Transposon-based mutagenesis identifies short RIP1 as an activator of NFκB

• Published in: Cell cycle (Georgetown, Tex.) Tex.), 2008-07, Vol.7 (14), p.2249-2256
• Main Authors: Dasgupta, Maupali, Agarwal, Mukesh K., Varley, Patrick, Lu, Tao, Stark, George R., Kandel, Eugene S.
• Format: Article
• Language: English
• Subjects: Binding; Biology; Bioscience; Calcium; Cancer; Cell; Cycle; Landes; Organogenesis; Proteins
• ISSN: 1538-4101; 1551-4005
• DOI: 10.4161/cc.7.14.6310

We used a vector based on the Sleeping Beauty transposon to search for constitutive activators of NF-κB in cultured cells. Dominant mutations were produced by random insertion of a tetracycline-regulated promoter, which provided robust and exceptionally well-regulatedexpression of downstream genes. The ability to regulate the mutant phenotype was used to attribute the latter to the insertional event. In one such mutant, the promoter was inserted in the middle of the gene encoding receptor-interacting protein kinase 1 (RIP1). The protein encoded by the hybrid transcript lacks the putative kinase domain of RIP1, but potently stimulates NF-κB, AP-1 and Ets-1 activity. Similarly to TNFα treatment, expression of the short RIP1 was toxic to cells that failed to up-regulate NF-κB. The effects of short RIP1 did not require endogenous RIP1 or cytokine treatment and coincided with reduced responsiveness to TNFα. Additional evidenceindicates that a similar short RIP1 could be produced naturally from the ripk1 locus. Interestingly, elevated expression of short RIP1 resulted in the loss of full length RIP1 from cells, pointing to a novel mechanism through which the abundance of RIP1 and the status of the related signaling cascades may be regulated.