TY - JOUR
T1 - PCNA interacts with hHusl/hRad9 in response to DNA damage and replication inhibition
AU - Komatsu, Kiyoshi
AU - Wharton, Walker
AU - Hang, Haiying
AU - Wu, Chun
AU - Singh, Sujay
AU - Lieberman, Howard B.
AU - Pledger, W. J.
AU - Wang, Hong-Gang
PY - 2000/11/2
Y1 - 2000/11/2
N2 - The hHus1 and several hRad proteins are involved in the control of DNA integrity checkpoints, although the mechanisms underlying these processes are unknown. Using a yeast two-hybrid system to detect protein-protein interactions, we found that human proliferating cell nuclear antigen (PCNA), a protein known to function in both DNA replication and repair, interacts with the human checkpoint-related protein Hus1 (hHus1). In human skin fibroblast cells, exposure to ionizing radiation of hydroxyurea triggers translocation of hHus1 from the cytosol to the nucleus, where it associates with PCNA as well as another checkpoint protein, hRad9. This nuclear translocation and the complex formation or hHus1 with PCNA and hRad9 correlate closely with changes in cell cycle distribution in response to radiation exposure. These results suggest that this multi-protein complex may be important for coordinating cell-cycle progression, DNA replication and repair of damaged DNA.
AB - The hHus1 and several hRad proteins are involved in the control of DNA integrity checkpoints, although the mechanisms underlying these processes are unknown. Using a yeast two-hybrid system to detect protein-protein interactions, we found that human proliferating cell nuclear antigen (PCNA), a protein known to function in both DNA replication and repair, interacts with the human checkpoint-related protein Hus1 (hHus1). In human skin fibroblast cells, exposure to ionizing radiation of hydroxyurea triggers translocation of hHus1 from the cytosol to the nucleus, where it associates with PCNA as well as another checkpoint protein, hRad9. This nuclear translocation and the complex formation or hHus1 with PCNA and hRad9 correlate closely with changes in cell cycle distribution in response to radiation exposure. These results suggest that this multi-protein complex may be important for coordinating cell-cycle progression, DNA replication and repair of damaged DNA.
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U2 - 10.1038/sj.onc.1203901
DO - 10.1038/sj.onc.1203901
M3 - Article
C2 - 11077446
AN - SCOPUS:0034597465
SN - 0950-9232
VL - 19
SP - 5291
EP - 5297
JO - Oncogene
JF - Oncogene
IS - 46
ER -