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. 2006 Nov 17;103(48):18083–18088. doi: 10.1073/pnas.0605247103

Fig. 1.

Fig. 1.

Survival of primary mouse fibroblasts after UV irradiation. The influence of mouse genotype on survival of primary dermal fibroblasts after irradiation with UV254 nm was measured by colony-forming ability, as described in Methods. The fluence required to reduce the survival of Polη+/++/+ cells to 37% of the unirradiated control (D37) was 8 J/m2. This was reduced to ≈2.8 J/m2 in the cells derived from Polη−/−+/+. In both Polη+/+ and Polη−/− backgrounds, disruption of Polι slightly reduced UV survival. The significance of the reduced survival of pol ι-deficient cells was determined by polynomial regression analysis (53), with the best fit provided by cubic polynomials. This analysis revealed that the percent survival for Polη+/+−/− cells was significantly lower than for Polη+/++/+ cells (P = 0.018), and that the percent survival for Polη−/−−/− cells was significantly lower than for Polη−/−+/+ cells (P = 0.001).