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

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...

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Veröffentlicht in:The Journal of cell biology 2009-09, Vol.186 (5), p.645-654
Hauptverfasser: Gilljam, Karin M, Feyzi, Emadoldin, Aas, Per A, Sousa, Mirta M.L, Müller, Rebekka, Vågbø, Cathrine B, Catterall, Tara C, Liabakk, Nina B, Slupphaug, Geir, Drabløs, Finn, Krokan, Hans E, Otterlei, Marit
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Sprache:eng
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Zusammenfassung: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.
ISSN:0021-9525
1540-8140
DOI:10.1083/jcb.200903138