Quantitative subproteomic analysis of germinating related changes in the scutellum oil bodies of Zea mays

Plant Science

Volumn 191-192, Issue , 2012, Pages 1-7

  Tnani, H ^a   Lopez I ^a   Jouenne, T ^b   Vicient, C M ^a  

^a CENTRE FOR RESEARCH IN AGRICULTURAL GENOMICS CRAG   (Spain)

^b UNIVERSITÉ DE ROUEN   (France)

Author keywords

Imbibition; Maize; Oil body; Proteomic; Scutellum

Indexed keywords

PROTEOME; VEGETABLE OIL; VEGETABLE PROTEIN;

AMINO ACID SEQUENCE; ARTICLE; CHEMISTRY; GERMINATION; GROWTH, DEVELOPMENT AND AGING; HISTOLOGY; LIQUID CHROMATOGRAPHY; MAIZE; MASS SPECTROMETRY; METABOLISM; METHODOLOGY; MOLECULAR GENETICS; PHYSIOLOGY; PLANT SEED; PROTEOMICS; TWO DIMENSIONAL GEL ELECTROPHORESIS;

AMINO ACID SEQUENCE; CHROMATOGRAPHY, LIQUID; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; GERMINATION; MASS SPECTROMETRY; MOLECULAR SEQUENCE DATA; PLANT OILS; PLANT PROTEINS; PROTEOME; PROTEOMICS; SEEDS; ZEA MAYS;

ZEA MAYS;

EID: 84860592393     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plantsci.2012.02.011     Document Type: Article

References (35)

1. Fujimoto T., Parton R.G. Not just fat: the structure and function of the lipid droplet. Cold Spring Harb. Perspect. Biol. 2011, 3:3.
2. Purkrtova Z.Z., Jolivet P., Miquel M., Chardot T. Structure and function of seed lipid-body-associated proteins. C. R. Biol. 2008, 331:746-754.
3. Pu J., Ha C.W., Zhang S., Jung J.P., Huh W.K., Liu P. Interactomic study on interaction between lipid droplets and mitochondria. Protein Cell 2011, 2:487-496.
4. Murphy D.J. The biogenesis and functions of lipid bodies in animals, plants and microorganisms. Prog. Lipid Res. 2001, 40:325-438.
5. Capuano F., Beaudoin F., Napier J.A., Shewry P.R. Properties and exploitation of oleosins. Biotechnol. Adv. 2007, 25:203-206.
6. Purkrtova Z., d'Andrea S., Jolivet P., Lipovova P., Kralova B., Kodicek M., Chardot Y. Structural properties of caleosin: a MS and CD study. Arch. Biochem. Biophys. 2007, 464:335-343.
7. Lin L.J., Tai S.S., Peng C.C., Tzen J.T. Steroleosin, a sterol-binding dehydrogenase in seed oil bodies. Plant Physiol. 2002, 128:1200-1211.
8. Bhatla S.C., Vandana S., Kaushik V. Recent developments in the localization of oil body-associated signaling molecules during lipolysis in oilseeds. Plant Signal. Behav. 2009, 4:176-182.
9. Yang M.F., Liu Y.J., Liu Y., Chen H., Chen F., Shen S.H. Proteomic analysis of oil mobilization in seed germination and postgermination development of Jatropha curcas. J. Proteome Res. 2009, 8:1441-1451.
10. Graham I.A. Seed storage oil mobilization. Annu. Rev. Plant Biol. 2008, 59:115-142.
11. Poxleitner M., Rogers S.W., Samuels A.L., Browse J., Rogers J.C. A role for caleosin in degradation of oil-body storage lipids during seed germination. Plant J. 2006, 47:917-933.
12. Jolivet P., Roux E., D'Andrea S., Davanture M., Negroni L., Zivy M., Chardot T. Protein composition of oil bodies in Arabidopsis thaliana ecotype WS. Plant Physiol. Biochem. 2004, 42:501-509.
13. Katavic V., Agrawal G.K., Hajduch M., Harris S.L., Thelen J.J. Protein and lipid composition analysis of oil bodies from two Brassica napus cultivars. Proteomics 2006, 6:4586-4598.
14. Tnani H., López I., Jouenne T., Vicient C.M. Protein composition analysis of oil bodies from maize embryos during germination. J. Plant Physiol. 2011, 168:510-513.
15. Jolivet P., Boulard C., Bellamy A., Larré C., Barre M., Rogniaux H., d'Andréa S., Chardot T., Nesi N. Protein composition of oil bodies from mature Brassica napus seeds. Proteomics 2009, 9:3268-3284.
16. Tzen J.T.C., Peng C.C., Cheng D.J., Chen E.C.F., Chiu J.M.H. A new method for seed oil body purification and examination of oil body integrity following germination. J. Biochem. 1997, 121:762-768.
17. Bradford M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 1976, 72:248-254.
18. Murcha M.W., Elhafez D., Millar A.H., Whelan J. The C-terminal region of TIM17 links the outer and inner mitochondrial membranes in Arabidopsis and is essential for protein import. J. Biol. Chem. 2005, 280:16476-16483.
19. Artal-Sanz M., Tavernarakis N. Prohibitin and mitochondrial biology. Trends Endocrinol. Metab. 2009, 20:394-401.
20. Wang Y., Ries A., Wu K., Yang A., Crawford N.M. The Arabidopsis prohibitin gene PHB3 functions in nitric oxide-mediated responses and in hydrogen peroxide-induced nitric oxide accumulation. Plant Cell 2010, 22:249-259.
21. Jackson C., Dench J., Moore A.L., Halliwell B., Foyer C.H., Hall D.O. Subcellular localisation and identification of superoxide dismutase in the leaves of higher plants. Eur. J. Biochem. 1978, 91:339-344.
22. Dunwell J.M., Purvis A., Khuri S. Cupins: the most functionally diverse protein superfamily. Phytochemistry 2004, 65:7-17.
23. Fernández D.E., Qu R., Huang A.H., Staehelin L.A. Immunogold localization of the L3 protein of maize lipid bodies during germination and seedling growth. Plant Physiol. 1988, 86:270-274.
24. Sadeghipour H.R., Bhatla S.C. Differential sensitivity of oleosins to proteolysis during oil body mobilization in sunflower seedlings. Plant Cell Physiol. 2002, 43:1117-1126.
25. Breiteneder H., Mills E.N. Plant food allergens - structural and functional aspects of allergenicity. Biotechnol. Adv. 2005, 23:395-399.
26. Shutov A.D., Kakhovskaya I.A. Evolution of seed storage globulins and cupin superfamily. Mol. Biol. 2011, 45:529-535.
27. Martinez-Caballero S., Grigoriev S.M., Herrmann J.M., Campo M.L., Kinnally K.W. Tim17p regulates the twin pore structure and voltage gating of the mitochondrial protein import complex TIM23. J. Biol. Chem. 2007, 282:3584-3593.
28. Nadimpalli R., Yalpani N., Johal G.S., Simmons C.R. Prohibitins, stomatins, and plant disease response genes compose a protein superfamily that controls cell proliferation, ion channel regulation and death,. J. Biol. Chem. 2000, 275:29579-29586.
29. Mishra S., Murphy L.C., Murphy L.J. The prohibitins: emerging roles in diverse functions. J. Cell. Mol. Med. 2006, 10:353-363.
30. Van Aken O., Whelan J., Van Breusegem F. Prohibitins: mitochondrial partners in development and stress response. Trends Plant Sci. 2010, 15:275-282.
31. Guan L., Scandalios J.G. Two structurally similar maize cytosolic superoxide dismutase genes, Sod4 and Sod4A, respond differentially to abscisic acid and high osmoticum. Plant Physiol. 1998, 117:217-224.
32. Levine T. Short-range intracellular trafficking of small molecules across endoplasmic reticulum junctions. Trends Cell Biol. 2004, 14:483-490.
33. Fujimoto T., Ohsaki Y., Cheng J., Suzuki M., Shinohara Y. Lipid droplets: a classic organelle with new outfits. Histochem. Cell Biol. 2008, 130:263-279.
34. Murphy S., Martin S., Parton R.G. Lipid droplet-organelle interactions; sharing the fats. Biochim. Biophys. Acta 2009, 1791:441-447.
35. Cermelli S., Guo Y., Gross S.P., Welte M.A. The lipid-droplet proteome reveals that droplets are a protein-storage depot. Curr. Biol. 2006, 16:1783-1795.