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[Cloning of ACA gene promoter and preliminary study of its function].

Identifieur interne : 000776 ( Main/Exploration ); précédent : 000775; suivant : 000777

[Cloning of ACA gene promoter and preliminary study of its function].

Auteurs : Zhao-Hua Liu [République populaire de Chine] ; Hong-Nian Guo ; Guang-Yu Zheng ; Ying-Chuan Tian

Source :

RBID : pubmed:15859344

Descripteurs français

English descriptors

Abstract

Using total DNA isolated from Amaranthus caudatus as the template, a DNA fragment of about 700bp upstream of the coding sequence of Amaranthus caudatus agglutinin (ACA) gene was amplified by TAIL-PCR and cloned. To examine the regulatory function of this DNA fragment, it was inserted into a plant expression vector containing GUS gene to substitute the CaMV 35S promoter and the resulted recombinant plasmid was designated as pBpAG. The expression vector pBpAG was transferred to different tissues of plants, via Agrobacterium-mediated transformation in vacuum condition. Transient expression of GUS in the transformed tissues was detected by histochemical GUS staining and the results showed that the GUS activity was expressed specifically in seeds. These preliminary results indicate that this DNA fragment upstream of the ACA coding sequence could very possibly be a promoter with seed specificity. Some putative cis-elements within the promoter were discussed.

PubMed: 15859344


Affiliations:


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Le document en format XML

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<title xml:lang="en">[Cloning of ACA gene promoter and preliminary study of its function].</title>
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<name sortKey="Liu, Zhao Hua" sort="Liu, Zhao Hua" uniqKey="Liu Z" first="Zhao-Hua" last="Liu">Zhao-Hua Liu</name>
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<nlm:affiliation>Institution of Microbiology Chinese Academy of Sciences, National Key Laboratory of Plant Genomics, Beijing 100080, China.</nlm:affiliation>
<country xml:lang="fr">République populaire de Chine</country>
<wicri:regionArea>Institution of Microbiology Chinese Academy of Sciences, National Key Laboratory of Plant Genomics, Beijing 100080</wicri:regionArea>
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<name sortKey="Guo, Hong Nian" sort="Guo, Hong Nian" uniqKey="Guo H" first="Hong-Nian" last="Guo">Hong-Nian Guo</name>
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<name sortKey="Zheng, Guang Yu" sort="Zheng, Guang Yu" uniqKey="Zheng G" first="Guang-Yu" last="Zheng">Guang-Yu Zheng</name>
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<name sortKey="Tian, Ying Chuan" sort="Tian, Ying Chuan" uniqKey="Tian Y" first="Ying-Chuan" last="Tian">Ying-Chuan Tian</name>
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<term>Base Sequence (MeSH)</term>
<term>Cloning, Molecular (MeSH)</term>
<term>Escherichia coli (genetics)</term>
<term>Escherichia coli (metabolism)</term>
<term>Molecular Sequence Data (MeSH)</term>
<term>Plant Lectins (genetics)</term>
<term>Promoter Regions, Genetic (genetics)</term>
<term>Rhizobium (genetics)</term>
<term>Rhizobium (metabolism)</term>
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<term>Amaranthus (génétique)</term>
<term>Clonage moléculaire (MeSH)</term>
<term>Données de séquences moléculaires (MeSH)</term>
<term>Escherichia coli (génétique)</term>
<term>Escherichia coli (métabolisme)</term>
<term>Lectines végétales (génétique)</term>
<term>Rhizobium (génétique)</term>
<term>Rhizobium (métabolisme)</term>
<term>Régions promotrices (génétique) (génétique)</term>
<term>Séquence nucléotidique (MeSH)</term>
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<term>Plant Lectins</term>
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<term>Amaranthus</term>
<term>Escherichia coli</term>
<term>Promoter Regions, Genetic</term>
<term>Rhizobium</term>
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<term>Amaranthus</term>
<term>Escherichia coli</term>
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<div type="abstract" xml:lang="en">Using total DNA isolated from Amaranthus caudatus as the template, a DNA fragment of about 700bp upstream of the coding sequence of Amaranthus caudatus agglutinin (ACA) gene was amplified by TAIL-PCR and cloned. To examine the regulatory function of this DNA fragment, it was inserted into a plant expression vector containing GUS gene to substitute the CaMV 35S promoter and the resulted recombinant plasmid was designated as pBpAG. The expression vector pBpAG was transferred to different tissues of plants, via Agrobacterium-mediated transformation in vacuum condition. Transient expression of GUS in the transformed tissues was detected by histochemical GUS staining and the results showed that the GUS activity was expressed specifically in seeds. These preliminary results indicate that this DNA fragment upstream of the ACA coding sequence could very possibly be a promoter with seed specificity. Some putative cis-elements within the promoter were discussed.</div>
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<AbstractText>Using total DNA isolated from Amaranthus caudatus as the template, a DNA fragment of about 700bp upstream of the coding sequence of Amaranthus caudatus agglutinin (ACA) gene was amplified by TAIL-PCR and cloned. To examine the regulatory function of this DNA fragment, it was inserted into a plant expression vector containing GUS gene to substitute the CaMV 35S promoter and the resulted recombinant plasmid was designated as pBpAG. The expression vector pBpAG was transferred to different tissues of plants, via Agrobacterium-mediated transformation in vacuum condition. Transient expression of GUS in the transformed tissues was detected by histochemical GUS staining and the results showed that the GUS activity was expressed specifically in seeds. These preliminary results indicate that this DNA fragment upstream of the ACA coding sequence could very possibly be a promoter with seed specificity. Some putative cis-elements within the promoter were discussed.</AbstractText>
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