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


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
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 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 CrossRef
Right arrow Citing Articles via Web of Science (70)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cellier, F.
Right arrow Articles by Casse, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cellier, F.
Right arrow Articles by Casse, F.
Agricola
Right arrow Articles by Cellier, F.
Right arrow Articles by Casse, F.

Molecular and Physiological Responses to Water Deficit in Drought-Tolerant and Drought-Sensitive Lines of Sunflower1
Accumulation of Dehydrin Transcripts Correlates with Tolerance

Françoise Cellier*, Geneviève Conéjéro, Jean-Christophe Breitler, and Francine Casse

Biochimie et Physiologie Moléculaire des Plantes, Ecole Nationale Supérieure Agronomique de Montpollier/Institut National de la Recherche Agronomique/Centre National de la Recherche Scientifique (Unité de Recherche Associée no. 2133), Université Montpellier II, place Viala 34060 Montpellier cedex 1, France

To investigate correlations between phenotypic adaptation to water limitation and drought-induced gene expression, we have studied a model system consisting of a drought-tolerant line (R1) and a drought-sensitive line (S1) of sunflowers (Helianthus annuus L.) subjected to progressive drought. R1 tolerance is characterized by the maintenance of shoot cellular turgor. Drought-induced genes (HaElip1, HaDhn1, and HaDhn2) were previously identified in the tolerant line. The accumulation of the corresponding transcripts was compared as a function of soil and leaf water status in R1 and S1 plants during progressive drought. In leaves of R1 plants the accumulation of HaDhn1 and HaDhn2 transcripts, but not HaElip1 transcripts, was correlated with the drought-adaptive response. Drought-induced abscisic acid (ABA) concentration was not associated with the varietal difference in drought tolerance. Stomata of both lines displayed similar sensitivity to ABA. ABA-induced accumulation of HaDhn2 transcripts was higher in the tolerant than in the sensitive genotype. HaDhn1 transcripts were similarly accumulated in the tolerant and in the sensitive plants in response to ABA, suggesting that additional factors involved in drought regulation of HaDhn1 expression might exist in tolerant plants.


1   This work was financially supported by the Bio Avenir program financed by Rhône-Poulenc and by Action Incitative Programmeé no. 924840 from the Institut National de la Recherche Agronomique.
*   Corresponding author; e-mail cellier{at}ensam.inra.fr; fax 33-467-525737.

Plant Physiol. (1998) 116: 319-328
Copyright Clearance Center:   0032-0889/98/116/0319/10
© 1998 American Society of Plant Physiologists




This article has been cited by other articles:


Home page
J Exp BotHome page
R. Aroca, P. Vernieri, and J. M. Ruiz-Lozano
Mycorrhizal and non-mycorrhizal Lactuca sativa plants exhibit contrasting responses to exogenous ABA during drought stress and recovery
J. Exp. Bot., May 9, 2008; (2008) ern057v1.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
R. Porcel, R. Azcon, and J. M. Ruiz-Lozano
Evaluation of the role of genes encoding for dehydrin proteins (LEA D-11) during drought stress in arbuscular mycorrhizal Glycine max and Lactuca sativa plants
J. Exp. Bot., July 1, 2005; 56(417): 1933 - 1942.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
P. Boominathan, R. Shukla, A. Kumar, D. Manna, D. Negi, P. K. Verma, and D. Chattopadhyay
Long Term Transcript Accumulation during the Development of Dehydration Adaptation in Cicer arietinum
Plant Physiology, July 1, 2004; 135(3): 1608 - 1620.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
A. H. A. Khedr, M. A. Abbas, A. A. A. Wahid, W. P. Quick, and G. M. Abogadallah
Proline induces the expression of salt-stress-responsive proteins and may improve the adaptation of Pancratium maritimum L. to salt-stress
J. Exp. Bot., November 1, 2003; 54(392): 2553 - 2562.
[Abstract] [Full Text] [PDF]


Home page
Crop Sci.Home page
C. G. Lopez, G. M. Banowetz, C. J. Peterson, and W. E. Kronstad
Dehydrin Expression and Drought Tolerance in Seven Wheat Cultivars
Crop Sci., March 1, 2003; 43(2): 577 - 582.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
J. L. Soulages, K. Kim, E. L. Arrese, C. Walters, and J. C. Cushman
Conformation of a Group 2 Late Embryogenesis Abundant Protein from Soybean. Evidence of Poly (L-Proline)-type II Structure
Plant Physiology, March 1, 2003; 131(3): 963 - 975.
[Abstract] [Full Text] [PDF]


Home page
Crop Sci.Home page
Y. Jiang and B. Huang
Protein Alterations in Tall Fescue in Response to Drought Stress and Abscisic Acid
Crop Sci., January 1, 2002; 42(1): 202 - 207.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
F. Cellier, G. Conejero, and F. Casse
Dehydrin transcript fluctuations during a day/night cycle in drought-stressed sunflower
J. Exp. Bot., February 2, 2000; 51(343): 299 - 304.
[Abstract] [Full Text] [PDF]


Home page
Crop Sci.Home page
A. A.C. Alves and T. L. Setter
Response of Cassava to Water Deficit: Leaf Area Growth and Abscisic Acid
Crop Sci., January 1, 2000; 40(1): 131 - 137.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 1998 by the American Society of Plant Biologists