Abstract
DNA synthesized in human cells within the first hour after ultraviolet (UV) irradiation is made in segments of lower molecular weight than in nonirradiated cells. The size of these segments approximates the average distance between pyrimidine dimers in the parental DNA. This suggests that the dimers interrupt normal DNA synthesis and result in gaps in the newly synthesized DNA. However, DNA synthesized in human cells at long times after irradiation is made in segments equal or nearly equal to those synthesized by nonirradiated cells. The recovery of the ability to synthesize DNA in segments of normal size occurs in normal human cells, where the dimers are excised, and also in cells of the human mutants xeroderma pigmentosum (XP), where the dimers remain in the DNA. This observation implies that the pyrimidine dimer may not be the lesion that causes DNA to be synthesized in smaller than normal segments.
MeSH Terms
Cell Line
Centrifugation, Density Gradient
Chromosome Aberrations/metabolism
Chromosome Disorders
DNA/biosynthesis,radiation effects
DNA Repair
DNA Replication
Dwarfism/metabolism
Fibroblasts/metabolism,radiation effects
Humans
Hypogonadism/metabolism
Intellectual Disability/metabolism
Isotope Labeling
Microcephaly/metabolism
Models, Biological
Radiation Effects
Species Specificity
Thymidine
Time Factors
Tritium
Ultraviolet Rays
Xeroderma Pigmentosum/metabolism
Chemicals
Tritium
DNA
Thymidine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Buhl S N
Setlow R B
Regan J D
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