The short-root mutation srt5 defines a sugar-mediated root growth in rice (Oryza sativa L.)

Plant Science

Volumn 167, Issue 1, 2004, Pages 49-54

  Yao, Shan Guo ^a   Mushika, Junko ^a   Taketa, Shin ^a   Ichii, Masahiko ^a  

^a KAGAWA UNIVERSITY   (Japan)

Author keywords

Abscisic acid; Rice; Root growth; srt5; Sugar

Indexed keywords

CROPS; FRUCTOSE; GLUCOSE; SEED; SUGAR (SUCROSE);

ENERGY DEFICIENCY; MUTATIONS; ROOT GROWTH;

PLANTS (BOTANY);

ORYZA SATIVA;

EID: 2442450577     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plantsci.2004.02.025     Document Type: Article

References (30)

1. Teo Y.H., Beyrouty C.A., Norman R.J., Gbur E.E. Nutrient uptake relationship to root characteristics of rice. Plant Soil. 171:1995;297-302
2. Terashima K., Ogata T., Akita S. Eco-physiological characteristics related with lodging tolerance of rice in direct sowing cultivation. Jpn. J. Crop Sci. 63:1994;34-41
3. Nemoto H., Suga R., Ishihara M., Okutsu Y. Deep rooted rice varieties detected through the observation of root characteristics using the trench method. Breed. Sci. 48:1998;321-324
4. Azhiri-Sigari T., Yamauchi A., Kamoshita A., Wade L.J. Genotypic variation in response of rainfed lowland rice to draught and rewatering. Plant Prod. Sci. 3:2000;180-188
5. Morita S., Suga T., Yamazaki K. The relationship between root length density and yield in rice plants. Jpn. J. Crop Sci. 57:1988;438-443
6. Kang S.Y., Morita S., Yamazaki K. Root growth and distribution in some Japonica-Indica hybrid and Japonica type rice cultivars under field conditions. Jpn. J. Crop Sci. 63:1994;118-124
7. Rolland F., Moore B., Sheen J. Sugar sensing and signaling in plants. Plant Cell. 14:2002;S185-S205
8. Zhou L., Jang J.-C., Jones T.L., Sheen J. Glucose and ethylene signal transduction crosstalk revealed by an Arabidopsis glucose-insensitive mutant. Proc. Natl. Acad. Sci. U.S.A. 95:1998;10294-10299
9. Nemeth K., Salchert K., Putnoky P., Bhalerao R., Koncz-Kalman Z., Stankovic-Stangeland B., Bako L., Mathur J., Okresz L., Stabel S., Geigenberger P., Stitt M., Redei G.P., Schell J., Koncz C. Pleiotropic control of glucose and hormone responses by PRL1, a nuclear WD protein, in Arabidopsis. Genes Dev. 12:1998;3059-3073
10. DeWald D., Sadka A., Mullet J. Sucrose modulation of soybean Vsp gene expression is inhibited by auxin. Plant Physiol. 104:1994;439-444
11. Perata P., Matsukura C., Vernieri P., Yamaguchi J. Sugar repression of a gibberellin-dependent signaling pathway in barley embryos. Plant Cell. 9:1997;2197-2208
12. Arenas-Huertero F., Arroyo A., Zhou L., Sheen J., Leon P. Analysis of Arabidopsis glucose insensitive mutants, gin5 and gin6, reveals a central role of the plant hormone ABA in the regulation of plant vegetative development by sugar. Genes Dev. 14:2000;2085-2096
13. Laby R.J., Kincaid M.S., Kim D., Gibson S.I. The Arabidopsis sugar-insensitive mutants sis4 and sis5 are defective in abscisic acid synthesis and response. Plant J. 23:2000;587-596
14. Huijser C., Korstee A., Pego J., Weisbeek P., Wisman E., Smeekens S. The Arabidopsis sucrose-uncoupled-6 gene is identical to abscisic acid insensitive-4: involvement of abscisic acid in sugar response. Plant J. 23:2000;577-585
15. Rook F., Corke F., Card R., Munz G., Smith C., Bevan M.W. Impaired sucrose-induction mutants reveal the modulation of sugar-induced starch biosynthetic gene expression by abscisic acid signaling. Plant J. 26:2001;421-433
16. Rook F., Bevan M.W. Genetic approaches to understanding sugar-response pathways. J. Exp. Bot. 54:2003;495-501
17. Yao S.-G., Taketa S., Ichii M. A novel short-root gene that affects specifically early root development in rice (Oryza sativa L.). Plant Sci. 163:2002;207-215
18. H.O.J. William, M.C. Tarczynski, Sucrose, in: H.U. Bergmeyer, J. Bergmeyer, M. Graß1 (Eds.), Methods of Enzymatic Analysis, vol. VIII, VCH Verlagsgesellschaft mbH, Weinheim, 1985, pp. 96-103.
19. Ikeda A., Sonoda Y., Vernieri P., Perata P., Hirochika H., Yamaguchi J. The slender rice mutant, with constitutively activated gibberellin signal transduction, has enhanced capacity for abscisic acid level. Plant Cell Physiol. 43:2002;974-979
20. Thomas B.R., Rodriguez R.L. Metabolite signals regulate gene expression and source/sink relations in cereal seedlings. Plant Physiol. 106:1994;1235-1239
21. Pego J.V., Weisbeek P.J., Smeekens S.C.M. Mannose inhibits Arabidopsis germination via a hexokinase-mediated step. Plant Physiol. 119:1999;1017-1023
22. Finkelstein R.R., Lynch T.J. Abscisic acid inhibition of radicle emergence but not seedling growth is suppressed by sugars. Plant Physiol. 122:2000;1179-1186
23. Jang J.-C., Leon P., Zhou L., Sheen J. Hexokinase as a sugar sensor in higher plants. Plant Cell. 9:1997;5-19
24. Ohto M., Onai K., Furukawa Y., Aoki E., Araki T., Nakamura K. Effects of sugar on vegetative development and floral transition in Arabidopsis. Plant Physiol. 127:2001;252-261
25. Quirino B.F., Noh Y.S., Himelblau E., Amasino R.M. Molecular aspects of leaf senescence. Trends Plant Sci. 5:2000;278-282
26. Eckardt N.A. Abscisic acid biosynthesis gene underscores the complexity of sugar, stress, and hormone interactions. Plant Cell. 14:2002;2645-2649
27. Garciarrubio A., Legaria J.P., Covarrubias A.A. Abscisic acid inhibits germination of mature Arabidopsis seeds by limiting the availability of energy and nutrients. Planta. 203:1997;182-187
28. Yoshida K.T., Fujiwara T., Naito S. The synergistic effects of sugar and abscisic acid on myo-inositol-1-phosphate synthase expression. Physiol. Plant. 114:2002;581-587
29. Cheng W.-H., Endo A., Zhou L., Penney J., Chen H.-C., Arroyo A., Leon P., Nambara E., Asami T., Seo M., Koshiba T., Sheen J. A unique short-chain dehydrogenase/reductase in Arabidopsis glucose signaling and abscisic acid biosynthesis and functions. Plant Cell. 14:2002;2723-2743
30. Smeekens S. Sugar-induced signal transduction in plants. Annu. Rev. Plant Physiol. Plant Mol. Biol. 54:2000;49-81