Abstract
Receptor-interacting protein (RIP) is a serine/threonine protein kinase that is critically involved in tumor necrosis factor receptor-1 (TNF-R1)-induced NF-kappaB activation. In a yeast two-hybrid screening for potential RIP-interacting proteins, we identified a novel protein designated as NKAP. Although NKAP interacts with RIP in yeast, NKAP does not interact with RIP in mammalian cells in co-immunoprecipitation experiments. When overexpressed in 293 cells, NKAP activated NF-kappaB in a dose-dependent manner. Moreover, down-regulation of NKAP by antisense RNA significantly inhibited TNF- and IL-1-induced NF-kappaB activation. Immunofluorescent staining indicated that NKAP was localized in the nucleus. Our findings suggest that NKAP is a novel nuclear regulator of TNF- and IL-1-induced NF-kappaB activation.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Antigens, CD / metabolism*
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Blotting, Western
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Cell Line
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Cell Nucleus / metabolism*
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Cloning, Molecular
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Co-Repressor Proteins
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DNA, Complementary / metabolism
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Dose-Response Relationship, Drug
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Down-Regulation
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Enzyme Activation
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Genes, Reporter
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Humans
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Luciferases / metabolism
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Mice
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Microscopy, Fluorescence
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Molecular Sequence Data
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NF-kappa B / metabolism*
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Nuclear Proteins / chemistry*
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Nuclear Proteins / genetics
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Nuclear Proteins / metabolism*
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Plasmids / metabolism
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Precipitin Tests
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Protein Binding
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Proteins / physiology*
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Receptor-Interacting Protein Serine-Threonine Kinases
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Receptors, Tumor Necrosis Factor / metabolism*
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Receptors, Tumor Necrosis Factor, Type I
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Recombinant Proteins / metabolism
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Repressor Proteins
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Sequence Homology, Amino Acid
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Transfection
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Two-Hybrid System Techniques
Substances
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Antigens, CD
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Co-Repressor Proteins
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DNA, Complementary
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NF-kappa B
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NKAP protein, human
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Nuclear Proteins
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Proteins
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Receptors, Tumor Necrosis Factor
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Receptors, Tumor Necrosis Factor, Type I
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Recombinant Proteins
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Repressor Proteins
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Luciferases
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RIPK1 protein, human
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Receptor-Interacting Protein Serine-Threonine Kinases
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Ripk1 protein, mouse