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A Chromatin Immunoprecipitation Assay to Identify Novel NFAT2 Target Genes in Chronic Lymphocytic Leukemia
Published on: December 4, 2018
Partners in transcription: NFAT and AP-1
F Macián1, C López-Rodríguez, A Rao
1Department of Pathology, Harvard Medical School and the Center for Blood Research, 200 Longwood Avenue, Boston, Massachusetts, MA 02115, USA.
Abstract:
Combinatorial regulation is a powerful mechanism that enables tight control of gene expression, via integration of multiple signaling pathways that induce different transcription factors required for enhanceosome assembly. The four calcium-regulated transcription factors of the NFAT family act synergistically with AP-1 (Fos/Jun) proteins on composite DNA elements which contain adjacent NFAT and AP-1 binding sites, where they form highly stable ternary complexes to regulate the expression of diverse inducible genes. Concomitant induction of NFAT and AP-1 requires concerted activation of two different signaling pathways: calcium/calcineurin, which promotes NFAT dephosphorylation, nuclear translocation and activation; and protein kinase C (PKC)/Ras, which promotes the synthesis, phosphorylation and activation of members of the Fos and Jun families of transcription factors. A fifth member of the NFAT family, NFAT5, controls the cellular response to osmotic stress, by a mechanism that requires dimer formation and is independent of calcineurin or of interaction with AP-1. Pharmacological interference with theNFAT:AP-1 interaction may be useful in selective manipulation of the immune response. Balanced activation of NFAT and AP-1 is known to be required for productive immune responses, but the role of NFAT:AP-1 interactions in other cell types and biological processes remains to be understood.
Insights
Nuclear Factor of Activated T-cells (NFAT) and Activator Protein-1 (AP-1) transcription factors synergize to control gene expression. Their interaction is crucial for immune responses, with potential for therapeutic targeting.
Area of Science:
- Molecular Biology
- Immunology
- Cell Signaling
Background:
- Combinatorial gene regulation integrates multiple signaling pathways for precise control.
- NFAT and AP-1 transcription factors form stable complexes on composite DNA elements.
- NFAT activation relies on calcium/calcineurin signaling, while AP-1 involves PKC/Ras pathways.
Purpose of the Study:
- To elucidate the synergistic mechanism of NFAT and AP-1 in gene regulation.
- To understand the distinct signaling pathways governing NFAT and AP-1 activation.
- To explore the therapeutic potential of targeting NFAT:AP-1 interactions.
Main Methods:
- Analysis of transcription factor synergy on composite DNA elements.
- Investigating calcium/calcineurin and PKC/Ras signaling pathways.
- Examining the role of NFAT5 in osmotic stress response.
Main Results:
- NFAT and AP-1 form stable ternary complexes, regulating inducible gene expression.
- Concerted activation of distinct signaling pathways drives NFAT and AP-1 induction.
- NFAT5 functions independently of calcineurin and AP-1 in osmotic stress response.
Conclusions:
- NFAT:AP-1 interaction is a key mechanism for regulating immune responses.
- Targeting NFAT:AP-1 interactions offers potential for immune modulation.
- Further research is needed to understand NFAT:AP-1 roles in other biological contexts.
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