Arabidopsis Cys2/His2-Type Zinc-Finger Proteins Function as Transcription Repressors under Drought, Cold, and High-Salinity Stress Conditions1

By H. Sakamoto, K. Maruyama, Y. Sakuma, T. Meshi, M. Iwabuchi, Kazuo Shinozaki, Kazuko Yamaguchi-Shinozaki. Plant Physiology, 2004

632 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/bfc2bb0df4301099611c4086389eac7affb2f2e5

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Citations in the corpus

Photosynthesis and antioxidative defense mechanisms in deciphering drought stress tolerance of crop plants (2016, background): “Zinc finger domain (C2H2) families of ZFPs are strongly induced in plants under osmotic stress (Sakamoto et al. 2004).”
Abiotic stress responsive proteins of wheat grain determined using proteomics technique. (2010, background): “Zinc finger or zinc finger motif was highly enhanced under drought, cold and salinity stress in Arabidopsis (Sakamoto et al., 2004).”
The AtGenExpress global stress expression data set: protocols, evaluation and model data analysis of UV-B light, drought and cold stress responses. (2007, background): “This immediate onset of a metabolic reprogramming may enable the adjustment of energy homeostasis to the stress conditions which is necessary for a successful stress defence (Ohta et al., 2001; Sakamoto et al., 2004).”
Transcriptional regulatory networks in cellular responses and tolerance to dehydration and cold stresses. (2006, background): “The product of one such downstream gene, STZ, functions as a transcriptional repressor, and its overexpression retards growth and induces tolerance to drought stress (89).”
Antioxidants and Antioxidant Enzymes in Higher Plants (2018, background): “In fact, it has been reported that, as a result of an increased generation of ROS, plants reduce the transcript levels of certain carbohydrate metabolism and photosynthesis-related genes that suppress plant growth (Sakamoto 2004).”
Genomics of Cold Hardiness in Woody Plants (2014, background): “, 1989), possibly via the salt tolerance zinc finger transcription factor (STZ; Sakamoto et al., 2004) and dwarfing, suggested to be related to an increase in gibberellin (GA)-regulated growth repressing”
Response of plants to water stress (2014, background): “Furthermore, recent findings on molecular mechanisms involved in protecting photosynthesis in order to adjust plant growth during water stress are discussed.”
Oxidative environment and redox homeostasis in plants: dissecting out significant contribution of major cellular organelles (2015, background): “Likewise, over-expression of transcription factors (Zat12 or JERF3, Zat10) control the expression of various ROSscavenging genes encoding enzymes showed higher tolerance to salt, drought or osmotic stresses (Sakamoto et al., 2004; Davletova et al., 2005).”
Coping with Stresses: Roles of Calcium- and Calcium/Calmodulin-Regulated Gene Expression[W][OA] (2011, background): “The C-repeat binding factors CBF1, 2, and 3, which are also called DREB1B, 1C, and 1A, respectively, are TFs that induce the expression of a large number of genes (CBF regulon) involved in cold acclimation (Riechmann et al., 2000; Maruyama et al., 2004; Sakamoto et al., 2004; Vogel et al., 2005).”
ABA-mediated transcriptional regulation in response to osmotic stress in plants (2011, background): “AZF2 was originally identified as an ABA-responsive transcriptional repressor under stress conditions (Sakamoto et al. 2004).”
Sensing and responding to excess light. (2009, result): “ZAT12 together with ZAT10 is strongly induced in response to seven out of nine ROS treatments (47), in agreement with previous and independent observations that these might code for general abiotic stress transcription factors (27, 28, 103, 133, 140).”
AREB1 Is a Transcription Activator of Novel ABRE-Dependent ABA Signaling That Enhances Drought Stress Tolerance in Arabidopsis[W][OA] (2005, methodology): “Drought tolerance assays were performed as described (Sakamoto et al., 2004) with minor modifications.”