1. Academic Validation
  2. Identification of a novel, widespread, and functionally important PCNA-binding motif

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

  • J Cell Biol. 2009 Sep 7;186(5):645-54. doi: 10.1083/jcb.200903138.
Karin M Gilljam 1 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
Affiliations

Affiliation

  • 1 Department of Cancer Research and Molecular Medicine, Faculty of Medicine, Norwegian University of Science and Technology, N-7489 Trondheim, Norway.
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.

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