Winged helix hepatocyte nuclear factor 3 and POU-domain protein Brn-2/N-Oct-3 bind overlapping sites on the neuronal promoter of human aromatic l-amino acid decarboxylase gene

The neuronal promoter of human aromatic l-amino acid decarboxylase gene has been analysed to elucidate the mechanisms of neuron type-specific expression. The (−560/+92) promoter segment was sufficient to direct luciferase expression at a higher level in SK-N-BE neuroblastoma cells, than in CHP126 ne...

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Veröffentlicht in:Brain research. Molecular brain research. 1998-05, Vol.56 (1), p.227-237
Hauptverfasser: Raynal, Jean-François, Dugast, Claire, Le Van Thaı̈, Agathe, Weber, Michel J.
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container_issue 1
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container_title Brain research. Molecular brain research.
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creator Raynal, Jean-François
Dugast, Claire
Le Van Thaı̈, Agathe
Weber, Michel J.
description The neuronal promoter of human aromatic l-amino acid decarboxylase gene has been analysed to elucidate the mechanisms of neuron type-specific expression. The (−560/+92) promoter segment was sufficient to direct luciferase expression at a higher level in SK-N-BE neuroblastoma cells, than in CHP126 neuroepithelia, HepG2 hepatoma or SK-Hep1 epithelioma cells. Deletions experiments showed that this segment contained a neuronal-specific (element T1) and a SK-N-BE-specific (element N1) cis-activating sequences. Element T1 (−72/−36) bound Sp1 and NF-Y proteins, and unidentified neuronal-specific factors. Element N1 (−102/−72) bound cell-specific factors, identified as HNF-3, N-Oct-3/Brn-2 and N-Oct-2. HNF-3 proteins recognized the sequence TCAGTAAATA that matches the consensus motif. Oct-1, N-Oct-2 and N-Oct-3 bound the AAATAATGC sequence that overlaps the HNF-3 binding site. In addition, we show that the HNF-3 binding sites from aldolase C and HNF-3β gene promoters also bind N-Oct-2 and N-Oct-3 proteins. These data suggest a functional interplay of winged helix/forkhead and POU-domain transcription factors on a variety of neuronal gene promoters.
doi_str_mv 10.1016/S0169-328X(98)00048-5
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Psychology ; Gene regulation ; Helix-Loop-Helix Motifs ; Hepatocyte Nuclear Factor 3-alpha ; Hepatocyte Nuclear Factor 3-beta ; Hepatocyte Nuclear Factor 3-gamma ; Homeodomain Proteins ; Humans ; Molecular and cellular biology ; Molecular genetics ; Neurons - cytology ; Neurons - metabolism ; NF-Y ; Nuclear Proteins - metabolism ; Nuclear Proteins - physiology ; POU Domain Factors ; Promoter Regions, Genetic - genetics ; Sp1 ; Transcription Factors - metabolism ; Transcription Factors - physiology ; Transcription. Transcription factor. Splicing. Rna processing ; Tumor Cells, Cultured</subject><ispartof>Brain research. 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Molecular brain research.</title><addtitle>Brain Res Mol Brain Res</addtitle><description>The neuronal promoter of human aromatic l-amino acid decarboxylase gene has been analysed to elucidate the mechanisms of neuron type-specific expression. The (−560/+92) promoter segment was sufficient to direct luciferase expression at a higher level in SK-N-BE neuroblastoma cells, than in CHP126 neuroepithelia, HepG2 hepatoma or SK-Hep1 epithelioma cells. Deletions experiments showed that this segment contained a neuronal-specific (element T1) and a SK-N-BE-specific (element N1) cis-activating sequences. Element T1 (−72/−36) bound Sp1 and NF-Y proteins, and unidentified neuronal-specific factors. Element N1 (−102/−72) bound cell-specific factors, identified as HNF-3, N-Oct-3/Brn-2 and N-Oct-2. HNF-3 proteins recognized the sequence TCAGTAAATA that matches the consensus motif. Oct-1, N-Oct-2 and N-Oct-3 bound the AAATAATGC sequence that overlaps the HNF-3 binding site. In addition, we show that the HNF-3 binding sites from aldolase C and HNF-3β gene promoters also bind N-Oct-2 and N-Oct-3 proteins. These data suggest a functional interplay of winged helix/forkhead and POU-domain transcription factors on a variety of neuronal gene promoters.</description><subject>Animals</subject><subject>Aromatic-L-Amino-Acid Decarboxylases - genetics</subject><subject>Binding Sites - genetics</subject><subject>Biological and medical sciences</subject><subject>COS Cells</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>DNA-Binding Proteins - physiology</subject><subject>DOPA decarboxylase</subject><subject>Dopamine</subject><subject>Drifter</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene regulation</subject><subject>Helix-Loop-Helix Motifs</subject><subject>Hepatocyte Nuclear Factor 3-alpha</subject><subject>Hepatocyte Nuclear Factor 3-beta</subject><subject>Hepatocyte Nuclear Factor 3-gamma</subject><subject>Homeodomain Proteins</subject><subject>Humans</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Neurons - cytology</subject><subject>Neurons - metabolism</subject><subject>NF-Y</subject><subject>Nuclear Proteins - metabolism</subject><subject>Nuclear Proteins - physiology</subject><subject>POU Domain Factors</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>Sp1</subject><subject>Transcription Factors - metabolism</subject><subject>Transcription Factors - physiology</subject><subject>Transcription. Transcription factor. Splicing. 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Psychology</topic><topic>Gene regulation</topic><topic>Helix-Loop-Helix Motifs</topic><topic>Hepatocyte Nuclear Factor 3-alpha</topic><topic>Hepatocyte Nuclear Factor 3-beta</topic><topic>Hepatocyte Nuclear Factor 3-gamma</topic><topic>Homeodomain Proteins</topic><topic>Humans</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Neurons - cytology</topic><topic>Neurons - metabolism</topic><topic>NF-Y</topic><topic>Nuclear Proteins - metabolism</topic><topic>Nuclear Proteins - physiology</topic><topic>POU Domain Factors</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>Sp1</topic><topic>Transcription Factors - metabolism</topic><topic>Transcription Factors - physiology</topic><topic>Transcription. Transcription factor. Splicing. 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Molecular brain research.</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raynal, Jean-François</au><au>Dugast, Claire</au><au>Le Van Thaı̈, Agathe</au><au>Weber, Michel J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Winged helix hepatocyte nuclear factor 3 and POU-domain protein Brn-2/N-Oct-3 bind overlapping sites on the neuronal promoter of human aromatic l-amino acid decarboxylase gene</atitle><jtitle>Brain research. Molecular brain research.</jtitle><addtitle>Brain Res Mol Brain Res</addtitle><date>1998-05-01</date><risdate>1998</risdate><volume>56</volume><issue>1</issue><spage>227</spage><epage>237</epage><pages>227-237</pages><issn>0169-328X</issn><eissn>1872-6941</eissn><abstract>The neuronal promoter of human aromatic l-amino acid decarboxylase gene has been analysed to elucidate the mechanisms of neuron type-specific expression. The (−560/+92) promoter segment was sufficient to direct luciferase expression at a higher level in SK-N-BE neuroblastoma cells, than in CHP126 neuroepithelia, HepG2 hepatoma or SK-Hep1 epithelioma cells. Deletions experiments showed that this segment contained a neuronal-specific (element T1) and a SK-N-BE-specific (element N1) cis-activating sequences. Element T1 (−72/−36) bound Sp1 and NF-Y proteins, and unidentified neuronal-specific factors. Element N1 (−102/−72) bound cell-specific factors, identified as HNF-3, N-Oct-3/Brn-2 and N-Oct-2. HNF-3 proteins recognized the sequence TCAGTAAATA that matches the consensus motif. Oct-1, N-Oct-2 and N-Oct-3 bound the AAATAATGC sequence that overlaps the HNF-3 binding site. In addition, we show that the HNF-3 binding sites from aldolase C and HNF-3β gene promoters also bind N-Oct-2 and N-Oct-3 proteins. These data suggest a functional interplay of winged helix/forkhead and POU-domain transcription factors on a variety of neuronal gene promoters.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>9602135</pmid><doi>10.1016/S0169-328X(98)00048-5</doi><tpages>11</tpages></addata></record>
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ispartof Brain research. Molecular brain research., 1998-05, Vol.56 (1), p.227-237
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subjects Animals
Aromatic-L-Amino-Acid Decarboxylases - genetics
Binding Sites - genetics
Biological and medical sciences
COS Cells
DNA-Binding Proteins - metabolism
DNA-Binding Proteins - physiology
DOPA decarboxylase
Dopamine
Drifter
Fundamental and applied biological sciences. Psychology
Gene regulation
Helix-Loop-Helix Motifs
Hepatocyte Nuclear Factor 3-alpha
Hepatocyte Nuclear Factor 3-beta
Hepatocyte Nuclear Factor 3-gamma
Homeodomain Proteins
Humans
Molecular and cellular biology
Molecular genetics
Neurons - cytology
Neurons - metabolism
NF-Y
Nuclear Proteins - metabolism
Nuclear Proteins - physiology
POU Domain Factors
Promoter Regions, Genetic - genetics
Sp1
Transcription Factors - metabolism
Transcription Factors - physiology
Transcription. Transcription factor. Splicing. Rna processing
Tumor Cells, Cultured
title Winged helix hepatocyte nuclear factor 3 and POU-domain protein Brn-2/N-Oct-3 bind overlapping sites on the neuronal promoter of human aromatic l-amino acid decarboxylase gene
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