Duplicated P5CS genes of Arabidopsis play distinct roles in stress regulation and developmental control of proline biosynthesis.
By G. Székely, E. Ábrahám, Á. Cséplő, G. Rigó, Laura Zsigmond, J. Csiszár, F. Ayaydin, N. Strizhov, J. Jásik, E. Schmelzer and 2 more. The Plant Journal, 2008
698 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/827a265207948886d8d8e27d47a7ec89759fbbca
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Citations in the corpus
- Proline accumulation in plants: a review (2008, background): “Recently Székely et al. (2008) provided first evidence about the specificity of cell type and subcellular localization patterns of P5CS1 and P5CS2 proteins in Arabidopsis.”
- Exogenous proline significantly affects the plant growth and nitrogen assimilation enzymes activities in rice (Oryza sativa) under salt stress (2016, methodology): “Szekely et al. (2008) reported that rapidly dividing and growing cells show high expression of AtP5CS2, a gene responsible for the synthesis of D1-pyrroline-5-carboxylate synthetase (P5CS) that involved in proline biosynthesis, indicating that active cells have a high demand for proline.”
- A R2R3-type MYB gene, OsMYB2, is involved in salt, cold, and dehydration tolerance in rice (2012, methodology): “In addition, proline can also function as a molecular chaperone to stabilize the structure of proteins as well as play a role in regulation of the antioxidant system (Hare et al., 1999; Szekely et al., 2008).”
- Drought-induced changes in development and function of grapevine (Vitis spp.) organs and in their hydraulic and non-hydraulic interactions at the whole-plant level: a physiological and molecular update (2010, background): “Of two family members included in the Arabidopsis genome, P5CS1 is induced by osmotic stress while P5CS2 is developmentally regulated and is required for embryo vitality (Székely et al. 2008).”
- Extreme climatic events: impacts of drought and high temperature on physiological processes in agronomically important plants (2014, background): “Usually one of the P5CS isoforms is osmo-regulated and the other is associated with developmentally governed processes (Hur et al., 2004; Székely et al., 2008; Pérez-Arellano et al., 2010).”
- Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “Transcriptional profiling analysis revealed a massive influence of salinity on proline metabolism, including induction of several key enzymes, such as pyrroline-5carboxylate synthetase (P5CS) (Székely et al., 2007).”
- Ornithine-δ-aminotransferase is essential for Arginine Catabolism but not for Proline Biosynthesis (2008, background): “In response to osmotic stress, P5CS1 becomes re-localised to plastids [14].”
- Exogenous proline induces soluble sugar accumulation and alleviates drought stress effects on photosystem II functioning of Arabidopsis thaliana leaves (2011, methodology): “One week before the DS A. thaliana plants were either sprayed (foliar application 4 times in total, day after day) with water or with 10 mM proline (Székely et al. 2008).”
- Proline Metabolism and Its Implications for Plant-Environment Interaction (2010, background): “Consistent with the upregulation of AtP5CS1, p5cs1 knockout mutants have greatly reduced proline levels during salt or low water potential stress (Szekely et al., 2008; Sharma and Verslues, 2010). p5cs1 mutants were also reported to have reduced growth and altered reactive oxygen levels, suggesting…”
- Utilization of genes encoding osmoprotectants in transgenic plants for enhanced abiotic stress tolerance (2015, background): “thaliana and other plant species, the P5CS, which is a rate-limiting factor in proline biosynthesis, is encoded by two genes [27,28], while P5CR is encoded by a single gene [29].”
- Reactive oxygen species homeostasis and signalling during drought and salinity stresses. (2010, background): “Pro synthesis from glutamate, previously documented in the cytosol, was recently shown to occur, at least in part, in the chloroplast (Szekely et al. 2008).”