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EMBO Rep. 2002 Aug;3(8):780-4. Epub 2002 Jul 15.

Human replication protein Cdc6 is selectively cleaved by caspase 3 during apoptosis.

Author information

1
MCR Cancer Cell Unit, Hutchison/MRC Research Centre, Cambridge, UK. cpelizon@yahoo.co.uk

Abstract

In eukaryotes, the initiation of DNA replication involves the ordered assembly on chromatin of pre-replicative complexes (pre-RCs), including the origin recognition complex (ORC), Cdc6, Cdt1 and the minichromosome maintenance proteins (MCMs). In light of its indispensable role in the formation of pre-RCs, Cdc6 binding to chromatin represents a key step in the regulation of DNA replication and cell proliferation. Here, we study the human Cdc6 (HuCdc6) protein during programmed cell death (apoptosis). We find that HuCdc6, but not HuOrc2 (a member of the ORC) or HuMcm5 (one of the MCMs), is specifically cleaved in several human cell lines induced to undergo apoptosis by a variety of stimuli. Expression of caspase-uncleavable mutant HuCdc6 attenuates apoptosis, delaying cell death. Therefore, an important function for cleavage of HuCdc6 is to prevent a wounded cell from replicating and to facilitate death.

PMID:
12151338
PMCID:
PMC1084215
DOI:
10.1093/embo/reports/kvf161
[Indexed for MEDLINE]
Free PMC Article

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