Issue 4, 2011

Identification and differential induction of the expression of aquaporins by salinity in broccoli plants

Abstract

Plant aquaporins belong to a large superfamily of conserved proteins called the major intrinsic proteins (MIPs). There is limited information about the diversity of MIPs and their water transport capacity in broccoli (Brassica oleracea) plants. In this study, the cDNAs of isoforms of Plasma Membrane Intrinsic Proteins (PIPs), a class of aquaporins, from broccoli roots have been partially sequenced. Thus, sequencing experiments led to the identification of eight PIP1 and three PIP2 genes encoding PIPs in B. oleracea plants. The occurrence of different gene products encoding PIPs suggests that they may play different roles in plants. The screening of their expression as well as the expression of two specific PIP2 isoforms (BoPIP2;2 and BoPIP2;3), in different organs and under different salt-stress conditions in two varieties, has helped to unravel the function and the regulation of PIPs in plants. Thus, a high degree of BoPIP2;3 expression in mature leaves suggests that this BoPIP2;3 isoform plays important roles, not only in root water relations but also in the physiology and development of leaves. In addition, differences between gene and protein patterns led us to consider that mRNA synthesis is inhibited by the accumulation of the corresponding encoded protein. Therefore, transcript levels, protein abundance determination and the integrated hydraulic architecture of the roots must be considered in order to interpret the response of broccoli to salinity.

Graphical abstract: Identification and differential induction of the expression of aquaporins by salinity in broccoli plants

Article information

Article type
Paper
Submitted
18 Nov 2010
Accepted
24 Jan 2011
First published
14 Feb 2011

Mol. BioSyst., 2011,7, 1322-1335

Identification and differential induction of the expression of aquaporins by salinity in broccoli plants

B. Muries, M. Faize, M. Carvajal and M. D. C. Martínez-Ballesta, Mol. BioSyst., 2011, 7, 1322 DOI: 10.1039/C0MB00285B

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