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    Proc Natl Acad Sci U S A. 2003 May 13;100(10):5991-6. Epub 2003 May 5.

    Caspase-mediated processing of the Drosophila NF-kappaB factor Relish.

    Stoven S, Silverman N, Junell A, Hedengren-Olcott M, Erturk D, Engstrom Y, Maniatis T, Hultmark D.

    Umeå Centre for Molecular Pathogenesis, Umeå University, S-901 87 Umeå, Sweden. Svenja.Stoven@ucmp.umu.se

    The NF-kappaB-like transcription factor Relish plays a central role in the innate immune response of Drosophila. Unlike other NF-kappaB proteins, Relish is activated by endoproteolytic cleavage to generate a DNA-binding Rel homology domain and a stable IkappaB-like fragment. This signal-induced endoproteolysis requires the activity of several gene products, including the IkappaB kinase complex and the caspase Dredd. Here we used mutational analysis and protein microsequencing to demonstrate that a caspase target site, located in the linker region between the Rel and the IkappaB-like domain, is the site of signal-dependent cleavage. We also show physical interaction between Relish and Dredd, suggesting that Dredd indeed is the Relish endoprotease. In addition to the caspase target site, the C-terminal 107 aa of Relish are required for endoproteolysis and signal-dependent phosphorylation by the Drosophila IkappaB kinase beta. Finally, an N-terminal serine-rich region in Relish and the PEST domain were found to negatively regulate Relish activation.

    PMID: 12732719 [PubMed - indexed for MEDLINE]

    PMCID: PMC156314

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