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Heterologous expression of the Hsp24 from Trichoderma asperellum improves antifungal ability of Populus transformant Pdpap-Hsp24 s to Cytospora chrysosperma and Alternaria alternate.

Identifieur interne : 001836 ( Main/Exploration ); précédent : 001835; suivant : 001837

Heterologous expression of the Hsp24 from Trichoderma asperellum improves antifungal ability of Populus transformant Pdpap-Hsp24 s to Cytospora chrysosperma and Alternaria alternate.

Auteurs : S D Ji [République populaire de Chine] ; Z Y Wang [République populaire de Chine] ; H J Fan [République populaire de Chine] ; R S Zhang [République populaire de Chine] ; Z Y Yu [République populaire de Chine] ; J J Wang [République populaire de Chine] ; Z H Liu [République populaire de Chine]

Source :

RBID : pubmed:27193371

Descripteurs français

English descriptors

Abstract

The tolerance of plants to biotic and abiotic stresses could be improved by transforming with fungal resistance-related genes. In this study, the cDNA sequence (GenBank Acc. No. KP337939) of the resistance-related gene Hsp24 encoding the 24 kD heat shock protein was obtained from the biocontrol fungus Trichoderma asperellum ACCC30536. The promoter region of Hsp24 contained many cis-regulators related to stresses response, such as "GCN4" and "GCR1" etc. Hsp24 transcription in T. asperellum was up-regulated under six different environmental stresses, compared with the control. Furthermore, following heterologous transformation into Populus davidiana × P. alba var. Pyramidalis (Pdpap), Hsp24 was successfully transcribed in transformant Pdpap-Hsp24s. Pathogen-related genes (PRs) in four Pdpap-Hsp24s were up-regulated compared with those in the control Pdpap (Pdpap-Con). After co-culture of Pdpap-Hsp24s with the weak parasite Cytospora chrysosperma, the transcription of genes related to hormone signal pathway (JA and SA) were up-regulated in Pdpap-Hsp24s, and ethidium bromide (EtBr) and Nitro-blue tetrazolium (NBT) staining assays indicated that the cell membrane permeability and the active oxygen content of Pdpap-Hsp24s leaves were lower than that of the control Pdpap-Con. And when the Pdpap-Hsp24s were under the Alternaria alternate stress, the activities of superoxide dismutase (SOD) and peroxidase (POD) got higher in Pdpap-Hsp24s than that in Pdpap-Con, and the disease spots in Pdpap-Con leaves were obviously larger than those in Pdpap-Hsp24s leaves. In summary, Hsp24 of T. asperellum ACCC30536 is an important defense response gene, and its heterologous expression improved the resistance of transformant Pdpap-Hsp24s to C. chrysosperma and A. alternate.

DOI: 10.1007/s10265-016-0829-9
PubMed: 27193371


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<term>Ascomycota (genetics)</term>
<term>Base Sequence (MeSH)</term>
<term>Cell Membrane Permeability (MeSH)</term>
<term>Cloning, Molecular (MeSH)</term>
<term>Fermentation (genetics)</term>
<term>Fungal Proteins (genetics)</term>
<term>Fungal Proteins (metabolism)</term>
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<term>Genes, Fungal (MeSH)</term>
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<term>Populus (microbiology)</term>
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<term>Stress, Physiological (genetics)</term>
<term>Superoxide Dismutase (metabolism)</term>
<term>Transcription, Genetic (MeSH)</term>
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<term>Ascomycota (génétique)</term>
<term>Clonage moléculaire (MeSH)</term>
<term>Fermentation (génétique)</term>
<term>Gènes fongiques (MeSH)</term>
<term>Myeloperoxidase (métabolisme)</term>
<term>Perméabilité des membranes cellulaires (MeSH)</term>
<term>Populus (génétique)</term>
<term>Populus (microbiologie)</term>
<term>Protéines fongiques (génétique)</term>
<term>Protéines fongiques (métabolisme)</term>
<term>Régions promotrices (génétique) (génétique)</term>
<term>Régulation de l'expression des gènes fongiques (MeSH)</term>
<term>Stress physiologique (génétique)</term>
<term>Superoxide dismutase (métabolisme)</term>
<term>Séquence nucléotidique (MeSH)</term>
<term>Transcription génétique (MeSH)</term>
<term>Transformation génétique (MeSH)</term>
<term>Trichoderma (génétique)</term>
<term>Trichoderma (métabolisme)</term>
<term>Végétaux génétiquement modifiés (MeSH)</term>
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<term>Fungal Proteins</term>
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<term>Antifungal Agents</term>
<term>Fungal Proteins</term>
<term>Peroxidase</term>
<term>Superoxide Dismutase</term>
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<term>Ascomycota</term>
<term>Fermentation</term>
<term>Populus</term>
<term>Promoter Regions, Genetic</term>
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<term>Trichoderma</term>
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<term>Ascomycota</term>
<term>Fermentation</term>
<term>Populus</term>
<term>Protéines fongiques</term>
<term>Régions promotrices (génétique)</term>
<term>Stress physiologique</term>
<term>Trichoderma</term>
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<term>Trichoderma</term>
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<term>Populus</term>
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<keywords scheme="MESH" qualifier="microbiology" xml:lang="en">
<term>Populus</term>
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<term>Antifongiques</term>
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<term>Base Sequence</term>
<term>Cell Membrane Permeability</term>
<term>Cloning, Molecular</term>
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<term>Plants, Genetically Modified</term>
<term>Transcription, Genetic</term>
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<term>Perméabilité des membranes cellulaires</term>
<term>Régulation de l'expression des gènes fongiques</term>
<term>Séquence nucléotidique</term>
<term>Transcription génétique</term>
<term>Transformation génétique</term>
<term>Végétaux génétiquement modifiés</term>
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<div type="abstract" xml:lang="en">The tolerance of plants to biotic and abiotic stresses could be improved by transforming with fungal resistance-related genes. In this study, the cDNA sequence (GenBank Acc. No. KP337939) of the resistance-related gene Hsp24 encoding the 24 kD heat shock protein was obtained from the biocontrol fungus Trichoderma asperellum ACCC30536. The promoter region of Hsp24 contained many cis-regulators related to stresses response, such as "GCN4" and "GCR1" etc. Hsp24 transcription in T. asperellum was up-regulated under six different environmental stresses, compared with the control. Furthermore, following heterologous transformation into Populus davidiana × P. alba var. Pyramidalis (Pdpap), Hsp24 was successfully transcribed in transformant Pdpap-Hsp24s. Pathogen-related genes (PRs) in four Pdpap-Hsp24s were up-regulated compared with those in the control Pdpap (Pdpap-Con). After co-culture of Pdpap-Hsp24s with the weak parasite Cytospora chrysosperma, the transcription of genes related to hormone signal pathway (JA and SA) were up-regulated in Pdpap-Hsp24s, and ethidium bromide (EtBr) and Nitro-blue tetrazolium (NBT) staining assays indicated that the cell membrane permeability and the active oxygen content of Pdpap-Hsp24s leaves were lower than that of the control Pdpap-Con. And when the Pdpap-Hsp24s were under the Alternaria alternate stress, the activities of superoxide dismutase (SOD) and peroxidase (POD) got higher in Pdpap-Hsp24s than that in Pdpap-Con, and the disease spots in Pdpap-Con leaves were obviously larger than those in Pdpap-Hsp24s leaves. In summary, Hsp24 of T. asperellum ACCC30536 is an important defense response gene, and its heterologous expression improved the resistance of transformant Pdpap-Hsp24s to C. chrysosperma and A. alternate. </div>
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