Regulation of the transcriptional activity of c-Fos by ERK. A novel role for the prolyl isomerase PIN1.
The activation of the activating protein-1 (AP-1) family of transcription factors, including c-Fos and c-Jun family members, is one of the earliest nuclear events induced by growth factors that stimulate extracellular signal-regulated kinases (ERKs). In the case of c-Fos, the activation of ERK leads to an increased expression of c-fos ... mRNA. In turn, we have recently shown that ERK phosphorylates multiple residues within the carboxylterminal transactivation domain (TAD) of c-Fos, thus resulting in its increased transcriptional activity. However, how ERK-dependent phosphorylation regulates c-Fos function is still poorly understood. In this regard, it has been recently observed that the prolyl isomerase Pin1 can interact with proteins phosphorylated on serine or threonine residues that precede prolines (pS/T-P), such as the transcription factors p53 and c-Jun, thereby controlling their activity by promoting the cis-trans isomerization of these pS/T-P bonds. Here, we found that Pin1 binds c-Fos through specific pS/T-P sites within the c-Fos TAD, and that this interaction results in an enhanced transcriptional response of c-Fos to polypeptide growth factors that stimulate ERK. Our findings suggest that c-Fos represents a novel target for the isomerizing activity of Pin1 and support a role for Pin1 in the mechanism by which c-Jun and c-Fos can cooperate to regulate AP-1-dependent gene transcription upon phosphorylation by mitogen-activated kinase (MAPK) family members.
Mesh Terms:
Animals, Cell Line, Cell Nucleus, DNA, Dose-Response Relationship, Drug, Enzyme Activation, Extracellular Signal-Regulated MAP Kinases, Glutathione Transferase, Humans, Ligands, MAP Kinase Signaling System, Mice, NIH 3T3 Cells, NIMA-Interacting Peptidylprolyl Isomerase, Peptidylprolyl Isomerase, Phosphorylation, Proline, Protein Binding, Protein Structure, Tertiary, Proto-Oncogene Proteins c-fos, Proto-Oncogene Proteins c-jun, Recombinant Fusion Proteins, Transcription Factor AP-1, Transcription, Genetic, Transcriptional Activation, Transfection, Tumor Suppressor Protein p53
Animals, Cell Line, Cell Nucleus, DNA, Dose-Response Relationship, Drug, Enzyme Activation, Extracellular Signal-Regulated MAP Kinases, Glutathione Transferase, Humans, Ligands, MAP Kinase Signaling System, Mice, NIH 3T3 Cells, NIMA-Interacting Peptidylprolyl Isomerase, Peptidylprolyl Isomerase, Phosphorylation, Proline, Protein Binding, Protein Structure, Tertiary, Proto-Oncogene Proteins c-fos, Proto-Oncogene Proteins c-jun, Recombinant Fusion Proteins, Transcription Factor AP-1, Transcription, Genetic, Transcriptional Activation, Transfection, Tumor Suppressor Protein p53
J. Biol. Chem.
Date: Oct. 21, 2005
PubMed ID: 16123044
View in: Pubmed Google Scholar
Download Curated Data For This Publication
214785
Switch View:
- Interactions 3