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Published September 7, 2012 | Published + Supplemental Material
Journal Article Open

EHMT1 Protein Binds to Nuclear Factor-κB p50 and Represses Gene Expression

Abstract

Transcriptional homeostasis relies on the balance between positive and negative regulation of gene transcription. Methylation of histone H3 lysine 9 (H3K9) is commonly correlated with gene repression. Here, we report that a euchromatic H3K9 methyltransferase, EHMT1, functions as a negative regulator in both the NF-κB- and type I interferon-mediated gene induction pathways. EHMT1 catalyzes H3K9 methylation at promoters of NF-κB target genes. Moreover, EHMT1 interacts with p50, and, surprisingly, p50 appears to repress the expression of type I interferon genes and genes activated by type I interferons by recruiting EHMT1 to catalyze H3K9 methylation at their promoter regions. Silencing the expression of EHMT1 by RNA interference enhances expression of a subset NF-κB-regulated genes, augments interferon production, and augments antiviral immunity.

Additional Information

© 2012 American Society for Biochemistry and Molecular Biology, Inc. Received March 22, 2012; Revision received July 14, 2012. First Published on July 16, 2012. This work was supported, in whole or in part, by National Institutes of Health Grant 2R01GM039458. This work was also supported by the University of Malaya HIR Grant UM.C/625/1/HIR/MOHE/CHAN-02; H-50001-A000022. We thank Dr. Yoichi Shinkai (Kyoto University, Japan) for EHMT1 plasmids, Dr. Jesse Bloom for the influenza virus and HEK293-PB1 and A549-PB1 cells, Dr. Shengli Hao, Dr. Michael Bethune and Dr. Parameswaran Ramakrishnan for critically reading the manuscript.

Attached Files

Published - J._Biol._Chem.-2012-Ea-31207-17.pdf

Supplemental Material - jbc.M112.365601-1.doc

Supplemental Material - jbc.M112.365601-2.xlsx

Supplemental Material - jbc.M112.365601-3.xlsx

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