A transposon-induced spontaneous mutation results in low β-amylase content in rice

Plant Science

Volumn 169, Issue 1, 2005, Pages 239-244

  Saika, Hiroaki ^a   Nakazono, Mikio ^a   Ikeda, Akira ^b   Yamaguchi, Junji ^b   Masaki, Shunpei ^c   Kanekatsu, Motoki ^c   Nemoto, Keisuke ^d  

^a UNIVERSITY OF TOKYO   (Japan)

^b HOKKAIDO UNIVERSITY   (Japan)

^c TOKYO UNIVERSITY OF AGRICULTURE AND TECHNOLOGY   (Japan)

^d UNIVERSITY OF TOKYO   (Japan)

Author keywords

Amylase; Germination; Mutator; Promoter; QTL; Rice (Oryza sativa L.)

Indexed keywords

CHROMOSOMES; ENZYMES; GENES; GENETIC ENGINEERING; SEED;

MUTATION RESULTS; QUANTITATIVE TRAIT LOCUS (QTL); RICE SEEDLINGS; TRANSPOSON-INDUCED SPONTANEOUS MUTATION;

CROPS;

CHROMOSOMES; ENZYMES; GENES; GERMINATION; MUTATION; RICE; SEEDLINGS; SEEDS;

HORDEUM VULGARE SUBSP. VULGARE; JAPONICA; ORYZA SATIVA;

EID: 19544376445     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plantsci.2005.03.022     Document Type: Article

References (27)

1. A. Scheidig, A. Fröhlich, S. Schulze, J.R. Lloyd, and J. Kossmann Downregulation of a chloroplast-targeted β-amylase leads to a starch-excess phenotype in leaves Plant J. 30 2002 581 591
2. W. Dreier, C. Schnarrenberger, and T. Börner Light- and stress-dependent enhancement of amylolytic activities in white and green barley leaves: β-amylases are stress-induced proteins J. Plant Physiol. 145 1995 342 348
3. T.H. Nielsen, U. Deiting, and M. Stitt A β-amylase in potato tubers is induced by storage at low temperature Plant Physiol. 113 1997 503 510
4. P. Ziegler Cereal beta-amylase J. Cereal Sci. 29 1999 195 204
5. D.E. Evans, L.C. MacLeod, J.K. Eglinton, C.E. Gibson, X. Zhang, W. Wallace, J.H. Skerritt, and R.C.M. Lance Measurement of beta-amylase in malting barley (Hordeum vulgare L.). I. Development of a quantitative ELISA for beta-amylase J. Cereal Sci. 26 1997 229 239
6. M. Kreis, M. Williamson, P.R. Shewry, P. Sharp, and M. Gale Identification of a second locus encoding β-amylase on chromosome 2 of barley Genet. Res. 51 1988 13 16
7. M.J. Erkkilä, R. Leah, H. Ahokas, and V. Cameron-Mills Allele-dependent barley grain β-amylase activity Plant Physiol. 117 1998 679 685
8. C.D. Li, P. Langridge, X.Q. Zhang, P.E. Eckstein, B.G. Rossnagel, R.C. Lance, E.B. Lefol, M.Y. Lu, B.L. Harvey, and G.J. Scoles Mapping barley (Hordeum vulgare L.) beta-amylase alleles in which an amino acid substitution determines beta-amylase isoenzyme type and the level of free beta-amylase J. Cereal Sci. 35 2002 39 50
9. T. Kaneko, M. Kihara, K. Ito, and K. Takeda Molecular and chemical analysis of β-amylase-less mutant barley in Tibet Plant Breeding 119 2000 383 387
10. S. Mitsunaga, O. Kawakami, T. Numata, J. Yamaguchi, K. Fukui, and T. Mitsui Polymorphism in rice amylases at an early stage of seed germination Biosci. Biotechnol. Biochem. 65 2001 662 665
11. J. Yamaguchi, S. Itoh, T. Saitoh, A. Ikeda, T. Tashiro, and Y. Nagato Characterization of β-amylase and its deficiency in various rice cultivars Theor. Appl. Genet. 98 1999 32 38
12. B. Yoon, N. Kim, and S. Akita The expression patterns of alpha- and beta-amylase genes in germinating rice seeds under low temperature and hypoxia conditions Korean J. Genet. 23 2001 333 339
13. M. Shiraishi, and H. Satoh Identification and gene analysis of amylase isozymes in germinating rice seeds Jpn. J. Breeding 40 Suppl. 1 1990 454 455
14. S.Y. Lin, T. Sasaki, and M. Yano Mapping quantitative trait loci controlling seed dormancy and heading date in rice, Oryza sativa L., using backcross inbred lines Theor. Appl. Genet. 96 1998 997 1003
15. M.M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding Ann. Biochem. 72 1976 248 254
16. E.S. Lander, P. Green, J. Abrahamson, A. Barlow, M.J. Daly, S.E. Lincoln, and L. Newburg MAPMAKER: an interactive computer package for constructing primary genetic linkage maps of experimental and natural populations Genomics 1 1987 174 181
17. S. Wang, C.J. Basten, Z.B. Zeng, Windows QTL Cartographer 2.0, Department of Statistics, North Carolina State University, Raleigh, NC, http://statgen.ncsu.edu/qtlcart/WWTLCart.htm, 2001-2003.
18. L. Guglielminetti, J. Yamaguchi, P. Perata, and A. Alpi Amylolytic activities in cereal seeds under aerobic and anaerobic conditions Plant Physiol. 109 1995 1069 1076
19. H. Zhu, F. Qu, and L.H. Zhu Isolation of genomic DNAs from plants, fungi and bacteria using benzyl chloride Nucleic Acids Res. 21 1993 5279 5280
20. M.A. Saghai Maroof, G.P. Yang, R.M. Biyashev, P.J. Maughan, and Q. Zhang Analysis of the barley and rice genomes by comparative RFLP linkage mapping Theor. Appl. Genet. 92 1996 541 551
21. S.M. Wang, W.L. Lue, K. Eimert, and J. Chen Phytohormone-regulated beta-amylase gene expression in rice Plant Mol. Biol. 31 1996 975 982
22. J. Daussant, J. Sadowski, T. Rorat, C. Mayer, and C. Lauriere Independent regulatory aspects and posttranscriptional modifications of two β-amylases of rye Plant Physiol. 96 1991 84 90
23. S.M. Wang, W.L. Lue, S.Y. Wu, H.W. Huang, and J. Chen Characterization of a maize β-amylase cDNA clone and its expression during seed germination Plant Physiol. 113 1997 403 409
24. D. Lisch Mutator transposons Trends Plant Sci. 7 2002 498 504
25. L. Mao, T.C. Wood, Y. Yu, M.A. Budiman, J. Tomkins, S.S. Woo, M. Sasinowski, G. Presting, D. Frisch, S. Goff, R.A. Dean, and R.A. Wing Rice transposable elements: A survey of 73,000 sequence-tagged connectors Genome Res. 10 2000 982 990
26. K. Turcotte, S. Srinvasan, and T. Bureau Survey of tranposable elements from rice genomic sequences Plant J. 25 2001 169 179
27. S. Yoshida, K. Tamaki, K. Watanabe, M. Fujino, and C. Nakamura A maize MuDR-like element expressed in rice callus subcultured with proline Hereditas 129 1998 95 99