| Literature DB >> 11927590 |
Hua Cheng1, Carlo Cenciarelli, Mingyuan Tao, Wade P Parks, Cecilia Cheng-Mayer.
Abstract
hTid-1, a human DnaJ protein, is a novel cellular target for HTLV-1 Tax. Here, we show that hTid-1 represses NF-kappaB activity induced by Tax as well as other activators such as tumor necrosis factor alpha (TNFalpha) and Bcl10. hTid-1 specifically suppresses serine phosphorylation of IkappaBalpha by activated IkappaB kinase beta (IKKbeta), but the activities of other serine kinases including p38, ERK2, and JNK1 are not affected. The suppressive activity of hTid-1 on IKKbeta requires a functional J domain that mediates association with heat shock proteins and results in prolonging the half-life of the NF-kappaB inhibitors IkappaBalpha and IkappaBbeta. Collectively, our data suggest that hTid-1, in association with heat shock proteins, exerts a negative regulatory effect on the NF-kappaB activity induced by various extracellular and intracellular activators including HTLV-1 Tax.Entities:
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Year: 2002 PMID: 11927590 DOI: 10.1074/jbc.M201204200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157