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Evidence for a mammalian late-G1 phase inhibitor of replication licensing distinct from geminin or Cdk activity.

Authors :
Sasaki T
Li A
Gillespie PJ
Blow JJ
Gilbert DM
Source :
Nucleus (Austin, Tex.) [Nucleus] 2011 Sep-Oct; Vol. 2 (5), pp. 455-64. Date of Electronic Publication: 2011 Sep 01.
Publication Year :
2011

Abstract

Pre-replication complexes (pre-RCs) are assembled onto DNA during late mitosis and G1 to license replication origins for use in S phase. In order to prevent re-replication of DNA, licensing must be completely shutdown prior to entry into S phase. While mechanisms preventing re-replication during S phase and mitosis have been elucidated, the means by which cells first prevent licensing during late G1 phase are poorly understood. We have employed a hybrid mammalian / Xenopus egg extract replication system to dissect activities that inhibit replication licensing at different stages of the cell cycle in Chinese Hamster Ovary (CHO) cells. We find that soluble extracts from mitotic cells inhibit licensing through a combination of geminin and Cdk activities, while extracts from S-phase cells inhibit licensing predominantly through geminin alone. Surprisingly however, geminin did not accumulate until after cells enter S phase. Unlike extracts from cells in early G1 phase, extracts from late G1 phase and early S phase cells contained an inhibitor of licensing that could not be accounted for by either geminin or Cdk. Moreover, inhibiting cyclin and geminin protein synthesis or inhibiting Cdk activity early in G1 phase did not prevent the appearance of inhibitory activity. These results suggest that a soluble inhibitor of replication licensing appears prior to entry into S phase that is distinct from either geminin or Cdk activity. Our hybrid system should permit the identification of this and other novel cell cycle regulatory activities.

Details

Language :
English
ISSN :
1949-1042
Volume :
2
Issue :
5
Database :
MEDLINE
Journal :
Nucleus (Austin, Tex.)
Publication Type :
Academic Journal
Accession number :
21983086
Full Text :
https://doi.org/10.4161/nucl.2.5.17859