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The replication kinase Cdc7-Dbf4 promotes the interaction of the p150 subunit of chromatin assembly factor 1 with proliferating cell nuclear antigen
被引:57
作者:
Gerard, Annabelle
Koundrioukoff, Stephane
Ramillon, Vincent
Sergere, Jean-Christophe
Mailand, Niels
Quivy, Jean-Pierre
Almouzni, Genevieve
机构:
[1] CNRS, UMR218, Inst Curie, Sect Rech, F-75248 Paris 05, France
[2] Danish Canc Soc, Inst Canc Biol, Copenhagen O, Denmark
[3] Danish Canc Soc, Ctr Genotox Stress Res, Copenhagen O, Denmark
来源:
关键词:
CAF1;
Cdc7-dbf4;
chromatin assembly;
replication;
PCNA;
D O I:
10.1038/sj.embor.7400750
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:
The coordination of chromatin assembly with DNA replication, which is essential for genomic stability, requires the combined activation of histone deposition with the firing of replication origins. We report here the direct interaction of chromatin assembly factor 1 (CAF1), a key factor involved in histone deposition, with the replication kinase Cdc7-Dbf4. We isolated a complex containing both the largest subunit of CAF1 (p150) and the Cdc7-Dbf4 kinase specifically in S phase and thus prove the existence of this interaction in vivo. We then show that the Cdc7-Dbf4 kinase efficiently phosphorylates p150. This event induces a change in p150 oligomerization state, which promotes binding to proliferating cell nuclear antigen (PCNA). Conversely, CAF1 recruitment is reduced in a PCNA/DNA loading assay using Cdc7-depleted extracts. Our data define p150 as a new target for this kinase with implications for the coordination between DNA replication and CAF1 functions.
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页码:817 / 823
页数:7
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