The role of Cdc6 in ensuring complete genome licensing and S phase checkpoint activation

J Cell Biol. 2004 Apr 26;165(2):181-90. doi: 10.1083/jcb.200311044. Epub 2004 Apr 19.

Abstract

Before S phase, cells license replication origins for initiation by loading them with Mcm2-7 heterohexamers. This process is dependent on Cdc6, which is recruited to unlicensed origins. Using Xenopus egg extracts we show that although each origin can load many Mcm2-7 hexamers, the affinity of Cdc6 for each origins drops once it has been licensed by loading the first hexamers. This encourages the distribution of at least one Mcm2-7 hexamer to each origin, and thereby helps to ensure that all origins are licensed. Although Cdc6 is not essential for DNA replication once licensing is complete, Cdc6 regains a high affinity for origins once replication forks are initiated and Mcm2-7 has been displaced from the origin DNA. We show that the presence of Cdc6 during S phase is essential for the checkpoint kinase Chk1 to become activated in response to replication inhibition. These results show that Cdc6 plays multiple roles in ensuring precise chromosome duplication.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aphidicolin / metabolism
  • Cell Cycle Proteins / metabolism*
  • Checkpoint Kinase 1
  • Chromatin / metabolism
  • DNA Replication*
  • DNA-Binding Proteins / metabolism
  • Enzyme Activation
  • Enzyme Inhibitors / metabolism
  • Female
  • Genome*
  • Humans
  • Male
  • Models, Genetic
  • Nuclear Proteins / metabolism
  • Oocytes / physiology
  • Origin Recognition Complex
  • Protein Binding
  • Protein Kinases / metabolism
  • Protein Structure, Quaternary
  • Protein Subunits / metabolism*
  • Replication Origin
  • S Phase / physiology*
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Spermatozoa / metabolism
  • Xenopus Proteins
  • Xenopus laevis

Substances

  • CDC6 protein, S cerevisiae
  • Cell Cycle Proteins
  • Chromatin
  • DNA-Binding Proteins
  • Enzyme Inhibitors
  • Nuclear Proteins
  • Origin Recognition Complex
  • Protein Subunits
  • Saccharomyces cerevisiae Proteins
  • Xenopus Proteins
  • Aphidicolin
  • Protein Kinases
  • CHEK1 protein, human
  • Checkpoint Kinase 1
  • Chek1 protein, Xenopus