Ectopic Expression of Grapevine Gene VaRGA1 in Arabidopsis Improves Resistance to Downy Mildew and Pseudomonas syringae pv. tomato DC3000 But Increases Susceptibility to Botrytis cinerea.
Identifieur interne : 000103 ( Main/Corpus ); précédent : 000102; suivant : 000104Ectopic Expression of Grapevine Gene VaRGA1 in Arabidopsis Improves Resistance to Downy Mildew and Pseudomonas syringae pv. tomato DC3000 But Increases Susceptibility to Botrytis cinerea.
Auteurs : Shanshan Tian ; Xiangjing Yin ; Peining Fu ; Wei Wu ; Jiang LuSource :
- International journal of molecular sciences [ 1422-0067 ] ; 2019.
English descriptors
- KwdEn :
- Arabidopsis (genetics), Arabidopsis (microbiology), Botrytis (pathogenicity), Disease Resistance (genetics), Ectopic Gene Expression (genetics), Gene Expression Regulation, Plant (genetics), Lycopersicon esculentum (genetics), Lycopersicon esculentum (microbiology), Oomycetes (genetics), Oomycetes (microbiology), Plant Diseases (genetics), Plant Diseases (microbiology), Plant Proteins (genetics), Promoter Regions, Genetic (genetics), Pseudomonas syringae (pathogenicity), Signal Transduction (genetics), Tobacco (genetics), Tobacco (microbiology), Vitis (genetics), Vitis (microbiology).
- MESH :
- chemical , genetics : Plant Proteins.
- genetics : Arabidopsis, Disease Resistance, Ectopic Gene Expression, Gene Expression Regulation, Plant, Lycopersicon esculentum, Oomycetes, Plant Diseases, Promoter Regions, Genetic, Signal Transduction, Tobacco, Vitis.
- microbiology : Arabidopsis, Lycopersicon esculentum, Oomycetes, Plant Diseases, Tobacco, Vitis.
- pathogenicity : Botrytis, Pseudomonas syringae.
Abstract
The protein family with nucleotide binding sites and leucine-rich repeat (NBS-LRR) in plants stimulates immune responses caused by effectors and can mediate resistance to hemi-biotrophs and biotrophs. In our previous study, a Toll-interleukin-1(TIR)-NBS-LRR gene cloned from Vitis amurensis "Shuanghong", VaRGA1, was induced by Plasmopara viticola and could improve the resistance of tobacco to Phytophthora capsici. In this study, VaRGA1 in "Shuanghong" was also induced by salicylic acid (SA), but inhibited by jasmonic acid (JA). To investigate whether VaRGA1 confers broad-spectrum resistance to pathogens, we transferred this gene into Arabidopsis and then treated with Hyaloperonospora arabidopsidis (Hpa), Botrytis cinerea (B. cinerea), and Pseudomonas syringae pv. tomato DC3000 (PstDC3000). Results showed that VaRGA1 improved transgenic Arabidopsis thaliana resistance to the biotrophic Hpa and hemi-biotrophic PstDC3000, but decreased resistance to the necrotrophic B. cinerea. Additionally, qPCR assays showed that VaRGA1 plays an important role in disease resistance by activating SA and inhibiting JA signaling pathways. A 1104 bp promoter fragment of VaRGA1 was cloned and analyzed to further elucidate the mechanism of induction of the gene at the transcriptional level. These results preliminarily confirmed the disease resistance function and signal regulation pathway of VaRGA1, and contributed to the identification of R-genes with broad-spectrum resistance function.
DOI: 10.3390/ijms21010193
PubMed: 31892116
PubMed Central: PMC6982372
Links to Exploration step
pubmed:31892116Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Ectopic Expression of Grapevine Gene <i>VaRGA1</i> in <i>Arabidopsis</i> Improves Resistance to Downy Mildew and <i>Pseudomonas syringae</i> pv. <i>tomato</i> DC3000 But Increases Susceptibility to <i>Botrytis cinerea</i>.</title><author><name sortKey="Tian, Shanshan" sort="Tian, Shanshan" uniqKey="Tian S" first="Shanshan" last="Tian">Shanshan Tian</name><affiliation><nlm:affiliation>Center for Viticulture and Enology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.</nlm:affiliation></affiliation></author><author><name sortKey="Yin, Xiangjing" sort="Yin, Xiangjing" uniqKey="Yin X" first="Xiangjing" last="Yin">Xiangjing Yin</name><affiliation><nlm:affiliation>Center for Viticulture and Enology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.</nlm:affiliation></affiliation></author><author><name sortKey="Fu, Peining" sort="Fu, Peining" uniqKey="Fu P" first="Peining" last="Fu">Peining Fu</name><affiliation><nlm:affiliation>Center for Viticulture and Enology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.</nlm:affiliation></affiliation></author><author><name sortKey="Wu, Wei" sort="Wu, Wei" uniqKey="Wu W" first="Wei" last="Wu">Wei Wu</name><affiliation><nlm:affiliation>Center for Viticulture and Enology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.</nlm:affiliation></affiliation></author><author><name sortKey="Lu, Jiang" sort="Lu, Jiang" uniqKey="Lu J" first="Jiang" last="Lu">Jiang Lu</name><affiliation><nlm:affiliation>Center for Viticulture and Enology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.</nlm:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2019">2019</date><idno type="RBID">pubmed:31892116</idno><idno 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Yin</name><affiliation><nlm:affiliation>Center for Viticulture and Enology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.</nlm:affiliation></affiliation></author><author><name sortKey="Fu, Peining" sort="Fu, Peining" uniqKey="Fu P" first="Peining" last="Fu">Peining Fu</name><affiliation><nlm:affiliation>Center for Viticulture and Enology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.</nlm:affiliation></affiliation></author><author><name sortKey="Wu, Wei" sort="Wu, Wei" uniqKey="Wu W" first="Wei" last="Wu">Wei Wu</name><affiliation><nlm:affiliation>Center for Viticulture and Enology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.</nlm:affiliation></affiliation></author><author><name sortKey="Lu, Jiang" sort="Lu, Jiang" uniqKey="Lu J" first="Jiang" last="Lu">Jiang Lu</name><affiliation><nlm:affiliation>Center for Viticulture and Enology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.</nlm:affiliation></affiliation></author></analytic><series><title level="j">International journal of molecular sciences</title><idno type="eISSN">1422-0067</idno><imprint><date when="2019" type="published">2019</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Arabidopsis (genetics)</term><term>Arabidopsis (microbiology)</term><term>Botrytis (pathogenicity)</term><term>Disease Resistance (genetics)</term><term>Ectopic Gene Expression (genetics)</term><term>Gene Expression Regulation, Plant (genetics)</term><term>Lycopersicon esculentum (genetics)</term><term>Lycopersicon esculentum (microbiology)</term><term>Oomycetes (genetics)</term><term>Oomycetes (microbiology)</term><term>Plant Diseases (genetics)</term><term>Plant Diseases (microbiology)</term><term>Plant Proteins (genetics)</term><term>Promoter Regions, Genetic (genetics)</term><term>Pseudomonas syringae (pathogenicity)</term><term>Signal Transduction (genetics)</term><term>Tobacco (genetics)</term><term>Tobacco (microbiology)</term><term>Vitis (genetics)</term><term>Vitis (microbiology)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Plant Proteins</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Arabidopsis</term><term>Disease Resistance</term><term>Ectopic Gene Expression</term><term>Gene Expression Regulation, Plant</term><term>Lycopersicon esculentum</term><term>Oomycetes</term><term>Plant Diseases</term><term>Promoter Regions, Genetic</term><term>Signal Transduction</term><term>Tobacco</term><term>Vitis</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Arabidopsis</term><term>Lycopersicon esculentum</term><term>Oomycetes</term><term>Plant Diseases</term><term>Tobacco</term><term>Vitis</term></keywords><keywords scheme="MESH" qualifier="pathogenicity" xml:lang="en"><term>Botrytis</term><term>Pseudomonas syringae</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The protein family with nucleotide binding sites and leucine-rich repeat (NBS-LRR) in plants stimulates immune responses caused by effectors and can mediate resistance to hemi-biotrophs and biotrophs. In our previous study, a Toll-interleukin-1(TIR)-NBS-LRR gene cloned from <i>Vitis amurensis</i> "Shuanghong", <i>VaRGA1</i>, was induced by <i>Plasmopara viticola</i> and could improve the resistance of tobacco to <i>Phytophthora capsici</i>. In this study, <i>VaRGA1</i> in "Shuanghong" was also induced by salicylic acid (SA), but inhibited by jasmonic acid (JA). To investigate whether <i>VaRGA1</i> confers broad-spectrum resistance to pathogens, we transferred this gene into <i>Arabidopsis</i> and then treated with <i>Hyaloperonospora arabidopsidis</i> (<i>Hpa</i>), <i>Botrytis cinerea</i> (<i>B. cinerea</i>), and <i>Pseudomonas syringae</i> pv. <i>tomato</i> DC3000 (<i>Pst</i>DC3000). Results showed that <i>VaRGA1</i> improved transgenic <i>Arabidopsis thaliana</i> resistance to the biotrophic <i>Hpa</i> and hemi-biotrophic <i>Pst</i>DC3000, but decreased resistance to the necrotrophic <i>B. cinerea</i>. Additionally, qPCR assays showed that <i>VaRGA1</i> plays an important role in disease resistance by activating SA and inhibiting JA signaling pathways. A 1104 bp promoter fragment of <i>VaRGA1</i> was cloned and analyzed to further elucidate the mechanism of induction of the gene at the transcriptional level. These results preliminarily confirmed the disease resistance function and signal regulation pathway of <i>VaRGA1</i>, and contributed to the identification of R-genes with broad-spectrum resistance function.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">31892116</PMID><DateCompleted><Year>2020</Year><Month>05</Month><Day>14</Day></DateCompleted><DateRevised><Year>2020</Year><Month>05</Month><Day>14</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">1422-0067</ISSN><JournalIssue CitedMedium="Internet"><Volume>21</Volume><Issue>1</Issue><PubDate><Year>2019</Year><Month>Dec</Month><Day>27</Day></PubDate></JournalIssue><Title>International journal of molecular sciences</Title><ISOAbbreviation>Int J Mol Sci</ISOAbbreviation></Journal><ArticleTitle>Ectopic Expression of Grapevine Gene <i>VaRGA1</i> in <i>Arabidopsis</i> Improves Resistance to Downy Mildew and <i>Pseudomonas syringae</i> pv. <i>tomato</i> DC3000 But Increases Susceptibility to <i>Botrytis cinerea</i>.</ArticleTitle><ELocationID EIdType="pii" ValidYN="Y">E193</ELocationID><ELocationID EIdType="doi" ValidYN="Y">10.3390/ijms21010193</ELocationID><Abstract><AbstractText>The protein family with nucleotide binding sites and leucine-rich repeat (NBS-LRR) in plants stimulates immune responses caused by effectors and can mediate resistance to hemi-biotrophs and biotrophs. In our previous study, a Toll-interleukin-1(TIR)-NBS-LRR gene cloned from <i>Vitis amurensis</i> "Shuanghong", <i>VaRGA1</i>, was induced by <i>Plasmopara viticola</i> and could improve the resistance of tobacco to <i>Phytophthora capsici</i>. In this study, <i>VaRGA1</i> in "Shuanghong" was also induced by salicylic acid (SA), but inhibited by jasmonic acid (JA). To investigate whether <i>VaRGA1</i> confers broad-spectrum resistance to pathogens, we transferred this gene into <i>Arabidopsis</i> and then treated with <i>Hyaloperonospora arabidopsidis</i> (<i>Hpa</i>), <i>Botrytis cinerea</i> (<i>B. cinerea</i>), and <i>Pseudomonas syringae</i> pv. <i>tomato</i> DC3000 (<i>Pst</i>DC3000). Results showed that <i>VaRGA1</i> improved transgenic <i>Arabidopsis thaliana</i> resistance to the biotrophic <i>Hpa</i> and hemi-biotrophic <i>Pst</i>DC3000, but decreased resistance to the necrotrophic <i>B. cinerea</i>. Additionally, qPCR assays showed that <i>VaRGA1</i> plays an important role in disease resistance by activating SA and inhibiting JA signaling pathways. A 1104 bp promoter fragment of <i>VaRGA1</i> was cloned and analyzed to further elucidate the mechanism of induction of the gene at the transcriptional level. These results preliminarily confirmed the disease resistance function and signal regulation pathway of <i>VaRGA1</i>, and contributed to the identification of R-genes with broad-spectrum resistance function.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Tian</LastName><ForeName>Shanshan</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Center for Viticulture and Enology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Yin</LastName><ForeName>Xiangjing</ForeName><Initials>X</Initials><AffiliationInfo><Affiliation>Center for Viticulture and Enology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Fu</LastName><ForeName>Peining</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>Center for Viticulture and Enology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Wu</LastName><ForeName>Wei</ForeName><Initials>W</Initials><AffiliationInfo><Affiliation>Center for Viticulture and Enology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Lu</LastName><ForeName>Jiang</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>Center for Viticulture and Enology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>CARS-29-yc-2</GrantID><Agency>Agriculture Research System of China</Agency><Country></Country></Grant><Grant><GrantID>WF107115001</GrantID><Agency>the Start-up Fund from Shanghai Jiao Tong University</Agency><Country></Country></Grant><Grant><GrantID>2013-3</GrantID><Agency>Guangxi Bagui Scholar Fund</Agency><Country></Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2019</Year><Month>12</Month><Day>27</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Int J Mol Sci</MedlineTA><NlmUniqueID>101092791</NlmUniqueID><ISSNLinking>1422-0067</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D010940">Plant Proteins</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D017360" MajorTopicYN="N">Arabidopsis</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D020171" MajorTopicYN="N">Botrytis</DescriptorName><QualifierName UI="Q000472" MajorTopicYN="N">pathogenicity</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D060467" MajorTopicYN="N">Disease Resistance</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000066630" MajorTopicYN="N">Ectopic Gene Expression</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018506" MajorTopicYN="N">Gene Expression Regulation, Plant</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018551" MajorTopicYN="N">Lycopersicon esculentum</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D009868" MajorTopicYN="N">Oomycetes</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010935" MajorTopicYN="N">Plant Diseases</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010940" MajorTopicYN="N">Plant Proteins</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011401" MajorTopicYN="N">Promoter Regions, Genetic</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D044224" MajorTopicYN="N">Pseudomonas syringae</DescriptorName><QualifierName UI="Q000472" MajorTopicYN="N">pathogenicity</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015398" MajorTopicYN="N">Signal Transduction</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014026" MajorTopicYN="N">Tobacco</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D027843" MajorTopicYN="N">Vitis</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">NBS-LRR</Keyword><Keyword MajorTopicYN="N">VaRGA1</Keyword><Keyword MajorTopicYN="N">broad-spectrum</Keyword><Keyword MajorTopicYN="N">disease resistance</Keyword><Keyword MajorTopicYN="N">histochemical staining</Keyword><Keyword MajorTopicYN="N">signaling pathways</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2019</Year><Month>10</Month><Day>10</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2019</Year><Month>12</Month><Day>20</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2019</Year><Month>12</Month><Day>22</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2020</Year><Month>1</Month><Day>2</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2020</Year><Month>1</Month><Day>2</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2020</Year><Month>5</Month><Day>15</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>epublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">31892116</ArticleId><ArticleId 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