AI Article Synopsis

  • TNF-induced NF-kappaB activity involves complex timing that affects different gene expression outcomes.
  • Researchers combined experiments and mathematical modeling to identify two key steps in this timing: one regulated by the negative feedback of IkappaBalpha and the other by the gene A20.
  • The study highlights the unique roles of IkappaBalpha and A20, showing that A20 helps modulate TNF responses by acting as a mediator for other inflammatory signals.

Article Abstract

TNF-induced NF-kappaB 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 IkappaBalpha-that define the duration of the first phase of NF-kappaB 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 ikappabalpha and a20, and identify the latter as a signaling cross-talk mediator controlling inflammatory and developmental responses.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2492747PMC
http://dx.doi.org/10.1101/gad.1680708DOI Listing

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