2017
DOI: 10.1007/s11103-017-0611-y
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An integrative overview of the molecular and physiological responses of sugarcane under drought conditions

Abstract: Drought is the main abiotic stress constraining sugarcane production. However, our limited understanding of the molecular mechanisms involved in the drought stress responses of sugarcane impairs the development of new technologies to increase sugarcane drought tolerance. Here, an integrated approach was performed to reveal the molecular and physiological changes in two closely related sugarcane cultivars, including the most extensively planted cultivar in Brazil (cv. RB867515), in response to moderate (-0.5 MP… Show more

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Cited by 34 publications
(20 citation statements)
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“…acetyl-CoA, propionyl-CoA, and acetoacetate, are potential energy sources for plants (Joshi et al, 2010). The global increase of numerous amino acids likely depicts increased degradation and synthesis of proteins (Vital et al, 2017). Similar observation was reported in crop cultivars, and shown to be linked to impact of osmotic stress on the proteasome (Vital et al, 2017).…”
Section: Early Signs Of Stress Responses In Elodea Nuttalli Treated Wmentioning
confidence: 66%
“…acetyl-CoA, propionyl-CoA, and acetoacetate, are potential energy sources for plants (Joshi et al, 2010). The global increase of numerous amino acids likely depicts increased degradation and synthesis of proteins (Vital et al, 2017). Similar observation was reported in crop cultivars, and shown to be linked to impact of osmotic stress on the proteasome (Vital et al, 2017).…”
Section: Early Signs Of Stress Responses In Elodea Nuttalli Treated Wmentioning
confidence: 66%
“…These studies bring a maximum of 25 proteins differentially accumulated which are mainly related to photosynthesis and homeostasis regulation. Recently, integrated transcriptomics, proteomics, and metabolomics data characterized the molecular responses of sugarcane leaves to drought stress . Although many changes in genes related to photosynthesis, carbohydrate, and amino acid metabolism, the proteome and transcriptome analyses were not always overlapped, which in part could be explained by the utilization of 2D gels.…”
Section: Introductionmentioning
confidence: 99%
“…The detection of the phosphorylated proteins was carried out by staining the 2DE gels using a Pro-Q ® Diamond Phosphoprotein Gel Stain kit (Invitrogen, Calrsbad, USA), according to the protocol described by Agrawal and Thelen [22]. The gels were then scanned with a FLA 5100 laser scanner and the images were analyzed as described by Vital [23].…”
Section: Gelsmentioning
confidence: 99%