Inhibition of Eukaryotic DNA Replication by Geminin Binding to Cdt1

Author:

Wohlschlegel James A.1,Dwyer Brian T.1,Dhar Suman K.1,Cvetic Christin2,Walter Johannes C.2,Dutta Anindya1

Affiliation:

1. Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, 75 Francis Street, Boston, MA 02115, USA.

2. Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, 240 Longwood Avenue, Boston, MA 02115, USA.

Abstract

In all eukaryotic organisms, inappropriate firing of replication origins during the G 2 phase of the cell cycle is suppressed by cyclin-dependent kinases. Multicellular eukaryotes contain a second putative inhibitor of re-replication called geminin. Geminin is believed to block binding of the mini-chromosome maintenance (MCM) complex to origins of replication, but the mechanism of this inhibition is unclear. Here we show that geminin interacts tightly with Cdt1, a recently identified replication initiation factor necessary for MCM loading. The inhibition of DNA replication by geminin that is observed in cell-free DNA replication extracts is reversed by the addition of excess Cdt1. In the normal cell cycle, Cdt1 is present only in G 1 and S, whereas geminin is present in S and G 2 phases of the cell cycle. Together, these results suggest that geminin inhibits inappropriate origin firing by targeting Cdt1.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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