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Close encounters of many kinds: Fos-Jun interactions that mediate transcription regulatory specificity.
- Source :
-
Oncogene [Oncogene] 2001 Apr 30; Vol. 20 (19), pp. 2438-52. - Publication Year :
- 2001
-
Abstract
- Fos and Jun family proteins regulate the expression of a myriad of genes in a variety of tissues and cell types. This functional versatility emerges from their interactions with related bZIP proteins and with structurally unrelated transcription factors. These interactions at composite regulatory elements produce nucleoprotein complexes with high sequence-specificity and regulatory selectivity. Several general principles including binding cooperativity and conformational adaptability have emerged from studies of regulatory complexes containing Fos-Jun family proteins. The structural properties of Fos-Jun family proteins including opposite orientations of heterodimer binding and the ability to bend DNA can contribute to the assembly and functions of such complexes. The cooperative recruitment of transcription factors, coactivators and chromatin remodeling factors to promoter and enhancer regions generates multiprotein transcription regulatory complexes with cell- and stimulus-specific transcriptional activities. The gene-specific architecture of these complexes can mediate the selective control of transcriptional activity.
- Subjects :
- Animals
Base Sequence
Basic-Leucine Zipper Transcription Factors
DNA metabolism
DNA-Binding Proteins metabolism
Enhancer Elements, Genetic
G-Box Binding Factors
Macromolecular Substances
Molecular Sequence Data
Promoter Regions, Genetic
Protein Structure, Tertiary
Proto-Oncogene Proteins c-fos physiology
Proto-Oncogene Proteins c-jun physiology
Transcription Factor AP-1 chemistry
Transcription Factor AP-1 metabolism
Transcription Factor AP-1 physiology
Transcription Factors metabolism
Transcriptional Activation
Proto-Oncogene Proteins c-fos chemistry
Proto-Oncogene Proteins c-fos metabolism
Proto-Oncogene Proteins c-jun chemistry
Proto-Oncogene Proteins c-jun metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0950-9232
- Volume :
- 20
- Issue :
- 19
- Database :
- MEDLINE
- Journal :
- Oncogene
- Publication Type :
- Academic Journal
- Accession number :
- 11402339
- Full Text :
- https://doi.org/10.1038/sj.onc.1204385