Abstract

BackgroundWheat (Triticum aestivum L.) serves as important grain crop widely cultivated in the world, which is often suffered by drought stress in natural conditions. As one of the most important post translation modifications, protein phosphorylation widely participates in plant abiotic stress regulation. In this study, we performed the first comparative analysis of phosphorylated protein characterization in flag leaves and developing grains of elite Chinese bread wheat cultivar Zhongmai 175 under water deficit by combining with proteomic approach and Pro-Q Diamond gel staining.ResultsField experiment showed that water deficit caused significant reduction of plant height, tiller number, ear length and grain yield. 2-DE and Pro-Q Diamond gel staining analysis showed that 58 proteins were phosphorylated among 112 differentially accumulated proteins in response to water deficit, including 20 in the flag leaves and 38 in the developing grains. The phosphorylated proteins from flag leaves mainly involved in photosynthesis, carbohydrate and energy metabolism, while those from developing grains were closely related with detoxification and defense, protein, carbohydrate and energy metabolism. Particularly, water deficit resulted in significant downregulation of phosphorylated modification level in the flag leaves, which could affect photosynthesis and grain yield. However, some important phosphorylated proteins involved in stress defense, energy metabolism and starch biosynthesis were upregulated under water deficit, which could benefit drought tolerance, accelerate grain filling and shorten grain developing time.ConclusionsThe modification level of those identified proteins from flag leaves and grains had great changes when wheat was suffered from water deficit, indicating that phosphoproteins played a key role in response to drought stress. Our results provide new insights into the molecular mechanisms how phosphoproteins respond to drought stress and thus reduce production.

Highlights

  • Wheat (Triticum aestivum L.) serves as important grain crop widely cultivated in the world, which is often suffered by drought stress in natural conditions

  • Subcellular localization showed that most of the differentially accumulated proteins (DAPs) in flag leaves and grains were located in chloroplast (73.17%) and cytoplasm (45.07%), respectively (Fig. 4b, c). These results indicate that the foremost function of Characterization of phosphorylated proteins in the developing flag leaves and grains under water deficit Through comparison of two-dimensional electrophoresis (2-DE) (Fig. 3), Pro-Q Diamond staining (Fig. 5), and tandem mass spectrometry results, 20 and 38 phosphorylated DAP spots in response to water deficit were respectively identified in flag leaves and developing grains, which were individually represented

  • We found that most phosphoproteins involved in carbon metabolism and energy metabolism were upregulated in flag leaves, but some important phosphoproteins participating in photosynthesis were downregulated

Read more

Summary

Introduction

Wheat (Triticum aestivum L.) serves as important grain crop widely cultivated in the world, which is often suffered by drought stress in natural conditions. As one of the most important post translation modifications, protein phosphorylation widely participates in plant abiotic stress regulation. As one of the most important grain crops, wheat (Triticum aestivum L.) is widely cultivated in the world due to its value as a stable source of saccharides and proteins, and its ability to adapt to different surviving environment. Most agricultural areas where wheat mainly spread over strongly depend on natural rainfall, Drought is one of the most common abiotic stresses, which significantly affects crop production (Fedoroff et al 2010). When encountered drought stress, plant root caps synthesize abscisic acid (ABA) to trigger a signaling cascade in guard cells, and leads to stomatal closure and reduction of water loss (MacRobbie 1998)

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.