Elicitor-responsive promoter regions in the tryptophan decarboxylase gene from Catharanthus roseus

Elicitor-responsive promoter regions in the tryptophan decarboxylase gene from Catharanthus roseus The tryptophan decarboxylase (Tdc) gene from Catharanthus roseus (Madagascar periwinkle) encodes a key enzyme in biosynthesis of terpenoid indole alkaloids. The expression of the Tdc gene is transcriptionally induced by fungal elicitors. Tdc upstream sequences from −1818 to +198 relative to the transcriptional start site were functionally analysed to identify cis-acting elements that determine basal expression or respond to elicitor. In a loss-of-function analysis promoter derivatives with 5′ or internal deletions fused to the gusA reporter gene were analysed in transgenic tobacco plants. Whereas promoter activity dropped considerably following deletion down to −160, this short promoter derivative was still elicitor-responsive. Subsequently, the −160 to −37 region was further studied by gain-of-function experiments, in which subfragments were tested as tetramers cloned on two different truncated promoters. Combination of the data resulted in the identification of three functional regions in the −160 promoter. The region between −160 to −99 was shown to act as the main transcriptional enhancer. Two separable elicitor-responsive elements were found to reside between −99 and −87 and between −87 and −37. These two elements are not redundant in the Tdc promoter, since their combination gave a distinct elicitor response. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Plant Molecular Biology Springer Journals

Elicitor-responsive promoter regions in the tryptophan decarboxylase gene from Catharanthus roseus

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Publisher
Kluwer Academic Publishers
Copyright
Copyright © 1999 by Kluwer Academic Publishers
Subject
Life Sciences; Biochemistry, general; Plant Sciences; Plant Pathology
ISSN
0167-4412
eISSN
1573-5028
D.O.I.
10.1023/A:1006138601744
Publisher site
See Article on Publisher Site

Abstract

The tryptophan decarboxylase (Tdc) gene from Catharanthus roseus (Madagascar periwinkle) encodes a key enzyme in biosynthesis of terpenoid indole alkaloids. The expression of the Tdc gene is transcriptionally induced by fungal elicitors. Tdc upstream sequences from −1818 to +198 relative to the transcriptional start site were functionally analysed to identify cis-acting elements that determine basal expression or respond to elicitor. In a loss-of-function analysis promoter derivatives with 5′ or internal deletions fused to the gusA reporter gene were analysed in transgenic tobacco plants. Whereas promoter activity dropped considerably following deletion down to −160, this short promoter derivative was still elicitor-responsive. Subsequently, the −160 to −37 region was further studied by gain-of-function experiments, in which subfragments were tested as tetramers cloned on two different truncated promoters. Combination of the data resulted in the identification of three functional regions in the −160 promoter. The region between −160 to −99 was shown to act as the main transcriptional enhancer. Two separable elicitor-responsive elements were found to reside between −99 and −87 and between −87 and −37. These two elements are not redundant in the Tdc promoter, since their combination gave a distinct elicitor response.

Journal

Plant Molecular BiologySpringer Journals

Published: Sep 29, 2004

References

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