Casein kinase 1alpha governs antigen-receptor-induced NF-kappaB activation and human lymphoma cell survival.

Abstract

The transcription factor NF-kappaB is required for lymphocyte activation and proliferation as well as the survival of certain lymphoma types. Antigen receptor stimulation assembles an NF-kappaB activating platform containing the scaffold protein CARMA1 (also called CARD11), the adaptor BCL10 and the paracaspase MALT1 (the CBM complex), linked to the inhibitor of NF-kappaB kinase complex, but signal transduction is not fully understood. We conducted parallel screens involving a mass spectrometry analysis of CARMA1 binding partners and an RNA interference screen for growth inhibition of the CBM-dependent 'activated B-cell-like' (ABC) subtype of diffuse large B-cell lymphoma (DLBCL). Here we report that both screens identified casein kinase 1alpha (CK1alpha) as a bifunctional regulator of NF-kappaB. CK1alpha dynamically associates with the CBM complex on T-cell-receptor (TCR) engagement to participate in cytokine production and lymphocyte proliferation. However, CK1alpha kinase activity has a contrasting role by subsequently promoting the phosphorylation and inactivation of CARMA1. CK1alpha has thus a dual 'gating' function which first promotes and then terminates receptor-induced NF-kappaB. ABC DLBCL cells required CK1alpha for constitutive NF-kappaB activity, indicating that CK1alpha functions as a conditionally essential malignancy gene-a member of a new class of potential cancer therapeutic targets.

DOI: 10.1038/nature07613

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@article{Bidre2009CaseinK1, title={Casein kinase 1alpha governs antigen-receptor-induced NF-kappaB activation and human lymphoma cell survival.}, author={Nicolas Bid{\`e}re and Vu N. Ngo and Jeansun Lee and Cailin T Collins and Lixin Zheng and Fengyi Wan and Ricardo E. Davis and Georg Lenz and Dane E. Anderson and Damien Arnoult and Aim{\'e} V{\'a}zquez and Keiko Sakai and Jun Zhang and Zhaojing Meng and Timothy D. Veenstra and Louis M . Staudt and Michael J. Lenardo}, journal={Nature}, year={2009}, volume={458 7234}, pages={92-6} }