The human homolog of Saccharomyces cerevisiae Mcm10 interacts with replication factors and dissociates from nuclease-resistant nuclear structures in G2 phase
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作者:
Izumi, M
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机构:RIKEN, Inst Phys & Chem Res, Div Radioisotope Techn, Cellular Physiol Lab, Wako, Saitama 3510198, Japan
Izumi, M
Yanagi, K
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机构:RIKEN, Inst Phys & Chem Res, Div Radioisotope Techn, Cellular Physiol Lab, Wako, Saitama 3510198, Japan
Yanagi, K
Mizuno, T
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机构:RIKEN, Inst Phys & Chem Res, Div Radioisotope Techn, Cellular Physiol Lab, Wako, Saitama 3510198, Japan
Mizuno, T
Yokoi, M
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机构:RIKEN, Inst Phys & Chem Res, Div Radioisotope Techn, Cellular Physiol Lab, Wako, Saitama 3510198, Japan
Yokoi, M
Kawasaki, Y
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机构:RIKEN, Inst Phys & Chem Res, Div Radioisotope Techn, Cellular Physiol Lab, Wako, Saitama 3510198, Japan
Kawasaki, Y
Moon, KY
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机构:RIKEN, Inst Phys & Chem Res, Div Radioisotope Techn, Cellular Physiol Lab, Wako, Saitama 3510198, Japan
Moon, KY
Hurwitz, J
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机构:RIKEN, Inst Phys & Chem Res, Div Radioisotope Techn, Cellular Physiol Lab, Wako, Saitama 3510198, Japan
Hurwitz, J
Yatagai, F
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机构:RIKEN, Inst Phys & Chem Res, Div Radioisotope Techn, Cellular Physiol Lab, Wako, Saitama 3510198, Japan
Yatagai, F
Hanaoka, F
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机构:RIKEN, Inst Phys & Chem Res, Div Radioisotope Techn, Cellular Physiol Lab, Wako, Saitama 3510198, Japan
Hanaoka, F
机构:
[1] RIKEN, Inst Phys & Chem Res, Div Radioisotope Techn, Cellular Physiol Lab, Wako, Saitama 3510198, Japan
[2] Osaka Univ, Inst Microbial Dis, Suita, Osaka 5650871, Japan
[3] Sloan Kettering Inst, Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
Mcm10 (Dna43), first identified in Saccharomyces cerevisiae, is an essential protein which functions in the initiation of DNA synthesis. Mcm10 is a nuclear protein that is localized to replication origins and mediates the interaction of the Mcm2-7 complex with replication origins. We identified and cloned a human cDNA whose product was structurally homologous to the yeast Mcm10 protein. Human Mcm10 (HsMcm10) is a 98-kDa protein of 874 amino acids which shows 23 and 21% overall similarity to Schizosaccharomyces pombe Cdc23 and S.cerevisiae Mcm10, respectively. The messenger RNA level of HsMcm10 increased at the G(1)/S-boundary when quiescent human NB1-RGB cells were induced to proliferate as is the case of many replication factors. HsMcm10 associated with nuclease-resistant nuclear structures throughout S phase and dissociated from it in G(2) phase. HsMcm10 associated with human Orc2 protein when over-expressed in COS-1 cells. HsMcm10 also interacted with Orc2, mcm2 and Mcm6 proteins in the yeast two-hybrid system. These results suggest that HsMcm10 may function in DNA replication through the interaction with Orc and Mcm2-7 complexes.