| Literature DB >> 26311312 |
Riku Fagerlund1, Marcelo Behar1, Karen T Fortmann1, Y Eason Lin2, Jesse D Vargas2, Alexander Hoffmann3.
Abstract
The magnitude, duration and oscillation of cellular signalling pathway responses are often limited by negative feedback loops, defined as an 'activator-induced inhibitor' regulatory motif. Within the NFκB signalling pathway, a key negative feedback regulator is IκBα. We show here that, contrary to current understanding, NFκB-inducible expression is not sufficient for providing effective negative feedback. We then employ computational simulations of NFκB signalling to identify IκBα molecular properties that are critical for proper negative feedback control and test the resulting predictions in biochemical and single-cell live-imaging studies. We identified nuclear import and nuclear export of IκBα and the IκBα-NFκB complex, as well as the free IκBα half-life, as key determinants of post-induction repression of NFκB and the potential for subsequent reactivation. Our work emphasizes that negative feedback is an emergent systems property determined by multiple molecular and biophysical properties in addition to the required 'activator-induced inhibitor' relationship.Entities:
Keywords: IκBα; NFκB; gene regulation; negative feedback; oscillation
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Year: 2015 PMID: 26311312 PMCID: PMC4614452 DOI: 10.1098/rsif.2015.0262
Source DB: PubMed Journal: J R Soc Interface ISSN: 1742-5662 Impact factor: 4.118