REVIEW

Cell Research (2008): 48-63
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XRCC1 and DNA polymerase β in cellular protection against cytotoxic DNA single-strand breaks

Julie K Horton¹, Mary Watson², Donna F Stefanick¹, Daniel T Shaughnessy², Jack A Taylor² and Samuel H Wilson¹

Correspondence: Samuel H Wilson Tel: +919-541-3201; Fax: +919-541-3592 E-mail: wilson5@niehs.nih.gov

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Single-strand breaks (SSBs) can occur in cells either directly, or indirectly following initiation of base excision repair (BER). SSBs generally have blocked termini lacking the conventional 5'-phosphate and 3'-hydroxyl groups and require further processing prior to DNA synthesis and ligation. XRCC1 is devoid of any known enzymatic activity, but it can physically interact with other proteins involved in all stages of the overlapping SSB repair and BER pathways, including those that conduct the rate-limiting end-tailoring, and in many cases can stimulate their enzymatic activities. XRCC1^-/- mouse fibroblasts are most hypersensitive to agents that produce DNA lesions repaired by monofunctional glycosylase-initiated BER and that result in formation of indirect SSBs. A requirement for the deoxyribose phosphate lyase activity of DNA polymerase β (pol β) is specific to this pathway, whereas pol β is implicated in gap-filling during repair of many types of SSBs. Elevated levels of strand breaks, and diminished repair, have been demonstrated in MMS-treated XRCC1^-/-, and to a lesser extent in pol β^-/- cell lines, compared with wild-type cells. Thus a strong correlation is observed between cellular sensitivity to MMS and the ability of cells to repair MMS-induced damage. Exposure of wild-type and pol β^-/- cells to an inhibitor of PARP activity dramatically potentiates MMS-induced cytotoxicity. XRCC1^-/- cells are also sensitized by PARP inhibition demonstrating that PARP-mediated poly(ADP-ribosyl)ation plays a role in modulation of cytotoxicity beyond recruitment of XRCC1 to sites of DNA damage.

Cell Research (2008) 18:48-63. doi: 10.1038/cr.2008.7; published online 1 January 2008

Keywords: DNA glycosylases, AP-endonuclease, covalent modification, BER subpathways, repair complex, BER interactome