A wheat gene encoding an aluminum-activated malate transporter.
By Takayuki Sasaki, Yoko Yamamoto, B. Ezaki, M. Katsuhara, S. Ahn, P. Ryan, E. Delhaize, H. Matsumoto. The Plant Journal, 2004
934 citations recorded by the source corpus.
Subfields: Plant Science
View Paper: https://www.semanticscholar.org/paper/647286e25a5a0724a25326d797ddb8345108de5a
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Citations in the corpus
- Physiology and molecular biology of stress tolerance in plants (2006, background): “Aluminium tolerance genes were isolated from Arabidopsis and wheat (Sivaguru et al., 2003; Sasaki et al., 2004).”
- Aluminum toxicity in plant cells: Mechanisms of cell death and inhibition of cell elongation (2018, background): “The OX transformants of TaALMT1 acquired the ability to release malate during Al treatment in Ca-sucrose solution, and exhibited a higher growth capacity than wild-type SL (Sasaki et al. 2004).”
- The rhizosphere microbiome: significance of plant beneficial, plant pathogenic, and human pathogenic microorganisms. (2013, background): “, 2007), to modulate organic anion efflux (Tesfaye et al., 2001; Anoop et al., 2003; Delhaize et al., 2004; Sasaki et al., 2004; Li et al., 2005), or to facilitate citrate efflux (Furukawa et al.”
- Effect of lime on root growth, morphology and the rhizosheath of cereal seedlings growing in an acid soil (2010, background): “In wheat, Al-activated efflux of malate from root tips is a primary Al resistance mechanism that is encoded by the TaALMT1 gene (Ryan et al. 1995; Sasaki et al. 2004).”
- Rhizosphere engineering and management for sustainable agriculture (2009, background): “Constitutive expression of TaALMT1 in plant and animal cells including tobacco suspension cells, rice (Oryza sativa) and Xenopus oocytes (Sasaki et al. 2004), barley (Hordeum vulgare) (Delhaize et al.”
- Genome-wide comparative diversity uncovers multiple targets of selection for improvement in hexaploid wheat landraces and cultivars (2013, background): “This process has included modification of vernalization and photoperiod requirements (3), adaptation to water-limiting conditions (4), low temperature (5), salt (6), and soil toxicity (7, 8).”
- Wheat physiology: a review of recent developments (2011, background): “Molecular markers for a major resistance gene were located (Riede and Anderson 1996), and the gene itself was identified (TaALMT1) in tolerant wheat and sequenced by Sasaki et al. (2004), the first ever such plant gene.”
- Physiological traits and cereal germplasm for sustainable agricultural systems (2007, background): “The work by Ryan, Delhaize and colleagues over the last ten years exemplifies how identifying diverse germplasm in the field, followed by careful physiology in the laboratory to understand the underlying mechanisms for acid soil tolerance in cereals led to a reliable screen, the discovery of a proce”
- Strategies and methods for studying the rhizosphere—the plant science toolbox (2009, background): “Citratepermeable channels in the plasma membrane of cluster roots of Lupinus albus have been identified (Zhang et al. 2004), and a gene encoding a malate channel that is activated by the presence of toxic levels of aluminium has been identified and cloned from wheat (Sasaki et al. 2004).”
- Plant Root Responses to Three Abundant Soil Minerals: Silicon, Aluminum and Iron (2005, methodology): “Recently, a gene (ALMT1) encoding this Al-activated malate transporter was cloned using a cDNA subtraction approach (Sasaki et al., 2004).”
- Plant and microbial strategies to improve the phosphorus efficiency of agriculture (2011, background): “For instance, barley genetically modified with the TaALMT1 gene from wheat showed at least a 20-fold greater Al3+- activated malate efflux than controls and this conferred greatly increased Al3+ resistance (Sasaki et al. 2004; Delhaize et al. 2004).”