The nuclear factor-?B (NF-?B) family of dimeric transcription factors controls key biological events such as innate and immune responses, and cell proliferation and programmed cell death, by regulating the expression of a wide range of genes that are directly involved in those biological processes. The NF-?B family is comprised of five subunits, p50 (NF-kappaB1), p52 (NF-kappaB2), p65 (RelA), c-Rel and RelB, which form functional NF-kappaB dimers in a combinatorial manner. The p52/RelB heterodimer is one of the combinatorial dimers which is a key player transcription factor in lymphoid cells. p52 is derived from the precursor protein p100 through processing by the proteasome in response to specific stimuli. The mechanism of this unusual, signal-dependent partial degradation of a molecule by the proteasome is unknown. The focus of this application is to study how the signal-dependent processing of p 100 to p52 occurs. We propose a model to explain the mechanism that underlies this processing event. It is known that RelB does not associate with itself or with p65 and c-Rel. However, it preferentially associates with p100. These observations lead us to hypothesize that hetero-dimerization with RelB is a pre-requisite event for p100 to be processed into p52 and the formation of the p52/RelB heterodimer. This proposal will test whether or not association with RelB is an obligatory step for p100 processing, and whether the p100/RelB dimer is a structurally unique dimer compared to other NF-kappaB dimers. Our preliminary experiments have shown that in RelB deficient cells, p100 processing to p52 is blocked. We have further revealed that the dimerization domain of RelB is relatively unstable and this lack of stability might be critical for the formation of the inactive p100/RelB heterodimer. This proposal will integrate in vitro biochemical and X-ray crystallographic studies with in vivo experiments using various NF-kappaB subunit knock out cells to understand the mechanism of activation of an important NF-kappaB heterodimer.
| Wang, Vivien Ya-Fan; Li, Yidan; Kim, Daniel et al. (2017) Bcl3 Phosphorylation by Akt, Erk2, and IKK Is Required for Its Transcriptional Activity. Mol Cell 67:484-497.e5 |
| Polley, Smarajit; Passos, Dario Oliveira; Huang, De-Bin et al. (2016) Structural Basis for the Activation of IKK1/?. Cell Rep 17:1907-1914 |
| Fusco, Amanda J; Mazumder, Anup; Wang, Vivien Ya-Fan et al. (2016) The NF-?B subunit RelB controls p100 processing by competing with the kinases NIK and IKK1 for binding to p100. Sci Signal 9:ra96 |
| Tao, Zhihua; Fusco, Amanda; Huang, De-Bin et al. (2014) p100/I?B? sequesters and inhibits NF-?B through kappaBsome formation. Proc Natl Acad Sci U S A 111:15946-51 |
| Vu, Don; Huang, De-Bin; Vemu, Annapurna et al. (2013) A structural basis for selective dimerization by NF-?B RelB. J Mol Biol 425:1934-1945 |
| Ghosh, Gourisankar; Wang, Vivien Ya-Fan; Huang, De-Bin et al. (2012) NF-?B regulation: lessons from structures. Immunol Rev 246:36-58 |
| Tao, Zhihua; Ghosh, Gourisankar (2012) Understanding NIK regulation from its structure. Structure 20:1615-7 |
| Wang, Vivien Ya-Fan; Huang, Wendy; Asagiri, Masataka et al. (2012) The transcriptional specificity of NF-?B dimers is coded within the ?B DNA response elements. Cell Rep 2:824-39 |
| Huxford, Tom; Hoffmann, Alexander; Ghosh, Gourisankar (2011) Understanding the logic of I?B:NF-?B regulation in structural terms. Curr Top Microbiol Immunol 349:1-24 |
| Savinova, Olga V; Hoffmann, Alexander; Ghosh, Gourisankar (2009) The Nfkb1 and Nfkb2 proteins p105 and p100 function as the core of high-molecular-weight heterogeneous complexes. Mol Cell 34:591-602 |
Showing the most recent 10 out of 14 publications
