Clamping the Mec1/ATR checkpoint kinase into action

Jerzy Majka, Peter M.J. Burgers

Research output: Contribution to journalReview article

14 Scopus citations

Abstract

The yeast checkpoint protein kinase Mec1, the ortholog of human ATR, is the essential upstream regulator of the cell cycle checkpoint in response to DNA damage and to stalling of DNA replication forks. The activity of Mec1/ATR is not directly regulated by the DNA substrates that signal checkpoint activation. Rather the signal appears to be transduced to Mec1 by factors that interact with the signaling DNA substrates. One of these factors, the DNA damage checkpoint clamp Rad17-Mec3-Ddc1 (human 9-1-1) is loaded onto gapped DNA resulting from the partial repair of DNA damage, and the Ddc1 subunit of this complex activates Mec1. In vertebrate cells, the TopBP1 protein (Cut5 in S. pombe and Dpb11 in S. cervisiae) that is also required for establishment of the replication fork, functions during replication fork dysfunction to activate ATR. Both mechanisms of activation generally upregulate the kinase activity towards all downstream targets.

Original languageEnglish
Pages (from-to)1157-1160
Number of pages4
JournalCell Cycle
Volume6
Issue number10
DOIs
StatePublished - May 15 2007

Keywords

  • Cell cycle checkpoint
  • Checkpoint kinase
  • Clamp
  • DNA damage
  • DNA replication

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