REV1 mediated mutagenesis in base excision repair deficient mouse fibroblast

The DNA polymerase β (Pol β) null background renders mouse embryonic fibroblast (MEF) cells base excision repair deficient and hyper-mutagenic upon treatment with the monofunctional alkylating agent, methyl methanesulfonate (MMS). This effect involves an increase in all types of base substitutions, with a modest predominance of G to A transitions. In the present study, we examined the hypothesis that the MMS-induced mutagenesis in the Pol β null MEF system is due to a lesion bypass mechanism. We studied the effect of RNAi mediated down-regulation of the lesion bypass factor REV1. The steady-state level of REV1 protein was reduced by more than 95% using stable expression of a siRNA construct in a Pol β null cell line. We found that REV1 expression is required for the MMS-induced mutagenesis phenotype of Pol β null MEF cells. In contrast, cell survival after MMS treatment is not reduced in the absence of REV1.