liguleless1 encodes a nuclear-localized protein required for induction of ligules and auricles during maize leaf organogenesis
The maize ligule and auricle are structures on the maize leaf that develop at the boundary of the sheath and blade. In the absence of liguleless1 (Ig1) gene expression, ligule and auricle are not formed, and the blade-sheath boundary does not develop as an exact line between sheath and blade. By usi...
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Veröffentlicht in: | Genes & development 1997-03, Vol.11 (5), p.616-628 |
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description | The maize ligule and auricle are structures on the maize leaf that develop at the boundary of the sheath and blade. In the absence of liguleless1 (Ig1) gene expression, ligule and auricle are not formed, and the blade-sheath boundary does not develop as an exact line between sheath and blade. By using the Activator (Ac) transposable element as a molecular tag, a novel Ig1 allele, Ig1-m1, was isolated and cloned. Analysis of somatic revertant sectors confirmed that the LG1 gene product functions in a cell-autonomous fashion. cDNA cloning as well as RT-PCR analysis of the LG1 mRNA indicate that the Ig1 gene is expressed at very low levels in the ligular region of developing maize leaf primordia, perhaps as early as plastochron 6 or earlier. Cellular localization studies in a heterologous system indicate that the LG1 product localizes exclusively to the nucleus. The predicted amino acid sequence of the LG1 protein is largely novel but contains an internal domain of 77 amino acids with significant similarity to a domain present in two recently identified SQUAMOSA PROMOTER-BINDING proteins 1 and 2 (SBP1 and SBP2) in Antirhinum majus. |
doi_str_mv | 10.1101/gad.11.5.616 |
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In the absence of liguleless1 (Ig1) gene expression, ligule and auricle are not formed, and the blade-sheath boundary does not develop as an exact line between sheath and blade. By using the Activator (Ac) transposable element as a molecular tag, a novel Ig1 allele, Ig1-m1, was isolated and cloned. Analysis of somatic revertant sectors confirmed that the LG1 gene product functions in a cell-autonomous fashion. cDNA cloning as well as RT-PCR analysis of the LG1 mRNA indicate that the Ig1 gene is expressed at very low levels in the ligular region of developing maize leaf primordia, perhaps as early as plastochron 6 or earlier. Cellular localization studies in a heterologous system indicate that the LG1 product localizes exclusively to the nucleus. The predicted amino acid sequence of the LG1 protein is largely novel but contains an internal domain of 77 amino acids with significant similarity to a domain present in two recently identified SQUAMOSA PROMOTER-BINDING proteins 1 and 2 (SBP1 and SBP2) in Antirhinum majus.</description><identifier>ISSN: 0890-9369</identifier><identifier>EISSN: 1549-5477</identifier><identifier>DOI: 10.1101/gad.11.5.616</identifier><identifier>PMID: 9119226</identifier><language>eng</language><publisher>United States</publisher><subject>Alleles ; Amino Acid Sequence ; Cell Nucleus - genetics ; Cell Nucleus - metabolism ; Cloning, Molecular ; DNA Transposable Elements - genetics ; DNA-Binding Proteins - genetics ; Gene Expression Regulation, Plant ; Germ-Line Mutation ; Molecular Sequence Data ; Mutation ; Phenotype ; Plant Leaves - genetics ; Plant Leaves - growth & development ; Plant Proteins - genetics ; Polymerase Chain Reaction ; Recombinant Fusion Proteins - genetics ; Recombinant Fusion Proteins - metabolism ; RNA, Messenger - biosynthesis ; RNA-Binding Proteins ; Sequence Homology, Amino Acid ; Zea mays ; Zea mays - genetics ; Zea mays - growth & development</subject><ispartof>Genes & development, 1997-03, Vol.11 (5), p.616-628</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-c7a3537e776cb457e685b3a7a2a8f372b4cf2909611bd6178518829cca6523ff3</citedby><cites>FETCH-LOGICAL-c421t-c7a3537e776cb457e685b3a7a2a8f372b4cf2909611bd6178518829cca6523ff3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9119226$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moreno, M A</creatorcontrib><creatorcontrib>Harper, L C</creatorcontrib><creatorcontrib>Krueger, R W</creatorcontrib><creatorcontrib>Dellaporta, S L</creatorcontrib><creatorcontrib>Freeling, M</creatorcontrib><title>liguleless1 encodes a nuclear-localized protein required for induction of ligules and auricles during maize leaf organogenesis</title><title>Genes & development</title><addtitle>Genes Dev</addtitle><description>The maize ligule and auricle are structures on the maize leaf that develop at the boundary of the sheath and blade. In the absence of liguleless1 (Ig1) gene expression, ligule and auricle are not formed, and the blade-sheath boundary does not develop as an exact line between sheath and blade. By using the Activator (Ac) transposable element as a molecular tag, a novel Ig1 allele, Ig1-m1, was isolated and cloned. Analysis of somatic revertant sectors confirmed that the LG1 gene product functions in a cell-autonomous fashion. cDNA cloning as well as RT-PCR analysis of the LG1 mRNA indicate that the Ig1 gene is expressed at very low levels in the ligular region of developing maize leaf primordia, perhaps as early as plastochron 6 or earlier. Cellular localization studies in a heterologous system indicate that the LG1 product localizes exclusively to the nucleus. The predicted amino acid sequence of the LG1 protein is largely novel but contains an internal domain of 77 amino acids with significant similarity to a domain present in two recently identified SQUAMOSA PROMOTER-BINDING proteins 1 and 2 (SBP1 and SBP2) in Antirhinum majus.</description><subject>Alleles</subject><subject>Amino Acid Sequence</subject><subject>Cell Nucleus - genetics</subject><subject>Cell Nucleus - metabolism</subject><subject>Cloning, Molecular</subject><subject>DNA Transposable Elements - genetics</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Gene Expression Regulation, Plant</subject><subject>Germ-Line Mutation</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Phenotype</subject><subject>Plant Leaves - genetics</subject><subject>Plant Leaves - growth & development</subject><subject>Plant Proteins - genetics</subject><subject>Polymerase Chain Reaction</subject><subject>Recombinant Fusion Proteins - genetics</subject><subject>Recombinant Fusion Proteins - metabolism</subject><subject>RNA, Messenger - biosynthesis</subject><subject>RNA-Binding Proteins</subject><subject>Sequence Homology, Amino Acid</subject><subject>Zea mays</subject><subject>Zea mays - genetics</subject><subject>Zea mays - growth & development</subject><issn>0890-9369</issn><issn>1549-5477</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkTtPBCEURonR6ProbE2orJyVOzPAUBrjK9nERusJw1wmGBYUdgot_O1idmNrxcfNuSeBj5BzYEsABteTHktY8qUAsUcWwFtV8VbKfbJgnWKVaoQ6Isc5vzHGBBPikBwqAFXXYkG-vZtmjx5zBorBxBEz1TTMxqNOlY9Ge_eFI31PcYMu0IQfs0tlYGOiLoyz2bgYaLR0ayrbYaR6Ts78XsYSwkTXukhoUVoa06RDnDBgdvmUHFjtM57tzhPyen_3cvtYrZ4fnm5vVpVpa9hURuqGNxKlFGZouUTR8aHRUte6s42sh9bYWjElAIZRgOw4dF2tjNGC1421zQm53HrLMz5mzJt-7bJB73XAOOdedgrK98G_IAgmuVKqgFdb0KSYc0Lbvye31umzB9b_9tKXXkroeV_EBb_YeedhjeMfvCui-QEhEIrr</recordid><startdate>19970301</startdate><enddate>19970301</enddate><creator>Moreno, M A</creator><creator>Harper, L C</creator><creator>Krueger, R W</creator><creator>Dellaporta, S L</creator><creator>Freeling, M</creator><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>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19970301</creationdate><title>liguleless1 encodes a nuclear-localized protein required for induction of ligules and auricles during maize leaf organogenesis</title><author>Moreno, M A ; Harper, L C ; Krueger, R W ; Dellaporta, S L ; Freeling, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-c7a3537e776cb457e685b3a7a2a8f372b4cf2909611bd6178518829cca6523ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Alleles</topic><topic>Amino Acid Sequence</topic><topic>Cell Nucleus - genetics</topic><topic>Cell Nucleus - metabolism</topic><topic>Cloning, Molecular</topic><topic>DNA Transposable Elements - genetics</topic><topic>DNA-Binding Proteins - genetics</topic><topic>Gene Expression Regulation, Plant</topic><topic>Germ-Line Mutation</topic><topic>Molecular Sequence Data</topic><topic>Mutation</topic><topic>Phenotype</topic><topic>Plant Leaves - genetics</topic><topic>Plant Leaves - growth & development</topic><topic>Plant Proteins - genetics</topic><topic>Polymerase Chain Reaction</topic><topic>Recombinant Fusion Proteins - genetics</topic><topic>Recombinant Fusion Proteins - metabolism</topic><topic>RNA, Messenger - biosynthesis</topic><topic>RNA-Binding Proteins</topic><topic>Sequence Homology, Amino Acid</topic><topic>Zea mays</topic><topic>Zea mays - genetics</topic><topic>Zea mays - growth & development</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moreno, M A</creatorcontrib><creatorcontrib>Harper, L C</creatorcontrib><creatorcontrib>Krueger, R W</creatorcontrib><creatorcontrib>Dellaporta, S L</creatorcontrib><creatorcontrib>Freeling, M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Genes & development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moreno, M A</au><au>Harper, L C</au><au>Krueger, R W</au><au>Dellaporta, S L</au><au>Freeling, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>liguleless1 encodes a nuclear-localized protein required for induction of ligules and auricles during maize leaf organogenesis</atitle><jtitle>Genes & development</jtitle><addtitle>Genes Dev</addtitle><date>1997-03-01</date><risdate>1997</risdate><volume>11</volume><issue>5</issue><spage>616</spage><epage>628</epage><pages>616-628</pages><issn>0890-9369</issn><eissn>1549-5477</eissn><abstract>The maize ligule and auricle are structures on the maize leaf that develop at the boundary of the sheath and blade. In the absence of liguleless1 (Ig1) gene expression, ligule and auricle are not formed, and the blade-sheath boundary does not develop as an exact line between sheath and blade. By using the Activator (Ac) transposable element as a molecular tag, a novel Ig1 allele, Ig1-m1, was isolated and cloned. Analysis of somatic revertant sectors confirmed that the LG1 gene product functions in a cell-autonomous fashion. cDNA cloning as well as RT-PCR analysis of the LG1 mRNA indicate that the Ig1 gene is expressed at very low levels in the ligular region of developing maize leaf primordia, perhaps as early as plastochron 6 or earlier. Cellular localization studies in a heterologous system indicate that the LG1 product localizes exclusively to the nucleus. The predicted amino acid sequence of the LG1 protein is largely novel but contains an internal domain of 77 amino acids with significant similarity to a domain present in two recently identified SQUAMOSA PROMOTER-BINDING proteins 1 and 2 (SBP1 and SBP2) in Antirhinum majus.</abstract><cop>United States</cop><pmid>9119226</pmid><doi>10.1101/gad.11.5.616</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alleles Amino Acid Sequence Cell Nucleus - genetics Cell Nucleus - metabolism Cloning, Molecular DNA Transposable Elements - genetics DNA-Binding Proteins - genetics Gene Expression Regulation, Plant Germ-Line Mutation Molecular Sequence Data Mutation Phenotype Plant Leaves - genetics Plant Leaves - growth & development Plant Proteins - genetics Polymerase Chain Reaction Recombinant Fusion Proteins - genetics Recombinant Fusion Proteins - metabolism RNA, Messenger - biosynthesis RNA-Binding Proteins Sequence Homology, Amino Acid Zea mays Zea mays - genetics Zea mays - growth & development |
title | liguleless1 encodes a nuclear-localized protein required for induction of ligules and auricles during maize leaf organogenesis |
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