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Published on: November 1, 2011
Identification of distal silencing elements in the murine interferon-A11 gene promoter
1Laboratoire de Régulation de l'Expression des Gènes Eucaryotes, UPR 37-CNRS, UFR Biomédicale, Université, René Descartes, Paris, France.
Abstract:
The murine interferon-A11 (Mu IFN-A11) gene is a member of the IFN-A multigenic family. In mouse L929 cells, the weak response of the gene's promoter to viral induction is due to a combination of both a point mutation in the virus responsive element (VRE) and the presence of negatively regulating sequences surrounding the VRE. In the distal part of the promoter, the negatively acting E1E2 sequence was delimited. This sequence displays an inhibitory effect in either orientation or position on the inducibility of a virus-responsive heterologous promoter. It selectively represses VRE-dependent transcription but is not able to reduce the transcriptional activity of a VRE-lacking promoter. In a transient transfection assay, an E1E2-containing DNA competitor was able to derepress the native Mu IFN-A11 promoter. Specific nuclear factors bind to this sequence; thus the binding of trans-regulators participates in the repression of the Mu IFN-A11 gene. The E1E2 sequence contains an IFN regulatory factor (IRF)-binding site. Recombinant IRF2 binds this sequence and anti-IRF2 antibodies supershift a major complex formed with nuclear extracts. The protein composing the complex is 50 kDa in size, indicating the presence of IRF2 or antigenically related proteins in the complex. The Mu IFN-A11 gene is the first example within the murine IFN-A family, in which a distal promoter element has been identified that can negatively modulate the transcriptional response to viral induction.
Insights
The murine interferon-A11 (Mu IFN-A11) gene
Area of Science:
- Immunology
- Molecular Biology
- Gene Regulation
Background:
- The murine interferon-A11 (Mu IFN-A11) gene is part of the IFN-A multigenic family.
- Its promoter shows weak viral induction response due to a mutation and negative regulatory sequences.
Purpose of the Study:
- To investigate the molecular mechanisms behind the weak viral inducibility of the Mu IFN-A11 gene promoter.
- To identify and characterize the negatively regulating sequences within the Mu IFN-A11 promoter.
Main Methods:
- Delimitation of the E1E2 negative regulatory sequence in the distal promoter.
- Transient transfection assays using heterologous promoters and DNA competitors.
- Electrophoretic mobility shift assays (EMSAs) with nuclear extracts and recombinant IRF2.
Main Results:
- A distal promoter element, E1E2, was identified that negatively regulates Mu IFN-A11 gene inducibility.
- E1E2 selectively represses virus-responsive element (VRE)-dependent transcription.
- IRF2 was identified as a specific nuclear factor binding to the E1E2 sequence, mediating repression.
Conclusions:
- The E1E2 sequence and its bound trans-regulators, including IRF2, are responsible for repressing the Mu IFN-A11 gene's response to viral induction.
- This study identifies the first distal negative regulatory element in the murine IFN-A family, elucidating a novel mechanism of interferon gene control.
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