Abstract
Tumor necrosis factor (TNF) receptor-associated factors (TRAFs) are mediators of many members of the TNF receptor superfamily and can activate both the nuclear factor κB (NF-κB) and stress-activated protein kinase (SAPK; also known as c-Jun N-terminal kinase) signal transduction pathways. We previously described the involvement of a TRAF-interacting molecule, TRAF-associated NF-κB activator (TANK), in TRAF2-mediated NF-κB activation. Here we show that TANK synergized with TRAF2, TRAF5, and TRAF6 but not with TRAF3 in SAPK activation. TRAF2 and TANK individually formed weak interactions with germinal center kinase (GCK)-related kinase (GCKR). However, when coexpressed, they formed a strong complex with GCKR, thereby providing a potential mechanism for TRAF and TANK synergy in GCKR-mediated SAPK activation, which is important in TNF family receptor signaling. Our results also suggest that TANK can form potential intermolecular as well as intramolecular interactions between its amino terminus and carboxyl terminus. This study suggests that TANK is a regulatory molecule controlling the threshold of NF-κB and SAPK activities in response to activation of TNF receptors. In addition, CD40 activated endogenous GCKR in primary B cells, implicating GCK family proteins in CD40-mediated B-cell functions.
ACKNOWLEDGMENTS
A. Chin, J. Shu, and C. Shi contributed equally to this work.
This work was supported by Boehringer Ingelheim Pharmaceuticals Inc. and National Institute of General Medical Sciences grant GM57559. A. Chin is a recipient of the UCLA Medical Science Training Program training grant GM 08042, and J. Shu is a postdoctoral fellow supported by Boehringer Ingelheim Pharmaceuticals Inc.
We thank R. Davis, M. Karin, and Z. Luo for various constructs, M. Kehry for soluble CD8-gp39, and T. Parks and K. Catron for helpful discussions.