Abstract
Members of the AP-1 transcription factor family, especially c-Jun and c-Fos, have long been known to mediate critical steps in the cellular response to ultraviolet (UV) irradiation. We sought to examine whether two newly discovered members of the AP-1 family, JDP-1 and JDP-2, also participate in the mammalian UV response. Here we report that JDP-2, but not JDP-1, is transiently induced upon UV challenge and that elevated levels of JDP-2 increase cell survival following UV exposure. This protective function of JDP-2 appears to be mediated through repression of p53 expression at the transcriptional level, via a conserved atypical AP-1 site in the p53promoter.
ACKNOWLEDGMENTS
We are grateful to E. Wagner and M. Oren for kindly providing c-jun+/+ and c-jun−/−fibroblasts and the p53 promoter construct, respectively. We acknowledge E. Shaulian for the gift of Saos-2 cells.
F.P. was a recipient of the Human Frontier Fellowship Program. This work was supported by the National Institute of Health, Department of Energy, and State of California Cancer Research Program.