p53 has pleiotropic functions including control of genomic plasticity
and integrity. Here we report that p53 can bind to several transcripti
on factor IIH-associated factors, including transcription-repair facto
rs, XPD (Rad3) and XPB, as well as CSB involved in strand-specific DNA
repair, via its C-terminal domain. We also found that wild-type, but
not Arg273His mutant p53 inhibits XPD (Rad3) and XPB DNA helicase acti
vities. Moreover, repair of UV-induced dimers is slower in Li-Fraumeni
syndrome cells (heterozygote p53 mutant) than in normal human cells.
Our findings indicate that p53 may play a direct role in modulating nu
cleotide excision repair pathways.