Regulation of NF-κB activity through lysine monomethylation of p65
- Creators
- Ea, Chee-Kwee
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Baltimore, David
Abstract
NF-κB is a key activator of inflammatory and immune responses with important pathological roles in cancer, heart disease, and autoimmune diseases. Transcriptional activity of NF-κB is regulated by different posttranslational modifications. Here, we report a novel mechanism of NF-κB regulation through lysine monomethylation by SET9 methyltransferase. Set9 specifically methylates p65 at lysine 37. Both TNFα and IL-1β treatments induced methylation of p65. Methylated p65 is restricted to the nucleus and this modification regulates the promoter binding of p65. Moreover, Set9 mediated methylation of p65 is required for the expression of a subset of NF-κB target genes in response to TNFα stimulation.
Additional Information
© 2009 by the National Academy of Sciences. Contributed by David Baltimore, September 14, 2009 (sent for review July 31, 2009). Published online before print October 28, 2009. We thank Dr. Danny Reinberg (NYU) for Set9 plasmids and Dr. Shengli Hao and Dr. Parameswaran Ramakrishnan for critically reading the manuscript. Author contributions: C.-K.E. and D.B. designed research; C.-K.E. performed research; C.-K.E. and D.B. analyzed data; and C.-K.E. and D.B. wrote the paper. This article contains supporting information online at www.pnas.org/cgi/content/full/0910439106/DCSupplemental. Freely available online through the PNAS open access option.Attached Files
Published - Ea2009p6440P_Natl_Acad_Sci_Usa.pdf
Supplemental Material - Ea2009p6440P_Natl_Acad_Sci_Usa_supp.pdf
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Additional details
- PMCID
- PMC2770010
- Eprint ID
- 16916
- Resolver ID
- CaltechAUTHORS:20091209-093326396
- Created
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2010-01-05Created from EPrint's datestamp field
- Updated
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2021-11-08Created from EPrint's last_modified field