The SHINE Clade of AP2 Domain Transcription Factors Activates Wax Biosynthesis, Alters Cuticle Properties, and Confers Drought Tolerance when Overexpressed in Arabidopsis w⃞

By A. Aharoni, Shital Dixit, R. Jetter, E. Thoenes, G. van Arkel, A. Pereira. The Plant Cell Online, 2004

806 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/6f646c9f8dd96b844f6d8f5574e7a4fa7def7de2

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Citations in the corpus

Genome-Wide Analysis of the ERF Gene Family in Arabidopsis and Rice[W] (2006, background): “…abiotic stresses (Stockinger et al., 1997; Liu et al., 1998; Dubouzet et al., 2003), and regulation of metabolism (van der Fits and Memelink, 2000; Aharoni et al., 2004; Broun et al., 2004; Zhang et al., 2005), and in developmental processes (van der Graaff et al., 2000; Banno et al., 2001; Chuck…”
Model legumes contribute to faba bean breeding (2010, neutral): “alfalfa (Aharoni et al., 2004; Zhang et al., 2005).”
Development and Utilization of Sorghum as a Bioenergy Crop (2008, background): “Overexpression of genes implicaded in wax production have resulted in increased resistance to drought in other plant species (Aharoni et al. 2004; Zhang et al. 2005).Dehydrins are proteins induced by osmotic stress and proposed to play a role in protecting the cell against the effects of desiccation”
Acyl-Lipid Metabolism (2013, background): “Overexpression of AP2/EREBP-type transcription factors SHN1/WIN1, SHN2, or SHN3 upregulates many wax biosynthetic genes and causes significant increases in all cuticular wax components (Aharoni et al., 2004; Broun et al., 2004).”
Breeding drought tolerant cowpea: constraints, accomplishments, and future prospects (2009, background): “AP2 transcription factor SHINE was shown to confer drought tolerance in Arabidopsis (Aharoni et al. 2004) using a different mechanism than that of the DREB/CBF genes.”
Recent molecular advances to combat abiotic stress tolerance in crop plants (2011, background): “Similarly, transgenic plants developed by expressing a droughtresponsive AP2-type TF, SHN1-3 or WXP1, induced several wax-related genes resulting in enhanced cuticular wax accumulation and increased drought tolerance (Aharoni et al., 2004; Zhang et al., 2005).”
The Formation and Function of Plant Cuticles1 (2013, positive): “Overexpression of this gene lead to glossy leaves with a greater wax load than the wild-type and lower transpiration, although this was likely due to a reduced density of stomata rather than the wax phenotype (Aharoni et al., 2004).”
General mechanisms of drought response and their application in drought resistance improvement in plants (2014, background): “The LOS5/ABA3 gene encodes a molybdenum cofactor (Moco) sulfurase which produces a cofactor (the sulfurylated MoCo) of AAO, which functions in the final step of ABA biosynthesis in Arabidopsis [181].”
The MYB96 Transcription Factor Regulates Cuticular Wax Biosynthesis under Drought Conditions in Arabidopsis[W] (2011, background): “Notably, recent studies strongly support the idea that cuticular wax accumulation is also closely associated with drought resistance responses (Aharoni et al., 2004; Zhang et al., 2005, 2007; Kosma et al., 2009).”
Regulation of Transpiration to Improve Crop Water Use (2009, background): “However, both mutations resulted in reduced transpirational water loss from detached leaves; this may be due to reduced stomatal density rather than altered wax accumulation in both mutants (Chen et al., 2003b; Aharoni et al., 2004).”
An insight into the drought stress induced alterations in plants (2011, background): “Transgenic plants expressing a drought-responsive AP2-type TF, SHINE transcription factor1-3(SHN1-3) or WAX inducible protein 1(WXP1), induced wax-related genes leading to enhanced cuticular wax accumulation and increased drought tolerance (Aharoni et al. 2004, Zhang et al. 2005).”
Genetic and biochemical evidence for involvement of HOTHEAD in the biosynthesis of long-chain α-,ω-dicarboxylic fatty acids and formation of extracellular matrix (2006, background): “Several other genes, ALE1, ACR4, WIN1/SHN, PAS2/PAP, and HTH, did not appear to be directly involved in biosynthesis of the cutin polyester based on their sequence similarities and expression pattern (Tanaka et al. 2001, 2002; Bellec et al. 2002; Haberer et al. 2002; Krolikowski et al. 2003; Aharoni”