2014
DOI: 10.1016/j.jprot.2014.07.010
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Phosphoproteome analysis reveals new drought response and defense mechanisms of seedling leaves in bread wheat (Triticum aestivum L.)

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Cited by 136 publications
(136 citation statements)
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“…Large-scale phosphoproteomic analyses have been conducted on several plant species, including Arabidopsis thaliana 454647484950, rice4851, Medicago truncatula 5253, soybean ( Glycine max L.)4954, canola ( Brassica napus )49, maize555657 Brachypodium distachyon 58 and wheat2659. However, further research on large-scale mining of the phosphorylation sites in starch biosynthetic enzymes has not been performed.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Large-scale phosphoproteomic analyses have been conducted on several plant species, including Arabidopsis thaliana 454647484950, rice4851, Medicago truncatula 5253, soybean ( Glycine max L.)4954, canola ( Brassica napus )49, maize555657 Brachypodium distachyon 58 and wheat2659. However, further research on large-scale mining of the phosphorylation sites in starch biosynthetic enzymes has not been performed.…”
Section: Discussionmentioning
confidence: 99%
“…Recently, we used LC-MS/MS to identify several phosphorylation sites present in GBSS I and SS I2324. Together with the development of phosphoproteomic approaches, TiO 2 enrichment-based large-scale phosphoproteomic analysis has been performed in wheat and Brachypodium distachyon 252627. However, large-scale phosphoproteomic analysis of starch granule-binding proteins in cereal crops has not been performed due to two major limitations.…”
mentioning
confidence: 99%
“…As reported in our earlier study (Hu et al, 2010), total proteins from the eighth leaf of the maize plants were extracted according to the method reported by Wang et al (2013) and Zhang et al (2014). Briefly, ~0.5 g fresh leaves from each biological replicate were ground into a fine power in liquid nitrogen using a mortar and pestle and further ground in 4 ml of SDS buffer (30% sucrose, 2% SDS, 100 mM Tris-HCl, pH 8.0, 50 mM EDTA-Na 2 , 20 mM DTT) and 4 ml phenol (Tris-buffered, pH 8.0), then 1 mM phenylmethanesulfonyl fluoride (PMSF) and PhosSTOP phosphatase inhibitor cocktail (one tablet/10 ml; Roche, Basel, Switzerland) was added to inhibit protease and phosphatase activity.…”
Section: Methodsmentioning
confidence: 99%
“…PP2C is known to be a negative regulator for plant drought tolerance in the abscisic acid (ABA) signaling pathway, which can inhibit the activity of SnRK, leading to a decrease of the phosphorylation of its substrates in the signaling cascade [83,84,85]. Both phosphorylation level [40,44] and abundance of PP2C [41,86] were obviously affected by drought stress. These data suggest that the PP2C-involved ABA signaling pathway is crucial for drought response.…”
Section: Drought Sensing and Signalingmentioning
confidence: 99%