A novel fibroblast growth factor gene expressed in the developing nervous system is a downstream target of the chimeric homeodomain oncoprotein E2A-Pbx1
Pbx1 is a homeodomain transcription factor that has the ability to form heterodimers with homeodomain proteins encoded by the homeotic selector (Hox) gene complexes and increase their DNA-binding affinity and specificity. A current hypothesis proposes that interactions with Pbx1 are necessary for Ho...
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Veröffentlicht in: | Development (Cambridge) 1997-09, Vol.124 (17), p.3221-3232 |
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description | Pbx1 is a homeodomain transcription factor that has the ability to form heterodimers with homeodomain proteins encoded by the homeotic selector (Hox) gene complexes and increase their DNA-binding affinity and specificity. A current hypothesis proposes that interactions with Pbx1 are necessary for Hox proteins to regulate downstream target genes that in turn control growth, differentiation and morphogenesis during development. In pre B cell leukemias containing the t(1;19) chromosome translocation, Pbx1 is converted into a strong transactivator by fusion to the activation domain of the bHLH transcription factor E2A. The E2A-Pbx1 fusion protein should therefore activate transcription of genes normally regulated by Pbx1. We have used the subtractive process of representational difference analysis to identify targets of E2A-Pbx1. We show that E2A-Pbx1 can directly activate transcription of a novel member of the fibroblast growth factor family of intercellular signalling molecules, FGF-15. The FGF-15 gene is expressed in a regionally restricted pattern in the developing nervous system, suggesting that FGF-15 may play an important role in regulating cell division and patterning within specific regions of the embryonic brain, spinal cord and sensory organs. |
doi_str_mv | 10.1242/dev.124.17.3221 |
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The FGF-15 gene is expressed in a regionally restricted pattern in the developing nervous system, suggesting that FGF-15 may play an important role in regulating cell division and patterning within specific regions of the embryonic brain, spinal cord and sensory organs.</description><identifier>ISSN: 0950-1991</identifier><identifier>EISSN: 1477-9129</identifier><identifier>DOI: 10.1242/dev.124.17.3221</identifier><identifier>PMID: 9310317</identifier><language>eng</language><publisher>England: The Company of Biologists Limited</publisher><subject>Amino Acid Sequence ; Animals ; Base Sequence ; Binding Sites - genetics ; Brain - embryology ; Brain - metabolism ; Central Nervous System - embryology ; Central Nervous System - growth & development ; Cloning, Molecular ; DNA Primers - genetics ; DNA, Complementary - genetics ; Fibroblast Growth Factors - genetics ; Gene Expression Regulation, Developmental ; Homeodomain Proteins - genetics ; Homeodomain Proteins - metabolism ; In Situ Hybridization ; Mice ; Molecular Sequence Data ; Oncogene Proteins, Fusion - genetics ; Oncogene Proteins, Fusion - metabolism ; Polymerase Chain Reaction ; Promoter Regions, Genetic ; Sequence Homology, Amino Acid ; Spinal Cord - embryology ; Spinal Cord - metabolism ; Transcriptional Activation</subject><ispartof>Development (Cambridge), 1997-09, Vol.124 (17), p.3221-3232</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-25820f6ef44b50ddb6ab98dabe676581f47c862c36d425ca9e8d4c1a805f5eff3</citedby><cites>FETCH-LOGICAL-c428t-25820f6ef44b50ddb6ab98dabe676581f47c862c36d425ca9e8d4c1a805f5eff3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3665,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9310317$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McWhirter, J R</creatorcontrib><creatorcontrib>Goulding, M</creatorcontrib><creatorcontrib>Weiner, J A</creatorcontrib><creatorcontrib>Chun, J</creatorcontrib><creatorcontrib>Murre, C</creatorcontrib><title>A novel fibroblast growth factor gene expressed in the developing nervous system is a downstream target of the chimeric homeodomain oncoprotein E2A-Pbx1</title><title>Development (Cambridge)</title><addtitle>Development</addtitle><description>Pbx1 is a homeodomain transcription factor that has the ability to form heterodimers with homeodomain proteins encoded by the homeotic selector (Hox) gene complexes and increase their DNA-binding affinity and specificity. A current hypothesis proposes that interactions with Pbx1 are necessary for Hox proteins to regulate downstream target genes that in turn control growth, differentiation and morphogenesis during development. In pre B cell leukemias containing the t(1;19) chromosome translocation, Pbx1 is converted into a strong transactivator by fusion to the activation domain of the bHLH transcription factor E2A. The E2A-Pbx1 fusion protein should therefore activate transcription of genes normally regulated by Pbx1. We have used the subtractive process of representational difference analysis to identify targets of E2A-Pbx1. We show that E2A-Pbx1 can directly activate transcription of a novel member of the fibroblast growth factor family of intercellular signalling molecules, FGF-15. The FGF-15 gene is expressed in a regionally restricted pattern in the developing nervous system, suggesting that FGF-15 may play an important role in regulating cell division and patterning within specific regions of the embryonic brain, spinal cord and sensory organs.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Binding Sites - genetics</subject><subject>Brain - embryology</subject><subject>Brain - metabolism</subject><subject>Central Nervous System - embryology</subject><subject>Central Nervous System - growth & development</subject><subject>Cloning, Molecular</subject><subject>DNA Primers - genetics</subject><subject>DNA, Complementary - genetics</subject><subject>Fibroblast Growth Factors - genetics</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Homeodomain Proteins - genetics</subject><subject>Homeodomain Proteins - metabolism</subject><subject>In Situ Hybridization</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>Oncogene Proteins, Fusion - genetics</subject><subject>Oncogene Proteins, Fusion - metabolism</subject><subject>Polymerase Chain Reaction</subject><subject>Promoter Regions, Genetic</subject><subject>Sequence Homology, Amino Acid</subject><subject>Spinal Cord - embryology</subject><subject>Spinal Cord - metabolism</subject><subject>Transcriptional Activation</subject><issn>0950-1991</issn><issn>1477-9129</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUT2P1DAQtRDoWA5qKiRXdNnzOE6clKvT8SGdBAXUlmOPE6MkXmzv7d0_4efiZVdIVBSjedK8efPxCHkLbAtc8BuLDyewBbmtOYdnZANCyqoH3j8nG9Y3rIK-h5fkVUo_GGN1K-UVueprYDXIDfm1o2t4wJk6P8QwzDplOsZwzBN12uQQ6YgrUnzcR0wJLfUrzRPSMhfnsPfrSFeMD-GQaHpKGRfqE9XUhuOackS90KzjiJkG96fPTH7B6A2dwoLBhkUXwbCasI8hY8F3fFd9HR7hNXnh9JzwzSVfk-8f7r7dfqruv3z8fLu7r4zgXa5403HmWnRCDA2zdmj10HdWD9jKtunACWm6lpu6tYI3RvfYWWFAd6xxDTpXX5P3Z92ywM8DpqwWnwzOs16xXKVkXzNR4r9EaAFqEG0h3pyJJoaUIjq1j37R8UkBUyfTVHneCSiQ6mRa6Xh3kT4MC9q__ItLpb491yc_TkcfUQ0-zGH0KSd1ceIfwd8BU6ZL</recordid><startdate>19970901</startdate><enddate>19970901</enddate><creator>McWhirter, J R</creator><creator>Goulding, M</creator><creator>Weiner, J A</creator><creator>Chun, J</creator><creator>Murre, C</creator><general>The Company of Biologists Limited</general><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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19970901</creationdate><title>A novel fibroblast growth factor gene expressed in the developing nervous system is a downstream target of the chimeric homeodomain oncoprotein E2A-Pbx1</title><author>McWhirter, J R ; Goulding, M ; Weiner, J A ; Chun, J ; Murre, C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-25820f6ef44b50ddb6ab98dabe676581f47c862c36d425ca9e8d4c1a805f5eff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Binding Sites - genetics</topic><topic>Brain - embryology</topic><topic>Brain - metabolism</topic><topic>Central Nervous System - embryology</topic><topic>Central Nervous System - growth & development</topic><topic>Cloning, Molecular</topic><topic>DNA Primers - genetics</topic><topic>DNA, Complementary - genetics</topic><topic>Fibroblast Growth Factors - genetics</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Homeodomain Proteins - genetics</topic><topic>Homeodomain Proteins - metabolism</topic><topic>In Situ Hybridization</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>Oncogene Proteins, Fusion - genetics</topic><topic>Oncogene Proteins, Fusion - metabolism</topic><topic>Polymerase Chain Reaction</topic><topic>Promoter Regions, Genetic</topic><topic>Sequence Homology, Amino Acid</topic><topic>Spinal Cord - embryology</topic><topic>Spinal Cord - metabolism</topic><topic>Transcriptional Activation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McWhirter, J R</creatorcontrib><creatorcontrib>Goulding, M</creatorcontrib><creatorcontrib>Weiner, J A</creatorcontrib><creatorcontrib>Chun, J</creatorcontrib><creatorcontrib>Murre, C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</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>Development (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McWhirter, J R</au><au>Goulding, M</au><au>Weiner, J A</au><au>Chun, J</au><au>Murre, C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A novel fibroblast growth factor gene expressed in the developing nervous system is a downstream target of the chimeric homeodomain oncoprotein E2A-Pbx1</atitle><jtitle>Development (Cambridge)</jtitle><addtitle>Development</addtitle><date>1997-09-01</date><risdate>1997</risdate><volume>124</volume><issue>17</issue><spage>3221</spage><epage>3232</epage><pages>3221-3232</pages><issn>0950-1991</issn><eissn>1477-9129</eissn><abstract>Pbx1 is a homeodomain transcription factor that has the ability to form heterodimers with homeodomain proteins encoded by the homeotic selector (Hox) gene complexes and increase their DNA-binding affinity and specificity. A current hypothesis proposes that interactions with Pbx1 are necessary for Hox proteins to regulate downstream target genes that in turn control growth, differentiation and morphogenesis during development. In pre B cell leukemias containing the t(1;19) chromosome translocation, Pbx1 is converted into a strong transactivator by fusion to the activation domain of the bHLH transcription factor E2A. The E2A-Pbx1 fusion protein should therefore activate transcription of genes normally regulated by Pbx1. We have used the subtractive process of representational difference analysis to identify targets of E2A-Pbx1. We show that E2A-Pbx1 can directly activate transcription of a novel member of the fibroblast growth factor family of intercellular signalling molecules, FGF-15. The FGF-15 gene is expressed in a regionally restricted pattern in the developing nervous system, suggesting that FGF-15 may play an important role in regulating cell division and patterning within specific regions of the embryonic brain, spinal cord and sensory organs.</abstract><cop>England</cop><pub>The Company of Biologists Limited</pub><pmid>9310317</pmid><doi>10.1242/dev.124.17.3221</doi><tpages>12</tpages></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection; Company of Biologists |
subjects | Amino Acid Sequence Animals Base Sequence Binding Sites - genetics Brain - embryology Brain - metabolism Central Nervous System - embryology Central Nervous System - growth & development Cloning, Molecular DNA Primers - genetics DNA, Complementary - genetics Fibroblast Growth Factors - genetics Gene Expression Regulation, Developmental Homeodomain Proteins - genetics Homeodomain Proteins - metabolism In Situ Hybridization Mice Molecular Sequence Data Oncogene Proteins, Fusion - genetics Oncogene Proteins, Fusion - metabolism Polymerase Chain Reaction Promoter Regions, Genetic Sequence Homology, Amino Acid Spinal Cord - embryology Spinal Cord - metabolism Transcriptional Activation |
title | A novel fibroblast growth factor gene expressed in the developing nervous system is a downstream target of the chimeric homeodomain oncoprotein E2A-Pbx1 |
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