Characterization of Cell-Death-Inducing Members of the Pectate Lyase Gene Family in Phytophthora capsici and Their Contributions to Infection of Pepper.
Identifieur interne : 000F13 ( Main/Exploration ); précédent : 000F12; suivant : 000F14Characterization of Cell-Death-Inducing Members of the Pectate Lyase Gene Family in Phytophthora capsici and Their Contributions to Infection of Pepper.
Auteurs : Li Fu [République populaire de Chine] ; Chunyuan Zhu [République populaire de Chine] ; Xiaomeng Ding [République populaire de Chine] ; Xiaoyan Yang [République populaire de Chine] ; Paul F. Morris [États-Unis] ; Brett M. Tyler [États-Unis] ; Xiuguo Zhang [République populaire de Chine]Source :
- Molecular plant-microbe interactions : MPMI [ 0894-0282 ] ; 2015.
Descripteurs français
- KwdFr :
- Capsicum (cytologie), Capsicum (microbiologie), Clonage moléculaire (MeSH), Données de séquences moléculaires (MeSH), Feuilles de plante (microbiologie), Interactions hôte-pathogène (génétique), Maladies des plantes (microbiologie), Mort cellulaire (MeSH), Phytophthora (génétique), Phytophthora (pathogénicité), Polysaccharide-lyases (génétique), Polysaccharide-lyases (métabolisme), Protéines fongiques (génétique), Régulation de l'expression des gènes fongiques (MeSH).
- MESH :
- cytologie : Capsicum.
- génétique : Interactions hôte-pathogène, Phytophthora, Polysaccharide-lyases, Protéines fongiques.
- microbiologie : Capsicum, Feuilles de plante, Maladies des plantes.
- métabolisme : Polysaccharide-lyases.
- pathogénicité : Phytophthora.
- Clonage moléculaire, Données de séquences moléculaires, Mort cellulaire, Régulation de l'expression des gènes fongiques.
English descriptors
- KwdEn :
- Capsicum (cytology), Capsicum (microbiology), Cell Death (MeSH), Cloning, Molecular (MeSH), Fungal Proteins (genetics), Gene Expression Regulation, Fungal (MeSH), Host-Pathogen Interactions (genetics), Molecular Sequence Data (MeSH), Phytophthora (genetics), Phytophthora (pathogenicity), Plant Diseases (microbiology), Plant Leaves (microbiology), Polysaccharide-Lyases (genetics), Polysaccharide-Lyases (metabolism).
- MESH :
- chemical , genetics : Fungal Proteins, Polysaccharide-Lyases.
- cytology : Capsicum.
- genetics : Host-Pathogen Interactions, Phytophthora.
- chemical , metabolism : Polysaccharide-Lyases.
- microbiology : Capsicum, Plant Diseases, Plant Leaves.
- pathogenicity : Phytophthora.
- Cell Death, Cloning, Molecular, Gene Expression Regulation, Fungal, Molecular Sequence Data.
Abstract
Pectate lyases (PL) play a critical role in pectin degradation. PL have been extensively studied in major bacterial and fungal pathogens of a wide range of plant species. However, the contribution of PL to infection by oomycete pathogens remains largely unknown. Here, we cloned 22 full-length pectate lyase (PcPL) genes from a highly aggressive strain of Phytophthora capsici SD33. Of these, PVX agroinfiltration revealed that 12 PcPL genes were found to be highly induced during infection of pepper by SD33 but the induction level was twofold less in a mildly aggressive strain, YN07. The four genes with the highest transcript levels as measured by by quantitative reverse-transcription polymerase chain reaction (PcPL1, PcPL15, PcPL16, and PcPL20) also produced a severe cell death response following transient expression in pepper leaves but the other eight PcPL genes did not. Overexpression of these four genes increased the virulence of SD33 on pepper slightly, and increased it more substantially during infection of tobacco. Overexpression of the genes in YN07 restored its aggressiveness to near that of SD33. Gene silencing experiments with the 12 PcPL genes produced diverse patterns of silencing of PcPL genes, from which it could be inferred from regression analysis that PcPL1, PcPL16, and PcPL20 could account for nearly all of the contributions of the PcPL genes to virulence.
DOI: 10.1094/MPMI-11-14-0352-R
PubMed: 25775270
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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PL have been extensively studied in major bacterial and fungal pathogens of a wide range of plant species. However, the contribution of PL to infection by oomycete pathogens remains largely unknown. Here, we cloned 22 full-length pectate lyase (PcPL) genes from a highly aggressive strain of Phytophthora capsici SD33. Of these, PVX agroinfiltration revealed that 12 PcPL genes were found to be highly induced during infection of pepper by SD33 but the induction level was twofold less in a mildly aggressive strain, YN07. The four genes with the highest transcript levels as measured by by quantitative reverse-transcription polymerase chain reaction (PcPL1, PcPL15, PcPL16, and PcPL20) also produced a severe cell death response following transient expression in pepper leaves but the other eight PcPL genes did not. Overexpression of these four genes increased the virulence of SD33 on pepper slightly, and increased it more substantially during infection of tobacco. Overexpression of the genes in YN07 restored its aggressiveness to near that of SD33. Gene silencing experiments with the 12 PcPL genes produced diverse patterns of silencing of PcPL genes, from which it could be inferred from regression analysis that PcPL1, PcPL16, and PcPL20 could account for nearly all of the contributions of the PcPL genes to virulence. </div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25775270</PMID><DateCompleted><Year>2015</Year><Month>12</Month><Day>03</Day></DateCompleted><DateRevised><Year>2015</Year><Month>07</Month><Day>29</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">0894-0282</ISSN><JournalIssue CitedMedium="Print"><Volume>28</Volume><Issue>7</Issue><PubDate><Year>2015</Year><Month>Jul</Month></PubDate></JournalIssue><Title>Molecular plant-microbe interactions : MPMI</Title><ISOAbbreviation>Mol Plant Microbe Interact</ISOAbbreviation></Journal><ArticleTitle>Characterization of Cell-Death-Inducing Members of the Pectate Lyase Gene Family in Phytophthora capsici and Their Contributions to Infection of Pepper.</ArticleTitle><Pagination><MedlinePgn>766-75</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1094/MPMI-11-14-0352-R</ELocationID><Abstract><AbstractText>Pectate lyases (PL) play a critical role in pectin degradation. PL have been extensively studied in major bacterial and fungal pathogens of a wide range of plant species. However, the contribution of PL to infection by oomycete pathogens remains largely unknown. Here, we cloned 22 full-length pectate lyase (PcPL) genes from a highly aggressive strain of Phytophthora capsici SD33. Of these, PVX agroinfiltration revealed that 12 PcPL genes were found to be highly induced during infection of pepper by SD33 but the induction level was twofold less in a mildly aggressive strain, YN07. The four genes with the highest transcript levels as measured by by quantitative reverse-transcription polymerase chain reaction (PcPL1, PcPL15, PcPL16, and PcPL20) also produced a severe cell death response following transient expression in pepper leaves but the other eight PcPL genes did not. Overexpression of these four genes increased the virulence of SD33 on pepper slightly, and increased it more substantially during infection of tobacco. Overexpression of the genes in YN07 restored its aggressiveness to near that of SD33. Gene silencing experiments with the 12 PcPL genes produced diverse patterns of silencing of PcPL genes, from which it could be inferred from regression analysis that PcPL1, PcPL16, and PcPL20 could account for nearly all of the contributions of the PcPL genes to virulence. </AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Fu</LastName><ForeName>Li</ForeName><Initials>L</Initials><AffiliationInfo><Affiliation>1 Department of Plant Pathology, Shandong Agricultural University, No. 61, Daizong Street, Taian, Shandong, 271018, China;</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Zhu</LastName><ForeName>Chunyuan</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>1 Department of Plant Pathology, Shandong Agricultural University, No. 61, Daizong Street, Taian, Shandong, 271018, China;</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Ding</LastName><ForeName>Xiaomeng</ForeName><Initials>X</Initials><AffiliationInfo><Affiliation>1 Department of Plant Pathology, Shandong Agricultural University, No. 61, Daizong Street, Taian, Shandong, 271018, China;</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Yang</LastName><ForeName>Xiaoyan</ForeName><Initials>X</Initials><AffiliationInfo><Affiliation>1 Department of Plant Pathology, Shandong Agricultural University, No. 61, Daizong Street, Taian, Shandong, 271018, China;</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Morris</LastName><ForeName>Paul F</ForeName><Initials>PF</Initials><AffiliationInfo><Affiliation>2 Department of Biological Sciences, Bowling Green State University, Bowling Green, OH 43403 U.S.A.;</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Tyler</LastName><ForeName>Brett M</ForeName><Initials>BM</Initials><AffiliationInfo><Affiliation>3 Center for Genome Research and Biocomputing, and Department of Botany and Plant Pathology, Oregon State University, Corvallis, 97331, U.S.A.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Zhang</LastName><ForeName>Xiuguo</ForeName><Initials>X</Initials><AffiliationInfo><Affiliation>1 Department of Plant Pathology, Shandong Agricultural University, No. 61, Daizong Street, Taian, Shandong, 271018, China;</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><DataBankList CompleteYN="Y"><DataBank><DataBankName>GENBANK</DataBankName><AccessionNumberList><AccessionNumber>KF133976</AccessionNumber><AccessionNumber>KF133977</AccessionNumber><AccessionNumber>KF133978</AccessionNumber><AccessionNumber>KF133979</AccessionNumber><AccessionNumber>KF133980</AccessionNumber></AccessionNumberList></DataBank></DataBankList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2015</Year><Month>07</Month><Day>08</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Mol Plant Microbe Interact</MedlineTA><NlmUniqueID>9107902</NlmUniqueID><ISSNLinking>0894-0282</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D005656">Fungal Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 4.2.2.-</RegistryNumber><NameOfSubstance UI="D011133">Polysaccharide-Lyases</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 4.2.2.2</RegistryNumber><NameOfSubstance UI="C023911">pectate lyase</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D002212" MajorTopicYN="N">Capsicum</DescriptorName><QualifierName UI="Q000166" MajorTopicYN="N">cytology</QualifierName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016923" MajorTopicYN="N">Cell Death</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003001" MajorTopicYN="N">Cloning, Molecular</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005656" MajorTopicYN="N">Fungal Proteins</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015966" MajorTopicYN="N">Gene Expression Regulation, Fungal</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D054884" MajorTopicYN="N">Host-Pathogen Interactions</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008969" MajorTopicYN="N">Molecular Sequence Data</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010838" MajorTopicYN="N">Phytophthora</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000472" MajorTopicYN="Y">pathogenicity</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010935" MajorTopicYN="N">Plant Diseases</DescriptorName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018515" MajorTopicYN="N">Plant Leaves</DescriptorName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011133" MajorTopicYN="N">Polysaccharide-Lyases</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2015</Year><Month>3</Month><Day>17</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2015</Year><Month>3</Month><Day>17</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2015</Year><Month>12</Month><Day>15</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">25775270</ArticleId><ArticleId IdType="doi">10.1094/MPMI-11-14-0352-R</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>République populaire de Chine</li><li>États-Unis</li></country><region><li>Ohio</li></region></list><tree><country name="République populaire de Chine"><noRegion><name sortKey="Fu, Li" sort="Fu, Li" uniqKey="Fu L" first="Li" last="Fu">Li Fu</name></noRegion><name sortKey="Ding, Xiaomeng" sort="Ding, Xiaomeng" uniqKey="Ding X" first="Xiaomeng" last="Ding">Xiaomeng Ding</name><name sortKey="Yang, Xiaoyan" sort="Yang, Xiaoyan" uniqKey="Yang X" first="Xiaoyan" last="Yang">Xiaoyan Yang</name><name sortKey="Zhang, Xiuguo" sort="Zhang, Xiuguo" uniqKey="Zhang X" first="Xiuguo" last="Zhang">Xiuguo Zhang</name><name sortKey="Zhu, Chunyuan" sort="Zhu, Chunyuan" uniqKey="Zhu C" first="Chunyuan" last="Zhu">Chunyuan Zhu</name></country><country name="États-Unis"><region name="Ohio"><name sortKey="Morris, Paul F" sort="Morris, Paul F" uniqKey="Morris P" first="Paul F" last="Morris">Paul F. Morris</name></region><name sortKey="Tyler, Brett M" sort="Tyler, Brett M" uniqKey="Tyler B" first="Brett M" last="Tyler">Brett M. Tyler</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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|texte= Characterization of Cell-Death-Inducing Members of the Pectate Lyase Gene Family in Phytophthora capsici and Their Contributions to Infection of Pepper.
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