Comparative proteomics of a lycopene-accumulating mutant reveals the important role of oxidative stress on carotenogenesis in sweet orange (Citrus sinensis [L.] osbeck)

Proteomics

Volumn 9, Issue 24, 2009, Pages 5455-5470

  Pan, Zhiyong ^a   Liu, Qing ^a   Yun, Ze ^a   Guan, Rui ^a   Zeng, Wenfang ^a   Xu, Qiang ^a   Deng, Xiuxin ^a  

^a HUAZHONG AGRICULTURAL UNIVERSITY   (China)

Author keywords

Citrus; Lycopene accumulation; Oxidative stress; Plant proteomics

Indexed keywords

CAROTENE; LYCOPENE; TERT BUTYL HYDROPEROXIDE;

ARTICLE; COMPARATIVE STUDY; CONTROLLED STUDY; FRUIT; GENE EXPRESSION PROFILING; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; OXIDATIVE STRESS; PHYTOCHEMISTRY; PLANT METABOLISM; PRIORITY JOURNAL; PROTEOMICS; SWEET ORANGE;

ANTIOXIDANTS; CAROTENOIDS; CITRUS SINENSIS; FRUIT; GENE EXPRESSION REGULATION, PLANT; GENES, PLANT; MUTATION; OXIDATIVE STRESS; PLANT PROTEINS; PROTEOMICS; SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION; TERT-BUTYLHYDROPEROXIDE; TRANSCRIPTION, GENETIC;

CITRUS; CITRUS SINENSIS;

EID: 73149100123     PISSN: 16159853     EISSN: 16159861     Source Type: Journal    
DOI: 10.1002/pmic.200900092     Document Type: Article

References (53)

1. Dimascio, P., Kaiser, S., Sies, H., Lycopene as the most efficient biological carotenoid singlet oxygen quencher. Arch. Biochem. Biophys. 1989, 274, 532-538.
2. Lindshield, B. L., Canene-Adams, K., Erdman, J. W., Lycopenoids: are lycopene metabolites bioactive? Arch. Biochem. Biophys. 2007, 458, 136-140.
3. Clinton, S. K., Lycopene: chemistry, biology, and implications for human health and disease. Nutrition Reviews 1998, 56, 35-51.
4. Saunt, J., Citrus Varieties of the World. Sinclair International Ltd., Norwich, England 2000, pp. 16-17.
5. Monselise, S. P., Halevy, A. H., Detection of lycopene in pink orange fruit. Science 1961, 133, 1478.
6. Liu, Q., Xu, J., Liu, Y. Z., Zhao, X. L. et al., A novel bud mutation that confers abnormal patterns of lycopene accumulation in sweet orange fruit (Citrus sinensis L. Osbeck). J. Exp. Bot. 2007, 58, 4161-4171.
7. Xu, C. J., Fraser, P. D., Wang, W. J., Bramley, P.M., Differences in the carotenoid content of ordinary citrus and lycopene-accumulating mutants. J. Agric. Food Chem. 2006, 54, 5474-5481.
8. Xu, J., Tao, N. G., Liu, Q., Deng, X. X., Presence of diverse ratios of lycopene/β-carotene in five pink or red-fleshed citrus cultivars. Sci. Hort. 2006, 108, 181-184.
9. Lee, H. S., Characterization of carotenoids in juice of red navel orange (Cara Cara). J. Agric. Food Chem. 2001, 49, 2563-2568.
10. Tao, N., Hu, Z., Liu, Q., Xu, J. et al., Expression of phytoene synthase gene (Psy) is enhanced during fruit ripening of Cara Cara navel orange (Citrus sinensis Osbeck). Plant Cell Rep. 2007, 26, 837-843.
11. Alquezar, B., Rodrigo, M. J., Zacarías, L., Regulation of carotenoid biosynthesis during fruit maturation in the red-fleshed orange mutant Cara Cara. Phytochemistry 2008, 69, 1997-2007.
12. Liu, Q., Zhu, A. D., Chai, L. J., Zhou, W. J. et al., Transcriptome analysis of a spontaneous mutant in sweet orange (Citrus sinensis L. Osbeck) during fruit development. J. Exp. Bot. 2009, 60, 801-813.
13. Ronen, G., Cohen, M., Zamir, D., Hirschberg, J., Regulation of carotenoid biosynthesis during tomato fruit development: expression of the gene for lycopene epsilon cyclase is down regulated during ripening and is elevated in the mutant delta. Plant J. 1999, 17, 341-351.
14. Bramley, P. M., Regulation of carotenoid formation during tomato fruit ripening and development. J. Exp. Bot. 2002, 53, 2107-2113.
15. Kolotilin, I., Koltai, H., Tadmor, Y., Bar-Or, C. et al., Transcriptional profiling of high pigment-2dg tomato mutant links early fruit plastid biogenesis with its overproduction of phytonutrients. Plant Physiol. 2007, 145, 389-401.
16. Deruere, J., Romer, S., d'Harlingue, A., Backhaus, R. A. et al., Fibril assembly and carotenoid overaccumulation in chromoplasts: a model for supramolecular lipoprotein structures. Plant Cell 1994, 6, 119-133.
17. Leitner-Dagan, Y., Ovadis, M., Shklarman, E., Elad, Y. et al., Expression and functional analyses of the plastid lipid-associated protein CHRC suggest its role in chromoplastogenesis and stress. Plant Physiol. 2006, 142, 233-244.
18. Simkin, A. J., Gaffé , J., Alcaraz, J. P., Carde, J. P. et al., Fibrillin influence on plastid ultrastructure and pigment content in tomato fruit. Phytochemistry 2007, 68, 1545-1556.
19. Li, L., Paolillo, D. J., Parthasarathy, M. V., DiMuzio, E. M. et al., A novel gene mutation that confers abnormal patterns of b-carotene accumulation in cauliflower (Brassica oleracea var. botrytis). Plant J. 2001, 26, 59-67.
20. Lu, S., Van Eck, J., Zhou, X., Lopez, A. B. et al., The cauliflower Or gene encodes a dnaJ cysteine-rich domain-containing protein that mediates high levels of β-carotene accumulation. Plant Cell 2006, 18, 3594-3605.
21. Bouvier, F., Backhaus, R. A., Camara, B., Induction and control of chromoplast-specific carotenoid genes by oxidative stress. J. Biol. Chem. 1998, 46, 30651-30659.
22. Kobayashi, M., Kakizono, T., Nagai, S., Enhanced carotenoid biosynthesis by oxidative stress in acetate-induced cyst cells of a green unicellular alga, Haematococcus pluvialis. Appl. Environ. Microbiol. 1993, 59, 867-873.
23. Boussiba, S., Carotenogenesis in the green alga Haematococcus pluvialis: cellular physiology and stress response. Physiol. Plant 2000, 108, 111-117.
24. Fang, J., Chai, C. L., Qian, Q., Li, C. L. et al., Mutations of genes in synthesis of the carotenoid precursors of ABA lead to pre-harvest sprouting and photo-oxidation in rice. Plant J. 2008, 54, 177-189.
25. Huang, R. H., Xia, R. X., Hu, L. M., Lu, Y. M., Wang, M. Y., Antioxidant activity and oxygen-scavenging system in orange pulp during fruit ripening and maturation. Sci. Hortic. 2007, 113, 166-172.
26. Faurobert, M., Mihr, C., Bertin, N., Pawlowski, T. et al., Major proteome variations associate with cherry tomato pericarp development and ripening. Plant Physiol. 2007, 143, 1327-1346.
27. Pan, Z. Y., Guan, R., Zhu, S. P., Deng, X. X., Proteomic analysis of somatic embryogenesis in Valencia sweet orange (Citrus sinensis Osbeck). Plant Cell Rep. 2009, 2, 281-289.
28. Giovanni, C., Maurizio, B., Luca, M., Laura, S. et al., Blue silver: a very sensitive colloidal coomassie G-250 staining for proteome analysis. Electrophoresis 2004, 25, 1327-1333.
29. Liu, Y. Z., Liu, Q., Tao, N. G., Deng, X. X., Efficient isolation of RNA from fruit peel and pulp of ripening navel orange (Citrus sinensis Osbeck). J. Huazhong Agric. Univ. 2006, 25, 300-304 (in Chinese).
30. Jiang, M. Y., Zhang, J. H., Water stress-induced abscisic acid accumulation triggers the increased generation of reactive oxygen species and up-regulates the activities of antioxidant enzymes in maize leaves. J. Exp. Bot. 2002, 53, 2401-2410.
31. Knöraer, O.C., Durner, J., Böger, P., Alterations in the antioxidative system of suspension-cultured soybean cells (Glycine max) induced by oxidative stress. Physiol. Plant 1996, 97, 388-396.
32. Vishnevetsky, M., Ovadis, M., Itzhaki, H., Levy, M. et al., Molecular cloning of a carotenoid-associated protein from Cucumis sativus corollas: homologous genes involved in carotenoid sequestration in chromoplasts. Plant J. 1996, 10, 1111-1118.
33. Vishnevetsky, M., Ovadis, M., Vainstein, A., Carotenoid sequestration in plants: the role of carotenoid-associated proteins. Trends Plant Sci. 1999, 4, 232-235.
34. Moriguchi, T., Kita, M., Endo-Inagaki, T., Ikoma, Y., Omura, M., Characterization of a cDNA homologous to carotenoid-associated protein in citrus fruits. Biochim. Biophys. Acta. 1998, 1442, 334-338.
35. Svensson, J., Ismail, A.M., Palva, E.T., Close, T., in: Storey, K.B. and Storey, J.M., (Eds.), Dehydrins. In Cell and Molecular Responses to Stress, Vol. 3, Sensing, Signaling and Cell Adaptation. Elsevier Press, Amsterdam 2002, pp. 155-171.
36. Close, T. J., Dehydrins: a commonality in the response of plants to dehydration and low temperature. Physiol. Plant 1997, 100, 291-296.
37. Hara, M., Terashima, T. F., Fukaya, T., Kuboi, T., Enhancement of cold tolerance and inhibition of lipid peroxidation by citrus dehydrin in transgenic tobacco. Planta 2003, 217, 290-298.
38. Roberts, M. R., Regulatory 14-3-3 protein-protein interactions in plant cells. Curr. Opin. Plant Biol. 2000, 3, 400-405.
39. Roberts, M. R., Salinas, J., Collinge, D. B., 14-3-3 proteins and the response to abiotic and biotic stress. Plant Mol. Biol. 2002, 1031, 1031-1039.
40. Roberts, M. R., 14-3-3 Proteins find new partners in plant cell signalling. Trends Plant Sci. 2003, 8, 218-223.
41. Coux, O., Tanaka, K., Goldberg, A. L., Structure and functions of the 20S and 26S Proteasomes. Ann. Rev. Biochem. 1996, 65, 801-847.
42. Wan, X. Y., Liu, J. Y., Comparative proteomic analysis reveals an intimate protein network provoked by hydrogen peroxide stress in rice seedling leaves. Mol. Cell Proteomics 2008, 7, 1469-1488.
43. Jaenicke, R., Creighton, T. E., Junior chaperones. Curr. Biol. 1993, 3, 234-235.
44. Howarth, C. J., Ougham, H. J., Gene expression under temperature stress. New Phytol.1993, 125, 1-26.
45. Storozhenko, S., De Pauw, P., Van Montagu, M., Kushnir, S., The heat shock element is a functional component of the Arabidopsis APX1 gene promoter. Plant Physiol. 1998, 116, 1005-1014.
46. Schett, G., Steiner, C. W., Groger, M., Winkler, S. et al., Activation of Fas inhibits heat induced activation of HSF1 and up-regulation of HSP70. FASEB J. 1999, 13, 833-842.
47. Vranová , E., Inzé , D., Van Breusegem, F., Signal transduction during oxidative stress. J. Exp. Bot. 2002, 53, 1227-1236.
48. Grumbach, K. H., Does the chloroplast envelope contain carotenoids and quinones in vivo? Physiol. Plant 1984, 60, 180-186.
49. Dalla Vecchia, F., Barbato, R., La Rocca, N., Mora, I., Rascio, N., Responses to bleaching herbicides by leaf chloroplasts of maize plants grown at different temperatures. J. Exp. Bot. 2001, 52, 811-820.
50. Zito, F., Gough, S., Marcato, C., Rascio, N., Casadoro, G., Expression of chloroplastic and cytosolic glutamine synthetase in barley leaves after cold-sensitive blocking of β-carotene synthesis by amitrole or mutation. Physiol. Plant 1995, 94, 535-544.
51. Rushing, J. W., Huber, D. J., Initiation of tomato fruit ripening with copper. J. Am. Soc. Hortic. Sci. 1985, 110, 316-318.
52. Sauret-Gueto, S., Botella-Pavia, P., Flores-Perez, U., Martinez-Garcia, J. F. et al., Plastid cues posttranscriptionally regulate the accumulation of key enzymes of the methylerythritol phosphate pathway in Arabidopsis. Plant Physiol. 2006, 141, 75-84.
53. Kato, M., Ikoma, Y., Matsumoro, H., Sugiura, M. et al., Accumulation of carotenoids and expression of carotenoid biosynthetic genes during maturation in citrus fruit. Plant Physiol. 2004, 134, 824-837.