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2011 | 33 | 1 |

Tytuł artykułu

Proteomic analysis of seed viability in maize

Autorzy

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
To identify specific proteins related to maize seed viability, seeds of Zhengdan 958 (one of the highyield maize hybrids in China) were sorted based on viability evaluation with triphenyltetrazolium chloride (TTC) assay and used for comparative proteomic analysis. After TTC staining, embryos of high-viability seeds were deep red (R type), while embryos of dead seeds were white (W type). Proteomic analysis revealed that 28 protein spots identified were differently expressed significantly between R and W embryos, of which 20 were up-regulated and 8 down-regulated in R embryos. Among them were proteins involved in stress response, protein folding, and stabilization, as wells as proteins related to nutrient reservoir and metabolism. Prominently, small heat shock proteins, late embryogenesis abundant (LEA) proteins, and antioxidant enzymes were highly up-regulated, while two proteases were highly down-regulated in R embryos compared to W embryos. One of LEA proteins was EMB564, which declined in abundance during artificial aging of seeds. Our results suggested an association of EMB564 with maize seed viability. It would be of interest to use these small proteins to develop quick tests for seed quality.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

33

Numer

1

Opis fizyczny

p.181-191,fig.,ref.

Twórcy

autor
  • College of Life Science, Henan Agricultural University, Zhengzhou, China
  • Huanghuaihai Regional Innovation Center for Maize Technology, Ministry of Agriculture, Zhengzhou, China
autor
  • College of Life Science, Henan Agricultural University, Zhengzhou, China
autor
  • College of Life Science, Henan Agricultural University, Zhengzhou, China
  • Huanghuaihai Regional Innovation Center for Maize Technology, Ministry of Agriculture, Zhengzhou, China
autor
  • College of Life Science, Henan Agricultural University, Zhengzhou, China
autor
  • College of Life Science, Henan Agricultural University, Zhengzhou, China
autor
  • Huanghuaihai Regional Innovation Center for Maize Technology, Ministry of Agriculture, Zhengzhou, China

Bibliografia

  • Alexandrov NN, Brover VV, Freidin S, Troukhan ME, Tatarinova TV, Zhang HY et al (2009) Insights into corn genes derived from large-scale cDNA sequencing. Plant Mol Biol 69:179–194
  • Battaglia M, Olvera-carrillo Y, Garciarrubio A, Campos F, Covarrubias AA (2008) The enigmatic LEA proteins and other hydrophilins. Plant Physiol 148:6–24
  • Bettey M, Finch-Savage WE, King GJ, Campos F, Covarrubias AA (2000) Quantitative genetic analysis of seed viability and preemergence seedling growth traits in Brassica oleracea. New Phytol 148:277–286
  • Boudet J, Buitink J, Hoekstra FA, Rogniaux H, Larre C, Satour P et al (2006) Comparative analysis of the heat stable proteome of radicles of Medicago truncatula seeds during germination identifies late embryogenesis abundant proteins associated with desiccation tolerance. Plant Physiol 140:1418–1436
  • Brini F, Hanin M, Lumbreras V, Amara I, Khoudi H, Hassairi A et al (2007) Overexpression of wheat dehydrin DHN-5 enhances tolerance to salt and osmotic stress in Arabidopsis thaliana. Plant Cell Rep 26:2017–2026
  • Campo S, Carrascal M, Coca M, Abian J, San Segundo B (2004) The defense response of germinating maize embryos against fungal infection: a proteomics approach. Proteomics 4:383–396
  • Catusse J, Strub JM, Job C, Van Dorsselaer A, Job D (2008) Proteome-wide characterization of sugar beet seed viability and its tissue specific expression. Proc Natl Acad Sci USA 105:10262–10267
  • Dure L, Crouch M, Harada JJ, Ho THD, Mundy J, Quatrano R et al (1989) Common amino acid sequence domains among the LEA proteins of higher plants. Plant Mol Biol 12:475–486
  • Espelund M, Saeboe-Larssen S, Hughes DW, Galau GA, Larsen F, Jakobsen KS (1992) Late embryogenesis-abundant genes encoding proteins with different numbers of hydrophilic repeats are regulated differentially by abscisic acid and osmotic stress. Plant J 2:241–252
  • Feder ME, Hofmann GE (1999) Heat-shock proteins, molecular chaperones, and the stress response: evolutionary and ecological physiology. Ann Rev Physiol 61:243–282
  • Fujita Y, Fujita M, Satoh R, Maruyama K, Parvez MM, Seki M et al (2005) AREB1 is a transcription activator of novel ABREdependent ABA signaling that enhances drought stress tolerance in Arabidopsis. Plant Cell 17:3470–3488
  • Gallardo K, Job C, Groot SPC, Puype M, Demol H, Vandekerckhove J et al (2001) Proteomic analysis of Arabidopsis seed germination and priming. Plant Physiol 126:835–848
  • Galleschi L, Capocchi A, Ghiringhelli S, Saviozzi F (2002) Antioxidants, free radicals, storage proteins, and proteolytic activities in wheat (Triticum durum) seeds during accelerated aging. J Agric Food Chem 50:5450–5457
  • Heath RL, Parker L (1968) Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198
  • Job CL, Lovigny Y, Belghazi M, Belghazi M, Job D (2005) Patterns of protein oxidation in Arabidopsis seeds and during germination. Plant Physiol 138:790–802
  • Kalemba EM, Pukacka S (2007) Possible roles of LEA proteins and sHSPs in seed protection: a short review. Biol Lett 44:3–16
  • Kocsy G, Von Ballmoos P, Ruegsegger A, Szalai G, Galiba G, Brunold C (2001) Increasing the glutathione content in a chilling-sensitive maize genotype using safeners increased protection against chilling-induced injury. Plant Physiol 127:1147–1156
  • Kumar GNM, Houtz RL, Knowles NR (1999) Age-induced protein modifications and increased proteolysis in potato seed-tubers. Plant Physiol 119:89–99
  • Kyte J, Doolittle RF (1982) A simple method for displaying the hydropathic character of a protein. J Mol Biol 157:105–132
  • Linding R, Russell RB, Neduva V, Gibson TJ (2003) GlobPlot: exploring protein sequences for globularity and disorder. Nucleic Acids Res 31:3701–3708
  • Linn SS, Pearce RS (1990) Changes in lipids in bean seeds (Phaseolus vulgaris) and corn caryopses (Zea mays) aged in contrasting environments. Ann Bot 65:452–456
  • Loreto F, Velikova V (2001) Isoprene produced by leaves protects the photosynthetic apparatus against ozone damage, quenches ozone products, and reduces lipid peroxidation of cellular membranes. Plant Physiol 127:1781–1787
  • Manfre AJ, Lanni LM, Marcotte WR (2006) The Arabidopsis group 1 late embryogenesis abundant protein ATEM6 is required for normal seed development. Plant Physiol 140:140–149
  • McDonald MB (1999) Seed deterioration: physiology, repair and assessment. Seed Sci Technol 27:177–237
  • McDonough CM, Floyd CD, Waniska RD, Rooney LW (2004) Effect of accelerated aging on maize, sorghum, and sorghum meal. J Cereal Sci 39:351–361
  • Melonia DA, Oliva MA, Martinez CA, Cambraia J (2003) Photosynthesis and activity of superoxide dismutase, peroxidase and glutathione reductase in cotton under salt stress. Environ Exp Bot 49:69–76
  • Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7:405–410
  • Ogé L, Bourdais G, Bove J, Collet B, Godin B, Granier F et al (2008) Protein repair L-isoaspartyl methyltransferase 1 is involved in both seed longevity and germination viability in Arabidopsis. Plant Cell 20:3022–3037
  • Pukacka S, Ratajczak E (2007) Age-related biochemical changes during storage of beech (Fagus sylvatica L.) seeds. Seed Sci Res 17:45–53
  • Rajesh S, Manickam A (2006) Prediction of functions for two LEA proteins from mung bean. Bioinformation 1:133–138
  • Rajjou L, Belghazi M, Huguet R, Robin C, Moreau A, Job C et al (2006) Proteomic investigation of the effect of salicylic acid on Arabidopsis seed germination and establishment of early defense mechanisms. Plant Physiol 141:910–923
  • Rajjou L, Lovigny Y, Groot SPC, Belghazi M, Job C, Job D (2008) Proteome-wide characterization of seed aging in Arabidopsis: a comparison between artificial and natural aging protocols. Plant Physiol 148:620–641
  • Ramanjulu S, Bartels D (2002) Drought- and desiccation-induced modulation of gene expression in plants. Plant Cell Environ 25:141–151
  • Revilla R, Butrón A, Rodríguez VM, Malvar RA, Ordás A (2009) Identification of genes related to germination in aged maize seed by screening natural variability. J Exp Bot 60:4151–4157
  • Richter AK, Frossard E, Brunner I (2007) Polyphenols in the woody roots of Norway spruce and European beech reduce TTC. Tree Physiol 27:155–160
  • Shin JH, KimSR, AnG (2009) Rice aldehyde dehydrogenase7 is needed for seed maturation and viability. Plant Physiol 149:905–915
  • Wang W, Vignani R, Scali M, Sensi E, Tiberi P, Cresti M (2006) A universal and rapid protocol for protein extraction from recalcitrant plant tissues for proteomic analysis. Electrophoresis 27:2782–2786
  • Wang JH, Chen SN, Bai B, Tang JH, Wang W (2009a) Effects of artificial aging on seed viability and proteome of maize seeds. J Henan Agric Univ 43:132–135
  • Wang W, Li CQ, Hu XL (2009b) Developmental expression of β-glucosidase in olive leaves. Biol Plant 53:138–140
  • Wang W, Bianchi L, Scali M, Liu LW, Bini L, Cresti M (2009c) Proteomic analysis of β-1, 3-glucanase in grape berry tissues. Acta Physiol Plant 31:597–604
  • Wehmeyer N, Vierling E (2000) The expression of small heat shock proteins in seeds responds to discrete development signals and suggests a general protective role in desiccation tolerance. Plant Physiol 122:1099–1108
  • Williams BA, Tsang A (1991) A maize gene expressed during embryogenesis is abscisic acid-inducible and highly conserved. Plant Mol Biol 16:919–923
  • Williams BA, Tsang A (1994) Analysis of multiple classes of abscisic acid responsive genes during embryogenesis in Zea mays. Dev Genet 15:415–424
  • Zhao PF, Zhu YH, Wang W (2010) Evaluation and improvement of spectrophotometric assays of TTC reduction: maize (Zea mays) embryo as an example. Acta Physiol Plant. doi:10.1007/s11738-009-0457-2 (in press)
  • Zolla L, Rinalducci S, Antonioli P, Righetti PG (2008) Proteomics as a complementary tool for identifying unintended side effects occurring in transgenic maize seeds as a result of genetic modifications. J Proteome Res 7:1850–1861
  • Zur Nieden U, Neumann D, Bucka A, Neumann D (1995) Tissuespecific localization of heat-stress proteins during embryo development. Planta 196:530–538

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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