Encoding NF-κB temporal control in response to TNF: distinct roles for the negative regulators IκBα and A20
Abstract
TNF-induced NF-κB activity shows complex temporal regulation whose different phases lead to distinct gene expression programs. Combining experimental studies and mathematical modeling, we identify two temporal amplification steps—one determined by the obligate negative feedback regulator IκBα—that define the duration of the first phase of NF-κB activity. The second phase is defined by A20, whose inducible expression provides for a rheostat function by which other inflammatory stimuli can regulate TNF responses. Our results delineate the nonredundant functions implied by the knockout phenotypes of iκbα and a20, and identify the latter as a signaling cross-talk mediator controlling inflammatory and developmental responses.
Additional Information
© 2008 by Cold Spring Harbor Laboratory Press. Received April 2, 2008; revised version accepted June 16, 2008. We acknowledge J. Hasty, B. Kholodenko, J. Faeder, and A. Levchenko for insightful discussions. This study was supported by National Institutes of Health R01 grant GM72024. S.L.W. is supported by the NSF Graduate Research Fellowship, and J.D.K. is supported by an American Heart Association Predoctoral Fellowship.Attached Files
Published - Genes_Dev.-2008-Werner-2093-101.pdf
Supplemental Material - WernerSuppMat.pdf
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Additional details
- PMCID
- PMC2492747
- Eprint ID
- 102677
- Resolver ID
- CaltechAUTHORS:20200421-065944620
- NIH
- R01 GM72024
- NSF Graduate Research Fellowship
- American Heart Association
- Created
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2020-04-21Created from EPrint's datestamp field
- Updated
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2021-11-16Created from EPrint's last_modified field