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XRCC1 and DNA polymerase β interaction contributes to cellular alkylating‐agent resistance and single‐strand break repair
Author(s) -
Wong HengKuan,
Wilson David M.
Publication year - 2005
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.20448
Subject(s) - xrcc1 , biology , dna repair , chinese hamster ovary cell , dna polymerase , protein fragment complementation assay , dna damage , polymerase , dna , microbiology and biotechnology , replication protein a , dna replication , genetics , complementation , dna binding protein , mutant , gene , transcription factor , cell culture , genotype , single nucleotide polymorphism
X‐ray cross complementing 1 (XRCC1) protein has been suggested to bind to DNA single‐strand breaks (SSBs) and organize protein interactions that facilitate efficient DNA repair. Using four site‐specifically modified human XRCC1 mutant expression systems and functional complementation assays in Chinese hamster ovary (CHO) XRCC1‐deficient EM9 cells, we evaluated the cellular contributions of XRCC1s proposed N‐terminal domain (NTD) DNA binding and DNA polymerase β (POLβ) interaction activities. Results within demonstrate that the interaction with POLβ is biologically important for alkylating agent resistance and SSB repair, whereas the proposed DNA binding function is not critical to these phenotypes. Our data favor a model where the interaction of XRCC1 with POLβ contributes to efficient DNA repair in vivo, whereas its interactions with target DNA is biologically less relevant. Published 2005 Wiley‐Liss, Inc.