Proteome analysis of maize seeds: the effect of artificial ageing.

Previous understanding of the mechanism of seed ageing is largely based on observations on imbibed seeds rather than dry seeds. The present research was conducted to investigate whether seed ageing has effects on the dry seeds through proteome analysis. Maize (Zea mays cv. Dabaitou) seeds were artificially aged at 50°C (13.58% moisture content) for 5 or 13 days, and the total protein was extracted from embryos of the dry seeds. Two-dimensional electrophoresis was performed and the differentially expressed proteins were identified by matrix-assisted laser desorption ionization-time of flight mass spectrometry. A total of 40 proteins were identified, in which 16 proteins were upregulated, indicating that artificial ageing affected the proteome of the dry seeds. Proteomic studies revealed that the signal transduction and transcription were disturbed by artificial ageing, which might lead to reduced protection against ageing. Artificial ageing also increased proteases and broke down stored proteins, impaired metabolism and energy supply, and ultimately resulted in seed deterioration. Proteins involved in metabolism and energy were the largest downregulated protein group, with regard to glycolysis, tricarboxylic acid cycle, the electron transport chain and oxidative phosphorylation. The downregulation of these proteins, together with reduction in the specific activity of glucose-6-phosphate dehydrogenase, and the content of glucose 6-phosphate, pyruvic acid and ATP in aged seeds, suggested the important roles of the mobilization of stored carbohydrates and energy supply in seed ageing and seed vigor. The present work provides new information about the proteomic changes during seed ageing and provides a possible mechanism for seed deterioration.

[1]  M. E. González-Benito,et al.  Characterization of volatile production during storage of lettuce (Lactuca sativa) seed. , 2010, Journal of experimental botany.

[2]  G. Qin,et al.  Mitochondrial damage in the soybean seed axis during imbibition at chilling temperatures. , 2009, Plant & cell physiology.

[3]  K. Kang,et al.  Developing rice embryo proteomics reveals essential role for embryonic proteins in regulation of seed germination. , 2009, Journal of proteome research.

[4]  C. Job,et al.  Proteome-Wide Characterization of Seed Aging in Arabidopsis: A Comparison between Artificial and Natural Aging Protocols[W][OA] , 2008, Plant Physiology.

[5]  Pingfang Yang,et al.  Proteomic analysis of rice (Oryza sativa) seeds during germination , 2007, Proteomics.

[6]  Yi Jin,et al.  Aldo-keto reductases and bioactivation/detoxication. , 2007, Annual review of pharmacology and toxicology.

[7]  C. Bailly,et al.  Sunflower seed deterioration as related to moisture content during ageing, energy metabolism and active oxygen species scavenging , 2006 .

[8]  H. Pritchard,et al.  Glutathione half-cell reduction potential: a universal stress marker and modulator of programmed cell death? , 2006, Free radical biology & medicine.

[9]  J. Zweier,et al.  Superoxide Generation from Mitochondrial NADH Dehydrogenase Induces Self-inactivation with Specific Protein Radical Formation* , 2005, Journal of Biological Chemistry.

[10]  Chenping Xu,et al.  Comparison of protein solubilization methods suitable for proteomic analysis of soybean seed proteins. , 2005, Analytical biochemistry.

[11]  M. Hajduch,et al.  A Systematic Proteomic Study of Seed Filling in Soybean. Establishment of High-Resolution Two-Dimensional Reference Maps, Expression Profiles, and an Interactive Proteome Database1[w] , 2005, Plant Physiology.

[12]  G. Leubner-Metzger,et al.  beta-1,3-Glucanase gene expression in low-hydrated seeds as a mechanism for dormancy release during tobacco after-ripening. , 2004, The Plant journal : for cell and molecular biology.

[13]  G. Goldman,et al.  The Aspergillus nidulans npkA Gene Encodes a Cdc2-Related Kinase That Genetically Interacts With the UvsBATR Kinase Sequence data from this article have been deposited with the NCBI under accession no. AY166593. , 2004, Genetics.

[14]  C. Bailly Active oxygen species and antioxidants in seed biology , 2004, Seed Science Research.

[15]  D. Barrett,et al.  Modified method for the determination of pyruvic acid with dinitrophenylhydrazine in the assessment of onion pungency , 2003 .

[16]  Yan-Lin Guo,et al.  Upregulation of Cdc2 and cyclin A during apoptosis of endothelial cells induced by cleaved high-molecular-weight kininogen. , 2003, American journal of physiology. Heart and circulatory physiology.

[17]  T. Penning,et al.  The aldo-keto reductase superfamily homepage. , 2003, Chemico-biological interactions.

[18]  A Khodjakov,et al.  Increased mitochondrial cytochrome c levels and mitochondrial hyperpolarization precede camptothecin-induced apoptosis in Jurkat cells , 2000, Cell Death and Differentiation.

[19]  J. Schlessinger,et al.  Cell Signaling by Receptor Tyrosine Kinases , 2000, Cell.

[20]  A. Weissman,et al.  RING Finger Proteins Mediators of Ubiquitin Ligase Activity , 2000, Cell.

[21]  M. Mcdonald Seed deterioration: Physiology, repair and assessment , 1999 .

[22]  C. Walters Understanding the mechanisms and kinetics of seed aging , 1998, Seed Science Research.

[23]  M. Corona,et al.  Heat-shock proteins in monitoring aging and heat-induced tolerance in germinating wheat and barley embryos , 1998, Seed Science Research.

[24]  J. Leahy,et al.  Fatty acid-induced beta cell hypersensitivity to glucose. Increased phosphofructokinase activity and lowered glucose-6-phosphate content. , 1998, The Journal of clinical investigation.

[25]  K. Stuhlmeier,et al.  Importance of Glucose-6-phosphate Dehydrogenase Activity for Cell Growth* , 1998, The Journal of Biological Chemistry.

[26]  P. Piffanelli,et al.  Analysis of 1.9 Mb of contiguous sequence from chromosome 4 of Arabidopsis thaliana , 1998, Nature.

[27]  K. Yeh,et al.  Expression of a gene encoding a 16.9-kDa heat-shock protein, Oshsp16.9, in Escherichia coli enhances thermotolerance. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[28]  W. Finch-Savage,et al.  Respiratory enzyme activities during germination in Brassica seed lots of differing vigour , 1996, Seed Science Research.

[29]  John C. Walker,et al.  Plant Protein Kinase Families and Signal Transduction , 1995, Plant physiology.

[30]  A. Dell'aquila Wheat seed ageing and embryo protein degradation , 1994, Seed Science Research.

[31]  Lianfa Shi,et al.  Premature p34cdc2 activation required for apoptosis. , 1994, Science.

[32]  R. H. Ellis,et al.  Seed and seedling vigour in relation to crop growth and yield , 1992, Plant Growth Regulation.

[33]  G. Rödel,et al.  Yeast SCO1 protein is required for a post-translational step in the accumulation of mitochondrial cytochrome c oxidase subunits I and II , 1990, Current Genetics.

[34]  R. L. Obendorf,et al.  Soybean Seed Respiration During Simulated Preharvest Deterioration , 1986 .

[35]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.

[36]  T. Ching,et al.  Physiological and Chemical Differences in Aged Seeds 1 , 1968 .

[37]  Knowles,et al.  Age-induced protein modifications and increased proteolysis in potato seed-tubers , 1999, Plant physiology.

[38]  Merrit Gj,et al.  Effects of seed ageing on early post-germination in root extension in maize: a spatial and histological analysis of the growth-zone , 1999 .

[39]  H. Shekar Shetty,et al.  Membrane deterioration and other biochemical changes, associated with accelerated ageing of maize seeds , 1991 .

[40]  P. M. Swamy,et al.  Contribution of the Pentose Phosphate Pathway and Glycolytic Pathway to Dormancy Breakage and Germination of Peanut (Arachis hypogaea L.) Seeds , 1986 .