Werner Shannon L, Kearns Jeffrey D, Zadorozhnaya Victoria, Lynch Candace, O'Dea Ellen, Boldin Mark P, Ma Averil, Baltimore David, Hoffmann Alexander
Signaling Systems Laboratory, Department of Chemistry and Biochemistry, University of California at San Diego, La Jolla, California 92093, USA.
Genes Dev. 2008 Aug 1;22(15):2093-101. doi: 10.1101/gad.1680708.
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.
肿瘤坏死因子(TNF)诱导的核因子κB(NF-κB)活性呈现出复杂的时间调控,其不同阶段会导致不同的基因表达程序。通过结合实验研究和数学建模,我们确定了两个时间放大步骤——一个由强制性负反馈调节因子IκBα决定,它定义了NF-κB活性第一阶段的持续时间。第二阶段由A20定义,其诱导性表达提供了一种变阻器功能,其他炎症刺激可借此调节TNF反应。我们的结果描绘了IκBα和A20基因敲除表型所暗示的非冗余功能,并确定A20是控制炎症和发育反应的信号转导交叉对话介质。