Identification of quantitative trait loci affecting ectomycorrhizal symbiosis in an interspecific F₁ poplar cross and differential expression of genes in ectomycorrhizas of the two parents: Populus deltoides and Populus trichocarpa
A Populus deltoides × Populus trichocarpa F₁ pedigree was analyzed for quantitative trait loci (QTLs) affecting ectomycorrhizal development and for microarray characterization of gene networks involved in this symbiosis. A 300 genotype progeny set was evaluated for its ability to form ectomycorrhiza...
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description | A Populus deltoides × Populus trichocarpa F₁ pedigree was analyzed for quantitative trait loci (QTLs) affecting ectomycorrhizal development and for microarray characterization of gene networks involved in this symbiosis. A 300 genotype progeny set was evaluated for its ability to form ectomycorrhiza with the basidiomycete Laccaria bicolor. The percentage of mycorrhizal root tips was determined on the root systems of all 300 progeny and their two parents. QTL analysis identified four significant QTLs, one on the P. deltoides and three on the P. trichocarpa genetic maps. These QTLs were aligned to the P. trichocarpa genome and each contained several megabases and encompass numerous genes. NimbleGen whole-genome microarray, using cDNA from RNA extracts of ectomycorrhizal root tips from the parental genotypes P. trichocarpa and P. deltoides, was used to narrow the candidate gene list. Among the 1,543 differentially expressed genes (p value ≤ 0.05; ≥5.0-fold change in transcript level) having different transcript levels in mycorrhiza of the two parents, 41 transcripts were located in the QTL intervals: 20 in Myc_d1, 14 in Myc_t1, and seven in Myc_t2, while no significant differences among transcripts were found in Myc_t3. Among these 41 transcripts, 25 were overrepresented in P. deltoides relative to P. trichocarpa; 16 were overrepresented in P. trichocarpa. The transcript showing the highest overrepresentation in P. trichocarpa mycorrhiza libraries compared to P. deltoides mycorrhiza codes for an ethylene-sensitive EREBP-4 protein which may repress defense mechanisms in P. trichocarpa while the highest overrepresented transcripts in P. deltoides code for proteins/genes typically associated with pathogen resistance. |
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(ORNL), Oak Ridge, TN (United States)</creatorcontrib><description>A Populus deltoides × Populus trichocarpa F₁ pedigree was analyzed for quantitative trait loci (QTLs) affecting ectomycorrhizal development and for microarray characterization of gene networks involved in this symbiosis. A 300 genotype progeny set was evaluated for its ability to form ectomycorrhiza with the basidiomycete Laccaria bicolor. The percentage of mycorrhizal root tips was determined on the root systems of all 300 progeny and their two parents. QTL analysis identified four significant QTLs, one on the P. deltoides and three on the P. trichocarpa genetic maps. These QTLs were aligned to the P. trichocarpa genome and each contained several megabases and encompass numerous genes. NimbleGen whole-genome microarray, using cDNA from RNA extracts of ectomycorrhizal root tips from the parental genotypes P. trichocarpa and P. deltoides, was used to narrow the candidate gene list. Among the 1,543 differentially expressed genes (p value ≤ 0.05; ≥5.0-fold change in transcript level) having different transcript levels in mycorrhiza of the two parents, 41 transcripts were located in the QTL intervals: 20 in Myc_d1, 14 in Myc_t1, and seven in Myc_t2, while no significant differences among transcripts were found in Myc_t3. Among these 41 transcripts, 25 were overrepresented in P. deltoides relative to P. trichocarpa; 16 were overrepresented in P. trichocarpa. The transcript showing the highest overrepresentation in P. trichocarpa mycorrhiza libraries compared to P. deltoides mycorrhiza codes for an ethylene-sensitive EREBP-4 protein which may repress defense mechanisms in P. trichocarpa while the highest overrepresented transcripts in P. deltoides code for proteins/genes typically associated with pathogen resistance.</description><identifier>ISSN: 1614-2942</identifier><identifier>EISSN: 1614-2950</identifier><identifier>DOI: 10.1007/s11295-010-0361-3</identifier><language>eng</language><publisher>Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag</publisher><subject>60 APPLIED LIFE SCIENCES ; Agricultural sciences ; BASIC BIOLOGICAL SCIENCES ; Biomedical and Life Sciences ; Biotechnology ; complementary DNA ; defense mechanisms ; ectomycorrhizae ; Forestry ; gene expression regulation ; GENES ; GENETICS ; GENOTYPE ; Laccaria bicolor ; Life Sciences ; microarray technology ; MYCORRHIZAS ; Original Paper ; parents ; PATHOGENS ; pedigree ; Plant Breeding/Biotechnology ; Plant Genetics and Genomics ; POPLARS ; Populus balsamifera subsp. trichocarpa ; Populus deltoides ; PROGENY ; PROTEINS ; quantitative analysis ; quantitative trait loci ; Quantitative trait loci . 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(ORNL), Oak Ridge, TN (United States)</creatorcontrib><title>Identification of quantitative trait loci affecting ectomycorrhizal symbiosis in an interspecific F₁ poplar cross and differential expression of genes in ectomycorrhizas of the two parents: Populus deltoides and Populus trichocarpa</title><title>Tree genetics & genomes</title><addtitle>Tree Genetics & Genomes</addtitle><description>A Populus deltoides × Populus trichocarpa F₁ pedigree was analyzed for quantitative trait loci (QTLs) affecting ectomycorrhizal development and for microarray characterization of gene networks involved in this symbiosis. A 300 genotype progeny set was evaluated for its ability to form ectomycorrhiza with the basidiomycete Laccaria bicolor. The percentage of mycorrhizal root tips was determined on the root systems of all 300 progeny and their two parents. QTL analysis identified four significant QTLs, one on the P. deltoides and three on the P. trichocarpa genetic maps. These QTLs were aligned to the P. trichocarpa genome and each contained several megabases and encompass numerous genes. NimbleGen whole-genome microarray, using cDNA from RNA extracts of ectomycorrhizal root tips from the parental genotypes P. trichocarpa and P. deltoides, was used to narrow the candidate gene list. Among the 1,543 differentially expressed genes (p value ≤ 0.05; ≥5.0-fold change in transcript level) having different transcript levels in mycorrhiza of the two parents, 41 transcripts were located in the QTL intervals: 20 in Myc_d1, 14 in Myc_t1, and seven in Myc_t2, while no significant differences among transcripts were found in Myc_t3. Among these 41 transcripts, 25 were overrepresented in P. deltoides relative to P. trichocarpa; 16 were overrepresented in P. trichocarpa. The transcript showing the highest overrepresentation in P. trichocarpa mycorrhiza libraries compared to P. deltoides mycorrhiza codes for an ethylene-sensitive EREBP-4 protein which may repress defense mechanisms in P. trichocarpa while the highest overrepresented transcripts in P. deltoides code for proteins/genes typically associated with pathogen resistance.</description><subject>60 APPLIED LIFE SCIENCES</subject><subject>Agricultural sciences</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>complementary DNA</subject><subject>defense mechanisms</subject><subject>ectomycorrhizae</subject><subject>Forestry</subject><subject>gene expression regulation</subject><subject>GENES</subject><subject>GENETICS</subject><subject>GENOTYPE</subject><subject>Laccaria bicolor</subject><subject>Life Sciences</subject><subject>microarray technology</subject><subject>MYCORRHIZAS</subject><subject>Original Paper</subject><subject>parents</subject><subject>PATHOGENS</subject><subject>pedigree</subject><subject>Plant Breeding/Biotechnology</subject><subject>Plant Genetics and Genomics</subject><subject>POPLARS</subject><subject>Populus balsamifera subsp. trichocarpa</subject><subject>Populus deltoides</subject><subject>PROGENY</subject><subject>PROTEINS</subject><subject>quantitative analysis</subject><subject>quantitative trait loci</subject><subject>Quantitative trait loci . Poplar . Symbiosis</subject><subject>RNA</subject><subject>root systems</subject><subject>root tips</subject><subject>Silviculture, forestry</subject><subject>SYMBIOSIS</subject><subject>Tree Biology</subject><issn>1614-2942</issn><issn>1614-2950</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9UcFu1DAUjBBIlMIHcMLixiHwnu3Eu9yqitJKK4EEPVuO7WxcZe1ge1uWG3wqN_4CpymVuPTiZ49n5j17quolwlsEEO8SIl03NSDUwFqs2aPqCFvkdUHh8f2e06fVs5SuALiAtj2q_lwY67PrnVbZBU9CT77tVUFyOV9bkqNymYxBO6L63urs_JaUEnYHHWIc3A81knTYdS4kl4jzRPmyZhvTZPXsS85-__pJpjCNKhIdQ0qFYohxxS7OvYuB_T5Fm9LdAFvr7a3V_33SfJeHMtNNIJOatek9-Rym_bhPxNgxB2fs4v4PzdHpIWgVJ_W8etKrMdkXd_W4ujz78PX0vN58-nhxerKpNUPK6gZWtNNci7VpOdWis0rjGlE0jCOq1ghD7YoaITQy1YHpWG845U0LnQW7YsfV68U3pOxk0i5bPejgfXmNRKCMMSikNwtpUKOcotupeJBBOXl-spEzBrRtKF2LayxcXLi3nxdtfy9AkHP4cglflvDlHL5kRUMXTSpcv7VRXoV99OXdD4peLaJeBam20SV5-YUCcgBgTDTwIAPbBpH9BcyGy38</recordid><startdate>2011</startdate><enddate>2011</enddate><creator>Labbé, Jessy</creator><creator>Jorge, Véronique</creator><creator>Kohler, Annegret</creator><creator>Vion, Patrice</creator><creator>Marçais, Benoît</creator><creator>Bastien, Catherine</creator><creator>Tuskan, Gerald A</creator><creator>Martin, Francis</creator><creator>Le Tacon, François</creator><general>Berlin/Heidelberg : Springer-Verlag</general><general>Springer-Verlag</general><general>Springer Verlag</general><scope>FBQ</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope><scope>OTOTI</scope><orcidid>https://orcid.org/0000-0002-9575-9567</orcidid><orcidid>https://orcid.org/0000-0002-5016-3006</orcidid><orcidid>https://orcid.org/0000-0002-4737-3715</orcidid><orcidid>https://orcid.org/0000-0002-8107-644X</orcidid></search><sort><creationdate>2011</creationdate><title>Identification of quantitative trait loci affecting ectomycorrhizal symbiosis in an interspecific F₁ poplar cross and differential expression of genes in ectomycorrhizas of the two parents: Populus deltoides and Populus trichocarpa</title><author>Labbé, Jessy ; Jorge, Véronique ; Kohler, Annegret ; Vion, Patrice ; Marçais, Benoît ; Bastien, Catherine ; Tuskan, Gerald A ; Martin, Francis ; Le Tacon, François</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3123-5082bc4c79d642c7beac1911753411a6d7d2e82d77c13ab0db3fd424560be0e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>60 APPLIED LIFE SCIENCES</topic><topic>Agricultural sciences</topic><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>complementary DNA</topic><topic>defense mechanisms</topic><topic>ectomycorrhizae</topic><topic>Forestry</topic><topic>gene expression regulation</topic><topic>GENES</topic><topic>GENETICS</topic><topic>GENOTYPE</topic><topic>Laccaria bicolor</topic><topic>Life Sciences</topic><topic>microarray technology</topic><topic>MYCORRHIZAS</topic><topic>Original Paper</topic><topic>parents</topic><topic>PATHOGENS</topic><topic>pedigree</topic><topic>Plant Breeding/Biotechnology</topic><topic>Plant Genetics and Genomics</topic><topic>POPLARS</topic><topic>Populus balsamifera subsp. trichocarpa</topic><topic>Populus deltoides</topic><topic>PROGENY</topic><topic>PROTEINS</topic><topic>quantitative analysis</topic><topic>quantitative trait loci</topic><topic>Quantitative trait loci . Poplar . Symbiosis</topic><topic>RNA</topic><topic>root systems</topic><topic>root tips</topic><topic>Silviculture, forestry</topic><topic>SYMBIOSIS</topic><topic>Tree Biology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Labbé, Jessy</creatorcontrib><creatorcontrib>Jorge, Véronique</creatorcontrib><creatorcontrib>Kohler, Annegret</creatorcontrib><creatorcontrib>Vion, Patrice</creatorcontrib><creatorcontrib>Marçais, Benoît</creatorcontrib><creatorcontrib>Bastien, Catherine</creatorcontrib><creatorcontrib>Tuskan, Gerald A</creatorcontrib><creatorcontrib>Martin, Francis</creatorcontrib><creatorcontrib>Le Tacon, François</creatorcontrib><creatorcontrib>Oak Ridge National Lab. 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(ORNL), Oak Ridge, TN (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of quantitative trait loci affecting ectomycorrhizal symbiosis in an interspecific F₁ poplar cross and differential expression of genes in ectomycorrhizas of the two parents: Populus deltoides and Populus trichocarpa</atitle><jtitle>Tree genetics & genomes</jtitle><stitle>Tree Genetics & Genomes</stitle><date>2011</date><risdate>2011</risdate><volume>7</volume><issue>3</issue><spage>617</spage><epage>627</epage><pages>617-627</pages><issn>1614-2942</issn><eissn>1614-2950</eissn><abstract>A Populus deltoides × Populus trichocarpa F₁ pedigree was analyzed for quantitative trait loci (QTLs) affecting ectomycorrhizal development and for microarray characterization of gene networks involved in this symbiosis. A 300 genotype progeny set was evaluated for its ability to form ectomycorrhiza with the basidiomycete Laccaria bicolor. The percentage of mycorrhizal root tips was determined on the root systems of all 300 progeny and their two parents. QTL analysis identified four significant QTLs, one on the P. deltoides and three on the P. trichocarpa genetic maps. These QTLs were aligned to the P. trichocarpa genome and each contained several megabases and encompass numerous genes. NimbleGen whole-genome microarray, using cDNA from RNA extracts of ectomycorrhizal root tips from the parental genotypes P. trichocarpa and P. deltoides, was used to narrow the candidate gene list. Among the 1,543 differentially expressed genes (p value ≤ 0.05; ≥5.0-fold change in transcript level) having different transcript levels in mycorrhiza of the two parents, 41 transcripts were located in the QTL intervals: 20 in Myc_d1, 14 in Myc_t1, and seven in Myc_t2, while no significant differences among transcripts were found in Myc_t3. Among these 41 transcripts, 25 were overrepresented in P. deltoides relative to P. trichocarpa; 16 were overrepresented in P. trichocarpa. The transcript showing the highest overrepresentation in P. trichocarpa mycorrhiza libraries compared to P. deltoides mycorrhiza codes for an ethylene-sensitive EREBP-4 protein which may repress defense mechanisms in P. trichocarpa while the highest overrepresented transcripts in P. deltoides code for proteins/genes typically associated with pathogen resistance.</abstract><cop>Berlin/Heidelberg</cop><pub>Berlin/Heidelberg : Springer-Verlag</pub><doi>10.1007/s11295-010-0361-3</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-9575-9567</orcidid><orcidid>https://orcid.org/0000-0002-5016-3006</orcidid><orcidid>https://orcid.org/0000-0002-4737-3715</orcidid><orcidid>https://orcid.org/0000-0002-8107-644X</orcidid></addata></record> |
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subjects | 60 APPLIED LIFE SCIENCES Agricultural sciences BASIC BIOLOGICAL SCIENCES Biomedical and Life Sciences Biotechnology complementary DNA defense mechanisms ectomycorrhizae Forestry gene expression regulation GENES GENETICS GENOTYPE Laccaria bicolor Life Sciences microarray technology MYCORRHIZAS Original Paper parents PATHOGENS pedigree Plant Breeding/Biotechnology Plant Genetics and Genomics POPLARS Populus balsamifera subsp. trichocarpa Populus deltoides PROGENY PROTEINS quantitative analysis quantitative trait loci Quantitative trait loci . Poplar . Symbiosis RNA root systems root tips Silviculture, forestry SYMBIOSIS Tree Biology |
title | Identification of quantitative trait loci affecting ectomycorrhizal symbiosis in an interspecific F₁ poplar cross and differential expression of genes in ectomycorrhizas of the two parents: Populus deltoides and Populus trichocarpa |
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