Activation and Autoregulation of DNA-PK from Structured Single-Stranded DNA and Coding End Hairpins

• Published in: Proceedings of the National Academy of Sciences - PNAS 2001-08, Vol.98 (17), p.9605-9610
• Main Authors: Soubeyrand, Sébastien, Torrance, Heather, Giffin, Ward, Gong, Wenrong, Schild-Poulter, Caroline, Robert J. G. Haché
• Format: Article
• Language: English
• Subjects: Antibodies; Base Sequence; Biochemistry; Biological Sciences; Deoxyribonucleic acid; DNA; DNA Nucleotidyltransferases - metabolism; DNA, Single-Stranded - metabolism; DNA-Activated Protein Kinase; DNA-Binding Proteins; DNA-dependent protein kinase; Enzyme Activation; Enzymes; Gels; Humans; Molecular Sequence Data; Molecules; Nuclear Proteins; Nucleic Acid Conformation; Nucleotides; Oligonucleotides; Peptide Fragments - metabolism; Phosphorylation; Protein Processing, Post-Translational; Protein-Serine-Threonine Kinases - metabolism; Proteins; Quantification; Recombinant Fusion Proteins - metabolism; Single stranded DNA; Structure-Activity Relationship; Substrate Specificity; Tumor Suppressor Protein p53 - metabolism; VDJ Recombinases
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.171211398

DNA-dependent protein kinase (DNA-PK) acts through an essential relationship with DNA to participate in the regulation of multiple cellular processes. Yet the role of DNA as a cofactor in kinase activity remains to be completely elucidated. For example, although DNA-PK activity appears to be required for the resolution of hairpin coding ends in variable diversity joining recombination, kinase activity remains to be demonstrated from hairpin ends or other DNA structures. In the present study we report that DNA-PK is strongly activated from hairpin ends and structured single-stranded DNA, but that the phosphorylation of many heterologous substrates is blocked efficiently by inactivation of the kinase through autophosphorylation. However, substrates that bound efficiently to single-stranded DNA such as p53 and replication protein A were efficiently phosphorylated by DNA-PK from structured DNA. DNA-PK also was found to be active toward heterologous substrates from hairpin ends on double-stranded DNA under conditions where autophosphorylation was minimized. These results suggest that the role of DNA-PK in resolving coding end hairpins is likely to be enzymatic rather than structural, expand understanding of how DNA-PK binding to structured DNA relates to enzyme activity, and suggest a mechanism for autoregulatory control of its kinase activity in the cell.