PoplarV1, Main, Exploration, bibRecord, 003257

Functional identification and regulation of the PtDrl02 gene promoter from triploid white poplar.

Identifieur interne : 003257 ( Main/Exploration ); précédent : 003256; suivant : 003258

Functional identification and regulation of the PtDrl02 gene promoter from triploid white poplar.

Auteurs : Huiquan Zheng [République populaire de Chine] ; Shanzhi Lin ; Qian Zhang ; Yang Lei ; Lu Hou ; Zhiyi Zhang

Source :

Plant cell reports [ 1432-203X ] ; 2010.

RBID : pubmed:20179934

Descripteurs français

English descriptors

KwdEn :
- Acetates (pharmacology), Cyclopentanes (pharmacology), Gene Expression Regulation, Plant (MeSH), Genes, Plant (MeSH), Genes, Reporter (MeSH), Oxylipins (pharmacology), Plant Leaves (genetics), Plant Leaves (metabolism), Plants, Genetically Modified (genetics), Plants, Genetically Modified (metabolism), Populus (genetics), Populus (metabolism), Promoter Regions, Genetic (MeSH), RNA, Plant (genetics), Salicylic Acid (pharmacology), Sodium Chloride (pharmacology), Tobacco (genetics), Tobacco (metabolism), Transcription Factors (metabolism), Transformation, Genetic (MeSH).
MESH :
- chemical , genetics : RNA, Plant.
- chemical , metabolism : Transcription Factors.
- chemical , pharmacology : Acetates, Cyclopentanes, Oxylipins, Salicylic Acid, Sodium Chloride.
- genetics : Plant Leaves, Plants, Genetically Modified, Populus, Tobacco.
- metabolism : Plant Leaves, Plants, Genetically Modified, Populus, Tobacco.
- Gene Expression Regulation, Plant, Genes, Plant, Genes, Reporter, Promoter Regions, Genetic, Transformation, Genetic.

Abstract

The PtDrl02 gene belongs to the TIR-NBS gene family in triploid white poplar (Populus tomentosa x P. bolleana) x P. tomentosa. Its expression pattern displays tissue-specificity, and the transcript level can be induced by wounding, methyl jasmonate (MeJA), and salicylic acid (SA). To understand the regulatory mechanism controlling PtDrl02 gene expression, we functionally characterized the PtDrl02 promoter region. Using the beta-glucuronidase as a reporter, we found that the PtDrl02 promoter directed gene expression mainly in the aerial parts of the plants and was confined to the cortex tissues of leaf veins, petioles, stems, and stem piths, showing a typical tissue-specific expression pattern. Deletion analysis revealed two positive regulatory regions (-985 to -669 and -669 to -467) responsible for the basal activity of the PtDrl02 promoter. Impressively, the sequence from -669 to -467 was shown to contain cis-element (s) responding to wounding and MeJA, while the promoter region between -244 and 0 could individually display wounding-responsiveness, and the fragment from -467 to -244 was required for SA- and NaCl-inducible expression of the PtDrl02 promoter. Additionally, it was found that the -985 to -669 sequence was the ABA-responding promoter fragment. These results suggested that the PtDrl02 promoter was modulated by multiple cis-regulatory elements in distinct and complex patterns to regulate PtDrl02 gene expression. Our study also suggested that the PtDrl02 gene 5' untranslated region, as well as a Populus WRKY transcription factor, PtWRKY1, was involved in the regulation of PtDrl02 promoter activities.

DOI: 10.1007/s00299-010-0834-8
PubMed: 20179934

Affiliations:

Links toward previous steps (curation, corpus...)

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Le document en format XML

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<term>Genes, Plant (MeSH)</term>
<term>Genes, Reporter (MeSH)</term>
<term>Oxylipins (pharmacology)</term>
<term>Plant Leaves (genetics)</term>
<term>Plant Leaves (metabolism)</term>
<term>Plants, Genetically Modified (genetics)</term>
<term>Plants, Genetically Modified (metabolism)</term>
<term>Populus (genetics)</term>
<term>Populus (metabolism)</term>
<term>Promoter Regions, Genetic (MeSH)</term>
<term>RNA, Plant (genetics)</term>
<term>Salicylic Acid (pharmacology)</term>
<term>Sodium Chloride (pharmacology)</term>
<term>Tobacco (genetics)</term>
<term>Tobacco (metabolism)</term>
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<term>Acide salicylique (pharmacologie)</term>
<term>Acétates (pharmacologie)</term>
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<term>Populus (métabolisme)</term>
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<term>Sodium Chloride</term>
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<term>Plants, Genetically Modified</term>
<term>Populus</term>
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<term>Tabac</term>
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<term>Plants, Genetically Modified</term>
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<front><div type="abstract" xml:lang="en">The PtDrl02 gene belongs to the TIR-NBS gene family in triploid white poplar (Populus tomentosa x P. bolleana) x P. tomentosa. Its expression pattern displays tissue-specificity, and the transcript level can be induced by wounding, methyl jasmonate (MeJA), and salicylic acid (SA). To understand the regulatory mechanism controlling PtDrl02 gene expression, we functionally characterized the PtDrl02 promoter region. Using the beta-glucuronidase as a reporter, we found that the PtDrl02 promoter directed gene expression mainly in the aerial parts of the plants and was confined to the cortex tissues of leaf veins, petioles, stems, and stem piths, showing a typical tissue-specific expression pattern. Deletion analysis revealed two positive regulatory regions (-985 to -669 and -669 to -467) responsible for the basal activity of the PtDrl02 promoter. Impressively, the sequence from -669 to -467 was shown to contain cis-element (s) responding to wounding and MeJA, while the promoter region between -244 and 0 could individually display wounding-responsiveness, and the fragment from -467 to -244 was required for SA- and NaCl-inducible expression of the PtDrl02 promoter. Additionally, it was found that the -985 to -669 sequence was the ABA-responding promoter fragment. These results suggested that the PtDrl02 promoter was modulated by multiple cis-regulatory elements in distinct and complex patterns to regulate PtDrl02 gene expression. Our study also suggested that the PtDrl02 gene 5' untranslated region, as well as a Populus WRKY transcription factor, PtWRKY1, was involved in the regulation of PtDrl02 promoter activities.</div>
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<Abstract><AbstractText>The PtDrl02 gene belongs to the TIR-NBS gene family in triploid white poplar (Populus tomentosa x P. bolleana) x P. tomentosa. Its expression pattern displays tissue-specificity, and the transcript level can be induced by wounding, methyl jasmonate (MeJA), and salicylic acid (SA). To understand the regulatory mechanism controlling PtDrl02 gene expression, we functionally characterized the PtDrl02 promoter region. Using the beta-glucuronidase as a reporter, we found that the PtDrl02 promoter directed gene expression mainly in the aerial parts of the plants and was confined to the cortex tissues of leaf veins, petioles, stems, and stem piths, showing a typical tissue-specific expression pattern. Deletion analysis revealed two positive regulatory regions (-985 to -669 and -669 to -467) responsible for the basal activity of the PtDrl02 promoter. Impressively, the sequence from -669 to -467 was shown to contain cis-element (s) responding to wounding and MeJA, while the promoter region between -244 and 0 could individually display wounding-responsiveness, and the fragment from -467 to -244 was required for SA- and NaCl-inducible expression of the PtDrl02 promoter. Additionally, it was found that the -985 to -669 sequence was the ABA-responding promoter fragment. These results suggested that the PtDrl02 promoter was modulated by multiple cis-regulatory elements in distinct and complex patterns to regulate PtDrl02 gene expression. Our study also suggested that the PtDrl02 gene 5' untranslated region, as well as a Populus WRKY transcription factor, PtWRKY1, was involved in the regulation of PtDrl02 promoter activities.</AbstractText>
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<name sortKey="Zhang, Qian" sort="Zhang, Qian" uniqKey="Zhang Q" first="Qian" last="Zhang">Qian Zhang</name>
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Functional identification and regulation of the PtDrl02 gene promoter from triploid white poplar.

Functional identification and regulation of the PtDrl02 gene promoter from triploid white poplar.

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