DNA end-independent activation of DNA-PK mediated via association with the DNA-binding protein C1D.
DNA-dependent protein kinase (DNA-PK), which is involved in DNA double-strand break repair and V(D)J recombination, is comprised of a DNA-targeting component termed Ku and an approximately 465-kD catalytic subunit, DNA-PKcs. Although DNA-PK phosphorylates proteins in the presence of DSBs or other discontinuities in the DNA double helix in vitro, the ... possibility exists that it is also activated in other circumstances via its association with additional proteins. Here, through use of the yeast two-hybrid screen, we discover that the recently identified high affinity DNA binding protein C1D interacts with the putative leucine zipper region of DNA-PKcs. Furthermore, we show that C1D can interact with DNA-PK in mammalian cells and that C1D is a very effective DNA-PK substrate in vitro. Finally, we establish that C1D directs the activation of DNA-PK in a manner that does not require DNA termini. Therefore, these studies provide a function for C1D and suggest novel mechanisms for DNA-PK activation in vivo.
Mesh Terms:
3T3 Cells, Amino Acid Sequence, Animals, COS Cells, Cell Line, Transformed, DNA, Superhelical, DNA-Activated Protein Kinase, DNA-Binding Proteins, Enzyme Activation, Hela Cells, Humans, Leucine Zippers, Mice, Molecular Sequence Data, Nuclear Proteins, Peptides, Phosphorylation, Plasmids, Protein-Serine-Threonine Kinases, Recombinant Fusion Proteins, Substrate Specificity
3T3 Cells, Amino Acid Sequence, Animals, COS Cells, Cell Line, Transformed, DNA, Superhelical, DNA-Activated Protein Kinase, DNA-Binding Proteins, Enzyme Activation, Hela Cells, Humans, Leucine Zippers, Mice, Molecular Sequence Data, Nuclear Proteins, Peptides, Phosphorylation, Plasmids, Protein-Serine-Threonine Kinases, Recombinant Fusion Proteins, Substrate Specificity
Genes Dev.
Date: Jul. 15, 1998
PubMed ID: 9679063
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