Expression and functional analysis of the rice plasma-membrane intrinsic protein gene family

Plasma membrane intrinsic proteins (PIPs) are a subfamily ofaquaporins that enable fast and controlled translocation of water across the membrane. In this study, we systematically identified and cloned ten PIP genes from rice. Based on the similarity of the amino acid sequences they encoded, these r...

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Bibliographic Details
Published inCell research Vol. 16; no. 3; pp. 277 - 286
Main Authors Guo, Lei, Wang, Zi Yi, Lin, Hong, Cui, Wei Er, Chen, Jun, Liu, Meihua, Chen, Zhang Liang, Qu, Li Jia, Gu, Hongya
Format Journal Article
LanguageEnglish
Published England Nature Publishing Group 01.03.2006
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Summary:Plasma membrane intrinsic proteins (PIPs) are a subfamily ofaquaporins that enable fast and controlled translocation of water across the membrane. In this study, we systematically identified and cloned ten PIP genes from rice. Based on the similarity of the amino acid sequences they encoded, these rice PIP genes were classified into two groups and designated as OsPIP1-1 to OsPIP1-3 and OsPIP2-1 to OsPIP2-7 following the nomenclature of PIP genes in maize. Quantitative RT-PCR analysis identified three root-specific and one leaf-specific OsPIP genes. Furthermore, the expression profile of each OsPIP gene in response to salt, drought and ABA treatment was examined in detail. Analysis on transgenic plants over-expressing of either OsPIP1 (OsPIP1-1) or OsPIP2 (OsPIP2-2) in wild-type Arabidopsis, showed enhanced tolerance to salt (100 mM of NaCl) and drought (200 mM ofmannitol), but not to salt treatment of higher concentration (150 mM of NaCl). Taken together, these data suggest a distinct role of each OsPIP gene in response to different stresses, and should add a new layer to the understanding of the physiological function of rice PIP genes.
Bibliography:S511
31-1568/Q
aquaporins, PIP, quantitative RT-PCR, Oryza sativa, organ-specific
ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 23
ISSN:1001-0602
1748-7838
DOI:10.1038/sj.cr.7310035