An Assay for Quantifying DNA Double-Strand Break Repair That Is Suitable for Small Numbers of Unlabeled Cells

• Published in: Radiation research 1997-01, Vol.147 (1), p.35-40
• Main Authors: Longo, John A., Nevaldine, Barbara, Longo, Sharon L., Winfield, Jeffrey A., Hahn, Peter J.
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Cell lines; CHO cells; Chromosomes, Fungal; Chromosomes, Human - radiation effects; DNA Damage; DNA Repair; DNA, Neoplasm - radiation effects; Dose-Response Relationship, Radiation; Dosimetry; Electrophoresis; Fundamental and applied biological sciences. Psychology; Gels; Glioblastoma - genetics; Humans; Kinetics; Molecular and cellular biology; Molecular genetics; Mutagenesis. Repair; Phosphors; Phosphorus Radioisotopes; Saccharomyces cerevisiae - genetics; Schizosaccharomyces - genetics; Solar X rays; Tumor cell line; Tumor Cells, Cultured; Tumors; X-Rays
• ISSN: 0033-7587; 1938-5404
• DOI: 10.2307/3579440

A system based on pulsed-field gel electrophoresis (PFGE) is described which measures the induction and repair of DNA double-strand breaks (DSBs) in a biologically relevant X-ray dose range (below 10 Gy) using as few as 125 cells per time. This system was used to measure repair in cells of a freshly obtained human glioblastoma multiforme tumor. No prelabeling of the cells is required, and many different cell types can be studied using this system. Under the pulsed-field conditions used, DNA in the range of 2 to 6 Mb enters the PFGE gel and forms an upper compression zone directly under each well. To quantify the DSBs after electrophoresis, the DNA was transferred to nylon membranes and hybridized with 32 P-labeled chromosomal DNA. Phosphor screens were exposed to the membranes and scanned on a phosphor imager. The kinetics of induction and repair was determined by measuring the amount of DNA in the compression zones compared to the amount in the wells. EMT-6 cells were used to demonstrate this method. Induction of DSBs by doses of 0-7.5 Gy X rays was assayed using approximately 12,500 cells per dose and was shown to be linear. Double-strand breaks from 1 Gy were detected above background. To determine a lower limit of the number of cells that could be used to measure DSB repair, cells were embedded in agarose at decreasing concentrations per plug, exposed to 7.5 Gy X irradiation and allowed to repair at 37°C for up to 60 min. DNA from approximately 12,500, 1,250 and 125 cells per time was loaded and subjected to PFGE. The average fast-repair half-time was 3 min and the slow-repair half-time was 35 min. The kinetics of DSB repair in glioblastoma multiforme cells was also determined using this system. Agarose plugs were prepared from a cell suspension, irradiated with 7.5 Gy X rays and allowed to repair for up to 90 min. DNA from approximately 1,250 tumor cells was electrophoresed and analyzed as described above for EMT-6 cells. For this particular tumor, approximately 75% of the induced DSBs were repaired after 90 min. Data presented show that this PFGE-based system is an extremely sensitive method for measuring DSB induction and repair after low doses of X rays using very few cells.