p53-mediated repression of nuclear factor-kappaB RelA via the transcriptional integrator p300

Autor: Ravi, R., Mookerjee, B., Hensbergen, Y., Bedi, Gc, Antonio Giordano, El Deiry WS, Fuchs, Ej, Bedi, A.
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Zdroj: Università degli Studi di Siena-IRIS
Popis: The p53 tumor suppressor gene plays an instrumental role in transcriptional regulation of target genes involved in cellular stress responses. p53-dependent transactivation and transrepression require its interaction with p300/CBP, a coactivator that also interacts with the RelA subunit of nuclear factor-kappaB. We find that p53 inhibits RelA-dependent transactivation without altering RelA expression or inducible kappaB-DNA binding. p53-mediated repression of RelA is relieved by p300 overexpression and the increased RelA activity conferred by p53-deficiency is counteracted by either transactivation domain-deficient p300 fragments that bind RelA or a transdominant mutant of IkappaB alpha. Our results suggest that p53 can regulate diverse kappaB-dependent cellular responses.
Databáze: OpenAIRE