Multiple conserved regulatory elements with overlapping functions determine Sox10 expression in mouse embryogenesis
Expression and function of the transcription factor Sox10 is predominant in neural crest cells, its derivatives and in oligodendrocytes. To understand how Sox10 expression is regulated during development, we analysed the potential of evolutionary conserved non-coding sequences in the Sox10 genomic r...
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Veröffentlicht in: | Nucleic acids research 2007-10, Vol.35 (19), p.6526-6538 |
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creator | Werner, Torsten Hammer, Alexander Wahlbuhl, Mandy Bösl, Michael R. Wegner, Michael |
description | Expression and function of the transcription factor Sox10 is predominant in neural crest cells, its derivatives and in oligodendrocytes. To understand how Sox10 expression is regulated during development, we analysed the potential of evolutionary conserved non-coding sequences in the Sox10 genomic region to function as enhancers. By linking these sequences to a β-galactosidase marker gene under the control of a minimal promoter, five regulatory regions were identified that direct marker gene expression in transgenic mice to Sox10 expressing cell types and tissues in a defined temporal pattern. These possible enhancers of the Sox10 gene mediate Sox10 expression in the otic vesicle, in oligodendrocytes and in several neural crest derivatives including the developing peripheral nervous system and the adrenal gland. They furthermore exhibit overlapping activities and share binding sites for Sox, Lef/Tcf, Pax and AP2 transcription factors. This may explain high level and robustness of Sox10 expression during embryonic development. |
doi_str_mv | 10.1093/nar/gkm727 |
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To understand how Sox10 expression is regulated during development, we analysed the potential of evolutionary conserved non-coding sequences in the Sox10 genomic region to function as enhancers. By linking these sequences to a β-galactosidase marker gene under the control of a minimal promoter, five regulatory regions were identified that direct marker gene expression in transgenic mice to Sox10 expressing cell types and tissues in a defined temporal pattern. These possible enhancers of the Sox10 gene mediate Sox10 expression in the otic vesicle, in oligodendrocytes and in several neural crest derivatives including the developing peripheral nervous system and the adrenal gland. They furthermore exhibit overlapping activities and share binding sites for Sox, Lef/Tcf, Pax and AP2 transcription factors. 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To understand how Sox10 expression is regulated during development, we analysed the potential of evolutionary conserved non-coding sequences in the Sox10 genomic region to function as enhancers. By linking these sequences to a β-galactosidase marker gene under the control of a minimal promoter, five regulatory regions were identified that direct marker gene expression in transgenic mice to Sox10 expressing cell types and tissues in a defined temporal pattern. These possible enhancers of the Sox10 gene mediate Sox10 expression in the otic vesicle, in oligodendrocytes and in several neural crest derivatives including the developing peripheral nervous system and the adrenal gland. They furthermore exhibit overlapping activities and share binding sites for Sox, Lef/Tcf, Pax and AP2 transcription factors. This may explain high level and robustness of Sox10 expression during embryonic development.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>Binding Sites</subject><subject>Birds - genetics</subject><subject>Cell Line</subject><subject>Conserved Sequence</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Embryo, Mammalian - metabolism</subject><subject>Embryonic Development - genetics</subject><subject>Enhancer Elements, Genetic</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Genomics</subject><subject>High Mobility Group Proteins - genetics</subject><subject>High Mobility Group Proteins - metabolism</subject><subject>Humans</subject><subject>Mammals - genetics</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>SOXE Transcription Factors</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0VuL1DAUB_AgijuuvvgBJAj6INTNrUn7Iuh6WWFcERXEl5Cmp7PZbZOatOPMtzfSYb086FMC55dDzvkjdJ-Sp5TU_MSbeLK5GhRTN9CKcskKUUt2E60IJ2VBiaiO0J2ULgmhgpbiNjqiqqpVNiuU3s395MYesA0-QdxCiyNs5t5MIe4x9DCAnxL-7qYLHLYQezOOzm9wN3s7ufwGtzBBHJwH_DHsKMGwGyOklGvYeTyEOQGGoYn7sAEPyaW76FZn-gT3Ducx-vz61afTs2L9_s3b0-frwpaETUVZq7ItwVgqTMWFaA2rheHEmq5rKim5avOdsK6tLDEURAUNA2qgtnWnmpYfo2dL33FuBmhtHiSaXo_RDSbudTBO_1nx7kJvwlYzUpd5Q7nB40ODGL7NkCY9uGSh742HPJaWVV60FOy_kBHOSiqrDB_-BS_DHH3eQjZEMiaVyOjJgmwMKUXorr9Mif6ZuM6J6yXxjB_8PuQveog4g0cLCPP470bF4lyaYHctTbzSUnFV6rMvX_WH86o-Vy_X-gX_ARsFyHE</recordid><startdate>20071001</startdate><enddate>20071001</enddate><creator>Werner, Torsten</creator><creator>Hammer, Alexander</creator><creator>Wahlbuhl, Mandy</creator><creator>Bösl, Michael R.</creator><creator>Wegner, Michael</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</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>7QL</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20071001</creationdate><title>Multiple conserved regulatory elements with overlapping functions determine Sox10 expression in mouse embryogenesis</title><author>Werner, Torsten ; 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subjects | Animals Base Sequence Binding Sites Birds - genetics Cell Line Conserved Sequence DNA-Binding Proteins - genetics DNA-Binding Proteins - metabolism Embryo, Mammalian - metabolism Embryonic Development - genetics Enhancer Elements, Genetic Gene Expression Regulation, Developmental Genomics High Mobility Group Proteins - genetics High Mobility Group Proteins - metabolism Humans Mammals - genetics Mice Mice, Transgenic SOXE Transcription Factors Transcription Factors - genetics Transcription Factors - metabolism |
title | Multiple conserved regulatory elements with overlapping functions determine Sox10 expression in mouse embryogenesis |
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