Cdt1 downregulation by proteolysis and geminin inhibition prevents DNA re-replication in Xenopus

Anatoliy Li, J. Julian Blow

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117 Citations (Scopus)


In late mitosis and G1, Mcm2–7 are assembled onto replication origins to 'license' them for initiation. At other cell cycle stages, licensing is inhibited, thus ensuring that origins fire only once per cell cycle. Three additional factors—the origin recognition complex, Cdc6 and Cdt1—are required for origin licensing. We examine here how licensing is regulated in Xenopus egg extracts. We show that Cdt1 is downregulated late in the cell cycle by two different mechanisms: proteolysis, which occurs in part due to the activity of the anaphase-promoting complex (APC/C), and inhibition by a protein called geminin. If both these regulatory mechanisms are abrogated, extracts undergo uncontrolled re-licensing and re-replication. The extent of re-replication is limited by checkpoint kinases that are activated as a consequence of re-replication itself. These results allow us to build a comprehensive model of how re-replication of DNA is prevented in Xenopus, with Cdt1 regulation being the key feature. The results also explain the original experiments that led to the proposal of a replication licensing factor.
Original languageEnglish
Pages (from-to)395-404
Number of pages10
JournalThe EMBO Journal
Issue number2
Publication statusPublished - 16 Dec 2004


  • Cdt1
  • DNA replication
  • Geminin
  • Replication licensing
  • Xenopus

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