Literature DB >> 8065921

The DNA target site for the Brn-3 POU family transcription factors can confer responsiveness to cyclic AMP and removal of serum in neuronal cells.

V Budhram-Mahadeo1, T Theil, P J Morris, K A Lillycrop, T Moroy, D S Latchman.   

Abstract

The POU factors Brn-3a and Brn-3b are closely related transcription factors which are expressed in neuronal cells. The levels of the transcripts encoding these factors are regulated in opposite directions in neuronal cells by specific cellular signalling pathways with dibutyryl cyclic AMP treatment and serum removal enhancing the level of Brn-3a and reducing the level of Brn-3b expression. This opposite expression pattern is paralleled by the ability of Brn-3a to specifically transactivate a target promoter bearing its DNA binding site whereas this promoter is repressed by Brn-3b. As predicted from these observations this target promoter is strongly activated by serum removal or addition of dibutyryl cyclic AMP. Therefore changes in Brn-3a and b expression can have a functional effect on promoter activity indicating that Brn-3a and Brn-3b can regulate gene expression via a specific binding site in response to the activation of specific cellular signalling pathways. The reasons for the differences in activity between these two related factors and their role in regulating gene activity in the nervous system are discussed.

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Year:  1994        PMID: 8065921      PMCID: PMC310280          DOI: 10.1093/nar/22.15.3092

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  38 in total

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Journal:  Nucleic Acids Res       Date:  1987-07-10       Impact factor: 16.971

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Journal:  Nature       Date:  1989-07-06       Impact factor: 49.962

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Journal:  Nature       Date:  1988-12-15       Impact factor: 49.962

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Journal:  Genes Dev       Date:  1988-12       Impact factor: 11.361

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Authors:  M Finney; G Ruvkun; H R Horvitz
Journal:  Cell       Date:  1988-12-02       Impact factor: 41.582

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Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1983-07-01       Impact factor: 3.365

9.  Mouse Brn-3 family of POU transcription factors: a new aminoterminal domain is crucial for the oncogenic activity of Brn-3a.

Authors:  T Theil; S McLean-Hunter; M Zörnig; T Möröy
Journal:  Nucleic Acids Res       Date:  1993-12-25       Impact factor: 16.971

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Authors:  A McCormick; H Brady; L E Theill; M Karin
Journal:  Nature       Date:  1990-06-28       Impact factor: 49.962

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  9 in total

1.  Alternative splicing of the Brn-3a and Brn-3b transcription factor RNAs is regulated in neuronal cells.

Authors:  Y Z Liu; S J Dawson; D S Latchman
Journal:  J Mol Neurosci       Date:  1996       Impact factor: 3.444

2.  The N-terminal domain unique to the long form of the Brn-3a transcription factor is essential to protect neuronal cells from apoptosis and for the activation of Bbcl-2 gene expression.

Authors:  M D Smith; S J Dawson; L M Boxer; D S Latchman
Journal:  Nucleic Acids Res       Date:  1998-09-15       Impact factor: 16.971

3.  The ability of POU family transcription factors to activate or repress gene expression is dependent on the spacing and context of their specific response elements.

Authors:  S J Dawson; Y Z Liu; B Rodel; T Möröy; D S Latchman
Journal:  Biochem J       Date:  1996-03-01       Impact factor: 3.857

4.  The Brn-3a transcription factor induces neuronal process outgrowth and the coordinate expression of genes encoding synaptic proteins.

Authors:  M D Smith; S J Dawson; D S Latchman
Journal:  Mol Cell Biol       Date:  1997-01       Impact factor: 4.272

5.  Activation of the herpes simplex virus immediate-early gene promoters by neuronally expressed POU family transcription factors.

Authors:  K A Lillycrop; Y Z Liu; T Theil; T Möröy; D S Latchman
Journal:  Biochem J       Date:  1995-04-15       Impact factor: 3.857

6.  Differential regulation of neuronal nicotinic acetylcholine receptor subunit gene promoters by Brn-3 POU family transcription factors.

Authors:  N G Milton; A Bessis; J P Changeux; D S Latchman
Journal:  Biochem J       Date:  1996-07-15       Impact factor: 3.857

7.  The HPV-activating cellular transcription factor Brn-3a is overexpressed in CIN3 cervical lesions.

Authors:  D Ndisdang; P J Morris; C Chapman; L Ho; A Singer; D S Latchman
Journal:  J Clin Invest       Date:  1998-04-15       Impact factor: 14.808

8.  POU transcription factors Brn-3a and Brn-3b interact with the estrogen receptor and differentially regulate transcriptional activity via an estrogen response element.

Authors:  V Budhram-Mahadeo; M Parker; D S Latchman
Journal:  Mol Cell Biol       Date:  1998-02       Impact factor: 4.272

9.  Cloning and initial characterization of an alternatively spliced transcript encoded by the bovine herpes virus 1 latency-related gene.

Authors:  Laxminarayana R Devireddy; Yange Zhang; Clinton J Jones
Journal:  J Neurovirol       Date:  2003-12       Impact factor: 2.643

  9 in total

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