Back to Search
Start Over
Activation of the alpha-internexin promoter by the Brn-3a transcription factor is dependent on the N-terminal region of the protein.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 1995 Feb 10; Vol. 270 (6), pp. 2853-8. - Publication Year :
- 1995
-
Abstract
- The Brn-3a, Brn-3b, and Brn-3c proteins are closely related POU (Pit-Oct-Unc) family transcription factors which are expressed predominantly in neuronal cells. We have identified the alpha-internexin gene as the first reported, neuronally expressed, target gene whose promoter activity is modulated by these factors. Both the Brn-3a and Brn-3c factors can activate the alpha-internexin promoter while Brn-3b represses it and can prevent activation by Brn-3a. Using chimeric constructs containing different regions of Brn-3a or Brn-3b, we show that activation of the alpha-internexin promoter requires the N-terminal region of Brn-3a. In contrast the activation by Brn-3a but not Brn-3b of an artificial promoter containing a synthetic Brn-3 binding site can be shown using the same constructs to be dependent on the POU domain of Brn-3a. Moreover, the isolated POU domain of Brn-3a can activate this artificial promoter but not the alpha-internexin promoter. Hence Brn-3a contains two distinct transactivation domains, at the N terminus and within the POU domain, whose effect is dependent upon the target promoter. The relationship of gene transactivation by Brn-3a to its ability to transform primary cells which is also dependent on the N-terminal region of the protein is discussed.
- Subjects :
- Base Sequence
Bucladesine pharmacology
Cell Line
Intermediate Filament Proteins
Molecular Sequence Data
Oligodeoxyribonucleotides
Protein Binding
Transcription Factor Brn-3
Transcription Factor Brn-3B
Transcription Factor Brn-3C
Carrier Proteins genetics
DNA-Binding Proteins metabolism
Promoter Regions, Genetic
Transcription Factors metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 270
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 7852360
- Full Text :
- https://doi.org/10.1074/jbc.270.6.2853