Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
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 Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (13)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Gollop, R.
Right arrow Articles by Perl, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gollop, R.
Right arrow Articles by Perl, A.
Agricola
Right arrow Articles by Gollop, R.
Right arrow Articles by Perl, A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Journal of Experimental Botany, Vol. 53, No. 373, pp. 1397-1409, June 2002
© 2002 Oxford University Press


Original Papers

Expression of the grape dihydroflavonol reductase gene and analysis of its promoter region1

Rachel Gollop2, Sylvie Even, Violeta Colova-Tsolova3 and Avihai Perl

Department of Fruit Tree Breeding and Molecular Genetics, ARO, The Volcani Center, PO Box 6, Bet-Dagan 50250, Israel

Dihydroflavonol reductase (DFR) is a key enzyme involved in anthocyanin biosynthesis and proanthocyanidin synthesis in grape. DFR catalyses the reduction of dihydroflavonols to leucoanthocyanidins in the anthocyanin pathway. The DFR products, the leucoanthocyanidins, are substrates for the next step in the anthocyanin pathway and are also the substrates for the proanthocyanidin pathway. In the present study the promoter of the grape dfr gene was cloned. Analysis of the dfr promoter sequence revealed the existence of several putative DNA binding motifs. The dfr promoter was fused to the uidA gene and the control of this fusion and the endogenous dfr gene expression, was studied in transformed plants and in red cell suspension originated from fruits. The dfr promoter–uidA gene fusion was expressed in leaves, roots and stems. Deletions of the dfr promoter influenced the specificity of the expression of the GUS gene fusion in plantlet roots and the level of expression in plants and in the red cell suspension originated from fruits. The deletion analysis of the dfr promoter suggests that a specific sequence located between -725 to -233 might be involved in expression of the dfr gene in fruits. Light, calcium and sucrose induced the dfr gene expression. In the transformed suspension cultures, expression of both the endogenous dfr gene and the dfr promoter–uidA gene fusions was induced by white light. The induction by both light and calcium suggests the possible involvement of a UV receptors signal transduction pathway in the induction of the dfr gene. The induction of the dfr gene and the dfr promoter–uidA gene fusions by light and sucrose indicates a close interaction between sucrose and light signalling pathways.

Key words: Developmental expression, dfr, grape, light signalling, sucrose signalling.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J Exp BotHome page
J. T. Matus, R. Loyola, A. Vega, A. Pena-Neira, E. Bordeu, P. Arce-Johnson, and J. A. Alcalde
Post-veraison sunlight exposure induces MYB-mediated transcriptional regulation of anthocyanin and flavonol synthesis in berry skins of Vitis vinifera
J. Exp. Bot., March 1, 2009; 60(3): 853 - 867.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
A. Zamboni, L. Minoia, A. Ferrarini, G. B. Tornielli, E. Zago, M. Delledonne, and M. Pezzotti
Molecular analysis of post-harvest withering in grape by AFLP transcriptional profiling
J. Exp. Bot., November 13, 2008; (2008) ern256v1.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
C. Solfanelli, A. Poggi, E. Loreti, A. Alpi, and P. Perata
Sucrose-Specific Induction of the Anthocyanin Biosynthetic Pathway in Arabidopsis
Plant Physiology, February 1, 2006; 140(2): 637 - 646.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
S. Teng, J. Keurentjes, L. Bentsink, M. Koornneef, and S. Smeekens
Sucrose-Specific Induction of Anthocyanin Biosynthesis in Arabidopsis Requires the MYB75/PAP1 Gene
Plant Physiology, December 1, 2005; 139(4): 1840 - 1852.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
O. Avsian-Kretchmer, Y. Gueta-Dahan, S. Lev-Yadun, R. Gollop, and G. Ben-Hayyim
The Salt-Stress Signal Transduction Pathway That Activates the gpx1 Promoter Is Mediated by Intracellular H2O2, Different from the Pathway Induced by Extracellular H2O2
Plant Physiology, July 1, 2004; 135(3): 1685 - 1696.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.