ISOLATION AND EXPRESSION ANALYSIS OF 2 RICE GENES ENCODING THE MAJOR INTRINSIC PROTEIN
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作者:
LIU, Q
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UNIV TOKYO, INST MOLEC & CELLULAR BIOSCI, CELLULAR FUNCT LAB, BUNKYO KU, TOKYO 113, JAPANUNIV TOKYO, INST MOLEC & CELLULAR BIOSCI, CELLULAR FUNCT LAB, BUNKYO KU, TOKYO 113, JAPAN
LIU, Q
[1
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UMEDA, M
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UNIV TOKYO, INST MOLEC & CELLULAR BIOSCI, CELLULAR FUNCT LAB, BUNKYO KU, TOKYO 113, JAPANUNIV TOKYO, INST MOLEC & CELLULAR BIOSCI, CELLULAR FUNCT LAB, BUNKYO KU, TOKYO 113, JAPAN
UMEDA, M
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UCHIMIYA, H
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UNIV TOKYO, INST MOLEC & CELLULAR BIOSCI, CELLULAR FUNCT LAB, BUNKYO KU, TOKYO 113, JAPANUNIV TOKYO, INST MOLEC & CELLULAR BIOSCI, CELLULAR FUNCT LAB, BUNKYO KU, TOKYO 113, JAPAN
UCHIMIYA, H
[1
]
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[1] UNIV TOKYO, INST MOLEC & CELLULAR BIOSCI, CELLULAR FUNCT LAB, BUNKYO KU, TOKYO 113, JAPAN
We isolated two rice cDNAs (rMip1 and rTip1) which are homologous to the genes encoding the major intrinsic protein (Mip) (soybean nod-26 and Arabidopsis gamma-Tip), respectively. Expression of rTip1 in shoots and roots of rice seedlings was enhanced by water stress, salt stress and exogenous ABA. rMip1 was expressed only in shoots. Although mRNA level of rMip1 in shoots was induced to a small extent by exogenous ABA, it did not show any increase under water or salt stress over the course of 12 h. On the basis of the differential expression patterns and evolutional distinctions, it is suggested that the possible channel proteins encoded by rMip1 and rTip1 genes may function in different transport systems.