Characterization of the silicon uptake system and molecular mapping of the silicon transporter gene in rice

被引:159
作者
Ma, JF [1 ]
Mitani, N
Nagao, S
Konishi, S
Tamai, K
Iwashita, T
Yano, M
机构
[1] Kagawa Univ, Fac Agr, Kagawa 7610795, Japan
[2] Inst Soc Technoinnovat Agr Forestry & Fisheries, Tsukuba, Ibaraki 3050854, Japan
[3] Suntory Inst Bioorgan Res, Osaka 6188503, Japan
[4] Natl Inst Agrobiotechnol Sci, Dept Mol Genet, Tsukuba, Ibaraki 3058602, Japan
关键词
D O I
10.1104/pp.104.047365
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Rice (Oryza sativa L. cv Oochikara) is a typical silicon-accumulating plant, but the mechanism responsible for the high silicon uptake by the roots is poorly understood. We characterized the silicon uptake system in rice roots by using a low-silicon rice mutant (Isi1) and wild-type rice. A kinetic study showed that the concentration of silicon in the root symplastic solution increased with increasing silicon concentrations in the external solution but saturated at a higher concentration in both lines. There were no differences in the silicon concentration of the symplastic solution between the wild-type rice and the mutant. The form of soluble silicon in the root, xylem, and leaf identified by Si-29-NMR was also the same in the two lines. However, the concentration of silicon in the xylem sap was much higher in the wild type than in the mutant. These results indicate that at least two transporters are involved in silicon transport from the external solution to the xylem and that the low-silicon rice mutant is defective in loading silicon into xylem rather than silicon uptake from external solution to cortical cells. To map the responsible gene, we performed a bulked segregant analysis by using both microsatellite and expressed sequence tag-based PCR markers. As a result, the gene was mapped to chromosome 2, flanked by microsatellite marker RM5303 and expressed sequence tag-based PCR marker E60168.
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页码:3284 / 3289
页数:6
相关论文
共 25 条
[1]  
[Anonymous], MINERAL NUTR HIGHER
[2]  
BERGMEYER HU, 1974, METHODEN ENZYMATISCH, V1, P649
[3]   THE ANOMALY OF SILICON IN PLANT BIOLOGY [J].
EPSTEIN, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (01) :11-17
[4]   Silicon [J].
Epstein, E .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1999, 50 :641-664
[5]   SILICON-RESPONSIVE CDNA CLONES ISOLATED FROM THE MARINE DIATOM CYLINDROTHECA-FUSIFORMIS [J].
HILDEBRAND, M ;
HIGGINS, DR ;
BUSSER, K ;
VOLCANI, BE .
GENE, 1993, 132 (02) :213-218
[6]   A gene family of silicon transporters [J].
Hildebrand, M ;
Volcani, BE ;
Gassmann, W ;
Schroeder, JI .
NATURE, 1997, 385 (6618) :688-689
[7]  
Kochian L.V., 2000, Biochemistry and Molecular Biology of Plants, P1204
[8]   Development of STS markers closely linked to the vrs1 locus in barley, Hordeum vulgare [J].
Komatsuda, T ;
Nakamura, I ;
Takaiwa, F ;
Oka, S .
GENOME, 1998, 41 (05) :680-685
[9]  
LANDER E S, 1987, Genomics, V1, P174, DOI 10.1016/0888-7543(87)90010-3
[10]  
MA J. F., 2002, SOIL FERTILIZER PLAN