We have determined that DNA damage is at least one of the signals generated
by ultraviolet radiation that stimulates pigmentation (tanning) in human s
kin. This photoprotective response is functionally similar to the SOS respo
nse described in bacteria. Here we present evidence that DNA damage stimula
tes pigmentation, at least in part, through up-regulation of tyrosinase mRN
A and protein levels. Furthermore, this response can be induced in the abse
nce of DNA damage by treatment of melanocytic cells and intact sl;in with s
mall DNA fragments, particularly thymidine dinucleotides, pTpT, Topical app
lication of these DNA fragments should provide a photoprotective tan to hum
an skin without the harmful effects of ultraviolet radiation.