Cyclin A Promotes S-Phase Entry via Interaction with the Replication Licensing Factor Mcm7

被引:35
|
作者
Chibazakura, Taku [1 ]
Kamachi, Kazuhiro [1 ]
Ohara, Mayu [1 ]
Tane, Shoji [1 ]
Yoshikawa, Hirofumi [1 ]
Roberts, James M. [2 ]
机构
[1] Tokyo Univ Agr, Dept Biosci, Setagaya Ku, Tokyo 1568502, Japan
[2] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
关键词
CDK-DEPENDENT PHOSPHORYLATION; DNA-REPLICATION; RETINOBLASTOMA PROTEIN; HETEROHEXAMERIC COMPLEXES; MAMMALIAN FIBROBLASTS; CHROMOSOMAL DNA; KINASE-ACTIVITY; BUDDING YEAST; CELL-CYCLE; BINDING;
D O I
10.1128/MCB.00630-10
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
Cyclin A is known to promote S-phase entry in mammals, but its critical targets in this process have not been defined. We derived a novel human cyclin A mutant (CycA-C1), which can activate cyclin-dependent kinase but cannot promote S-phase entry, and isolated replication licensing factor Mcm7 as a factor that interacts with the wild-type cyclin A but not with the mutant. We demonstrated that human cyclin A and Mcm7 interact in the chromatin fraction. To address the physiological significance of the cyclin A-Mcm7 interaction, we isolated an Mcm7 mutant (Mcm7-3) that is capable of association with CycA-C1 and found that it can also suppress the deficiency of CycA-C1 in promoting S-phase entry. Finally, RNA interference experiments showed that the CycA-C1 mutant is defective for the endogenous cyclin A function in S-phase entry and that this defect can be suppressed by the Mcm7-3 mutant. Our findings demonstrate that interaction with Mcm7 is essential for the function of cyclin A in promoting S-phase entry.
引用
收藏
页码:248 / 255
页数:8
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