Regulatory metabolic networks in drought stress responses.
By Motoaki Seki, T. Umezawa, Kaoru Urano, Kazuo Shinozaki. Current opinion in plant biology, 2007
903 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/d7831320331c393d71a84f8e8ef54c9f96a350b5
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Citations in the corpus
- Complexity of the Alternative Splicing Landscape in Plants[C][W][OPEN] (2013, background): “Several recent studies provide evidence in support of such adominant regulatory role for truncated proteins produced by splice variants in plants (Gagete et al., 2009; Penfield et al., 2010; James et al., 2012; Seo et al., 2012; Wang et al., 2012; Liu et al., 2013).”
- Plant Growth Promoting Rhizobacterial Mitigation of Drought Stress in Crop Plants: Implications for Sustainable Agriculture (2019, background): “One major response of plants is the adjustment of the osmotic potential of cells through the accrual of compatible solutes such as phenolics, proline (amino acids), trehalose (sugar), glycine betaine, amongst others [49,50], in response to drought stress [35,51].”
- Hydrogen peroxide pretreatment induces osmotic stress tolerance by influencing osmolyte and abscisic acid levels in maize leaves (2014, background): “ABA was known as a factor responsible for stomatal closure (Seki et al. 2007).”
- Nitric oxide, stomatal closure, and abiotic stress. (2007, background): “1) (Zhu, 2002; Chaves et al., 2003; Seki et al., 2007).”
- General mechanisms of drought response and their application in drought resistance improvement in plants (2014, background): “As stress conditions increase, some osmolytes such as prolines, soluble sugars, spermines, and betaine accumulate in plant cells to maintain the cell turgor pressure [12].”
- Simultaneous phenotyping of leaf growth and chlorophyll fluorescence via GROWSCREEN FLUORO allows detection of stress tolerance in Arabidopsis thaliana and other rosette plants. (2009, background): “It is mediated via osmotic changes, triggering a signal transduction network in the plant cells (Knight and Knight 2001; Zhu 2002; Seki et al. 2007 ).”
- Global transcriptome analysis reveals circadian regulation of key pathways in plant growth and development (2008, background): “Circadian regulation of abiotic stress responses Multiple plant hormones have been implicated in stress responses [67,75-77] and many acute abiotic stresses are the direct result of daily light/dark cycles.”
- The MYB96 Transcription Factor Regulates Cuticular Wax Biosynthesis under Drought Conditions in Arabidopsis[W] (2011, background): “Plant resistance responses to drought conditions are exerted via several distinct mechanisms, such as synthesis of osmopro- tectants and antioxidants, maintenance of root growth andwater uptake, and adjustments of aerial development (Schroeder et al., 2001; Seki et al., 2007; Mouillon et al., 2008).”
- Early abscisic acid signal transduction mechanisms: newly discovered components and newly emerging questions. (2010, background): “ABA treatment induces changes in gene expression in more than ;10% of the Arabidopsis genome (Sánchez et al. 2004; Seki et al. 2007; Yang et al. 2008; Zeller et al. 2009), resulting in the increased expression of stressassociated and signaling component transcripts.”
- Proline accumulation in plants: a review (2008, background): “This has been achieved by the genetic manipulation of osmolytes, transcriptions factors and more recently of the cytokinin hormone ( Seki et al. 2007; Rivero et al. 2007).”
- Role of sugars under abiotic stress. (2016, background): “…plant species, it was observed that raffinose, stachyose, and verbascose accumulates during desiccation of seeds (Peterbauer and Richter, 2001; Seki et al., 2007; Mohammadkhani andHeidari, 2008) and also accumulates markedly in leaves when the plant is exposed to chilling, temperature or…”