|
Plant Physiol, February 2002, Vol. 128, pp. 734-741
Control of Gibberellin Levels and Gene Expression during
De-Etiolation in Pea1
James B.
Reid,*
Natasha A.
Botwright,
Jennifer J.
Smith,
Damian P.
O'Neill, and
L. Huub J.
Kerckhoffs
School of Plant Science, University of Tasmania, G.P.O. Box
252-55, Hobart, Tasmania, 7001, Australia
Gibberellin A1 (GA1) levels drop
significantly in wild-type pea (Pisum sativum) plants
within 4 h of exposure to red, blue, or far-red light. This
response is controlled by phytochrome A (phyA) (and not phyB) and a
blue light receptor. GA8 levels are increased in response
to 4 h of red light, whereas the levels of GA19,
GA20, and GA29 do not vary substantially. Red
light appears to control GA1 levels by down-regulating the
expression of Mendel's LE (PsGA3ox1)
gene that controls the conversion of GA20 to
GA1, and by up-regulating PsGA2ox2, which
codes for a GA 2-oxidase that converts GA1 to
GA8. This occurs within 0.5 to 1 h of exposure to red
light. Similar responses occur in blue light. The major GA 20-oxidase
gene expressed in shoots, PsGA20ox1, does not show substantial light regulation, but does show up-regulation after 4 h of red light, probably as a result of feedback regulation. Expression
of PsGA3ox1 shows a similar feedback response, whereas PsGA2ox2 shows a feed-forward response. These results
add to our understanding of how light reduces shoot elongation during
de-etiolation.
1
This work was supported by the
Australian Research Council.
*
Corresponding author; e-mail Jim.Reid{at}utas.edu.au; fax
61-3-6226-2698.
© 2002 American Society of Plant Physiologists
This article has been cited by other articles:

|
 |

|
 |
 
F. Vandenbussche, B. Vancompernolle, I. Rieu, M. Ahmad, A. Phillips, T. Moritz, P. Hedden, and D. Van Der Straeten
Ethylene-induced Arabidopsis hypocotyl elongation is dependent on but not mediated by gibberellins
J. Exp. Bot.,
December 1, 2007;
58(15-16):
4269 - 4281.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
X. Zhao, X. Yu, E. Foo, G. M. Symons, J. Lopez, K. T. Bendehakkalu, J. Xiang, J. L. Weller, X. Liu, J. B. Reid, et al.
A Study of Gibberellin Homeostasis and Cryptochrome-Mediated Blue Light Inhibition of Hypocotyl Elongation
Plant Physiology,
September 1, 2007;
145(1):
106 - 118.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Prisic and R. J. Peters
Synergistic Substrate Inhibition of ent-Copalyl Diphosphate Synthase: A Potential Feed-Forward Inhibition Mechanism Limiting Gibberellin Metabolism
Plant Physiology,
May 1, 2007;
144(1):
445 - 454.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
X. Johnson, T. Brcich, E. A. Dun, M. Goussot, K. Haurogne, C. A. Beveridge, and C. Rameau
Branching Genes Are Conserved across Species. Genes Controlling a Novel Signal in Pea Are Coregulated by Other Long-Distance Signals
Plant Physiology,
November 1, 2006;
142(3):
1014 - 1026.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. J. Benschop, J. Bou, A. J.M. Peeters, N. Wagemaker, K. Guhl, D. Ward, P. Hedden, T. Moritz, and L. A.C.J. Voesenek
Long-Term Submergence-Induced Elongation in Rumex palustris Requires Abscisic Acid-Dependent Biosynthesis of Gibberellin1
Plant Physiology,
August 1, 2006;
141(4):
1644 - 1652.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. D. Platten, E. Foo, R. C. Elliott, V. Hecht, J. B. Reid, and J. L. Weller
Cryptochrome 1 Contributes to Blue-Light Sensing in Pea
Plant Physiology,
November 1, 2005;
139(3):
1472 - 1482.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. A. Stavang, B. Lindgard, A. Erntsen, S. E. Lid, R. Moe, and J. E. Olsen
Thermoperiodic Stem Elongation Involves Transcriptional Regulation of Gibberellin Deactivation in Pea
Plant Physiology,
August 1, 2005;
138(4):
2344 - 2353.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
T. Hisamatsu, R. W. King, C. A. Helliwell, and M. Koshioka
The Involvement of Gibberellin 20-Oxidase Genes in Phytochrome-Regulated Petiole Elongation of Arabidopsis
Plant Physiology,
June 1, 2005;
138(2):
1106 - 1116.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
T.-S. Tseng, P. A. Salome, C. R. McClung, and N. E. Olszewski
SPINDLY and GIGANTEA Interact and Act in Arabidopsis thaliana Pathways Involved in Light Responses, Flowering, and Rhythms in Cotyledon Movements
PLANT CELL,
June 1, 2004;
16(6):
1550 - 1563.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. Oda, C. Sakuta, S. Masuda, T. Mizoguchi, H. Kamada, and S. Satoh
Possible Involvement of Leaf Gibberellins in the Clock-Controlled Expression of XSP30, a Gene Encoding a Xylem Sap Lectin, in Cucumber Roots
Plant Physiology,
December 1, 2003;
133(4):
1779 - 1790.
[Abstract]
[Full Text]
|
 |
|

|
 |

|
 |
 
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]
|
 |
|

|
 |

|
 |
 
N. Olszewski, T.-p. Sun, and F. Gubler
Gibberellin Signaling: Biosynthesis, Catabolism, and Response Pathways
PLANT CELL,
May 1, 2002;
14(90001):
S61 - 80.
[Full Text]
[PDF]
|
 |
|
|
|