Molecular cloning and functional analysis of two phosphate transporter genes from Rhizopogon luteolus and Leucocortinarius bulbiger, two ectomycorrhizal fungi of Pinus tabulaeformis.
Identifieur interne : 001102 ( Main/Corpus ); précédent : 001101; suivant : 001103Molecular cloning and functional analysis of two phosphate transporter genes from Rhizopogon luteolus and Leucocortinarius bulbiger, two ectomycorrhizal fungi of Pinus tabulaeformis.
Auteurs : Rong Zheng ; Jugang Wang ; Min Liu ; Guozhen Duan ; Xiaomin Gao ; Shulan Bai ; Yachao HanSource :
- Mycorrhiza [ 1432-1890 ] ; 2016.
English descriptors
- KwdEn :
- Basidiomycota (genetics), Basidiomycota (metabolism), Cloning, Molecular (methods), Fungal Proteins (genetics), Fungal Proteins (metabolism), Gene Expression Regulation, Fungal (physiology), Hydrogen-Ion Concentration (MeSH), Mycorrhizae (genetics), Mycorrhizae (metabolism), Phylogeny (MeSH), Pinus (microbiology), Protein Transport (MeSH).
- MESH :
- chemical , genetics : Fungal Proteins.
- genetics : Basidiomycota, Mycorrhizae.
- metabolism : Basidiomycota, Fungal Proteins, Mycorrhizae.
- methods : Cloning, Molecular.
- microbiology : Pinus.
- physiology : Gene Expression Regulation, Fungal.
- Hydrogen-Ion Concentration, Phylogeny, Protein Transport.
Abstract
Inorganic phosphorus (Pi) is essential for plant growth, and phosphate (P) deficiency is a primary limiting factor in Pinus tabulaeformis development in northern China. P acquisition in mycorrhizal plants is highly dependent on the activities of phosphate transporters of their root-associated fungi. In the current study, two phosphate transporter genes, RlPT and LbPT, were isolated from Rhizopogon luteolus and Leucocortinarius bulbiger, respectively, two ectomycorrhizal fungi forming symbiotic interactions with the P. tabulaeformis. Phylogenetic analysis suggested that the sequence of the phosphate transporter of L. bulbiger is most closely related to a phosphate transporter of Hebeloma cylindrosporum, whereas the phosphate transporter of R. luteolus is most closely related to that of Piloderma croceum. The subcellular localization indicated that RlPT and LbPT were expressed in the plasma membrane. The complementation assay in yeast indicated that both RlPT and LbPT partially compensated for the absence of phosphate transporter activity in the MB192 yeast strain, with a K m value of 57.90 μmol/L Pi for RlPT and 35.87 μmol/L Pi for LbPT. qPCR analysis revealed that RlPT and LbPT were significantly up-regulated at lower P availability, which may enhance P uptake and transport under Pi starvation. Our results suggest that RlPT and LbPT presumably play a key role in Pi acquisition by P. tabulaeformis via ectomycorrhizal fungi.
DOI: 10.1007/s00572-016-0702-7
PubMed: 27098350
Links to Exploration step
pubmed:27098350Le document en format XML
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China.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>South Subtropical Crops Research Institute, Chinese Academy of Tropical Agricultural Science, Zhanjiang, 524091, Guangdong, China.</nlm:affiliation></affiliation></author><author><name sortKey="Liu, Min" sort="Liu, Min" uniqKey="Liu M" first="Min" last="Liu">Min Liu</name><affiliation><nlm:affiliation>College of Forestry, Inner Mongolia Agricultural University, Hohhot, 010019, Inner Mongolia, China.</nlm:affiliation></affiliation></author><author><name sortKey="Duan, Guozhen" sort="Duan, Guozhen" uniqKey="Duan G" first="Guozhen" last="Duan">Guozhen Duan</name><affiliation><nlm:affiliation>College of Forestry, Inner Mongolia Agricultural University, Hohhot, 010019, Inner Mongolia, China.</nlm:affiliation></affiliation></author><author><name sortKey="Gao, Xiaomin" sort="Gao, Xiaomin" uniqKey="Gao X" first="Xiaomin" last="Gao">Xiaomin Gao</name><affiliation><nlm:affiliation>South Subtropical Crops Research Institute, 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wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">001102</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Molecular cloning and functional analysis of two phosphate transporter genes from Rhizopogon luteolus and Leucocortinarius bulbiger, two ectomycorrhizal fungi of Pinus tabulaeformis.</title><author><name sortKey="Zheng, Rong" sort="Zheng, Rong" uniqKey="Zheng R" first="Rong" last="Zheng">Rong Zheng</name><affiliation><nlm:affiliation>College of Forestry, Inner Mongolia Agricultural University, Hohhot, 010019, Inner Mongolia, China.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>College of Life Science and Technology, Inner Mongolia Normal University, Hohhot, 010020, Inner Mongolia, China.</nlm:affiliation></affiliation></author><author><name sortKey="Wang, Jugang" sort="Wang, Jugang" uniqKey="Wang J" first="Jugang" last="Wang">Jugang Wang</name><affiliation><nlm:affiliation>College of Forestry, Inner Mongolia Agricultural University, Hohhot, 010019, Inner Mongolia, China.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>South Subtropical Crops Research Institute, Chinese Academy of Tropical Agricultural Science, Zhanjiang, 524091, Guangdong, China.</nlm:affiliation></affiliation></author><author><name sortKey="Liu, Min" sort="Liu, Min" uniqKey="Liu M" first="Min" last="Liu">Min Liu</name><affiliation><nlm:affiliation>College of Forestry, Inner Mongolia Agricultural University, Hohhot, 010019, Inner Mongolia, China.</nlm:affiliation></affiliation></author><author><name sortKey="Duan, Guozhen" sort="Duan, Guozhen" uniqKey="Duan G" first="Guozhen" last="Duan">Guozhen Duan</name><affiliation><nlm:affiliation>College of Forestry, Inner Mongolia Agricultural University, Hohhot, 010019, Inner Mongolia, China.</nlm:affiliation></affiliation></author><author><name sortKey="Gao, Xiaomin" sort="Gao, Xiaomin" uniqKey="Gao X" first="Xiaomin" last="Gao">Xiaomin Gao</name><affiliation><nlm:affiliation>South Subtropical Crops Research Institute, Chinese Academy of Tropical Agricultural Science, Zhanjiang, 524091, Guangdong, China.</nlm:affiliation></affiliation></author><author><name sortKey="Bai, Shulan" sort="Bai, Shulan" uniqKey="Bai S" first="Shulan" last="Bai">Shulan Bai</name><affiliation><nlm:affiliation>College of Forestry, Inner Mongolia Agricultural University, Hohhot, 010019, Inner Mongolia, China. baishulan2004@163.com.</nlm:affiliation></affiliation></author><author><name sortKey="Han, Yachao" sort="Han, Yachao" uniqKey="Han Y" first="Yachao" last="Han">Yachao Han</name><affiliation><nlm:affiliation>Fuyang Vocational and Technical College, Fuyang, 236031, Anhui, China.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Mycorrhiza</title><idno type="eISSN">1432-1890</idno><imprint><date when="2016" type="published">2016</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Basidiomycota (genetics)</term><term>Basidiomycota (metabolism)</term><term>Cloning, Molecular (methods)</term><term>Fungal Proteins (genetics)</term><term>Fungal Proteins (metabolism)</term><term>Gene Expression Regulation, Fungal (physiology)</term><term>Hydrogen-Ion Concentration (MeSH)</term><term>Mycorrhizae (genetics)</term><term>Mycorrhizae (metabolism)</term><term>Phylogeny (MeSH)</term><term>Pinus (microbiology)</term><term>Protein Transport (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Fungal Proteins</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Basidiomycota</term><term>Mycorrhizae</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Basidiomycota</term><term>Fungal Proteins</term><term>Mycorrhizae</term></keywords><keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Cloning, Molecular</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Pinus</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Gene Expression Regulation, Fungal</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Hydrogen-Ion Concentration</term><term>Phylogeny</term><term>Protein Transport</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Inorganic phosphorus (Pi) is essential for plant growth, and phosphate (P) deficiency is a primary limiting factor in Pinus tabulaeformis development in northern China. P acquisition in mycorrhizal plants is highly dependent on the activities of phosphate transporters of their root-associated fungi. In the current study, two phosphate transporter genes, RlPT and LbPT, were isolated from Rhizopogon luteolus and Leucocortinarius bulbiger, respectively, two ectomycorrhizal fungi forming symbiotic interactions with the P. tabulaeformis. Phylogenetic analysis suggested that the sequence of the phosphate transporter of L. bulbiger is most closely related to a phosphate transporter of Hebeloma cylindrosporum, whereas the phosphate transporter of R. luteolus is most closely related to that of Piloderma croceum. The subcellular localization indicated that RlPT and LbPT were expressed in the plasma membrane. The complementation assay in yeast indicated that both RlPT and LbPT partially compensated for the absence of phosphate transporter activity in the MB192 yeast strain, with a K m value of 57.90 μmol/L Pi for RlPT and 35.87 μmol/L Pi for LbPT. qPCR analysis revealed that RlPT and LbPT were significantly up-regulated at lower P availability, which may enhance P uptake and transport under Pi starvation. Our results suggest that RlPT and LbPT presumably play a key role in Pi acquisition by P. tabulaeformis via ectomycorrhizal fungi. </div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">27098350</PMID><DateCompleted><Year>2017</Year><Month>02</Month><Day>22</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1432-1890</ISSN><JournalIssue CitedMedium="Internet"><Volume>26</Volume><Issue>7</Issue><PubDate><Year>2016</Year><Month>Oct</Month></PubDate></JournalIssue><Title>Mycorrhiza</Title><ISOAbbreviation>Mycorrhiza</ISOAbbreviation></Journal><ArticleTitle>Molecular cloning and functional analysis of two phosphate transporter genes from Rhizopogon luteolus and Leucocortinarius bulbiger, two ectomycorrhizal fungi of Pinus tabulaeformis.</ArticleTitle><Pagination><MedlinePgn>633-44</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1007/s00572-016-0702-7</ELocationID><Abstract><AbstractText>Inorganic phosphorus (Pi) is essential for plant growth, and phosphate (P) deficiency is a primary limiting factor in Pinus tabulaeformis development in northern China. P acquisition in mycorrhizal plants is highly dependent on the activities of phosphate transporters of their root-associated fungi. In the current study, two phosphate transporter genes, RlPT and LbPT, were isolated from Rhizopogon luteolus and Leucocortinarius bulbiger, respectively, two ectomycorrhizal fungi forming symbiotic interactions with the P. tabulaeformis. Phylogenetic analysis suggested that the sequence of the phosphate transporter of L. bulbiger is most closely related to a phosphate transporter of Hebeloma cylindrosporum, whereas the phosphate transporter of R. luteolus is most closely related to that of Piloderma croceum. The subcellular localization indicated that RlPT and LbPT were expressed in the plasma membrane. The complementation assay in yeast indicated that both RlPT and LbPT partially compensated for the absence of phosphate transporter activity in the MB192 yeast strain, with a K m value of 57.90 μmol/L Pi for RlPT and 35.87 μmol/L Pi for LbPT. qPCR analysis revealed that RlPT and LbPT were significantly up-regulated at lower P availability, which may enhance P uptake and transport under Pi starvation. Our results suggest that RlPT and LbPT presumably play a key role in Pi acquisition by P. tabulaeformis via ectomycorrhizal fungi. </AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Zheng</LastName><ForeName>Rong</ForeName><Initials>R</Initials><AffiliationInfo><Affiliation>College of Forestry, Inner Mongolia Agricultural University, Hohhot, 010019, Inner Mongolia, China.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>College of Life Science and Technology, Inner Mongolia Normal University, Hohhot, 010020, Inner Mongolia, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Wang</LastName><ForeName>Jugang</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>College of Forestry, Inner Mongolia Agricultural University, Hohhot, 010019, Inner Mongolia, China.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>South Subtropical Crops Research Institute, Chinese Academy of Tropical Agricultural Science, Zhanjiang, 524091, Guangdong, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Liu</LastName><ForeName>Min</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>College of Forestry, Inner Mongolia Agricultural University, Hohhot, 010019, Inner Mongolia, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Duan</LastName><ForeName>Guozhen</ForeName><Initials>G</Initials><AffiliationInfo><Affiliation>College of Forestry, Inner Mongolia Agricultural University, Hohhot, 010019, Inner Mongolia, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Gao</LastName><ForeName>Xiaomin</ForeName><Initials>X</Initials><AffiliationInfo><Affiliation>South Subtropical Crops Research Institute, Chinese Academy of Tropical Agricultural Science, Zhanjiang, 524091, Guangdong, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Bai</LastName><ForeName>Shulan</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>College of Forestry, Inner Mongolia Agricultural University, Hohhot, 010019, Inner Mongolia, China. baishulan2004@163.com.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Han</LastName><ForeName>Yachao</ForeName><Initials>Y</Initials><AffiliationInfo><Affiliation>Fuyang Vocational and Technical College, Fuyang, 236031, Anhui, China.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2016</Year><Month>04</Month><Day>21</Day></ArticleDate></Article><MedlineJournalInfo><Country>Germany</Country><MedlineTA>Mycorrhiza</MedlineTA><NlmUniqueID>100955036</NlmUniqueID><ISSNLinking>0940-6360</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D005656">Fungal Proteins</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D001487" MajorTopicYN="N">Basidiomycota</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003001" MajorTopicYN="N">Cloning, Molecular</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005656" MajorTopicYN="N">Fungal Proteins</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015966" MajorTopicYN="N">Gene Expression Regulation, Fungal</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006863" MajorTopicYN="N">Hydrogen-Ion Concentration</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D038821" MajorTopicYN="N">Mycorrhizae</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010802" MajorTopicYN="N">Phylogeny</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D028223" MajorTopicYN="N">Pinus</DescriptorName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D021381" MajorTopicYN="N">Protein Transport</DescriptorName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Ectomycorrhizae</Keyword><Keyword MajorTopicYN="N">Gene expression</Keyword><Keyword MajorTopicYN="N">Heterologous characterization</Keyword><Keyword MajorTopicYN="N">Phosphate transporter</Keyword><Keyword MajorTopicYN="N">Pinus tabulaeformis</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2015</Year><Month>11</Month><Day>01</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2016</Year><Month>04</Month><Day>14</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2016</Year><Month>4</Month><Day>22</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2016</Year><Month>4</Month><Day>22</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate 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|flux= Main
|étape= Corpus
|type= RBID
|clé= pubmed:27098350
|texte= Molecular cloning and functional analysis of two phosphate transporter genes from Rhizopogon luteolus and Leucocortinarius bulbiger, two ectomycorrhizal fungi of Pinus tabulaeformis.
}}
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| NlmPubMed2Wicri -a MycorrhizaeV1
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