The human homolog of Saccharomyces cerevisiae Mcm10 interacts with replication factors and dissociates from nuclease-resistant nuclear structures in G2 phase

被引:76
作者
Izumi, M
Yanagi, K
Mizuno, T
Yokoi, M
Kawasaki, Y
Moon, KY
Hurwitz, J
Yatagai, F
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
关键词
D O I
10.1093/nar/28.23.4769
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页码:4769 / 4777
页数:9
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