作者: K. W. Caldecott , S. Aoufouchi , P. Johnson , S. Shall
关键词: Biochemistry 、 DNA polymerase II 、 In vitro recombination 、 DNA polymerase mu 、 Polymerase 、 DNA polymerase 、 DNA polymerase I 、 DNA ligase 、 DNA clamp 、 Biology
摘要: The DNA repair proteins XRCC1 and ligase III are physically associated in human cells directly interact vitro vivo. Here, we demonstrate that is additionally with polymerase-beta these polypeptides also interact. We present data suggesting poly (ADP-ribose) polymerase can XRCC1. Finally, shares the novel function of a molecular nick-sensor, inhibit activity latter polypeptide vitro. Taken together, suggest four described above may be co-ordinated within single multiprotein complex.