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Multiple phosphorylation events control chicken ovalbumin upstream promoter transcription factor I orphan nuclear
Frédérique Gay1, Peter Baráth, Christine Desbois-Le Péron
1Equipe Information et Programmation Cellulaire, Unité Mixte de Recherche 6026 Centre National de la Recherche Scientifique, Université de Rennes I, Campus de Beaulieu, 35042 Rennes Cedex, France.
Abstract:
Chicken ovalbumin upstream promoter transcription factor I (COUP-TFI) is an orphan member of the nuclear hormone receptor superfamily that comprises key regulators of many biological functions, such as embryonic development, metabolism, homeostasis, and reproduction. Although COUP-TFI can both actively silence gene transcription and antagonize the functions of various other nuclear receptors, the COUP-TFI orphan receptor also acts as a transcriptional activator in certain contexts. Moreover, COUP-TFI has recently been shown to serve as an accessory factor for some ligand-bound nuclear receptors, suggesting that it may modulate, both negatively and positively, a wide range of hormonal responses. In the absence of any identified cognate ligand, the mechanisms involved in the regulation of COUP-TFI activity remain unclear. The elucidation of several putative phosphorylation sites for MAPKs, PKC, and casein kinase II within the sequence of this orphan receptor led us to investigate phosphorylation events regulating the various COUP-TFI functions. After showing that COUP-TFI is phosphorylated in vivo, we provide evidence that in vivo inhibition of either MAPK or PKC signaling pathway leads to a specific and pronounced decrease in COUP-TFI-dependent transcriptional activation of the vitronectin gene promoter. Focusing on the molecular mechanisms underlying the MAPK- and PKC-mediated regulation of COUP-TFI activity, we show that COUP-TFI can be directly targeted by PKC and MAPK. These phosphorylation events differentially modulate COUP-TFI functions: PKC-mediated phosphorylation enhances COUP-TFI affinity for DNA and MAPK-mediated phosphorylation positively regulates the transactivation function of COUP-TFI, possibly through enhancing specific coactivator recruitment. These data provide evidence that COUP-TFI is likely to integrate distinct signaling pathways and raise the possibility that multiple extracellular signals influence biological processes controlled by COUP-TFI.
Insights
Chicken ovalbumin upstream promoter transcription factor I (COUP-TFI) is phosphorylated by MAPK and PKC, affecting its gene regulation. These modifications enhance DNA binding and coactivator recruitment, integrating signaling pathways for biological control.
Area of Science:
- Molecular Biology
- Gene Regulation
- Signal Transduction
Background:
- Chicken ovalbumin upstream promoter transcription factor I (COUP-TFI) is a nuclear receptor regulating development, metabolism, and reproduction.
- COUP-TFI acts as a transcriptional repressor, activator, and modulator of other nuclear receptors.
- Mechanisms regulating COUP-TFI activity are unclear, especially in the absence of a known ligand.
Purpose of the Study:
- To investigate the role of phosphorylation in regulating COUP-TFI functions.
- To elucidate the molecular mechanisms of MAPK and PKC in modulating COUP-TFI activity.
Main Methods:
- In vivo phosphorylation analysis of COUP-TFI.
- Inhibition of MAPK and PKC signaling pathways.
- Reporter gene assays for vitronectin gene promoter activity.
- In vitro kinase assays to determine direct targeting by PKC and MAPK.
Main Results:
- COUP-TFI is phosphorylated in vivo.
- Inhibition of MAPK or PKC significantly reduces COUP-TFI-dependent vitronectin gene promoter activation.
- PKC enhances COUP-TFI DNA binding affinity.
- MAPK positively regulates COUP-TFI transactivation function, likely via coactivator recruitment.
Conclusions:
- COUP-TFI activity is regulated by phosphorylation events mediated by MAPK and PKC.
- Phosphorylation differentially modulates COUP-TFI's DNA binding and transactivation capabilities.
- COUP-TFI integrates distinct signaling pathways, suggesting extracellular signals influence its biological roles.