Using immunodepletion of cyclin E and the inhibitor protein p21WAF/CIP1, we demonstrate that the cyclin E protein, in association with Cdk2, is required for the elongation phase of replication on single-stranded substrates. Although cyclin E/Cdk2 is likely to be the major target by which p21 inhibits the initiation of sperm DNA replication, p21 can inhibit single-stranded replication through a mechanism dependent on PCNA. While the cyclin E/Cdk2 complex appears to have a role in the initiation of DNA replication, another Cdk kinase, possibly cyclin A/Cdk, may be involved in a later step controlling the switch from initiation to elongation. The provision of a large maternal pool of cyclin E protein shows that regulators of replication are constitutively present, which explains the lack of a protein synthesis requirement for replication in the early embryonic cell cycle.
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15 August 1995
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August 15 1995
Early events in DNA replication require cyclin E and are blocked by p21CIP1.
P K Jackson,
P K Jackson
Harvard Medical School, Department of Cell Biology, Boston, Massachusetts 02115, USA.
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S Chevalier,
S Chevalier
Harvard Medical School, Department of Cell Biology, Boston, Massachusetts 02115, USA.
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M Philippe,
M Philippe
Harvard Medical School, Department of Cell Biology, Boston, Massachusetts 02115, USA.
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M W Kirschner
M W Kirschner
Harvard Medical School, Department of Cell Biology, Boston, Massachusetts 02115, USA.
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P K Jackson
Harvard Medical School, Department of Cell Biology, Boston, Massachusetts 02115, USA.
S Chevalier
Harvard Medical School, Department of Cell Biology, Boston, Massachusetts 02115, USA.
M Philippe
Harvard Medical School, Department of Cell Biology, Boston, Massachusetts 02115, USA.
M W Kirschner
Harvard Medical School, Department of Cell Biology, Boston, Massachusetts 02115, USA.
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1995) 130 (4): 755–769.
Citation
P K Jackson, S Chevalier, M Philippe, M W Kirschner; Early events in DNA replication require cyclin E and are blocked by p21CIP1.. J Cell Biol 15 August 1995; 130 (4): 755–769. doi: https://doi.org/10.1083/jcb.130.4.755
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