Overexpression of the Arabidopsis CBF3 transcriptional activator mimics multiple biochemical changes associated with cold acclimation.

By S. J. Gilmour, A. Sebolt, Maite P. Salazar, J. Everard, M. Thomashow. Plant Physiology, 2000

1,134 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/c8692bfcefd966ecc78146164758fea24f875d99

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Citations in the corpus

Exploring the Temperature-Stress Metabolome of Arabidopsis1[w] (2004, background): “…process involving a number of physiological and biochemical changes, including changes in membrane structure and function, tissue water content, global gene expression, protein, lipid, and primary and secondary metabolite composition (Levitt, 1972; Gilmour et al., 2000; Shinozaki and Dennis, 2003).”
Transcription Factor CBF4 Is a Regulator of Drought Adaptation in Arabidopsis1 (2002, methodology): “Similar to earlier observations of CBF3/DREB1a overexpression using the 35S promoter (Kasuga et al., 1999; Gilmour et al., 2000), the 35S::CBF4 plants showed retarded growth compared with the wild-type controls (Fig.”
Arabidopsis CBF3/DREB1A and ABF3 in Transgenic Rice Increased Tolerance to Abiotic Stress without Stunting Growth1[w] (2005, background): “The presence of multiple CRT/DRE elements is a common characteristic of Arabidopsis genes that are induced by CBF3 (Gilmour et al., 2000; Dubouzet et al., 2003; Maruyama et al., 2004).”
Role of Plant Transcription Factors in Abiotic Stress Tolerance (2011, background): “…Drought Sakuma et al., 2006 AtCBF1 Arabidopsis Salinity Jaglo-Ottosen et al.,1998 AtCBF2 Tomato Freezing Hseih et al., 2002 AtCBF3 Arabidopsis Freezing Gilmour et al., 2000 AtCBF4 Arabidopsis Freezing Haake et al., 2002 BNCBF5 Brassica napus Freezing Savitch et al., 2005 BNCBF17 Brassica napus…”
The role of dehydrins in plant response to cold (2007, background): “Similarly, the overexpression of CBF3 led to the increase in FT characterised by enhanced expression of several Cor genes in transgenic Arabidopsis (Gilmour et al. 2000).”
Plant abiotic stress response and nutrient use efficiency (2020, background): “For instance, the constitutive overexpression of CBFs adversely affects plant growth under normal growth conditions (Gilmour et al., 2000; Jaglo-Ottosen et al., 1998).”
The Cold-Inducible CBF1 Factor–Dependent Signaling Pathway Modulates the Accumulation of the Growth-Repressing DELLA Proteins via Its Effect on Gibberellin Metabolism[W] (2008, background): “…cold and dehydration-responsive cis-element, designated the CRT (C-repeat)/DRE (dehydration response element), present in the promoter of COR (cold-regulated) and a multitude of other stress-responsive genes known as the CBF regulon (Stockinger et al., 1997; Gilmour et al., 1998; Liu et al., 1998).”
A combination of the Arabidopsis DREB1A gene and stress-inducible rd29A promoter improved drought- and low-temperature stress tolerance in tobacco by gene transfer. (2004, background): “…of the DREB1A (CBF3) cDNA under the control of the CaMV 35S promoter resulted in strong expression of target stress-inducible genes and the transgenic plants acquired higher tolerance to drought, high-salt, and freezing stresses (Liu et al. 1998, Kasuga et al. 1999, Gilmour et al. 2000).”
Over-expression of miR397 improves plant tolerance to cold stress in Arabidopsis thaliana (2014, background): “Ectopic overexpression of CBF1 or CBF3 in Arabidopsis results in constitutive expression of downstream cold-inducible genes, high levels of proline and soluble sugars, and increased freezing tolerance (Liu et al. 1998; Jaglo-Ottosen et al. 1998; Kasuga et al. 1999; Gilmour et al. 2000).”
Hydrogen sulfide is involved in the chilling stress response in Vitis vinifera L. (2013, background): “Ectopically expression of AtCBFs and AtICE1 in different plant species can enhance chilling tolerance [41,42], and ectopically expression of CBFs from other plants is able to enhance the freezing tolerance of transgenic Arabidopsis [20,43].”