• Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

TANK potentiates tumor necrosis factor receptor-associated factor-mediated c-Jun N-terminal kinase/stress-activated protein kinase activation through the germinal center kinase pathway.

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 kappaB (NF-kappaB) 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-kappaB activator (TANK), in TRAF2-mediated NF-kappaB 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-kappaB 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.

Pubmed ID: 10490605

Authors

  • Chin AI
  • Shu J
  • Shan Shi C
  • Yao Z
  • Kehrl JH
  • Cheng G

Journal

Molecular and cellular biology

Publication Data

October 3, 1999

Associated Grants

  • Agency: NIGMS NIH HHS, Id: GM 08042
  • Agency: NIGMS NIH HHS, Id: GM57559

Mesh Terms

  • Adaptor Proteins, Signal Transducing
  • Antigens, CD40
  • B-Lymphocytes
  • Enzyme Activation
  • Germinal Center
  • Humans
  • Lymphocytes
  • MAP Kinase Kinase 4
  • MAP Kinase Kinase Kinase 1
  • MAP Kinase Kinase Kinases
  • MAP Kinase Signaling System
  • Mitogen-Activated Protein Kinase Kinases
  • Mitogen-Activated Protein Kinases
  • Palatine Tonsil
  • Peptide Fragments
  • Protein-Serine-Threonine Kinases
  • Proteins
  • Receptors, Tumor Necrosis Factor
  • T-Lymphocytes
  • TNF Receptor-Associated Factor 2
  • TNF Receptor-Associated Factor 5
  • TNF Receptor-Associated Factor 6