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  6. Keywords
  7. Topics
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We are analyzing https://link.springer.com/article/10.1007/bf02736784.

Title:
Three related brain nuclear receptors, NGFI-B, Nurr1, and NOR-1, as transcriptional activators | Journal of Molecular Neuroscience
Description:
Three related orphan nuclear receptors that are expressed in the brain, NGFI-B, Nurr1, and NOR-1, were studied to compare their function as transcriptional activators. NGFI-B was able to activate (in the absence of added hormone) in CV1 cells both an NGFI-B-responsive luciferase reporter gene (containing eight copies of a response element for NGFI-B upstream of a basal prolactin promoter driving the luciferase gene, NBRE8-LUC), a similar thyroid hormone-receptor-responsive reporter gene (TRE3-LUC), and a reporter gene with an authentic promoter from aXenopus vitellogenin gene containing two binding sites for the estrogen receptor (vit-LUC). NGFI-B activated NBRE8-LUC and TRE3-LUC (but not the vit-LUC) with an amino-terminal activation domain. Nurr1 was less promiscuous as a transcriptional activator, activating the NBRE8-LUC better than NGFI-B, but less than NGFI-B at the other reporter genes. NOR-1 activated only the NBRE8-LUC reporter gene. These results indicate that closely related nuclear receptors may differentiate between response elements or promoters and that different activation mechanisms exist depending on the promoter. This may contribute to regulation of specificity of target gene expression in the brain.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
  • Education
  • Telecommunications

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We can't figure out the monetization strategy.

Websites don't always need to be profitable; some serve as platforms for education or personal expression. Websites can serve multiple purposes. And this might be one of them. Link.springer.com could be getting rich in stealth mode, or the way it's monetizing isn't detectable.

Keywords {🔍}

article, google, scholar, pubmed, cas, gene, ngfib, receptor, nuclear, receptors, related, transcriptional, paulsen, hormone, reporter, response, access, milbrandt, nurr, orphan, factor, steroid, privacy, cookies, content, journal, brain, element, binding, expression, transcription, growth, cell, dna, publish, research, search, molecular, nbreluc, thyroid, activation, genes, regulation, open, biol, data, information, log, activators, december,

Topics {✒️}

brain-specific transcription factor month download article/chapter nuclear hormone receptors simple phase-extraction assay nuclear orphan receptors reporter gene responsive nbre8-luc reporter gene amino-terminal activation domain response elements reporter genes related subjects t-cell hybrid require glucocorticoid receptor gene full article pdf growth factor treatment nuclear receptor ngfi privacy choices/manage cookies response element human estrogen receptor firefly luciferase gene axenopus vitellogenin gene transcriptional activators published chloramphenicol acyltransferase activity reporter gene t-cell receptor december 1995 volume 6 european economic area 3disco-based immunocytochemistry apoptotic signals delivered chain terminating inhibitors zinc finger residues conditions privacy policy molecular neuroscience aims male mice revealed target gene expression t-cell hybridomas accepting optional cookies article journal nucleic acids res transcriptionally inducible member genes check access instant access journal finder publish added hormone main content log dna binding site estrogen receptor luciferase gene article paulsen

Schema {🗺️}

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         headline:Three related brain nuclear receptors, NGFI-B, Nurr1, and NOR-1, as transcriptional activators
         description:Three related orphan nuclear receptors that are expressed in the brain, NGFI-B, Nurr1, and NOR-1, were studied to compare their function as transcriptional activators. NGFI-B was able to activate (in the absence of added hormone) in CV1 cells both an NGFI-B-responsive luciferase reporter gene (containing eight copies of a response element for NGFI-B upstream of a basal prolactin promoter driving the luciferase gene, NBRE8-LUC), a similar thyroid hormone-receptor-responsive reporter gene (TRE3-LUC), and a reporter gene with an authentic promoter from aXenopus vitellogenin gene containing two binding sites for the estrogen receptor (vit-LUC). NGFI-B activated NBRE8-LUC and TRE3-LUC (but not the vit-LUC) with an amino-terminal activation domain. Nurr1 was less promiscuous as a transcriptional activator, activating the NBRE8-LUC better than NGFI-B, but less than NGFI-B at the other reporter genes. NOR-1 activated only the NBRE8-LUC reporter gene. These results indicate that closely related nuclear receptors may differentiate between response elements or promoters and that different activation mechanisms exist depending on the promoter. This may contribute to regulation of specificity of target gene expression in the brain.
         datePublished:
         dateModified:
         pageStart:249
         pageEnd:255
         sameAs:https://doi.org/10.1007/BF02736784
         keywords:
            Gene regulation
            NGFI-B
            NOR-1
            Nurr1
            transcription factor
            Neurosciences
            Neurochemistry
            Cell Biology
            Proteomics
            Neurology
         image:
         isPartOf:
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            volumeNumber:6
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               name:Ragnhild E. Paulsen
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                        type:PostalAddress
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                     name:University of Oslo, Biotechnology Centre of Oslo
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                        name:Institute of Pharmacy, University of Oslo, Biotechnology Centre of Oslo, Oslo, Norway
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      headline:Three related brain nuclear receptors, NGFI-B, Nurr1, and NOR-1, as transcriptional activators
      description:Three related orphan nuclear receptors that are expressed in the brain, NGFI-B, Nurr1, and NOR-1, were studied to compare their function as transcriptional activators. NGFI-B was able to activate (in the absence of added hormone) in CV1 cells both an NGFI-B-responsive luciferase reporter gene (containing eight copies of a response element for NGFI-B upstream of a basal prolactin promoter driving the luciferase gene, NBRE8-LUC), a similar thyroid hormone-receptor-responsive reporter gene (TRE3-LUC), and a reporter gene with an authentic promoter from aXenopus vitellogenin gene containing two binding sites for the estrogen receptor (vit-LUC). NGFI-B activated NBRE8-LUC and TRE3-LUC (but not the vit-LUC) with an amino-terminal activation domain. Nurr1 was less promiscuous as a transcriptional activator, activating the NBRE8-LUC better than NGFI-B, but less than NGFI-B at the other reporter genes. NOR-1 activated only the NBRE8-LUC reporter gene. These results indicate that closely related nuclear receptors may differentiate between response elements or promoters and that different activation mechanisms exist depending on the promoter. This may contribute to regulation of specificity of target gene expression in the brain.
      datePublished:
      dateModified:
      pageStart:249
      pageEnd:255
      sameAs:https://doi.org/10.1007/BF02736784
      keywords:
         Gene regulation
         NGFI-B
         NOR-1
         Nurr1
         transcription factor
         Neurosciences
         Neurochemistry
         Cell Biology
         Proteomics
         Neurology
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            1559-1166
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         name:Humana Press
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            name:Ragnhild E. Paulsen
            affiliation:
                  name:Division for Environmental Toxicology
                  address:
                     name:Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller, Norway
                     type:PostalAddress
                  type:Organization
                  name:University of Oslo, Biotechnology Centre of Oslo
                  address:
                     name:Institute of Pharmacy, University of Oslo, Biotechnology Centre of Oslo, Oslo, Norway
                     type:PostalAddress
                  type:Organization
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            name:Kjersti Granås
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                  name:Division for Environmental Toxicology
                  address:
                     name:Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller, Norway
                     type:PostalAddress
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            name:Helge Johnsen
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                  name:Division for Environmental Toxicology
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                     name:Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller, Norway
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      address:
         name:Institute of Pharmacy, University of Oslo, Biotechnology Centre of Oslo, Oslo, Norway
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      address:
         name:Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller, Norway
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         name:Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller, Norway
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         name:Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller, Norway
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            name:University of Oslo, Biotechnology Centre of Oslo
            address:
               name:Institute of Pharmacy, University of Oslo, Biotechnology Centre of Oslo, Oslo, Norway
               type:PostalAddress
            type:Organization
      name:Kjersti Granås
      affiliation:
            name:Division for Environmental Toxicology
            address:
               name:Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller, Norway
               type:PostalAddress
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            name:Division for Environmental Toxicology
            address:
               name:Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller, Norway
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            name:Division for Environmental Toxicology
            address:
               name:Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller, Norway
               type:PostalAddress
            type:Organization
      name:Sigrun Sterri
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            name:Division for Environmental Toxicology
            address:
               name:Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller, Norway
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      name:Institute of Pharmacy, University of Oslo, Biotechnology Centre of Oslo, Oslo, Norway
      name:Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller, Norway
      name:Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller, Norway
      name:Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller, Norway
      name:Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller, Norway
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