iTRAQ-based quantitative proteome and phosphoprotein characterization reveals the central metabolism changes involved in wheat grain development
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  • 作者:Chaoying Ma (81)
    Jianwen Zhou (81)
    Guanxing Chen (81)
    Yanwei Bian (81)
    Dongwen Lv (81)
    Xiaohui Li (81)
    Zhimin Wang (82)
    Yueming Yan (81)

    81. College of Life Sciences
    ; Capital Normal University ; Beijing ; 100048 ; China
    82. College of Agriculture and Biotechnology
    ; China Agricultural University ; Beijing ; 100094 ; China
  • 关键词:Wheat ; Grain proteome ; iTRAQ ; Phosphoproteins ; qRT ; PCR
  • 刊名:BMC Genomics
  • 出版年:2014
  • 出版时间:December 2014
  • 年:2014
  • 卷:15
  • 期:1
  • 全文大小:3,325 KB
  • 参考文献:1. Brenchley, R, Spannagl, M, Pfeifer, M, Barker, GLA, Amore, RD, Allen, AM, McKenzie, N, Kramer, M, Kerhornou, A, Bolser, D, Kay, S, Waite, D, Trick, M, Bancroft, I, Gu, Y, Huo, N, Luo, MC, Sehgal, S, Gill, B, Kianian, S, Anderson, O, Kersey, P, Dvorak, J, McCombie, WR, Hall, A, Mayer, KFX, Edwards, KJ, Bevan, MW, Hall, N (2012) Analysis of the breadwheat genome using whole-genome shotgun sequencing. Nature 491: pp. 705-710 CrossRef
    2. Song, Y, Zheng, Q (2007) Dynamic rheological properties of wheat flour dough and proteins. Trends Food Sci Technol 18: pp. 132-138 CrossRef
    3. Singh, NK, Donovan, GR, Batey, IL, MacRitchie, F (1990) Use of sonication and size-exclusion high-performance liquid chromatography in the study of wheat flour proteins. I. Dissolution of total proteins in the absence of reducing agents. Cereal Chem 67: pp. 150-161
    4. Wiesner, H, Seilmeier, W, Belitz, HD (1980) Vergleichende untersuchungen 眉ber partielle aminosauresequenzen von prolaminen und glutelinen verschriedener getreidearten. Z Lebensm Unters Forsch 170: pp. 17-26 CrossRef
    5. Shewry, PR, Mitchell, RAC, Tosi, P, Wan, Y, Toscano-Underwood, C, Lovegrove, A, Freeman, J, Toole, GA, Mills, ENC, Ward, JL (2012) An integrated study of grain development of wheat (cv. Hereward). J Cereal Sci 56: pp. 21-30 CrossRef
    6. Bechtel, DB, Wilson, JD (2003) Amyloplast formation and starch granule development in hard red winter wheat. Cereal Chem 80: pp. 175-183 CrossRef
    7. Parker, ML (1985) The relationship between A-type and B-type starch granules in the developing endosperm of wheat. J Cereal Sci 3: pp. 271-278 CrossRef
    8. Wan, Y, Poole, RL, Huttly, AK, Toscano-Underwood, C, Feeney, K, Welham, S, Gooding, MJ, Mills, C, Edwards, KJ, Shewry, PR, Mitchell, RAC (2008) Transcriptome analysis of grain development in hexaploid wheat. BMC Genomics 9: pp. 121 CrossRef
    9. Howarth, JR, Parmar, S, Jones, J, Shepherd, CE, Corol, DI, Galster, AM, Hawkins, ND, Miller, SJ, Baker, JM, Verrier, PJ, Ward, JL, Beale, MH, Barraclough, PB, Hawkesford, MJ (2008) Co-ordinated expression of amino acid metabolism in response to N and S deficiency during wheat grain filling. J Exp Bot 59: pp. 3675-3689 CrossRef
    10. Dong, K, Ge, P, Ma, C, Wang, K, Yan, X, Gao, L, Li, X, Liu, J, Ma, W, Yan, Y (2012) Albumin and globulin dynamics during grain development of elite Chinese wheat cultivar Xiaoyan 6. J Cereal Sci 56: pp. 615-622 CrossRef
    11. Ruuska, SA, Girke, T, Benning, C, Ohlrogge, JB (2002) Contrapuntal networks of gene expression during Arabidopsis seed filling. Plant Cell 14: pp. 1191-1206 CrossRef
    12. Zhang, A, Lu, Q, Yin, Y, Ding, S, Wen, X, Lu, C (2010) Comparative proteomic analysis provides new insights into the regulation of carbon metabolism during leaf senescence of rice grown under field conditions. J Plant Physiol 167: pp. 1380-1389 CrossRef
    13. Mechin, V, Thevenot, C, Le Guilloux, M, Prioul, JL, Damerval, C (2007) Developmental analysis of maize endosperm proteome suggests a pivotal role for pyruvate orthophosphate dikinase. Plant Physiol 143: pp. 1203-1219 CrossRef
    14. Xu, SB, Li, T, Deng, ZY, Chong, K, Xue, YB, Wang, T (2008) Dynamic proteomic analysis reveals a switch between central carbon metabolism and alcoholic fermentation in rice filling grains. Plant Physiol 148: pp. 908-925 CrossRef
    15. Gao, L, Wang, A, Li, X, Dong, K, Wang, K, Appels, R, Ma, W, Yan, Y (2009) Wheat quality related differential expressions of album ins and globulins revealed by two-dimensional difference gel electrophoresis (2-D DIGE). J Proteomics 73: pp. 279-296 CrossRef
    16. Lesage, VS, Merlino, M, Chambon, C, Bouchet, B, Marion, D, Branlard, G (2012) Proteomes of hard and soft near-isogenic wheat lines reveal that kernel hardness is related to the amplification of a stress response during endosperm development. J Exp Bot 63: pp. 1001-1011 CrossRef
    17. Ge, P, Ma, C, Wang, S, Gao, L, Li, X, Guo, G, Ma, W, Yan, Y (2012) Comparative proteomic analysis of grain development in two spring wheat varieties under drought stress. Anal Bioanal Chem 402: pp. 1297-1313 CrossRef
    18. Guo, G, Ge, P, Ma, C, Li, X, Lv, D, Wang, S, Ma, W, Yan, Y (2012) Comparative proteomic analysis of salt response proteins in seedling roots of two wheat varieties. J Proteomics 75: pp. 1867-1885 CrossRef
    19. Molloy, MP, Herbert, BR, Walsh, BJ, Tyler, MI, Traini, M, Sanchez, JC, Hochstrasser, DF, Williams, KL, Gooley, AA (1998) Extraction of membrane proteins by differential solubilization for separation using two-dimensional gel electrophoresis. Electrophoresis 19: pp. 837-844 CrossRef
    20. Ge, P, Hao, P, Cao, M, Guo, G, Lv, D, Subburaj, S, Li, X, Yan, X, Xiao, J, Ma, W, Yan, Y (2013) iTRAQ-based quantitative proteomic analysis reveals new metabolic pathways of wheat seedling growth under hydrogen peroxide stress. Proteomics 13: pp. 3046-3058
    21. Karp, NA, Huber, W, Sadowski, PG, Charles, PD, Hseter, SV, Lilley, KS (2010) Addressing accuracy and precision issues in iTRAQ quantitation. Mol Cell Proteomics 9: pp. 1885-97 CrossRef
    22. Wang, M, You, J (2012) Mass spectrometry for protein quantification in biomarker discovery. Methods Mol Biol 815: pp. 199-225 CrossRef
    23. Ford, KL, Cassin, A, Bacic, A (2011) Quantitative proteomic analysis of wheat cultivars with differing drought stress tolerance. Front Plant Sci 2: pp. 44 CrossRef
    24. Thingholm, TE, Jensen, ON, Larsen, MR (2009) Analytical strategies for phosphoproteomics. Proteomics 9: pp. 1451-1468 CrossRef
    25. Khan, M, Takasaki, H, Komatsu, S (2005) Comprehensive phosphoproteome analysis in rice and identification of phosphoproteins responsive to different hormones/stresses. J Proteome Res 4: pp. 1592-1599 CrossRef
    26. Kline, KG, Barrett-Wilt, GA, Sussman, MR (2010) In planta changes in protein phosphorylation induced by the plant hormone abscisic acid. Proc Natl Acad Sci 107: pp. 5986-5991 CrossRef
    27. Bonhomme, L, Valot, B, Tardieu, F, Zivy, M (2012) Phosphoproteome dynamics upon changes in plant water status reveal early events associated with rapid growth adjustment in maize leaves. Mol Cell Proteomics 1: pp. 957-972 CrossRef
    28. Lv, D, Subburaj, S, Cao, M, Yan, X, Li, X, Appels, R, Sun, D, Ma, W, Yan, Y (2014) Proteome and phosphoproteome characterization reveals new response and defense mechanisms of Brachypodium distachyon leaves under salt stress. Mol Cell Proteomics 13: pp. 632-652 CrossRef
    29. Lv, D, Ge, P, Zhang, M, Cheng, Z, Li, X, Yan, Y (2014) Integrative network analysis of the signaling cascades in seedling leaves of bread wheat by large-scale phosphoproteomic profiling. J Proteome Res 13: pp. 2381-2395 CrossRef
    30. Tetlow, IJ, Beisel, KG, Cameron, S, Makhmoudova, A, Liu, FS, Bresolin, NS, Wait, R, Morell, MK, Emes, MJ (2008) Analysis of protein complexes in wheat amyloplasts reveals functional interactions among starch biosynthetic enzymes. Plant Physiol 146: pp. 1878-1891 CrossRef
    31. Tetlow, IJ, Wait, R, Lu, Z, Akkasaeng, R, Bowsher, CG, Esposito, S, Kosar-Hashemi, B, Morell, MK, Emes, MJ (2004) Protein phosphorylation in amyloplasts regulates starch branching enzyme activity and protein-protein interactions. Plant Cell 16: pp. 694-708 CrossRef
    32. Tada, Y, Kashimura, T (2009) Proteomic Analysis of Salt-Responsive Proteins in the Mangrove Plant, Bruguiera gymnorhiza. Plant Cell Physiol 50: pp. 439-446 CrossRef
    33. Ni, W, Trelease, RN (1991) Post-Transcriptional Regulation of Catalase lsozyme Expression in Cotton Seeds. Plant Cell 3: pp. 737-744 CrossRef
    34. Tian, Q, Stepaniants, SB, Mao, M, Weng, L, Feetham, MC, Doyle, MJ, Yi, EC, Dai, H, Thorsson, V, Eng, J, Goodlett, D, Berger, JP, Gunter, B, Linseley, PS, Stoughton, RB, Aebersold, R, Collins, SJ, Hanlon, WA, Hood, LE (2004) Integrated genomic and proteomics analyses of gene expression in mammalian cells. Mol Cell Proteomics 3: pp. 960-969 CrossRef
    35. Kelley, LA, Sternberg, MJ (2009) Protein structure prediction on the Web: a case study using the Phyre server. Nat Protoc 4: pp. 363-71 CrossRef
    36. Fluhra, R, Lampl, N, Roberts, TH (2012) Serpin protease inhibitors in plant biology. Physiol Plantarum 145: pp. 95-102 CrossRef
    37. Keeling, PL, Wood, JR, Tyson, RH, Bridges, LG (1988) Starch biosynthesis in developing wheat grain Evidence against the Direct Involvement of Triose Phosphates in the Metabolic Pathway. Plant Physiol 87: pp. 311-319 CrossRef
    38. Liang, J, Zhang, J, Cao, X (2001) Grain Sink Strength May Be Related to the Poor Grain Filling of indica-japonica Rice (Oryza sativa) Hybrids. Physiol Plantarum 112: pp. 470-477 CrossRef
    39. Wang, F, Sanz, A, Brenner, ML, Smith, A (1993) Sucrose synthase, starch accumulation, and tomato fruit sink strength. Plant Physiol 101: pp. 321-327
    40. Tschiersch, H, Borisjuk, L, Rutten, T, Rolletschek, H (2010) Gradients of seed photosynthesis and its role for oxygen balancing. Biosystems 103: pp. 302-308 CrossRef
    41. Martin, C, Smith, AM (1995) Starch biosynthesis. Plant Cell 7: pp. 971-985 CrossRef
    42. Sullivan, DT, Kaneko, Y (1995) The maize brittlel gene encodes amyloplast membrane polypeptides. Planta 196: pp. 477-484 CrossRef
    43. Geigenberger, P (2011) Regulation of starch biosynthesis in response to a fluctuating environment. Plant Physiol 155: pp. 1566-1577 CrossRef
    44. Commuri, PD, Keeling, PL (2001) Chain-length specificities of maize starch synthase I enzyme: studies of glucan affinity and catalytic properties. Plant J 25: pp. 475-486 CrossRef
    45. Grimaud, F, Rogniaux, H, James, MG, Myers, AM, Planchot, V (2008) Proteome and phosphoproteome analysis of starch granule-associated proteins from normal maize andmutants affected in starch biosynthesis. J Exp Bot 59: pp. 3395-3406 CrossRef
    46. Reiland, S, Messerli, G, Baerenfaller, K, Gerrits, B, Endler, A, Grossmann, J, Gruissem, W, Baginsky, S (2009) Large-scale Arabidopsis phosphoproteome profiling reveals novel chloroplast kinase substrates and phosphorylation networks. Plant Physiol 150: pp. 889-903 CrossRef
    47. Deutscher, D The current status of breeding for protein quality in corn. In: Friedman, M eds. (1978) Nutritional Improvement of Food and Feed Proteins. Plenum, New York, pp. 281-300 CrossRef
    48. Miflin, BJ, Habash, DZ (2002) The role of glutamine synthetase and glutamate dehydrogenase in nitrogen assimilation and possibilities for improvement in the nitrogen utilization of crops. J Exp Bot 53: pp. 979-987 CrossRef
    49. Bernard, SM, Habash, DZ (2009) The importance of cytosolic glutamine synthetase in nitrogen assimilation and recycling. New Phytol 182: pp. 608-620 CrossRef
    50. Martin, A, Lee, J, Kichey, T, Gerentes, D, Zivy, M, Tatout, C, Dubois, F, Balliau, T, Valot, B, Davanture, M, Terc茅-Laforgue, T, Quiller茅, I, Coque, M, Gallais, A, Gonzalez-Moro, MB, Bethencourt, L, Habash, DZ, Lea, PJ, Charcosset, A, Perez, P, Murigneux, A, Sakakibara, H, Edwards, KJ, Hirel, B (2006) Two cytosolic glutamine synthetase isoforms of maize are specifically involved in the control of grain production. Plant Cell 18: pp. 3252-3274 CrossRef
    51. Wilkinson, B, Gilbert, HF (2004) Protein disulfide isomerase. Biochim Biophys Acta 1699: pp. 35-44 CrossRef
    52. Houston, NL, Fan, C, Xiang, Q, Schulze, JM, Jung, R, Boston, RS (2005) Phylogenetic analyses identify 10 classes of the protein disulfide isomerase family in plants, including single-domain protein disulfide isomerase-related proteins. Plant Physiol 137: pp. 762-778 CrossRef
    53. Takemoto, Y, Couglan, SJ, Okita, TW, Satoh, H, Ogawa, M, Kumamaru, T (2002) The rice mutant esp2 greatly accumulates the glutelin precursor and deletes the protein disulfide isomerase. Plant Physiol 128: pp. 1212-1222 CrossRef
    54. d鈥橝loisio, E, Paolacci, AR, Dhanapal, AP, Tanzarella, OA, Porceddu, E, Ciaffi, M (2010) The protein disulfide isomerase gene family in bread wheat (T. aestivum L.). BMC Plant Biol 10: pp. 101 CrossRef
    55. Bollini, R, Chrispeels, MJ (1979) The rough endoplasmic reticulum is the site of reserve-protein synthesis in developing Phaseolus vulgaris cotyledons. Planta 146: pp. 487-501 CrossRef
    56. Shewry, PR, Tatham, AS (1997) Disulphide bonds in wheat gluten proteins. J Cereal Sci 25: pp. 207-227 CrossRef
    57. Gianibelli, MC, Larroque, OR, MacRitchie, F, Wrigley, CW (2001) Biochemical, genetic and molecular characterization of wheat glutenin and its component subunits. Cereal Chem 78: pp. 635-646 CrossRef
    58. Gupta, RB, Masci, S, Lafiandra, D, Bariana, HS, MacRitchie, F (1996) Accumulation of protein subunits and their polymers in developing grains of hexaploid wheats. J Exp Bot 47: pp. 1377-1385 CrossRef
    59. Morris, CF, Rose, SP Wheat. In: Henry, RJ, Kettlewell, PS eds. (1996) Cereal grain quality. Chapman and Hall, New York, pp. 3-54 CrossRef
    60. Hogg, AC, Sripo, T, Beecher, B, Martin, JM, Giroux, MJ (2004) Wheat puroindolines interact to form friabilin and control wheat grain hardness. Theor Appl Genet 108: pp. 1089-1097 CrossRef
    61. Thomashow, MF (1999) Plant cold acclimation: freezing tolerance genes and regulatory mechanisms. Annu Rev Plant Physiol Plant Mol Biol 50: pp. 571-599 CrossRef
    62. Kr眉ger, C, Berkowitz, O, Stephan, UW, Hell, R (2002) A metal-binding member of the late embryogenesis abundant protein family transports iron in the phloem of Ricinus communis L. J Biol Chem 277: pp. 25062-25069 CrossRef
    63. Coppolino, MG, Woodside, MJ, Demaurex, N, Grinstein, S, St-Arnaud, R, Dedhar, S (1997) Calreticulin is essential for integrin-mediated calcium signalling and cell adhesion. Nature 386: pp. 843-847 CrossRef
    64. Cuming, AC (1984) Developmental regulation of gene expression in wheat embryos. Molecular cloning of a DNA sequence encoding the early-methionine-labelled (Em) polypeptide. Eur J Biochem 145: pp. 351-357 CrossRef
    65. Roberts, TH, Hejgaard, J (2008) Serpins in plants and green algae. Funct Integr Genomic 8: pp. 1-27 CrossRef
    66. Vensel, WH, Tanaka, CK, Cai, N, Wong, JH, Buchanan, BB, Hurkman, WJ (2005) Developmental changes in the metabolic protein profiles of wheat endosperm. Proteomics 5: pp. 1594-1611 CrossRef
    67. Lampl, N, Budai-Hadrian, O, Davydov, O, Joss, TV, Harrop, SJ, Curmi, PM, Roberts, TH, Fluhr, R (2010) Arabidopsis AtSerpin1: crystal structure and in vivo interaction with its target protease responsive to desiccation-21 (RD21). J Biol Chem 285: pp. 13550-13560 CrossRef
    68. Longhi, TM, Cella, N (2012) Tyrosine phosphorylation plays a role in increasing maspin protein levels and its cytoplasmic accumulation. FEBS Open Bio 2: pp. 93-97 CrossRef
    69. Congote, LF, Temmel, N (2004) The C-terminal 26-residue peptide of serpin A1 stimulates proliferation of breast and liver cancer cells: role of protein kinase C and CD47. FBES Letters 576: pp. 343-347 CrossRef
    70. Neuwald, AF, Aravind, L, Spouge, JL, Koonin, EV (1999) AAA+: a class of chaperone-like ATPases associated with the assembly, operation, and disassembly of protein complexes. Genome Res 9: pp. 27-43
    71. Mollapour, M, Tsutsumi, S, Donnelly, AC, Beebe, K, Tokita, MJ, Lee, MJ, Lee, S, Morra, G, Bourboulia, D, Scroggins, BT, Colombo, G, Blagg, BS, Panaretou, B, Stetler-Stevenson, WG, Trepel, JB, Piper, PW, Prodromou, C, Pearl, LH, Neckers, L (2010) Swe1Wee1-dependent tyrosine phosphorylation of Hsp90 regulates distinct facets of chaperone function. Mol Cell 37: pp. 333-343 CrossRef
    72. Wang, W, Vinocur, B, Shoseyov, O, Altman, A (2004) Role of plant heat-shock proteins and molecular chaperones in the abiotic stress response. Trends Plant Sci 9: pp. 244-252 CrossRef
    73. Ito, J, Taylor, NL, Castleden, I, Weckwerth, W, Millar, AH, Heazlewood, JL (2009) A survey of the Arabidopsis thaliana mitochondrial phosphoproteome. Proteomics 17: pp. 4229-4240 CrossRef
    74. Mollapour, M, Neckers, L (1823) Post-translational modifications of Hsp90 and their contributions to chaperone regulation. Biochim Biophys Acta 2012: pp. 648-655
    75. Mhamdi, A, Queval, G, Chaouch, S, Vanderauwera, S, Breusegem, FV, Noctor, G (2011) Catalase function in plants: a focus on Arabidopsis mutants as stress-mimic models. J Exp Bot 61: pp. 4197-4220 CrossRef
    76. Wood, ZA, Schr枚der, E, Harris, JR, Poole, LB (2003) Structure, mechanism and regulation of peroxiredoxins. Trends Biochem Sci 28: pp. 32-40 CrossRef
    77. Serrato, AJ, Cejudo, FJ (2003) Type-h thioredoxins accumulate in the nucleus of developing wheat seed tissues suffering oxidative stress. Planta 217: pp. 392-399 CrossRef
    78. Manevich, Y, Sweitzer, T, Pak, JH, Feinstein, SI, Muzykantov, V, Fisher, AB (2002) 1-Cys peroxiredoxin overexpression protects cells against phospholipid peroxidation-mediated membrane damage. Proc Natl Acad Sci 99: pp. 11599-11604 CrossRef
    79. Manevich, Y, Feinstein, SI, Fisher, AB (2004) Activation of the antioxidant enzyme 1-CYS peroxiredoxin requires glutathionylation mediated by heterodimerization with 蟺GST. Proc Natl Acad Sci 101: pp. 3780-3785 CrossRef
    80. Barrs, HD, Weatherley, PE (1962) A re-examination of the relative turgidity technique for estimating water deficit in leaves. Aust J Biol Sci 15: pp. 413-428
    81. Bates, LS, Waldren, RP, Teare, ID (1973) Rapid determination of free proline for water-stress studies. Plant Soil 39: pp. 205-207 CrossRef
    82. Zhang, J, Dell, B, Conocono, E, Waters, I, Setter, T, Appels, R (2009) Water deficits in wheat: fructan exohydrolase (1-FEH) mRNA expression and relationship to soluble carbohydrate concentrations in two varieties. New Phytol 181: pp. 843-850 CrossRef
    83. Olsen, JV, Blagoev, B, Gnad, F, Macek, B, Kumar, C, Mortensen, P, Mann, M (2006) Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. Cell 127: pp. 635-648 CrossRef
    84. Cox, J, Mann, M (2008) MaxQuant enables high peptide identification rates, individualized ppb-range mass accuracies and proteome-wide protein quantification. Nat Biotechnol 26: pp. 1367-1372 CrossRef
    85. Du, Z, Zhou, X, Ling, Y, Zhang, Z, Su, Z (2010) agriGO: a GO analysis toolkit for the agricultural community. Nucleic Acids Res 38: pp. W64-W70 CrossRef
  • 刊物主题:Life Sciences, general; Microarrays; Proteomics; Animal Genetics and Genomics; Microbial Genetics and Genomics; Plant Genetics & Genomics;
  • 出版者:BioMed Central
  • ISSN:1471-2164
文摘
Background Wheat (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. Results The 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. Conclusions Our 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.

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