Identification and characterization of a Xenopus homolog of Dbf4, a regulatory subunit of the Cdc7 protein kinase required for the initiation of DNA replication

被引:20
作者
Furukohri, A
Sato, N
Masai, H
Arai, K
Sugino, A
Waga, S
机构
[1] Osaka Univ, Grad Sch Frontier Biosci, Labs Biomol Network, Chromosome Replicat Grp, Osaka 5650871, Japan
[2] Osaka Univ, Microbial Dis Res Inst, Osaka 5650871, Japan
[3] Osaka Univ, Grad Sch Sci, Osaka 5650871, Japan
[4] Univ Tokyo, Inst Med Sci, Tokyo 1088639, Japan
[5] Tokyo Metropolitan Inst Med Sci, Tokyo 1138613, Japan
关键词
cell cycle; Dbf4-Cdc7; kinase; DNA replication; protein phosphorylation; Xenopus egg extract;
D O I
10.1093/jb/mvg163
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
Dbf4 is a regulatory subunit for the Cdc7 protein kinase that is required for the initiation of eukaryotic DNA replication, but the precise roles of Dbf4-Cdc7 remain to be determined. Here we identified a Xenopus homolog of Dbf4 (XDbf4) and characterized XDbf4 and Xenopus Cdc7 (XCdc7) in Xenopus egg extracts. XDbf4 formed a complex with XCdc7 in egg extracts and activated XCdc7 kinase activity in vitro. In contrast with Dbf4 in yeast and mammalian cultured cells, the XDbf4 levels in egg extracts did not change during the cell cycle progression. XDbf4 was a phosphoprotein in interphase extracts, and was apparently hyperphosphorylated in cytostatic factor (CSF)mediated, metaphase-arrested extracts and in mitotic extracts. However, the hyperphosphorylation. of XDbf4 did not seem to affect the level of kinase activation, or chromatin binding of the XDbf4-XCdc7 complex. Upon release from CSF-arrest, XDbf4 was partially dephosphorylated and bound to chromatin. Interestingly, XDbf4 was loaded onto chromatin before XCdc7 during DNA replication in egg extracts. These results suggest that the function of XDbf4-XCdc7 during the early embryonic cell cycle is regulated in a manner distinct from that during the somatic cell cycle.
引用
收藏
页码:447 / 457
页数:11
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