Ubiquitin binding mediates the NF-κB inhibitory potential of ABIN proteins

Deregulated nuclear factor κB (NF-κB) activation plays an important role in inflammation and tumorigenesis. ABIN proteins have been characterized as negative regulators of NF-κB signaling. However, their mechanism of NF-κB inhibition remained unclear. With the help of a yeast two-hybrid screen, we i...

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Bibliographic Details
Published inOncogene Vol. 27; no. 26; pp. 3739 - 3745
Main Authors Wagner, S, Carpentier, I, Rogov, V, Kreike, M, Ikeda, F, Löhr, F, Wu, C-J, Ashwell, J D, Dötsch, V, Dikic, I, Beyaert, R
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 12.06.2008
Nature Publishing Group
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Summary:Deregulated nuclear factor κB (NF-κB) activation plays an important role in inflammation and tumorigenesis. ABIN proteins have been characterized as negative regulators of NF-κB signaling. However, their mechanism of NF-κB inhibition remained unclear. With the help of a yeast two-hybrid screen, we identified ABIN proteins as novel ubiquitin-interacting proteins. The minimal ubiquitin-binding domain (UBD) corresponds to the ABIN homology domain 2 (AHD2) and is highly conserved in ABIN-1, ABIN-2 and ABIN-3. Moreover, this region is also present in NF-κB essential modulator/IκB kinase γ (NEMO/IKKγ) and the NEMO-like protein optineurin, and is therefore termed UB D in A BIN proteins and N EMO (UBAN). Nuclear magnetic resonance studies of the UBAN domain identify it as a novel type of UBD, with the binding surface on ubiquitin being significantly different from the binding surface of other UBDs. ABIN-1 specifically binds ubiquitinated NEMO via a bipartite interaction involving its UBAN and NEMO-binding domain. Mutations in the UBAN domain led to a loss of ubiquitin binding and impaired the NF-κB inhibitory potential of ABINs. Taken together, these data illustrate an important role for ubiquitin binding in the negative regulation of NF-κB signaling by ABINs and identify UBAN as a novel UBD.
ISSN:0950-9232
1476-5594
DOI:10.1038/sj.onc.1211042