PhytophthoraV1, Main, Exploration, bibRecord, 001A30

Systemic acquired resistance in soybean is regulated by two proteins, Orthologous to Arabidopsis NPR1.

Identifieur interne : 001A30 ( Main/Exploration ); précédent : 001A29; suivant : 001A31

Systemic acquired resistance in soybean is regulated by two proteins, Orthologous to Arabidopsis NPR1.

Auteurs : Devinder Sandhu [États-Unis] ; I Made Tasma ; Ryan Frasch ; Madan K. Bhattacharyya

Source :

BMC plant biology [ 1471-2229 ] ; 2009.

RBID : pubmed:19656407

Descripteurs français

KwdFr :
- ADN des plantes (génétique), Acides isonicotiniques (pharmacologie), Alignement de séquences (MeSH), Analyse de séquence d'ADN (MeSH), Banque de gènes (MeSH), Clonage moléculaire (MeSH), Données de séquences moléculaires (MeSH), Génome végétal (MeSH), Maladies des plantes (génétique), Phytophthora (pathogénicité), Protéines d'Arabidopsis (génétique), Protéines d'Arabidopsis (métabolisme), Protéines végétales (génétique), Protéines végétales (métabolisme), Régulation de l'expression des gènes végétaux (MeSH), Soja (génétique), Soja (métabolisme), Séquence d'acides aminés (MeSH), Test de complémentation (MeSH), Transduction du signal (MeSH), Végétaux génétiquement modifiés (génétique), Végétaux génétiquement modifiés (métabolisme).
MESH :
- génétique : ADN des plantes, Maladies des plantes, Protéines d'Arabidopsis, Protéines végétales, Soja, Végétaux génétiquement modifiés.
- métabolisme : Protéines d'Arabidopsis, Protéines végétales, Soja, Végétaux génétiquement modifiés.
- pathogénicité : Phytophthora.
- pharmacologie : Acides isonicotiniques.
- Alignement de séquences, Analyse de séquence d'ADN, Banque de gènes, Clonage moléculaire, Données de séquences moléculaires, Génome végétal, Régulation de l'expression des gènes végétaux, Séquence d'acides aminés, Test de complémentation, Transduction du signal.

English descriptors

KwdEn :
- Amino Acid Sequence (MeSH), Arabidopsis Proteins (genetics), Arabidopsis Proteins (metabolism), Cloning, Molecular (MeSH), DNA, Plant (genetics), Gene Expression Regulation, Plant (MeSH), Gene Library (MeSH), Genetic Complementation Test (MeSH), Genome, Plant (MeSH), Isonicotinic Acids (pharmacology), Molecular Sequence Data (MeSH), Phytophthora (pathogenicity), Plant Diseases (genetics), Plant Proteins (genetics), Plant Proteins (metabolism), Plants, Genetically Modified (genetics), Plants, Genetically Modified (metabolism), Sequence Alignment (MeSH), Sequence Analysis, DNA (MeSH), Signal Transduction (MeSH), Soybeans (genetics), Soybeans (metabolism).
MESH :
- chemical , genetics : Arabidopsis Proteins, DNA, Plant, Plant Proteins.
- chemical , metabolism : Arabidopsis Proteins, Plant Proteins.
- chemical , pharmacology : Isonicotinic Acids.
- genetics : Plant Diseases, Plants, Genetically Modified, Soybeans.
- metabolism : Plants, Genetically Modified, Soybeans.
- pathogenicity : Phytophthora.
- Amino Acid Sequence, Cloning, Molecular, Gene Expression Regulation, Plant, Gene Library, Genetic Complementation Test, Genome, Plant, Molecular Sequence Data, Sequence Alignment, Sequence Analysis, DNA, Signal Transduction.

Abstract

BACKGROUND

Systemic acquired resistance (SAR) is induced in non-inoculated leaves following infection with certain pathogenic strains. SAR is effective against many pathogens. Salicylic acid (SA) is a signaling molecule of the SAR pathway. The development of SAR is associated with the induction of pathogenesis related (PR) genes. Arabidopsis non-expressor of PR1 (NPR1) is a regulatory gene of the SA signal pathway 123. SAR in soybean was first reported following infection with Colletotrichum trancatum that causes anthracnose disease. We investigated if SAR in soybean is regulated by a pathway, similar to the one characterized in Arabidopsis.

RESULTS

Pathogenesis-related gene GmPR1 is induced following treatment of soybean plants with the SAR inducer, 2,6-dichloroisonicotinic acid (INA) or infection with the oomycete pathogen, Phytophthora sojae. In P. sojae-infected plants, SAR was induced against the bacterial pathogen, Pseudomonas syringae pv. glycinea. Soybean GmNPR1-1 and GmNPR1-2 genes showed high identities to Arabidopsis NPR1. They showed similar expression patterns among the organs, studied in this investigation. GmNPR1-1 and GmNPR1-2 are the only soybean homologues of NPR1and are located in homoeologous regions. In GmNPR1-1 and GmNPR1-2 transformed Arabidopsis npr1-1 mutant plants, SAR markers: (i) PR-1 was induced following INA treatment and (ii) BGL2 following infection with Pseudomonas syringae pv. tomato (Pst), and SAR was induced following Pst infection. Of the five cysteine residues, Cys82, Cys150, Cys155, Cys160, and Cys216 involved in oligomer-monomer transition in NPR1, Cys216 in GmNPR1-1 and GmNPR1-2 proteins was substituted to Ser and Leu, respectively.

CONCLUSION

Complementation analyses in Arabidopsis npr1-1 mutants revealed that homoeologous GmNPR1-1 and GmNPR1-2 genes are orthologous to Arabidopsis NPR1. Therefore, SAR pathway in soybean is most likely regulated by GmNPR1 genes. Substitution of Cys216 residue, essential for oligomer-monomer transition of Arabidopsis NPR1, with Ser and Leu residues in GmNPR1-1 and GmNPR1-2, respectively, suggested that there may be differences between the regulatory mechanisms of GmNPR1 and Arabidopsis NPR proteins.

DOI: 10.1186/1471-2229-9-105
PubMed: 19656407
PubMed Central: PMC2738679

Affiliations:

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<term>DNA, Plant (genetics)</term>
<term>Gene Expression Regulation, Plant (MeSH)</term>
<term>Gene Library (MeSH)</term>
<term>Genetic Complementation Test (MeSH)</term>
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<term>Plant Proteins (metabolism)</term>
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<term>Plants, Genetically Modified (metabolism)</term>
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<term>Analyse de séquence d'ADN (MeSH)</term>
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<term>Clonage moléculaire (MeSH)</term>
<term>Données de séquences moléculaires (MeSH)</term>
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<term>Protéines d'Arabidopsis (métabolisme)</term>
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<term>Gene Library</term>
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<term>Clonage moléculaire</term>
<term>Données de séquences moléculaires</term>
<term>Génome végétal</term>
<term>Régulation de l'expression des gènes végétaux</term>
<term>Séquence d'acides aminés</term>
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<front><div type="abstract" xml:lang="en"><p><b>BACKGROUND</b>
</p>
<p>Systemic acquired resistance (SAR) is induced in non-inoculated leaves following infection with certain pathogenic strains. SAR is effective against many pathogens. Salicylic acid (SA) is a signaling molecule of the SAR pathway. The development of SAR is associated with the induction of pathogenesis related (PR) genes. Arabidopsis non-expressor of PR1 (NPR1) is a regulatory gene of the SA signal pathway 123. SAR in soybean was first reported following infection with Colletotrichum trancatum that causes anthracnose disease. We investigated if SAR in soybean is regulated by a pathway, similar to the one characterized in Arabidopsis.</p>
</div>
<div type="abstract" xml:lang="en"><p><b>RESULTS</b>
</p>
<p>Pathogenesis-related gene GmPR1 is induced following treatment of soybean plants with the SAR inducer, 2,6-dichloroisonicotinic acid (INA) or infection with the oomycete pathogen, Phytophthora sojae. In P. sojae-infected plants, SAR was induced against the bacterial pathogen, Pseudomonas syringae pv. glycinea. Soybean GmNPR1-1 and GmNPR1-2 genes showed high identities to Arabidopsis NPR1. They showed similar expression patterns among the organs, studied in this investigation. GmNPR1-1 and GmNPR1-2 are the only soybean homologues of NPR1and are located in homoeologous regions. In GmNPR1-1 and GmNPR1-2 transformed Arabidopsis npr1-1 mutant plants, SAR markers: (i) PR-1 was induced following INA treatment and (ii) BGL2 following infection with Pseudomonas syringae pv. tomato (Pst), and SAR was induced following Pst infection. Of the five cysteine residues, Cys82, Cys150, Cys155, Cys160, and Cys216 involved in oligomer-monomer transition in NPR1, Cys216 in GmNPR1-1 and GmNPR1-2 proteins was substituted to Ser and Leu, respectively.</p>
</div>
<div type="abstract" xml:lang="en"><p><b>CONCLUSION</b>
</p>
<p>Complementation analyses in Arabidopsis npr1-1 mutants revealed that homoeologous GmNPR1-1 and GmNPR1-2 genes are orthologous to Arabidopsis NPR1. Therefore, SAR pathway in soybean is most likely regulated by GmNPR1 genes. Substitution of Cys216 residue, essential for oligomer-monomer transition of Arabidopsis NPR1, with Ser and Leu residues in GmNPR1-1 and GmNPR1-2, respectively, suggested that there may be differences between the regulatory mechanisms of GmNPR1 and Arabidopsis NPR proteins.</p>
</div>
</front>
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<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Systemic acquired resistance (SAR) is induced in non-inoculated leaves following infection with certain pathogenic strains. SAR is effective against many pathogens. Salicylic acid (SA) is a signaling molecule of the SAR pathway. The development of SAR is associated with the induction of pathogenesis related (PR) genes. Arabidopsis non-expressor of PR1 (NPR1) is a regulatory gene of the SA signal pathway 123. SAR in soybean was first reported following infection with Colletotrichum trancatum that causes anthracnose disease. We investigated if SAR in soybean is regulated by a pathway, similar to the one characterized in Arabidopsis.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Pathogenesis-related gene GmPR1 is induced following treatment of soybean plants with the SAR inducer, 2,6-dichloroisonicotinic acid (INA) or infection with the oomycete pathogen, Phytophthora sojae. In P. sojae-infected plants, SAR was induced against the bacterial pathogen, Pseudomonas syringae pv. glycinea. Soybean GmNPR1-1 and GmNPR1-2 genes showed high identities to Arabidopsis NPR1. They showed similar expression patterns among the organs, studied in this investigation. GmNPR1-1 and GmNPR1-2 are the only soybean homologues of NPR1and are located in homoeologous regions. In GmNPR1-1 and GmNPR1-2 transformed Arabidopsis npr1-1 mutant plants, SAR markers: (i) PR-1 was induced following INA treatment and (ii) BGL2 following infection with Pseudomonas syringae pv. tomato (Pst), and SAR was induced following Pst infection. Of the five cysteine residues, Cys82, Cys150, Cys155, Cys160, and Cys216 involved in oligomer-monomer transition in NPR1, Cys216 in GmNPR1-1 and GmNPR1-2 proteins was substituted to Ser and Leu, respectively.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Complementation analyses in Arabidopsis npr1-1 mutants revealed that homoeologous GmNPR1-1 and GmNPR1-2 genes are orthologous to Arabidopsis NPR1. Therefore, SAR pathway in soybean is most likely regulated by GmNPR1 genes. Substitution of Cys216 residue, essential for oligomer-monomer transition of Arabidopsis NPR1, with Ser and Leu residues in GmNPR1-1 and GmNPR1-2, respectively, suggested that there may be differences between the regulatory mechanisms of GmNPR1 and Arabidopsis NPR proteins.</AbstractText>
</Abstract>
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<ForeName>Ryan</ForeName>
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Systemic acquired resistance in soybean is regulated by two proteins, Orthologous to Arabidopsis NPR1.

Systemic acquired resistance in soybean is regulated by two proteins, Orthologous to Arabidopsis NPR1.

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