Pyramided QTL underlying tolerance to Phytophthora root rot in mega-environments from soybean cultivars ‘Conrad' and ‘Hefeng 25'

Phytophthora root rot (PRR) of soybean (Glycine max (L.) Merr.) is the second most important cause of yield loss by disease in North America, surpassed only by soybean cyst nematode (Wrather et al. in Can J Plant Pathol 23:115-121, 2001). Tolerance can provide economically useful disease control, co...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Theoretical and applied genetics 2010-08, Vol.121 (4), p.651-658
Hauptverfasser: Li, Xiuping, Han, Yingpeng, Teng, Weili, Zhang, Shuzheng, Yu, Kangfu, Poysa, Vaino, Anderson, Terry, Ding, Junjie, Li, Wenbin
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 658
container_issue 4
container_start_page 651
container_title Theoretical and applied genetics
container_volume 121
creator Li, Xiuping
Han, Yingpeng
Teng, Weili
Zhang, Shuzheng
Yu, Kangfu
Poysa, Vaino
Anderson, Terry
Ding, Junjie
Li, Wenbin
description Phytophthora root rot (PRR) of soybean (Glycine max (L.) Merr.) is the second most important cause of yield loss by disease in North America, surpassed only by soybean cyst nematode (Wrather et al. in Can J Plant Pathol 23:115-121, 2001). Tolerance can provide economically useful disease control, conditioning partial resistance of soybean to PRR. The aims of this study were to identify new quantitative trait loci (QTL) underlying tolerance to PRR, and to evaluate the effects of pyramided or stacked loci on the level of tolerance. A North American cultivar ‘Conrad' (tolerant to PRR) was crossed with a northeastern China cultivar ‘Hefeng 25' (tolerant to PRR). Through single-seed descent, 140 F₂:₅ and F₂:₆ recombinant inbred lines were advanced. A total of 164 simple sequence repeat (SSR) markers were used to construct a genetic linkage map. The percentage of seedling death was measured over 2 years (2007 and 2008) in the field at four naturally infested locations in Canada and China following additional soil infestation and in the greenhouse following inoculation with Phytophthora sojae isolate. A total of eight QTL underlying tolerance to PRR were identified, located in five linkage groups (F, D1b+w, A2, B1, and C2). The phenotypic variation contributed by the loci ranged from 4.24 to 27.98%. QPRR-1 (anchored in the interval of SSR markers Satt325 and Satt343 of LG F), QPRR-2 (anchored in the interval of Satt005 and Satt600 of LG D1b+w), and QPRR-3 (anchored in the interval of Satt579 and Sat_089 of LG D1b+w) derived their beneficial allele from ‘Conrad'. They were located at chromosomal locations known to underlie PRR tolerance in diverse germplasm. Five QTL that derived beneficial alleles from ‘Hefeng 25' were identified. The QTL (QPRR-1 to QPRR-7) that were detected across at least three environments were selected for loci stacking and to analyze the relationship between number of tolerance loci and disease loss percentage. The accumulation of tolerance loci was positively correlated with decreases in disease loss percentage. The pyramid of loci underlying tolerance to PRR provided germplasm useful for crop improvement by marker-assisted selection and may provide durable cultivar tolerance against the PRR disease.
doi_str_mv 10.1007/s00122-010-1337-2
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_902364857</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A361351484</galeid><sourcerecordid>A361351484</sourcerecordid><originalsourceid>FETCH-LOGICAL-c623t-774b34fa9dc1c00d3dc10ac3155b683482c19320f0b98a7db488c15b04fb2c283</originalsourceid><addsrcrecordid>eNqFkt-K1DAUxoso7rj6AN5oUGTwouvJv2l7uQzqLgy4urvXIU3TTpc2GZN0sXde-BA-n09iSkeXEVECyUny-75wwpckTzGcYIDsjQfAhKSAIcWUZim5lywwoyQlhJH7yQKAQcozTo6SR97fAADhQB8mRwRoAYSxRfLtYnSybytdoY9XGzSYSrtubE2Dgu20k0bpWKGL7Rjsbhu21knkrA1xCqg1qNeNTLW5bZ01vTbBo9rZHnk7lloapIYutLfSefTj6_e1NU5WSyRNNW3PdK3jO4QvHycPatl5_WS_HifX795erc_SzYf35-vTTapWhIY0y1hJWS2LSmEFUNG4glQUc16ucspyonBBCdRQFrnMqpLlucK8BFaXRJGcHifL2Xfn7OdB-yD61ivdddJoO3gR_4SuWM6z_5IZm1jMJ88Xf5A3dnAmtiGyVc7ygrHJ7uUMNbLTojW1DU6qyVKc0hWmHLOcRerkL1Qcle5bZY2u23h-IHh9IIhM0F9CIwfvxfnlp0MWz6xy1nuna7FzbS_dKDCIKU1iTpOAaR_TJEjUPNv3NpS9rn4rfsUnAq_2gPRKdvWUl9bfcRQyzIupfzJzPl6ZRru7T_rX689nUS2tkI2LxteXBDAFnGcUx-InXV7pQg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>768489447</pqid></control><display><type>article</type><title>Pyramided QTL underlying tolerance to Phytophthora root rot in mega-environments from soybean cultivars ‘Conrad' and ‘Hefeng 25'</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Li, Xiuping ; Han, Yingpeng ; Teng, Weili ; Zhang, Shuzheng ; Yu, Kangfu ; Poysa, Vaino ; Anderson, Terry ; Ding, Junjie ; Li, Wenbin</creator><creatorcontrib>Li, Xiuping ; Han, Yingpeng ; Teng, Weili ; Zhang, Shuzheng ; Yu, Kangfu ; Poysa, Vaino ; Anderson, Terry ; Ding, Junjie ; Li, Wenbin</creatorcontrib><description>Phytophthora root rot (PRR) of soybean (Glycine max (L.) Merr.) is the second most important cause of yield loss by disease in North America, surpassed only by soybean cyst nematode (Wrather et al. in Can J Plant Pathol 23:115-121, 2001). Tolerance can provide economically useful disease control, conditioning partial resistance of soybean to PRR. The aims of this study were to identify new quantitative trait loci (QTL) underlying tolerance to PRR, and to evaluate the effects of pyramided or stacked loci on the level of tolerance. A North American cultivar ‘Conrad' (tolerant to PRR) was crossed with a northeastern China cultivar ‘Hefeng 25' (tolerant to PRR). Through single-seed descent, 140 F₂:₅ and F₂:₆ recombinant inbred lines were advanced. A total of 164 simple sequence repeat (SSR) markers were used to construct a genetic linkage map. The percentage of seedling death was measured over 2 years (2007 and 2008) in the field at four naturally infested locations in Canada and China following additional soil infestation and in the greenhouse following inoculation with Phytophthora sojae isolate. A total of eight QTL underlying tolerance to PRR were identified, located in five linkage groups (F, D1b+w, A2, B1, and C2). The phenotypic variation contributed by the loci ranged from 4.24 to 27.98%. QPRR-1 (anchored in the interval of SSR markers Satt325 and Satt343 of LG F), QPRR-2 (anchored in the interval of Satt005 and Satt600 of LG D1b+w), and QPRR-3 (anchored in the interval of Satt579 and Sat_089 of LG D1b+w) derived their beneficial allele from ‘Conrad'. They were located at chromosomal locations known to underlie PRR tolerance in diverse germplasm. Five QTL that derived beneficial alleles from ‘Hefeng 25' were identified. The QTL (QPRR-1 to QPRR-7) that were detected across at least three environments were selected for loci stacking and to analyze the relationship between number of tolerance loci and disease loss percentage. The accumulation of tolerance loci was positively correlated with decreases in disease loss percentage. The pyramid of loci underlying tolerance to PRR provided germplasm useful for crop improvement by marker-assisted selection and may provide durable cultivar tolerance against the PRR disease.</description><identifier>ISSN: 0040-5752</identifier><identifier>EISSN: 1432-2242</identifier><identifier>DOI: 10.1007/s00122-010-1337-2</identifier><identifier>PMID: 20390244</identifier><identifier>CODEN: THAGA6</identifier><language>eng</language><publisher>Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag</publisher><subject>Adaptation, Physiological - genetics ; Agriculture ; Alleles ; Atmospheric carbon dioxide ; Biochemistry ; Biological and medical sciences ; Biomedical and Life Sciences ; Biotechnology ; Chromosomes ; Classical genetics, quantitative genetics, hybrids ; Cultivars ; Environment ; Fundamental and applied biological sciences. Psychology ; Genes ; Genetic Linkage ; Genetics of eukaryotes. Biological and molecular evolution ; Germplasm ; Glycine max ; Glycine max - genetics ; Glycine max - microbiology ; Inbreeding ; Life Sciences ; Nematoda ; Original Paper ; Pathogens ; Phenotype ; Phytophthora - physiology ; Phytophthora sojae ; Plant Biochemistry ; Plant Breeding/Biotechnology ; Plant Diseases - genetics ; Plant Diseases - microbiology ; Plant Genetics and Genomics ; Plant Roots - genetics ; Plant Roots - microbiology ; Pteridophyta, spermatophyta ; Quantitative trait loci ; Quantitative Trait Loci - genetics ; Soybean ; Soybeans ; Vegetals</subject><ispartof>Theoretical and applied genetics, 2010-08, Vol.121 (4), p.651-658</ispartof><rights>Springer-Verlag 2010</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2010 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c623t-774b34fa9dc1c00d3dc10ac3155b683482c19320f0b98a7db488c15b04fb2c283</citedby><cites>FETCH-LOGICAL-c623t-774b34fa9dc1c00d3dc10ac3155b683482c19320f0b98a7db488c15b04fb2c283</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00122-010-1337-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00122-010-1337-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=23071597$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20390244$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Xiuping</creatorcontrib><creatorcontrib>Han, Yingpeng</creatorcontrib><creatorcontrib>Teng, Weili</creatorcontrib><creatorcontrib>Zhang, Shuzheng</creatorcontrib><creatorcontrib>Yu, Kangfu</creatorcontrib><creatorcontrib>Poysa, Vaino</creatorcontrib><creatorcontrib>Anderson, Terry</creatorcontrib><creatorcontrib>Ding, Junjie</creatorcontrib><creatorcontrib>Li, Wenbin</creatorcontrib><title>Pyramided QTL underlying tolerance to Phytophthora root rot in mega-environments from soybean cultivars ‘Conrad' and ‘Hefeng 25'</title><title>Theoretical and applied genetics</title><addtitle>Theor Appl Genet</addtitle><addtitle>Theor Appl Genet</addtitle><description>Phytophthora root rot (PRR) of soybean (Glycine max (L.) Merr.) is the second most important cause of yield loss by disease in North America, surpassed only by soybean cyst nematode (Wrather et al. in Can J Plant Pathol 23:115-121, 2001). Tolerance can provide economically useful disease control, conditioning partial resistance of soybean to PRR. The aims of this study were to identify new quantitative trait loci (QTL) underlying tolerance to PRR, and to evaluate the effects of pyramided or stacked loci on the level of tolerance. A North American cultivar ‘Conrad' (tolerant to PRR) was crossed with a northeastern China cultivar ‘Hefeng 25' (tolerant to PRR). Through single-seed descent, 140 F₂:₅ and F₂:₆ recombinant inbred lines were advanced. A total of 164 simple sequence repeat (SSR) markers were used to construct a genetic linkage map. The percentage of seedling death was measured over 2 years (2007 and 2008) in the field at four naturally infested locations in Canada and China following additional soil infestation and in the greenhouse following inoculation with Phytophthora sojae isolate. A total of eight QTL underlying tolerance to PRR were identified, located in five linkage groups (F, D1b+w, A2, B1, and C2). The phenotypic variation contributed by the loci ranged from 4.24 to 27.98%. QPRR-1 (anchored in the interval of SSR markers Satt325 and Satt343 of LG F), QPRR-2 (anchored in the interval of Satt005 and Satt600 of LG D1b+w), and QPRR-3 (anchored in the interval of Satt579 and Sat_089 of LG D1b+w) derived their beneficial allele from ‘Conrad'. They were located at chromosomal locations known to underlie PRR tolerance in diverse germplasm. Five QTL that derived beneficial alleles from ‘Hefeng 25' were identified. The QTL (QPRR-1 to QPRR-7) that were detected across at least three environments were selected for loci stacking and to analyze the relationship between number of tolerance loci and disease loss percentage. The accumulation of tolerance loci was positively correlated with decreases in disease loss percentage. The pyramid of loci underlying tolerance to PRR provided germplasm useful for crop improvement by marker-assisted selection and may provide durable cultivar tolerance against the PRR disease.</description><subject>Adaptation, Physiological - genetics</subject><subject>Agriculture</subject><subject>Alleles</subject><subject>Atmospheric carbon dioxide</subject><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Chromosomes</subject><subject>Classical genetics, quantitative genetics, hybrids</subject><subject>Cultivars</subject><subject>Environment</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes</subject><subject>Genetic Linkage</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>Germplasm</subject><subject>Glycine max</subject><subject>Glycine max - genetics</subject><subject>Glycine max - microbiology</subject><subject>Inbreeding</subject><subject>Life Sciences</subject><subject>Nematoda</subject><subject>Original Paper</subject><subject>Pathogens</subject><subject>Phenotype</subject><subject>Phytophthora - physiology</subject><subject>Phytophthora sojae</subject><subject>Plant Biochemistry</subject><subject>Plant Breeding/Biotechnology</subject><subject>Plant Diseases - genetics</subject><subject>Plant Diseases - microbiology</subject><subject>Plant Genetics and Genomics</subject><subject>Plant Roots - genetics</subject><subject>Plant Roots - microbiology</subject><subject>Pteridophyta, spermatophyta</subject><subject>Quantitative trait loci</subject><subject>Quantitative Trait Loci - genetics</subject><subject>Soybean</subject><subject>Soybeans</subject><subject>Vegetals</subject><issn>0040-5752</issn><issn>1432-2242</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkt-K1DAUxoso7rj6AN5oUGTwouvJv2l7uQzqLgy4urvXIU3TTpc2GZN0sXde-BA-n09iSkeXEVECyUny-75wwpckTzGcYIDsjQfAhKSAIcWUZim5lywwoyQlhJH7yQKAQcozTo6SR97fAADhQB8mRwRoAYSxRfLtYnSybytdoY9XGzSYSrtubE2Dgu20k0bpWKGL7Rjsbhu21knkrA1xCqg1qNeNTLW5bZ01vTbBo9rZHnk7lloapIYutLfSefTj6_e1NU5WSyRNNW3PdK3jO4QvHycPatl5_WS_HifX795erc_SzYf35-vTTapWhIY0y1hJWS2LSmEFUNG4glQUc16ucspyonBBCdRQFrnMqpLlucK8BFaXRJGcHifL2Xfn7OdB-yD61ivdddJoO3gR_4SuWM6z_5IZm1jMJ88Xf5A3dnAmtiGyVc7ygrHJ7uUMNbLTojW1DU6qyVKc0hWmHLOcRerkL1Qcle5bZY2u23h-IHh9IIhM0F9CIwfvxfnlp0MWz6xy1nuna7FzbS_dKDCIKU1iTpOAaR_TJEjUPNv3NpS9rn4rfsUnAq_2gPRKdvWUl9bfcRQyzIupfzJzPl6ZRru7T_rX689nUS2tkI2LxteXBDAFnGcUx-InXV7pQg</recordid><startdate>20100801</startdate><enddate>20100801</enddate><creator>Li, Xiuping</creator><creator>Han, Yingpeng</creator><creator>Teng, Weili</creator><creator>Zhang, Shuzheng</creator><creator>Yu, Kangfu</creator><creator>Poysa, Vaino</creator><creator>Anderson, Terry</creator><creator>Ding, Junjie</creator><creator>Li, Wenbin</creator><general>Berlin/Heidelberg : Springer-Verlag</general><general>Springer-Verlag</general><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7SS</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20100801</creationdate><title>Pyramided QTL underlying tolerance to Phytophthora root rot in mega-environments from soybean cultivars ‘Conrad' and ‘Hefeng 25'</title><author>Li, Xiuping ; Han, Yingpeng ; Teng, Weili ; Zhang, Shuzheng ; Yu, Kangfu ; Poysa, Vaino ; Anderson, Terry ; Ding, Junjie ; Li, Wenbin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c623t-774b34fa9dc1c00d3dc10ac3155b683482c19320f0b98a7db488c15b04fb2c283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adaptation, Physiological - genetics</topic><topic>Agriculture</topic><topic>Alleles</topic><topic>Atmospheric carbon dioxide</topic><topic>Biochemistry</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Chromosomes</topic><topic>Classical genetics, quantitative genetics, hybrids</topic><topic>Cultivars</topic><topic>Environment</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes</topic><topic>Genetic Linkage</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Germplasm</topic><topic>Glycine max</topic><topic>Glycine max - genetics</topic><topic>Glycine max - microbiology</topic><topic>Inbreeding</topic><topic>Life Sciences</topic><topic>Nematoda</topic><topic>Original Paper</topic><topic>Pathogens</topic><topic>Phenotype</topic><topic>Phytophthora - physiology</topic><topic>Phytophthora sojae</topic><topic>Plant Biochemistry</topic><topic>Plant Breeding/Biotechnology</topic><topic>Plant Diseases - genetics</topic><topic>Plant Diseases - microbiology</topic><topic>Plant Genetics and Genomics</topic><topic>Plant Roots - genetics</topic><topic>Plant Roots - microbiology</topic><topic>Pteridophyta, spermatophyta</topic><topic>Quantitative trait loci</topic><topic>Quantitative Trait Loci - genetics</topic><topic>Soybean</topic><topic>Soybeans</topic><topic>Vegetals</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Xiuping</creatorcontrib><creatorcontrib>Han, Yingpeng</creatorcontrib><creatorcontrib>Teng, Weili</creatorcontrib><creatorcontrib>Zhang, Shuzheng</creatorcontrib><creatorcontrib>Yu, Kangfu</creatorcontrib><creatorcontrib>Poysa, Vaino</creatorcontrib><creatorcontrib>Anderson, Terry</creatorcontrib><creatorcontrib>Ding, Junjie</creatorcontrib><creatorcontrib>Li, Wenbin</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Theoretical and applied genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Xiuping</au><au>Han, Yingpeng</au><au>Teng, Weili</au><au>Zhang, Shuzheng</au><au>Yu, Kangfu</au><au>Poysa, Vaino</au><au>Anderson, Terry</au><au>Ding, Junjie</au><au>Li, Wenbin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pyramided QTL underlying tolerance to Phytophthora root rot in mega-environments from soybean cultivars ‘Conrad' and ‘Hefeng 25'</atitle><jtitle>Theoretical and applied genetics</jtitle><stitle>Theor Appl Genet</stitle><addtitle>Theor Appl Genet</addtitle><date>2010-08-01</date><risdate>2010</risdate><volume>121</volume><issue>4</issue><spage>651</spage><epage>658</epage><pages>651-658</pages><issn>0040-5752</issn><eissn>1432-2242</eissn><coden>THAGA6</coden><abstract>Phytophthora root rot (PRR) of soybean (Glycine max (L.) Merr.) is the second most important cause of yield loss by disease in North America, surpassed only by soybean cyst nematode (Wrather et al. in Can J Plant Pathol 23:115-121, 2001). Tolerance can provide economically useful disease control, conditioning partial resistance of soybean to PRR. The aims of this study were to identify new quantitative trait loci (QTL) underlying tolerance to PRR, and to evaluate the effects of pyramided or stacked loci on the level of tolerance. A North American cultivar ‘Conrad' (tolerant to PRR) was crossed with a northeastern China cultivar ‘Hefeng 25' (tolerant to PRR). Through single-seed descent, 140 F₂:₅ and F₂:₆ recombinant inbred lines were advanced. A total of 164 simple sequence repeat (SSR) markers were used to construct a genetic linkage map. The percentage of seedling death was measured over 2 years (2007 and 2008) in the field at four naturally infested locations in Canada and China following additional soil infestation and in the greenhouse following inoculation with Phytophthora sojae isolate. A total of eight QTL underlying tolerance to PRR were identified, located in five linkage groups (F, D1b+w, A2, B1, and C2). The phenotypic variation contributed by the loci ranged from 4.24 to 27.98%. QPRR-1 (anchored in the interval of SSR markers Satt325 and Satt343 of LG F), QPRR-2 (anchored in the interval of Satt005 and Satt600 of LG D1b+w), and QPRR-3 (anchored in the interval of Satt579 and Sat_089 of LG D1b+w) derived their beneficial allele from ‘Conrad'. They were located at chromosomal locations known to underlie PRR tolerance in diverse germplasm. Five QTL that derived beneficial alleles from ‘Hefeng 25' were identified. The QTL (QPRR-1 to QPRR-7) that were detected across at least three environments were selected for loci stacking and to analyze the relationship between number of tolerance loci and disease loss percentage. The accumulation of tolerance loci was positively correlated with decreases in disease loss percentage. The pyramid of loci underlying tolerance to PRR provided germplasm useful for crop improvement by marker-assisted selection and may provide durable cultivar tolerance against the PRR disease.</abstract><cop>Berlin/Heidelberg</cop><pub>Berlin/Heidelberg : Springer-Verlag</pub><pmid>20390244</pmid><doi>10.1007/s00122-010-1337-2</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0040-5752
ispartof Theoretical and applied genetics, 2010-08, Vol.121 (4), p.651-658
issn 0040-5752
1432-2242
language eng
recordid cdi_proquest_miscellaneous_902364857
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Adaptation, Physiological - genetics
Agriculture
Alleles
Atmospheric carbon dioxide
Biochemistry
Biological and medical sciences
Biomedical and Life Sciences
Biotechnology
Chromosomes
Classical genetics, quantitative genetics, hybrids
Cultivars
Environment
Fundamental and applied biological sciences. Psychology
Genes
Genetic Linkage
Genetics of eukaryotes. Biological and molecular evolution
Germplasm
Glycine max
Glycine max - genetics
Glycine max - microbiology
Inbreeding
Life Sciences
Nematoda
Original Paper
Pathogens
Phenotype
Phytophthora - physiology
Phytophthora sojae
Plant Biochemistry
Plant Breeding/Biotechnology
Plant Diseases - genetics
Plant Diseases - microbiology
Plant Genetics and Genomics
Plant Roots - genetics
Plant Roots - microbiology
Pteridophyta, spermatophyta
Quantitative trait loci
Quantitative Trait Loci - genetics
Soybean
Soybeans
Vegetals
title Pyramided QTL underlying tolerance to Phytophthora root rot in mega-environments from soybean cultivars ‘Conrad' and ‘Hefeng 25'
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T00%3A48%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pyramided%20QTL%20underlying%20tolerance%20to%20Phytophthora%20root%20rot%20in%20mega-environments%20from%20soybean%20cultivars%20%E2%80%98Conrad'%20and%20%E2%80%98Hefeng%2025'&rft.jtitle=Theoretical%20and%20applied%20genetics&rft.au=Li,%20Xiuping&rft.date=2010-08-01&rft.volume=121&rft.issue=4&rft.spage=651&rft.epage=658&rft.pages=651-658&rft.issn=0040-5752&rft.eissn=1432-2242&rft.coden=THAGA6&rft_id=info:doi/10.1007/s00122-010-1337-2&rft_dat=%3Cgale_proqu%3EA361351484%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=768489447&rft_id=info:pmid/20390244&rft_galeid=A361351484&rfr_iscdi=true