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


     


Plant Physiology 92:1094-1100 (1990)
© 1990 American Society of Plant Biologists

This Article
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 (66)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Talon, M.
Right arrow Articles by Zeevaart, J. A. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Talon, M.
Right arrow Articles by Zeevaart, J. A. D.
Agricola
Right arrow Articles by Talon, M.
Right arrow Articles by Zeevaart, J. A. D.
Development and Growth Regulation

Gibberellins and Stem Growth as Related to Photoperiod in Silene armeria L. 1

Manuel Talon and Jan A. D. Zeevaart

Michigan State University-Department of Energy Plant Research Laboratory, Michigan State University, East Lansing, Michigan 48824

Stem growth and flowering in the long-day plant Silene armeria L. are induced by exposure to a minimum of 3 to 6 long days (LD). Stem growth continues in subsequent short days (SD), albeit at a reduced rate. The growth retardant tetcyclacis inhibited stem elongation induced by LD, but had no effect on flowering. This indicates that photoperiodic control of stem growth in Silene is mediated by gibberellins (GA). The objective of this study was to analyze the effects of photoperiod on the levels and distribution of endogenous GAs in Silene and to determine the nature of the photoperiodic after-effect on stem growth in this plant. The GAs identified in extracts from Silene by full-scan combined gas chromatography-mass spectrometry (GC-MS), GA12, GA53, GA44, GA17, GA19, GA20, GA1, GA29, and GA8, are members of the early 13-hydroxylation pathway. All of these GAs were present in plants under SD as well as under LD conditions. The GA53 level was highest in plants in SD, and decreased in plants transferred to LD conditions. By contrast, GA19, GA20, and GA1 initially increased in plants transferred to LD, and then declined. Likewise, when Silene plants were returned from LD to SD, there was an increase in GA53, and a decrease in GA19, GA20, and GA1 which ultimately reached levels similar to those found in plants kept in SD. Thus, measurements of GA levels in whole shoots of Silene as well as in individual parts of the plant suggest that the photoperiod modulates GA metabolism mainly through the rate of conversion of GA53. As a result of LD induction, GA1 accumulates at its highest level in shoot tips which, in turn, results in stem elongation. In addition, LD also appear to increase the sensitivity of the tissue to GA, and this effect is presumably responsible for the photoperiodic after-effect on stem elongation in Silene.


1 Supported by a fellowship from the Spanish Ministry of Agriculture (I.N.I.A.) to M. T., by the U.S. Department of Energy under contract DE-AC02-76ERO-1338, and by U.S. Department of Agriculture grant No. 88-37261-3434 to J. A. D. Z.




This article has been cited by other articles:


Home page
Mol PlantHome page
R. W. King, L. N. Mander, T. Asp, C. P. MacMillan, C. A. Blundell, and L. T. Evans
Selective Deactivation of Gibberellins below the Shoot Apex is Critical to Flowering but Not to Stem Elongation of Lolium
Mol Plant, March 1, 2008; 1(2): 295 - 307.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
S. Eriksson, H. Bohlenius, T. Moritz, and O. Nilsson
GA4 Is the Active Gibberellin in the Regulation of LEAFY Transcription and Arabidopsis Floral Initiation
PLANT CELL, September 1, 2006; 18(9): 2172 - 2181.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
C. P. MacMillan, C. A. Blundell, and R. W. King
Flowering of the Grass Lolium perenne. Effects of Vernalization and Long Days on Gibberellin Biosynthesis and Signaling
Plant Physiology, July 1, 2005; 138(3): 1794 - 1806.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
D. J. Lee and J. A.D. Zeevaart
Molecular Cloning of GA 2-Oxidase3 from Spinach and Its Ectopic Expression in Nicotiana sylvestris
Plant Physiology, May 1, 2005; 138(1): 243 - 254.
[Abstract] [Full Text] [PDF]


Home page
ANN BOT (LOND)Home page
E. THINGNAES, S. TORRE, A. ERNSTSEN, and R. MOE
Day and Night Temperature Responses in Arabidopsis: Effects on Gibberellin and Auxin Content, Cell Size, Morphology and Flowering Time
Ann. Bot., October 1, 2003; 92(4): 601 - 612.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
D. J. Lee and J. A.D. Zeevaart
Differential Regulation of RNA Levels of Gibberellin Dioxygenases by Photoperiod in Spinach
Plant Physiology, December 1, 2002; 130(4): 2085 - 2094.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
R. W. King, T. Moritz, L. T. Evans, O. Junttila, and A. J. Herlt
Long-Day Induction of Flowering in Lolium temulentum Involves Sequential Increases in Specific Gibberellins at the Shoot Apex
Plant Physiology, October 1, 2001; 127(2): 624 - 632.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 1990 by the American Society of Plant Biologists