Forskning ved Københavns Universitet - Københavns Universitet


Direct interaction between XRCC1 and UNG2 facilitates rapid repair of uracil in DNA by XRCC1 complexes

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  • Akbari, Mansour
  • Karin Solvang-Garten
  • Audun Hanssen-Bauer
  • Nora Valeska Lieske
  • Henrik Sahlin Pettersen
  • Grete Klippenvåg Pettersen
  • David M Wilson
  • Hans E Krokan
  • Marit Otterlei

Uracil-DNA glycosylase, UNG2, interacts with PCNA and initiates post-replicative base excision repair (BER) of uracil in DNA. The DNA repair protein XRCC1 also co-localizes and physically interacts with PCNA. However, little is known about whether UNG2 and XRCC1 directly interact and participate in a same complex for repair of uracil in replication foci. Here, we examine localization pattern of these proteins in live and fixed cells and show that UNG2 and XRCC1 are likely in a common complex in replication foci. Using pull-down experiments we demonstrate that UNG2 directly interacts with the nuclear localization signal-region (NLS) of XRCC1. Western blot and functional analysis of immunoprecipitates from whole cell extracts prepared from S-phase enriched cells demonstrate the presence of XRCC1 complexes that contain UNG2 in addition to separate XRCC1 and UNG2 associated complexes with distinct repair features. XRCC1 complexes performed complete repair of uracil with higher efficacy than UNG2 complexes. Based on these results, we propose a model for a functional role of XRCC1 in replication associated BER of uracil.

TidsskriftDNA Repair
Udgave nummer7
Sider (fra-til)785-95
Antal sider11
StatusUdgivet - 1 jul. 2010
Eksternt udgivetJa

Bibliografisk note

2010 Elsevier B.V. All rights reserved.

ID: 213362186