Plant Physiol.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


First published online November 14, 2002; 10.1104/pp.009019

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
130/4/2101    most recent
pp.009019v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (65)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Martre, P.
Right arrow Articles by Chrispeels, M. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Martre, P.
Right arrow Articles by Chrispeels, M. J.
Agricola
Right arrow Articles by Martre, P.
Right arrow Articles by Chrispeels, M. J.

Plant Physiol, December 2002, Vol. 130, pp. 2101-2110

Plasma Membrane Aquaporins Play a Significant Role during Recovery from Water Deficit1

Pierre Martre,23* Raphaël Morillon,2 François Barrieu, Gretchen B. North, Park S. Nobel, and Maarten J. Chrispeels

Department of Organismic Biology, Ecology, and Evolution, University of California, Los Angeles, California 90095-1606 (P.M., P.S.N.); Division of Biology, University of California, La Jolla, California 92093-0116 (R.M., M.J.C.); Institut de Biologie Moléculaire Végétale-Unité Mixte de Recherche Physiologie et Biotechnologies Végétales Centre INRA de Bordeaux, BP81, 33883 Villenave d'Ornon cedex (F.B.); and Department of Biology, Occidental College, Los Angeles, California 90041 (G.B.N.)

The role of plasma membrane aquaporins (PIPs) in water relations of Arabidopsis was studied by examining plants with reduced expression of PIP1 and PIP2 aquaporins, produced by crossing two different antisense lines. Compared with controls, the double antisense (dAS) plants had reduced amounts of PIP1 and PIP2 aquaporins, and the osmotic hydraulic conductivity of isolated root and leaf protoplasts was reduced 5- to 30-fold. The dAS plants had a 3-fold decrease in the root hydraulic conductivity expressed on a root dry mass basis, but a compensating 2.5-fold increase in the root to leaf dry mass ratio. The leaf hydraulic conductance expressed on a leaf area basis was similar for the dAS compared with the control plants. As a result, the hydraulic conductance of the whole plant was unchanged. Under sufficient and under water-deficient conditions, stomatal conductance, transpiration rate, plant hydraulic conductance, leaf water potential, osmotic pressure, and turgor pressure were similar for the dAS compared with the control plants. However, after 4 d of rewatering following 8 d of drying, the control plants recovered their hydraulic conductance and their transpiration rates faster than the dAS plants. Moreover, after rewatering, the leaf water potential was significantly higher for the control than for the dAS plants. From these results, we conclude that the PIPs play an important role in the recovery of Arabidopsis from the water-deficient condition.


1 This work was supported in part by the U.S. Department of Agriculture National Research Initiative Competitive Grants Program (to M.J.C.) and by the National Science Foundation (grant no. IBN-9975163 to P.S.N.).

2 These authors contributed equally to the paper.

3 Present address: Unité d'Agronomie, Site de Crouël, Institut National de la Recherche Agronomique Clermont-Ferrand, 63 039 Clermont-Ferrand cedex 2, France.

* Corresponding author; e-mail pmartre{at}clermont.inra.fr; fax 33-473-624-457.

© 2002 American Society of Plant Biologists



This article has been cited by other articles:


Home page
Plant Cell PhysiolHome page
M. Mahdieh, A. Mostajeran, T. Horie, and M. Katsuhara
Drought Stress Alters Water Relations and Expression of PIP-Type Aquaporin Genes in Nicotiana tabacum Plants
Plant Cell Physiol., May 1, 2008; 49(5): 801 - 813.
[Abstract] [Full Text] [PDF]


Home page
ANN BOT (LOND)Home page
N. Uehlein and R. Kaldenhoff
Aquaporins and Plant Leaf Movements
Ann. Bot., January 1, 2008; 101(1): 1 - 4.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
M. Levin, J. H. Lemcoff, S. Cohen, and Y. Kapulnik
Low air humidity increases leaf-specific hydraulic conductance of Arabidopsis thaliana (L.) Heynh (Brassicaceae)
J. Exp. Bot., October 10, 2007; (2007) erm220v1.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
J. Y. Jang, J. Y. Rhee, D. G. Kim, G. C. Chung, J. H. Lee, and H. Kang
Ectopic Expression of a Foreign Aquaporin Disrupts the Natural Expression Patterns of Endogenous Aquaporin Genes and Alters Plant Responses to Different Stress Conditions
Plant Cell Physiol., September 1, 2007; 48(9): 1331 - 1339.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
V. Gloser, M. A. Zwieniecki, C. M. Orians, and N. M. Holbrook
Dynamic changes in root hydraulic properties in response to nitrate availability
J. Exp. Bot., July 1, 2007; 58(10): 2409 - 2415.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
H. Cochard, J.-S. Venisse, T. S. Barigah, N. Brunel, S. Herbette, A. Guilliot, M. T. Tyree, and S. Sakr
Putative Role of Aquaporins in Variable Hydraulic Conductance of Leaves in Response to Light
Plant Physiology, January 1, 2007; 143(1): 122 - 133.
[Abstract] [Full Text] [PDF]


Home page
ANN BOT (LOND)Home page
R. AROCA, A. FERRANTE, P. VERNIERI, and M. J. CHRISPEELS
Drought, Abscisic Acid and Transpiration Rate Effects on the Regulation of PIP Aquaporin Gene Expression and Abundance in Phaseolus vulgaris Plants
Ann. Bot., December 1, 2006; 98(6): 1301 - 1310.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
C. Zhu, D. Schraut, W. Hartung, and A. R. Schaffner
Differential responses of maize MIP genes to salt stress and ABA
J. Exp. Bot., November 1, 2005; 56(421): 2971 - 2981.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
Y. Boursiac, S. Chen, D.-T. Luu, M. Sorieul, N. van den Dries, and C. Maurel
Early Effects of Salinity on Water Transport in Arabidopsis Roots. Molecular and Cellular Features of Aquaporin Expression
Plant Physiology, October 1, 2005; 139(2): 790 - 805.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
K. Matsui, K. Hiratsu, T. Koyama, H. Tanaka, and M. Ohme-Takagi
A Chimeric AtMYB23 Repressor Induces Hairy Roots, Elongation of Leaves and Stems, and Inhibition of the Deposition of Mucilage on Seed Coats in Arabidopsis
Plant Cell Physiol., January 15, 2005; 46(1): 147 - 155.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
M. Bots, R. Feron, N. Uehlein, K. Weterings, R. Kaldenhoff, and T. Mariani
PIP1 and PIP2 aquaporins are differentially expressed during tobacco anther and stigma development
J. Exp. Bot., January 1, 2005; 56(409): 113 - 121.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
R. Vera-Estrella, B. J. Barkla, H. J. Bohnert, and O. Pantoja
Novel Regulation of Aquaporins during Osmotic Stress
Plant Physiology, August 1, 2004; 135(4): 2318 - 2329.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
L. Sack, C. M. Streeter, and N. M. Holbrook
Hydraulic Analysis of Water Flow through Leaves of Sugar Maple and Red Oak
Plant Physiology, April 1, 2004; 134(4): 1824 - 1833.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
K. Fetter, V. Van Wilder, M. Moshelion, and F. Chaumont
Interactions between Plasma Membrane Aquaporins Modulate Their Water Channel Activity
PLANT CELL, January 1, 2004; 16(1): 215 - 228.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY THE PLANT CELL
Copyright © 2002 by the American Society of Plant Biologists