Format

Send to

Choose Destination
Trends Biochem Sci. 2011 Aug;36(8):405-14. doi: 10.1016/j.tibs.2011.05.002. Epub 2011 Jun 7.

How dormant origins promote complete genome replication.

Author information

1
Wellcome Trust Centre for Gene Regulation & Expression, University of Dundee Dow Street, Dundee DD1 5EH, UK. j.j.blow@dundee.ac.uk

Abstract

Many replication origins that are licensed by loading MCM2-7 complexes in G1 are not normally used. Activation of these dormant origins during S phase provides a first line of defence for the genome if replication is inhibited. When replication forks fail, dormant origins are activated within regions of the genome currently engaged in replication. At the same time, DNA damage-response kinases activated by the stalled forks preferentially suppress the assembly of new replication factories, thereby ensuring that chromosomal regions experiencing replicative stress complete synthesis before new regions of the genome are replicated. Mice expressing reduced levels of MCM2-7 have fewer dormant origins, are cancer-prone and are genetically unstable, demonstrating the importance of dormant origins for preserving genome integrity. We review the function of dormant origins, the molecular mechanism of their regulation and their physiological implications.

PMID:
21641805
PMCID:
PMC3329722
DOI:
10.1016/j.tibs.2011.05.002
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Elsevier Science Icon for PubMed Central
Loading ...
Support Center