DNA Replication and Postreplication Mismatch Repair in Cell-Free Extracts from Cultured Human Neuroblastoma and Fibroblast Cells

• Published in: The Journal of neuroscience 1997-11, Vol.17 (22), p.8711-8720
• Main Authors: David, Pascale, Efrati, Edna, Tocco, Georges, Krauss, Sharon Wald, Goodman, Myron F
• Format: Article
• Language: English
• Subjects: Antineoplastic Agents - pharmacology; Cell Differentiation - drug effects; Cell Differentiation - genetics; Cell Extracts - genetics; DNA Ligases - physiology; DNA Polymerase beta - metabolism; DNA Polymerase I - metabolism; DNA Repair - physiology; DNA Replication - physiology; DNA, Viral - genetics; Fibroblasts - cytology; Fibroblasts - enzymology; HeLa Cells; Humans; Neuroblastoma; Replication Origin - genetics; Simian virus 40 - genetics; Tretinoin - pharmacology
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/jneurosci.17-22-08711.1997

DNA synthesis and postreplication mismatch repair were measured in vitro using cell-free extracts from cultured human SY5Y neuroblastoma and WI38 fibroblast cells in different growth states. All extracts, including differentiated SY5Y and quiescent WI38 fibroblasts, catalyzed SV40 origin-dependent DNA synthesis, totally dependent on SV40 T-antigen. Thus, although differentiated neuroblastoma and quiescent fibroblasts cells were essentially nondividing, their extracts were competent for DNA replication using DNA polymerases delta, alpha, and possibly epsilon, with proliferating cell nuclear antigen. Nonreplicative DNA synthesis and lesion bypass by either alpha- or beta-polymerases were detected independently in extracts using primed or gapped single-stranded DNA templates. Long-patch postreplication mismatch repair was measured for the first time in neuroblastoma cell-free extracts. Extracts from subconfluent and high-density SY5Y cells catalyzed postreplication mismatch repair with efficiencies comparable to those of HeLa cell extracts. No significant differences were observed in repair between SY5Y differentiated and undifferentiated cell extracts. Mismatch repair efficiencies were threefold lower in extracts from subconfluent WI38 cells, and repair in WI38 quiescent cells was fourfold less than in subconfluent cells, suggesting that mismatch repair may be regulated. The spectrum of mismatch repair in SY5Y extracts closely resembled the mismatch removal specificities of HeLa extracts: T . G and G . G mismatches were repaired most efficiently; C . A, A . A, A . G and a five-base loop were repaired with intermediate efficiency; repair of G . A, C . C, and T . T mismatches was extremely inefficient.