کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1980109 | 1539402 | 2015 | 7 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: DNA polymerase β-dependent cell survival independent of XRCC1 expression DNA polymerase β-dependent cell survival independent of XRCC1 expression](/preview/png/1980109.png)
• Pol β- and XRCC1-deficient mouse fibroblasts are hypersensitive to MMS.
• Pol β and XRCC1 interaction is important for recruitment of pol β to DNA damage.
• Pol β shRNA was used to knock down pol β in Xrcc1+/+ and Xrcc1−/− mouse fibroblasts.
• Studies provide evidence for pol β-dependent survival independent of XRCC1.
• PAR imaging data are consistent with decreased repair in pol β knock down variants.
Base excision repair (BER) is a primary mechanism for repair of base lesions in DNA such as those formed by exposure to the DNA methylating agent methyl methanesulfonate (MMS). Both DNA polymerase β (pol β)- and XRCC1-deficient mouse fibroblasts are hypersensitive to MMS. This is linked to a repair deficiency as measured by accumulation of strand breaks and poly(ADP-ribose) (PAR). The interaction between pol β and XRCC1 is important for recruitment of pol β to sites of DNA damage. Endogenous DNA damage can substitute for MMS-induced damage such that BER deficiency as a result of either pol β- or XRCC1-deletion is associated with sensitivity to PARP inhibitors. Pol β shRNA was used to knock down pol β in Xrcc1+/+ and Xrcc1−/− mouse fibroblasts. We determined whether pol β-mediated cellular resistance to MMS and PARP inhibitors resulted entirely from coordination with XRCC1 within the same BER sub-pathway. We find evidence for pol β-dependent cell survival independent of XRCC1 expression for both types of agents. The results suggest a role for pol β-dependent, XRCC1-independent repair. PAR immunofluorescence data are consistent with the hypothesis of a decrease in repair in both pol β knock down cell variants.
Journal: DNA Repair - Volume 26, February 2015, Pages 23–29