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  • Identification of a novel, widespread, and functionally important PCNA-binding motif.

Identification of a novel, widespread, and functionally important PCNA-binding motif.

The Journal of cell biology (2009-09-09)
Karin M Gilljam, Emadoldin Feyzi, Per A Aas, Mirta M L Sousa, Rebekka Müller, Cathrine B Vågbø, Tara C Catterall, Nina B Liabakk, Geir Slupphaug, Finn Drabløs, Hans E Krokan, Marit Otterlei
ABSTRACT

Numerous proteins, many essential for the DNA replication machinery, interact with proliferating cell nuclear antigen (PCNA) through the PCNA-interacting peptide (PIP) sequence called the PIP box. We have previously shown that the oxidative demethylase human AlkB homologue 2 (hABH2) colocalizes with PCNA in replication foci. In this study, we show that hABH2 interacts with a posttranslationally modified PCNA via a novel PCNA-interacting motif, which we term AlkB homologue 2 PCNA-interacting motif (APIM). We identify APIM in >200 other proteins involved in DNA maintenance, transcription, and cell cycle regulation, and verify a functional APIM in five of these. Expression of an APIM peptide increases the cellular sensitivity to several cytostatic agents not accounted for by perturbing only the hABH2-PCNA interaction. Thus, APIM is likely to mediate PCNA binding in many proteins involved in DNA repair and cell cycle control during genotoxic stress.