4.7 Article

The functional role of Cdc6 in S-G2/M in mammalian cells

Journal

EMBO REPORTS
Volume 7, Issue 4, Pages 425-430

Publisher

WILEY
DOI: 10.1038/sj.embor.7400624

Keywords

Cdc6; DNA replication; Chk1 checkpoint mitotic lethality

Funding

  1. NCI NIH HHS [T32 CA077109, CA97950, R01 CA097950, 2T32 CA77109-06A2] Funding Source: Medline
  2. NIGMS NIH HHS [GM67859, R01 GM067859] Funding Source: Medline

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The Cdc6 protein is required for licensing of replication origins before the onset of DNA replication in eukaryotic cells. Here, we examined whether Cdc6 has other roles in mammalian cell-cycle progression from S to G2/M phase. Using RNA interference, we showed that depletion of Cdc6 in synchronous G1 cells blocks G1 to S transition, confirming the essential role of Cdc6 in the initiation of DNA replication. In contrast, depletion of Cdc6 in synchronous S-phase cells slowed DNA replication and led to mitotic lethality. The Cdc6-depleted S-phase cells showed fewer newly fired origins; however, established replication forks remained active, even during chromatin condensation. Despite such DNA replication abnormalities, loss of Cdc6 failed to activate Chk1 kinase. These results show that Cdc6 is not only required for G1 origin licensing, but is also crucial for proper S-phase DNA replication that is essential for DNA segregation during mitosis.

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