RelA repression of RelB activity induces selective gene activation downstream of TNF receptors

Abstract

TNF-α is a potent proinflammatory cytokine that regulates immune and inflammatory responses and programmed cell death. TNF-α stimulation causes nuclear translocation of several NF-κB dimers, including RelA/p50 and RelB/p50. However, contrary to RelA, RelB entering the nucleus in response to TNF-α cannot bind to DNA in mouse embryonic fibroblasts, strongly suggesting that RelB DNA-binding activity is modulated by additional nuclear mechanisms. Here, we demonstrate that TNF-α promotes the association of RelA with RelB in the nucleus and that TNF-α-induced RelA/RelB heterodimers do not bind to κB sites. Remarkably, we show that RelA serine-276, the phosphorylation of which is induced by TNF receptor ligation, is crucial for RelA/RelB complex formation and subsequent inhibition of RelB DNA binding. In the absence of RelA phosphorylation on serine-276, TNF-α stimulation leads to a strong increase in the expression of endogenous NF-κB-responsive genes, such as Bcl-xL, whose transcriptional up-regulation is mainly controlled by RelB. Our findings demonstrate that RelA has a major regulatory role serving to dampen RelB activity in response to TNF-α and define a previously unrecognized mechanism that represents an essential step leading to selective NF-κB target gene expression.

• NF-κB
• phosphorylation
• target gene expression