Potato expressed sequence tag generation and analysis using standard and unique cDNA libraries
To help develop an understanding of the genes that govern the developmental characteristics of the potato (Solanum tuberosum), as well as the genes associated with responses to specified pathogens and storage conditions, The Canadian Potato Genome Project (CPGP) carried out 5' end sequencing of...
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Veröffentlicht in: | Plant molecular biology 2005-10, Vol.59 (3), p.407-433 |
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description | To help develop an understanding of the genes that govern the developmental characteristics of the potato (Solanum tuberosum), as well as the genes associated with responses to specified pathogens and storage conditions, The Canadian Potato Genome Project (CPGP) carried out 5' end sequencing of regular, normalized and full-length cDNA libraries of the Shepody potato cultivar, generating over 66,600 expressed sequence tags (ESTs). Libraries sequenced represented tuber developmental stages, pathogen-challenged tubers, as well as leaf, floral developmental stages, suspension cultured cells and roots. All libraries analysed to date have contributed unique sequences, with the normalized libraries high on the list. In addition, a low molecular weight library has enhanced the 3' ends of our sequence assemblies. Using the combined assembly dataset, unique tuber developmental, cold storage and pathogen-challenged sequences have been identified. A comparison of the ESTs specific to the pathogen-challenged tuber and foliar libraries revealed minimal overlap between these libraries. Mixed assemblies using over 189,000 potato EST sequences from CPGP and The Institute for Genomics Research (TIGR) has revealed common sequences, as well as CPGP- and TIGR-unique sequences. |
doi_str_mv | 10.1007/s11103-005-0185-y |
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Libraries sequenced represented tuber developmental stages, pathogen-challenged tubers, as well as leaf, floral developmental stages, suspension cultured cells and roots. All libraries analysed to date have contributed unique sequences, with the normalized libraries high on the list. In addition, a low molecular weight library has enhanced the 3' ends of our sequence assemblies. Using the combined assembly dataset, unique tuber developmental, cold storage and pathogen-challenged sequences have been identified. A comparison of the ESTs specific to the pathogen-challenged tuber and foliar libraries revealed minimal overlap between these libraries. Mixed assemblies using over 189,000 potato EST sequences from CPGP and The Institute for Genomics Research (TIGR) has revealed common sequences, as well as CPGP- and TIGR-unique sequences.</description><identifier>ISSN: 0167-4412</identifier><identifier>EISSN: 1573-5028</identifier><identifier>DOI: 10.1007/s11103-005-0185-y</identifier><identifier>PMID: 16235108</identifier><language>eng</language><publisher>Netherlands: Springer Nature B.V</publisher><subject>bacterial diseases of plants ; blight ; cDNA libraries ; cold storage ; common scab ; Cultivars ; Developmental stages ; disease resistance ; DNA, Complementary - chemistry ; DNA, Complementary - genetics ; Expressed Sequence Tags ; fungal diseases of plants ; Gene Expression Regulation, Developmental ; Gene Expression Regulation, Plant ; Gene Library ; genomic libraries ; Genomics ; Genomics - methods ; Libraries ; Molecular weight ; Pathogens ; Phytophthora infestans ; plant development ; Potatoes ; Sequence Analysis, DNA ; Solanum tuberosum ; Solanum tuberosum - genetics ; Solanum tuberosum - growth & development ; Streptomyces scabiei ; tuber development ; tubers ; Vegetables</subject><ispartof>Plant molecular biology, 2005-10, Vol.59 (3), p.407-433</ispartof><rights>Springer 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c447t-fb989914ecbb5c56e68790711dacdf68701bbf2d1fb453901a2187fa45a47e2f3</citedby><cites>FETCH-LOGICAL-c447t-fb989914ecbb5c56e68790711dacdf68701bbf2d1fb453901a2187fa45a47e2f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16235108$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Flinn, B</creatorcontrib><creatorcontrib>Rothwell, C</creatorcontrib><creatorcontrib>Griffiths, R</creatorcontrib><creatorcontrib>Lague, M</creatorcontrib><creatorcontrib>DeKoeyer, D</creatorcontrib><creatorcontrib>Sardana, R</creatorcontrib><creatorcontrib>Audy, P</creatorcontrib><creatorcontrib>Goyer, C</creatorcontrib><creatorcontrib>Li, X.Q</creatorcontrib><creatorcontrib>Wang-Pruski, G</creatorcontrib><title>Potato expressed sequence tag generation and analysis using standard and unique cDNA libraries</title><title>Plant molecular biology</title><addtitle>Plant Mol Biol</addtitle><description>To help develop an understanding of the genes that govern the developmental characteristics of the potato (Solanum tuberosum), as well as the genes associated with responses to specified pathogens and storage conditions, The Canadian Potato Genome Project (CPGP) carried out 5' end sequencing of regular, normalized and full-length cDNA libraries of the Shepody potato cultivar, generating over 66,600 expressed sequence tags (ESTs). Libraries sequenced represented tuber developmental stages, pathogen-challenged tubers, as well as leaf, floral developmental stages, suspension cultured cells and roots. All libraries analysed to date have contributed unique sequences, with the normalized libraries high on the list. In addition, a low molecular weight library has enhanced the 3' ends of our sequence assemblies. Using the combined assembly dataset, unique tuber developmental, cold storage and pathogen-challenged sequences have been identified. A comparison of the ESTs specific to the pathogen-challenged tuber and foliar libraries revealed minimal overlap between these libraries. Mixed assemblies using over 189,000 potato EST sequences from CPGP and The Institute for Genomics Research (TIGR) has revealed common sequences, as well as CPGP- and TIGR-unique sequences.</description><subject>bacterial diseases of plants</subject><subject>blight</subject><subject>cDNA libraries</subject><subject>cold storage</subject><subject>common scab</subject><subject>Cultivars</subject><subject>Developmental stages</subject><subject>disease resistance</subject><subject>DNA, Complementary - chemistry</subject><subject>DNA, Complementary - genetics</subject><subject>Expressed Sequence Tags</subject><subject>fungal diseases of plants</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Gene Expression Regulation, Plant</subject><subject>Gene Library</subject><subject>genomic libraries</subject><subject>Genomics</subject><subject>Genomics - methods</subject><subject>Libraries</subject><subject>Molecular weight</subject><subject>Pathogens</subject><subject>Phytophthora infestans</subject><subject>plant development</subject><subject>Potatoes</subject><subject>Sequence Analysis, DNA</subject><subject>Solanum tuberosum</subject><subject>Solanum tuberosum - genetics</subject><subject>Solanum tuberosum - growth & development</subject><subject>Streptomyces scabiei</subject><subject>tuber development</subject><subject>tubers</subject><subject>Vegetables</subject><issn>0167-4412</issn><issn>1573-5028</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkcFu1DAQhi0EotvCA3ABiwO3wIwd28mxaqEgVYAEvWI5yXjlKpssnkRi3x6XXQmJCwfLsv39o_F8QrxAeIsA7h0jIugKwFSAjakOj8QGjdOVAdU8FhtA66q6RnUmzpnvAUpK26fiDK3SBqHZiB9f5yUss6Rf-0zMNEimnytNPcklbOWWJsphSfMkwzSUFcYDJ5Yrp2kreSmXIQ9_3tYplaDsrz9fyjF1OeRE_Ew8iWFken7aL8Tdh_ffrz5Wt19uPl1d3lZ9Xbulil3btC3W1Hed6Y0l27gWHOIQ-iGWA2DXRTVg7GqjW8CgsHEx1CbUjlTUF-LNse4-z6ULXvwucU_jGCaaV_a2sa3TDfwXRKfK7Jwu4Ot_wPt5zeX_7J1trTZluAXCI9TnmTlT9PucdiEfPIJ_UOSPinxR5B8U-UPJvDwVXrsdDX8TJycFeHUEYph92ObE_u6bAtRFn1WqYL8BURSVlQ</recordid><startdate>20051001</startdate><enddate>20051001</enddate><creator>Flinn, B</creator><creator>Rothwell, C</creator><creator>Griffiths, R</creator><creator>Lague, M</creator><creator>DeKoeyer, D</creator><creator>Sardana, R</creator><creator>Audy, P</creator><creator>Goyer, C</creator><creator>Li, X.Q</creator><creator>Wang-Pruski, G</creator><general>Springer Nature B.V</general><scope>FBQ</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>3V.</scope><scope>7TM</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>8G5</scope><scope>ABUWG</scope><scope>AEUYN</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>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7QO</scope><scope>7X8</scope></search><sort><creationdate>20051001</creationdate><title>Potato expressed sequence tag generation and analysis using standard and unique cDNA libraries</title><author>Flinn, B ; Rothwell, C ; Griffiths, R ; Lague, M ; DeKoeyer, D ; Sardana, R ; Audy, P ; Goyer, C ; Li, X.Q ; Wang-Pruski, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-fb989914ecbb5c56e68790711dacdf68701bbf2d1fb453901a2187fa45a47e2f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>bacterial diseases of plants</topic><topic>blight</topic><topic>cDNA libraries</topic><topic>cold storage</topic><topic>common scab</topic><topic>Cultivars</topic><topic>Developmental stages</topic><topic>disease resistance</topic><topic>DNA, Complementary - 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Academic</collection><jtitle>Plant molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Flinn, B</au><au>Rothwell, C</au><au>Griffiths, R</au><au>Lague, M</au><au>DeKoeyer, D</au><au>Sardana, R</au><au>Audy, P</au><au>Goyer, C</au><au>Li, X.Q</au><au>Wang-Pruski, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Potato expressed sequence tag generation and analysis using standard and unique cDNA libraries</atitle><jtitle>Plant molecular biology</jtitle><addtitle>Plant Mol Biol</addtitle><date>2005-10-01</date><risdate>2005</risdate><volume>59</volume><issue>3</issue><spage>407</spage><epage>433</epage><pages>407-433</pages><issn>0167-4412</issn><eissn>1573-5028</eissn><abstract>To help develop an understanding of the genes that govern the developmental characteristics of the potato (Solanum tuberosum), as well as the genes associated with responses to specified pathogens and storage conditions, The Canadian Potato Genome Project (CPGP) carried out 5' end sequencing of regular, normalized and full-length cDNA libraries of the Shepody potato cultivar, generating over 66,600 expressed sequence tags (ESTs). Libraries sequenced represented tuber developmental stages, pathogen-challenged tubers, as well as leaf, floral developmental stages, suspension cultured cells and roots. All libraries analysed to date have contributed unique sequences, with the normalized libraries high on the list. In addition, a low molecular weight library has enhanced the 3' ends of our sequence assemblies. Using the combined assembly dataset, unique tuber developmental, cold storage and pathogen-challenged sequences have been identified. A comparison of the ESTs specific to the pathogen-challenged tuber and foliar libraries revealed minimal overlap between these libraries. Mixed assemblies using over 189,000 potato EST sequences from CPGP and The Institute for Genomics Research (TIGR) has revealed common sequences, as well as CPGP- and TIGR-unique sequences.</abstract><cop>Netherlands</cop><pub>Springer Nature B.V</pub><pmid>16235108</pmid><doi>10.1007/s11103-005-0185-y</doi><tpages>27</tpages></addata></record> |
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subjects | bacterial diseases of plants blight cDNA libraries cold storage common scab Cultivars Developmental stages disease resistance DNA, Complementary - chemistry DNA, Complementary - genetics Expressed Sequence Tags fungal diseases of plants Gene Expression Regulation, Developmental Gene Expression Regulation, Plant Gene Library genomic libraries Genomics Genomics - methods Libraries Molecular weight Pathogens Phytophthora infestans plant development Potatoes Sequence Analysis, DNA Solanum tuberosum Solanum tuberosum - genetics Solanum tuberosum - growth & development Streptomyces scabiei tuber development tubers Vegetables |
title | Potato expressed sequence tag generation and analysis using standard and unique cDNA libraries |
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