Dissemination of the highly expressed Bx7 glutenin subunit (Glu-B1al allele) in wheat as revealed by novel PCR markers and RP-HPLC
Increased expression of the high molecular weight glutenin subunit (HMW-GS) Bx7 is associated with improved dough strength of wheat (Triticum aestivum L.) flour. Several cultivars and landraces of widely different genetic backgrounds from around the world have now been found to contain this so-calle...
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description | Increased expression of the high molecular weight glutenin subunit (HMW-GS) Bx7 is associated with improved dough strength of wheat (Triticum aestivum L.) flour. Several cultivars and landraces of widely different genetic backgrounds from around the world have now been found to contain this so-called 'over-expressing' allelic form of the Bx7 subunit encoded by Glu-B1al. Using three methods of identification, SDS-PAGE, RP-HPLC and PCR marker analysis, as well as pedigree information, we have traced the distribution and source of this allele from a Uruguayan landrace, Americano 44D, in the mid-nineteenth century. Results are supported by knowledge of the movement of wheat lines with migrants. All cultivars possessing the Glu-B1al allele can be identified by the following attributes: (1) the elution of the By sub-unit peak before the Dx sub-unit peak by RP-HPLC, (2) high expression levels of Bx7 (>39% Mol % Bx), (3) a 43 bp insertion in the matrix-attachment region (MAR) upstream of the gene promoter relative to Bx7 and an 18 bp nucleotide duplication in the coding region of the gene. Evidence is presented indicating that these 18 and 43 bp sequence insertions are not causal for the high expression levels of Bx7 as they were also found to be present in a small number of hexaploid species, including Chinese Spring, and species expressing Glu-B1ak and Glu-B1a alleles. In addition, these sequence inserts were found in different isolates of the tetraploid wheat, T. turgidum, indicating that these insertion/deletion events occurred prior to hexaploidization. |
doi_str_mv | 10.1007/s00122-004-1776-8 |
format | Article |
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Several cultivars and landraces of widely different genetic backgrounds from around the world have now been found to contain this so-called 'over-expressing' allelic form of the Bx7 subunit encoded by Glu-B1al. Using three methods of identification, SDS-PAGE, RP-HPLC and PCR marker analysis, as well as pedigree information, we have traced the distribution and source of this allele from a Uruguayan landrace, Americano 44D, in the mid-nineteenth century. Results are supported by knowledge of the movement of wheat lines with migrants. All cultivars possessing the Glu-B1al allele can be identified by the following attributes: (1) the elution of the By sub-unit peak before the Dx sub-unit peak by RP-HPLC, (2) high expression levels of Bx7 (>39% Mol % Bx), (3) a 43 bp insertion in the matrix-attachment region (MAR) upstream of the gene promoter relative to Bx7 and an 18 bp nucleotide duplication in the coding region of the gene. Evidence is presented indicating that these 18 and 43 bp sequence insertions are not causal for the high expression levels of Bx7 as they were also found to be present in a small number of hexaploid species, including Chinese Spring, and species expressing Glu-B1ak and Glu-B1a alleles. In addition, these sequence inserts were found in different isolates of the tetraploid wheat, T. turgidum, indicating that these insertion/deletion events occurred prior to hexaploidization.</description><identifier>ISSN: 0040-5752</identifier><identifier>EISSN: 1432-2242</identifier><identifier>DOI: 10.1007/s00122-004-1776-8</identifier><identifier>PMID: 15340686</identifier><identifier>CODEN: THAGA6</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>alleles ; Base Sequence ; Biological and medical sciences ; Chromatography, High Pressure Liquid - methods ; Classical genetics, quantitative genetics, hybrids ; cultivars ; DNA Primers ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation, Plant ; Genes ; Genetic Markers ; genetic variation ; Genetics of eukaryotes. Biological and molecular evolution ; Geography ; glutenins ; Glutens - analogs & derivatives ; Glutens - genetics ; Molecular Weight ; nucleotide sequence insertions ; nucleotide sequences ; polymerase chain reaction ; Polymerase Chain Reaction - methods ; Polyploidy ; Protein Subunits - genetics ; Pteridophyta, spermatophyta ; reversed-phase high performance liquid chromatography ; Triticum - genetics ; Triticum aestivum ; Vegetals ; Wheat</subject><ispartof>Theoretical and applied genetics, 2004-11, Vol.109 (7), p.1525-1535</ispartof><rights>2005 INIST-CNRS</rights><rights>Springer-Verlag 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-55091509da241890120d1ec96bb642851c89921e21e5e5f5faabbd643422d13b3</citedby><cites>FETCH-LOGICAL-c411t-55091509da241890120d1ec96bb642851c89921e21e5e5f5faabbd643422d13b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16268099$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15340686$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Butow, B.J</creatorcontrib><creatorcontrib>Gale, K.R</creatorcontrib><creatorcontrib>Ikea, J</creatorcontrib><creatorcontrib>Juhasz, A</creatorcontrib><creatorcontrib>Bedo, Z</creatorcontrib><creatorcontrib>Tamas, L</creatorcontrib><creatorcontrib>Gianibelli, M.C</creatorcontrib><title>Dissemination of the highly expressed Bx7 glutenin subunit (Glu-B1al allele) in wheat as revealed by novel PCR markers and RP-HPLC</title><title>Theoretical and applied genetics</title><addtitle>Theor Appl Genet</addtitle><description>Increased expression of the high molecular weight glutenin subunit (HMW-GS) Bx7 is associated with improved dough strength of wheat (Triticum aestivum L.) flour. Several cultivars and landraces of widely different genetic backgrounds from around the world have now been found to contain this so-called 'over-expressing' allelic form of the Bx7 subunit encoded by Glu-B1al. Using three methods of identification, SDS-PAGE, RP-HPLC and PCR marker analysis, as well as pedigree information, we have traced the distribution and source of this allele from a Uruguayan landrace, Americano 44D, in the mid-nineteenth century. Results are supported by knowledge of the movement of wheat lines with migrants. All cultivars possessing the Glu-B1al allele can be identified by the following attributes: (1) the elution of the By sub-unit peak before the Dx sub-unit peak by RP-HPLC, (2) high expression levels of Bx7 (>39% Mol % Bx), (3) a 43 bp insertion in the matrix-attachment region (MAR) upstream of the gene promoter relative to Bx7 and an 18 bp nucleotide duplication in the coding region of the gene. Evidence is presented indicating that these 18 and 43 bp sequence insertions are not causal for the high expression levels of Bx7 as they were also found to be present in a small number of hexaploid species, including Chinese Spring, and species expressing Glu-B1ak and Glu-B1a alleles. In addition, these sequence inserts were found in different isolates of the tetraploid wheat, T. turgidum, indicating that these insertion/deletion events occurred prior to hexaploidization.</description><subject>alleles</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Classical genetics, quantitative genetics, hybrids</subject><subject>cultivars</subject><subject>DNA Primers</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation, Plant</subject><subject>Genes</subject><subject>Genetic Markers</subject><subject>genetic variation</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>Geography</subject><subject>glutenins</subject><subject>Glutens - analogs & derivatives</subject><subject>Glutens - genetics</subject><subject>Molecular Weight</subject><subject>nucleotide sequence insertions</subject><subject>nucleotide sequences</subject><subject>polymerase chain reaction</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Polyploidy</subject><subject>Protein Subunits - genetics</subject><subject>Pteridophyta, spermatophyta</subject><subject>reversed-phase high performance liquid chromatography</subject><subject>Triticum - genetics</subject><subject>Triticum aestivum</subject><subject>Vegetals</subject><subject>Wheat</subject><issn>0040-5752</issn><issn>1432-2242</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkUtv1DAUhSMEokPhB7ABCwlEF4F7_Uq8pEMfSCMxKnRtOcnNTIonGeykdLb8clzNSJW6QbLlxfnO0b0-WfYa4RMCFJ8jAHKeA8gci0Ln5ZNshlLwnHPJn2azJECuCsWPshcx3gAAVyCeZ0eohARd6ln292sXI2263o3d0LOhZeOa2Lpbrf2O0d02UJIbdnpXsJWfRuq7nsWpmvpuZB8v_JSfovPMeU-eTlgS_6zJjcxFFuiWnE_easf64ZY8W86v2MaFXxQic33Drpb55XIxf5k9a52P9OrwHmfX52c_55f54vvFt_mXRV5LxDFXCgym2zgusTRpc2iQaqOrSkteKqxLYzhSOopUq1rnqqrRUkjOGxSVOM4-7HO3Yfg9URztpos1ee96GqZodYHCCK7_C2IhjYSySOC7R-DNMIU-LWFLDikLBCYI91AdhhgDtXYbuvQNO4tg72u0-xptasve12jL5HlzCJ6qDTUPjkNvCXh_AFysnW-D6-suPnCa6xKMSdzbPde6wbpVSMz1Dw4oAIzmaUjxD1Xuq3g</recordid><startdate>20041101</startdate><enddate>20041101</enddate><creator>Butow, B.J</creator><creator>Gale, K.R</creator><creator>Ikea, J</creator><creator>Juhasz, A</creator><creator>Bedo, Z</creator><creator>Tamas, L</creator><creator>Gianibelli, M.C</creator><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>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>RC3</scope><scope>7X8</scope></search><sort><creationdate>20041101</creationdate><title>Dissemination of the highly expressed Bx7 glutenin subunit (Glu-B1al allele) in wheat as revealed by novel PCR markers and RP-HPLC</title><author>Butow, B.J ; Gale, K.R ; Ikea, J ; Juhasz, A ; Bedo, Z ; Tamas, L ; Gianibelli, M.C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-55091509da241890120d1ec96bb642851c89921e21e5e5f5faabbd643422d13b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>alleles</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Classical genetics, quantitative genetics, hybrids</topic><topic>cultivars</topic><topic>DNA Primers</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation, Plant</topic><topic>Genes</topic><topic>Genetic Markers</topic><topic>genetic variation</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Geography</topic><topic>glutenins</topic><topic>Glutens - analogs & derivatives</topic><topic>Glutens - genetics</topic><topic>Molecular Weight</topic><topic>nucleotide sequence insertions</topic><topic>nucleotide sequences</topic><topic>polymerase chain reaction</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Polyploidy</topic><topic>Protein Subunits - genetics</topic><topic>Pteridophyta, spermatophyta</topic><topic>reversed-phase high performance liquid chromatography</topic><topic>Triticum - genetics</topic><topic>Triticum aestivum</topic><topic>Vegetals</topic><topic>Wheat</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Butow, B.J</creatorcontrib><creatorcontrib>Gale, K.R</creatorcontrib><creatorcontrib>Ikea, J</creatorcontrib><creatorcontrib>Juhasz, A</creatorcontrib><creatorcontrib>Bedo, Z</creatorcontrib><creatorcontrib>Tamas, L</creatorcontrib><creatorcontrib>Gianibelli, M.C</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>ProQuest Central (Corporate)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Health & 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 & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & 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>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>Butow, B.J</au><au>Gale, K.R</au><au>Ikea, J</au><au>Juhasz, A</au><au>Bedo, Z</au><au>Tamas, L</au><au>Gianibelli, M.C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dissemination of the highly expressed Bx7 glutenin subunit (Glu-B1al allele) in wheat as revealed by novel PCR markers and RP-HPLC</atitle><jtitle>Theoretical and applied genetics</jtitle><addtitle>Theor Appl Genet</addtitle><date>2004-11-01</date><risdate>2004</risdate><volume>109</volume><issue>7</issue><spage>1525</spage><epage>1535</epage><pages>1525-1535</pages><issn>0040-5752</issn><eissn>1432-2242</eissn><coden>THAGA6</coden><abstract>Increased expression of the high molecular weight glutenin subunit (HMW-GS) Bx7 is associated with improved dough strength of wheat (Triticum aestivum L.) flour. Several cultivars and landraces of widely different genetic backgrounds from around the world have now been found to contain this so-called 'over-expressing' allelic form of the Bx7 subunit encoded by Glu-B1al. Using three methods of identification, SDS-PAGE, RP-HPLC and PCR marker analysis, as well as pedigree information, we have traced the distribution and source of this allele from a Uruguayan landrace, Americano 44D, in the mid-nineteenth century. Results are supported by knowledge of the movement of wheat lines with migrants. All cultivars possessing the Glu-B1al allele can be identified by the following attributes: (1) the elution of the By sub-unit peak before the Dx sub-unit peak by RP-HPLC, (2) high expression levels of Bx7 (>39% Mol % Bx), (3) a 43 bp insertion in the matrix-attachment region (MAR) upstream of the gene promoter relative to Bx7 and an 18 bp nucleotide duplication in the coding region of the gene. Evidence is presented indicating that these 18 and 43 bp sequence insertions are not causal for the high expression levels of Bx7 as they were also found to be present in a small number of hexaploid species, including Chinese Spring, and species expressing Glu-B1ak and Glu-B1a alleles. In addition, these sequence inserts were found in different isolates of the tetraploid wheat, T. turgidum, indicating that these insertion/deletion events occurred prior to hexaploidization.</abstract><cop>Heidelberg</cop><cop>Berlin</cop><pub>Springer</pub><pmid>15340686</pmid><doi>10.1007/s00122-004-1776-8</doi><tpages>11</tpages></addata></record> |
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subjects | alleles Base Sequence Biological and medical sciences Chromatography, High Pressure Liquid - methods Classical genetics, quantitative genetics, hybrids cultivars DNA Primers Fundamental and applied biological sciences. Psychology Gene Expression Regulation, Plant Genes Genetic Markers genetic variation Genetics of eukaryotes. Biological and molecular evolution Geography glutenins Glutens - analogs & derivatives Glutens - genetics Molecular Weight nucleotide sequence insertions nucleotide sequences polymerase chain reaction Polymerase Chain Reaction - methods Polyploidy Protein Subunits - genetics Pteridophyta, spermatophyta reversed-phase high performance liquid chromatography Triticum - genetics Triticum aestivum Vegetals Wheat |
title | Dissemination of the highly expressed Bx7 glutenin subunit (Glu-B1al allele) in wheat as revealed by novel PCR markers and RP-HPLC |
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