Abstract

BackgroundWheat (Triticum aestivum L.) is an economically important grain crop. Two-dimensional gel-based approaches are limited by the low identification rate of proteins and lack of accurate protein quantitation. The recently developed isobaric tag for relative and absolute quantitation (iTRAQ) method allows sensitive and accurate protein quantification. Here, we performed the first iTRAQ-based quantitative proteome and phosphorylated proteins analyses during wheat grain development.ResultsThe proteome profiles and phosphoprotein characterization of the metabolic proteins during grain development of the elite Chinese bread wheat cultivar Yanyou 361 were studied using the iTRAQ-based quantitative proteome approach, TiO2 microcolumns, and liquid chromatography-tandem mass spectrometry (LC-MS/MS). Among 1,146 non-redundant proteins identified, 421 showed at least 2-fold differences in abundance, and they were identified as differentially expressed proteins (DEPs), including 256 upregulated and 165 downregulated proteins. Of the 421 DEPs, six protein expression patterns were identified, most of which were up, down, and up-down expression patterns. The 421 DEPs were classified into nine functional categories mainly involved in different metabolic processes and located in the membrane and cytoplasm. Hierarchical clustering analysis indicated that the DEPs involved in starch biosynthesis, storage proteins, and defense/stress-related proteins significantly accumulated at the late grain development stages, while those related to protein synthesis/assembly/degradation and photosynthesis showed an opposite expression model during grain development. Quantitative real-time polymerase chain reaction (qRT-PCR) analysis of 12 representative genes encoding different metabolic proteins showed certain transcriptional and translational expression differences during grain development. Phosphorylated proteins analyses demonstrated that 23 DEPs such as AGPase, sucrose synthase, Hsp90, and serpins were phosphorylated in the developing grains and were mainly involved in starch biosynthesis and stress/defense.ConclusionsOur results revealed a complex quantitative proteome and phosphorylation profile during wheat grain development. Numerous DEPs are involved in grain starch and protein syntheses as well as adverse defense, which set an important basis for wheat yield and quality. Particularly, some key DEPs involved in starch biosynthesis and stress/defense were phosphorylated, suggesting their roles in wheat grain development.Electronic supplementary materialThe online version of this article (doi:10.1186/1471-2164-15-1029) contains supplementary material, which is available to authorized users.

Highlights

  • Wheat (Triticum aestivum L.) is an economically important grain crop

  • Physiological changes of flag leaves during grain development The dynamic changes of relative water content (RWC), total chlorophyll content, water soluble content (WSC), and proline content of flag leaf at five grain developmental stages (7, 14, 18, 21, and 28 days post-anthesis (DPA)) of the Yanyou 361 cultivar are shown in Additional file 1: Figure S1

  • The results showed that RWC gradually decreased along with grain development, while total chlorophyll content increased from 14 to 18 DPA and decreased dramatically until grain maturation

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Summary

Introduction

Wheat (Triticum aestivum L.) is an economically important grain crop. Wheat (Triticum aestivum L., 2n =6× =42, AABBDD) is one of the most important grain crops in the world. It is well known that wheat grain proteins are classified into two major categories: non-prolamins, including water-soluble albumins, and salt-soluble globulins and prolamins, including gliadins and glutenins. Albumins and globulins, which include various enzymes and their inhibitors that play important roles in plant growth and development, are soluble proteins [3]. These proteins are relatively well balanced for human nutrition because of their high level of essential amino acids such as lysine, tryptophan, and methionine [4]

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