata et al. 2006; Fujii et al. 2009; Fujita et al. 2009; Sirichandra et al. 2010).”
- An insight into the drought stress induced alterations in plants (2011, background): “…responsive element binding protein) with multisite mutations also resulted in the induction of many ABA-responsive genes without exogenous ABA application suggesting that altered TFs activation by point mutations may have the potential to enhance drought tolerance ability (Furihata et al. 2006).”
- ABA signaling in stress-response and seed development (2013, background): “The phosphorylation recognition motif (RXXS/T) of the AREB/ABFs is frequently present in sites phosphorylated by general Ser/Thr protein kinases, such as SnRK2 and calcium-dependent protein kinases (CPKs) (Kagaya et al. 2002; Furihata et al. 2006).”
- Molecular Basis of the Core Regulatory Network in ABA Responses: Sensing, Signaling and Transport (2010, background): “Several studies have demonstrated that AREB/ABFs are highly phosphorylated in response to ABA, and this phosphorylation is suffi cient for their activation ( Uno et al. 2000 , Kagaya et al. 2002 , Furihata et al. 2006 ).”