Proteomic characterization of tissue expansion of rice scutellum stimulated by abscisic acid

Bioscience, Biotechnology and Biochemistry

Volumn 71, Issue 5, 2007, Pages 1260-1268

  Asakura, Tsuyoshi ^a   Hirose, Shota ^a   Asatsuma, Satoru ^a,c   Nanjo, Yohei ^a,d   Nakaizumi, Tetsuyo ^a   Itoh, Kimiko ^a   Hori, Hidetaka ^a   Komatsu, Setsuko ^b   Mitsui, Toshiaki ^a  

^a NIIGATA UNIVERSITY   (Japan)

^b NATIONAL INSTITUTE OF AGROBIOLOGICAL SCIENCES   (Japan)

^c RIKEN Center for Sustainable Resource Science   (Japan)

^d EHIME UNIVERSITY   (Japan)

Author keywords

Abscisic acid (ABA); Germination; Oryza sativa; Proteome; Scutellum

Indexed keywords

ADENOSINETRIPHOSPHATE; CHARACTERIZATION; CROPS; ORGANIC ACIDS; PROTEINS; TWO DIMENSIONAL;

ABSCISIC ACID (ABA); ORYZA SATIVA; PROTEOMES; SCUTELLUM;

TISSUE;

ORYZA SATIVA;

ABSCISIC ACID; DRUG DERIVATIVE; PHYTOHORMONE; PROTEOME; STARCH; VEGETABLE PROTEIN;

ARTICLE; BIOSYNTHESIS; DRUG EFFECT; GROWTH, DEVELOPMENT AND AGING; METABOLISM; METHODOLOGY; PROTEOMICS; RICE; SEEDLING; STANDARD;

ABSCISIC ACID; ORYZA SATIVA; PLANT GROWTH REGULATORS; PLANT PROTEINS; PROTEOME; PROTEOMICS; REFERENCE STANDARDS; SEEDLING; STARCH;

EID: 34347369371     PISSN: 09168451     EISSN: 13476947     Source Type: Journal    
DOI: 10.1271/bbb.60675     Document Type: Article

References (34)

1. Nomura, T., Kono, Y., and Akazawa, T., Enzymic mechanism of starch breakdown in germinating rice seeds. II. Scutellum as the site of sucrose synthesis. Plant Physiol., 44, 765-769 (1969).
2. Kaneko, M., Itoh, H., Ueguchi-Tanaka, M., Ashikari, M., and Matsuoka, M., The α-amylase induction in endosperm during rice seed germination is caused by gibberellin synthesized in epithelium. Plant Physiol., 128, 1264-1270 (2002).
3. Mitsui, T., and Itoh, K., The α-amylase multigene family. Trends Plant Sci., 2, 255-261 (1997).
4. Ritchie, S., and Gilroy, S., Tansley review no. 100. Gibberellins: regulating genes and germination. New Phytol., 140, 363-383 (1998).
5. Rock, C. D., Tansley review no. 120. Pathways to abscisic acid-regulated gene expression. New Phytol., 148, 357-396 (2000).
6. Cheng, W.-H., Endo, A., Zhou, L., Penney, J., Chen, H.-C., Arroyo, A., León, P., Nambara, E., Asami, T., Seo, M., Koshiba, T., and Sheen, J., A unique short-chain dehydrogenase/reductase in Arabidopsis glucose signaling and abscisic acid. Plant Cell, 14, 2723-2743 (2002).
7. Eckardt, N. C., Abscisic acid biosynthesis gene underscores the complexity of sugar, stress, and hormone interactions. Plant Cell, 14, 2645-2649 (2002).
8. Kobayashi, M., Gomi, M., Agematsu, J., Asami, T., Yoshida, S., and Sakurai, A., Fluctuation of endogenous gibberellin and abscisic acid levels in germinating seeds of barley. Biosci. Biotechnol. Biochem., 59, 1969-1970 (1995).
9. 1 level and α-amylase in germinating rice seeds. J. Plant Growth Regul., 15, 147-151 (1996).
10. Bethke, P. V., Schuurink, R., and Jones, R. L., Hormonal signalling in cereal aleurone. J. Exp. Bot., 48, 1337-1356 (1997).
11. Kashem, M. A., Hori, H., Itoh, K., Hayakawa, T., Todoroki, Y., Hirai, N., Ohigashi, H., and Mitsui, T., Effects of (+)-8′,8′,8′- trifluoroabscisic acid on α-amylase expression and sugar accumulation in rice cells. Planta, 205, 319-326 (1998).
12. Todoroki, Y., Hirai, N., and Koshimizu, K., 8′,8′, -Difluoro- and 8′,8′,8′,-trifluoroabscisic acids as highly potent, long-lasting analogues of abscisic acid. Phytochemistry, 38, 561-568 (1995).
13. Mitsui, T., Yamaguchi, J., and Akazawa, T., Physicochemical and serological characterization of rice α-amylase isoforms and identification of their corresponding genes. Plant Physiol., 110, 1395-1404 (1996).
14. Bradford, M. M., A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem., 72, 248-254 (1976).
15. Matsukura, C., Saitoh, T., Hirose, T., Ohsugi, R., Perata, P., and Yamaguchi, J., Sugar uptake and transport in rice embryo: expression of companion cell-specific sucrose transporter (OsSUT1) induced by sugar and light. Plant Physiol., 124, 85-93 (2000).
16. Cleveland, D. W., Fischer, S. G., Kirschner, M. W., and Laemmli, U. K., Peptide mapping by limited proteolysis in sodium dodecyl sulfate and analysis by gel electrophoresis. J. Biol. Chem., 252, 1102-1106 (1977).
17. Pearson, W. R., and Lipman, D. J., Improved tools for biological sequence comparison. Proc. Natl. Acad. Sci. USA, 985, 11969-11974 (1988).
18. Altschul, S. F., Madden, T. L., Schaffer, A. A., Zhang, J., Zhang, Z., Miller, W., and Lipman, D. J., Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res., 25, 3389-3402 (1997).
19. Asatsuma, S., Sawada, C., Itoh, K., Okito, M., Kitajima, A., and Mitsui, T., Involvement of α-amylase I-1 in starch degradation in rice chloroplasts. Plant Cell Physiol., 46, 858-869 (2005).
20. Moons, A., Gielen, J., Vandekerckhove, J., Straeten, D. V. D., Gheysen, G., and Montagu, M. V., An abscisic-acid-and salt-stress-responsive rice cDNA from a novel plant gene family. Planta, 202, 443-454 (1997).
21. Kawasaki, S., Borchert, C., Deyholos, M., Wang, H., Brazille, S., Kawai, K., Galbraith, D., and Bohnert, H. J., Gene expression profiles during the initial phase of salt stress in rice. Plant Cell, 13, 889-905 (2001).
22. Sharp, R. E., LeNoble, M. E., Else, M. A., Thorne, E. T., and Gherardi, F., Endogenous ABA maintains shoot growth in tomato independently of effects on plant water balance: evidence for an interaction with ethylene. J. Exp. Bot., 51, 1575-1584 (2000).
23. Spollen, W. G., LeNoble, M. E., Samuels, T. D., Bernstein, N., and Sharp, R. E., Abscisic acid accumulation maintains maize primary root elongation at low water potentials by restricting ethylene production. Plant Physiol., 122, 967-976 (2000).
24. Rolland, F., Baena-Gonzalez, E., and Sheen, J., Sugar sensing and signaling in plants: conserved and novel mechanisms. Annu. Rev. Plant Biol., 57, 675-709 (2006).
25. Schussler, J. R., Brenner, M. L., and Brun, W. A., Relationship of endogenous abscisic acid to sucrose level and seed growth rate of soybeans. Plant Physiol., 96, 1308-1313 (1991).
26. León, P., and Sheen, J., Sugar and hormone connections. Trends Plant Sci., 8, 110-116 (2003).
27. Nambara, E., and Marion-Poll, A., ABA action and interactions in seeds. Trends Plant Sci., 8, 213-217 (2003).
28. Casaretto, J., and Ho, T.-H. D., The transcription factors HvABI5 and HvVP1 are required for the abscisic acid induction of gene expression in barley aleurone cells. Plant Cell, 15, 271-284 (2002).
29. Higo, K., Ugawa, Y., Iwamoto, M., and Korenaga, T., Plant cis-acting regulatory DNA elements (PLACE) database. Nucleic Acids Res., 27, 297-300 (1999).
30. Shen, Q., and Ho, T.-H. D., Promoter switches specific for abscisic acid (ABA)-induced gene expression in cereals. Physiol. Plant., 101, 653-664 (1997).
31. Kang, J.-Y., Choi, H.-I., Im, M.-Y., and Kim, S. Y., Arabidopsis basic leucine zipper proteins that mediate stress-responsive abscisic acid signaling. Plant Cell, 14, 343-357 (2002).
32. Velasco, B., Salamini, F., and Bartels, D., Dehydration and ABA increase mRNA levels and enzyme activity of cytosolic GAPDH in the resurrection plant Craterostingma plantagineum. Plant Mol. Biol., 26, 541-546 (1994).
33. Forsthoefel, N. R., Cushman, M. A. F., and Cushman, J. C., Posttranscriptional and posttranslational control of enolase expression in the facultative crassulacean acid metabolism plant Mesembryanthemum crystallium L. Plant Physiol., 108, 1185-1195 (1995).
34. Plaxton, W. C., The organization and regulation of plant glycolysis. Annu. Rev. Plant Physiol. Plant Mol. Biol., 47, 185-214 (1996).