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Cyclin e is recruited to the nuclear matrix during differentiation, but is not recruited in cancer cells

  • Jennifer Munkley
  • , Nikki A. Copeland
  • , Victoria Moignard
  • , John R.P. Knight
  • , Erin Greaves
  • , Simon A. Ramsbottom
  • , Mary E. Pownall
  • , Jennifer Southgate
  • , Justin F.X. Ainscough
  • , Dawn Coverley*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Cyclin E supports pre-replication complex (pre-RC) assembly, while cyclin A-associated kinase activates DNA synthesis. We show that cyclin E, but not A, is mounted upon the nuclear matrix in sub-nuclear foci in differentiated vertebrate cells, but not in undifferentiated cells or cancer cells. In murine embryonic stem cells, Xenopus embryos and human urothelial cells, cyclin E is recruited to the nuclear matrix as cells differentiate and this can be manipulated in vitro. This suggests that pre-RC assembly becomes spatially restricted as template usage is defined. Furthermore, failure to become restricted may contribute to the plasticity of cancer cells.

Original languageEnglish
Pages (from-to)2671-2677
Number of pages7
JournalNucleic acids research
Volume39
Issue number7
DOIs
Publication statusPublished - Apr 2011

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Research Beacons, Institutes and Platforms

  • Manchester Cancer Research Centre

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