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The Y-family DNA polymerase κ (pol κ) functions in mammalian nucleotide-excision repair

Abstract

DNA polymerase κ (pol κ) is a member of the Y-family of DNA polymerases that are thought to function in translesion synthesis (TLS) past different types of DNA damage. Here, we show that pol κ-deficient mouse cells have substantially reduced (but not absent) levels of nucleotide excision repair (NER) of UV damage, as measured by several methods. Our results provide evidence for an unexpected role for pol κ in mammalian NER.

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Figure 1: Polk-deficient MEFs have a defective NER phenotype.
Figure 2: NER is reduced in Polk-deficient cells.

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Acknowledgements

We are grateful to H. Ohmori for helpful comments and for the Polk-deficient MEFs, and to H. Fawcett and L. Ju for technical assistance. This work was supported by a Medical Research Council (MRC) programme grant to A.R.L. and an Uehara Memorial Foundation grant to T.O.

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Correspondence to Alan R. Lehmann.

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Ogi, T., Lehmann, A. The Y-family DNA polymerase κ (pol κ) functions in mammalian nucleotide-excision repair. Nat Cell Biol 8, 640–642 (2006). https://doi.org/10.1038/ncb1417

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