A novel mechanism of nuclear factor-kappaB regulation by adenoviral protein 14.7K

Carmody, R. J. , Maguschak, K. and Chen, Y. H. (2006) A novel mechanism of nuclear factor-kappaB regulation by adenoviral protein 14.7K. Immunology, 117(2), pp. 188-95. (doi:10.1111/j.1365-2567.2005.02277.) (PMID:16423054) (PMCID:PMC1782211)

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Viruses have evolved many different ways to evade immune attacks. The adenoviral E3 protein 14.7K effectively inhibits antiviral immunity and inflammation. However, the underlying mechanism for this effect is unclear. Here we show that 14.7K is a potent inhibitor of nuclear factor (NF)-kappaB transcriptional activity following Toll-like receptor (TLR) or tumour necrosis factor (TNF) receptor signalling. The inhibition of the NF-kappaB activity occurs downstream of IkappaBalpha degradation and NF-kappaB translocation into the nucleus. Analysis of NF-kappaB DNA binding reveals that 14.7K specifically inhibits p50 homodimer DNA binding and that this inhibition is mediated through the interaction of 14.7K with p50. We propose that 14.7K inhibits NF-kappaB activity through directly blocking p50 binding to DNA and that this is the basis for its anti-inflammatory properties. Our data also indicate a role for p50 homodimer-dependent transcription in inflammation.

Item Type:Articles
Glasgow Author(s) Enlighten ID:Carmody, Dr Ruaidhri
Authors: Carmody, R. J., Maguschak, K., and Chen, Y. H.
Subjects:Q Science > Q Science (General)
College/School:College of Medical Veterinary and Life Sciences > Institute of Infection Immunity and Inflammation
Journal Name:Immunology
ISSN (Online):1365-2567

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