The repair of cyclobutane pyrimidine dimers (CPDs), DNA lesions induce
d by ultraviolet light, was studied at nucleotide resolution. Human fi
broblasts were irradiated with ultraviolet light and allowed to repair
. The DNA was enzymatically cleaved at the CPDs, and the induced break
s along the promoter and exon 1 of the PGK1 gene were mapped by ligati
on-mediated polymerase chain reaction. Repair rates within the nontran
scribed strand varied as much as 15-fold, depending on nucleotide posi
tion. Preferential repair of the transcribed strand began just downstr
eam of the transcription start site but was most pronounced beginning
at nucleotide +140 in exon 1. The promoter contained two slowly repair
ed regions that coincided with two transcription factor binding sites.