FoxM1 is required for execution of the mitotic programme and chromosome stability

  • Jamila Laoukili
  • , Matthijs R.H. Kooistra
  • , Alexandra Brás
  • , Jos Kauw
  • , Ron M. Kerkhoven
  • , Ashby Morrison
  • , Hans Clevers
  • , René H. Medema

Research output: Contribution to journalArticlepeer-review

714 Citations (Scopus)

Abstract

Transcriptional induction of cell-cycle regulatory proteins ensures proper timing of subsequent cell-cycle events. Here we show that the Forkhead transcription factor FoxM1 regulates expression of many G2-specific genes and is essential for chromosome stability. Loss of FoxM1 leads to pleiotropic cell-cycle defects, including a delay in G2, chromosome mis-segregation and frequent failure of cytokinesis. We show that transcriptional activation of cyclin B by FoxM1 is essential for timely mitotic entry, whereas CENP-F, another direct target of FoxM1 identified here, is essential for precise functioning of the mitotic spindle checkpoint. Thus, our data uncover a transcriptional cluster regulated by FoxM1 that is essential for proper mitotic progression.

Original languageEnglish
Pages (from-to)126-136
Number of pages11
JournalNature Cell Biology
Volume7
Issue number2
DOIs
Publication statusPublished - Feb 2005
Externally publishedYes

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