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Chromatin control during the cell cycle

Jonathan B Weitzman

Author Affiliations

Genome Biology 2002, 3:spotlight-20020514-01  doi:10.1186/gb-spotlight-20020514-01

The electronic version of this article is the complete one and can be found online at:


Published:14 May 2002

© 2002 BioMed Central Ltd

Research news

Maintaining cells in the quiescent G0 phase of the cell division cycle is achieved by suppressing the expression of genes required for cell-cycle progression. In the May 10 Science, Hidesato Ogawa and colleagues at the Dana-Farber Cancer Institute in Boston describe a repressive mechanism in quiescent cells involving the E2F-6 transcription factor (Science 2002, 296:1132-1136). They immunopurified protein complexes that include E2F-6 from human cells and analysed co-purifying protein bands by mass spectrometry. They detected the DP-1, Mga and Max transcription factors and showed that the E2F-6 complex can bind to E2F- and Myc-binding sites on DNA; they also found two associated histone methyltransferase enzymes. In addition, Ogawa et al. detected the HP1γ protein that binds to methylated lysine 9 residues in the tails of histone proteins. Finally, they also found evidence for Polycomb-group-like, ring-finger proteins in the same complex. The authors propose that E2F- and Myc-regulated genes are repressed in quiescent cells by E2F-6 and recruitment of a complex that modifies chromatin structure.

References

  1. [http://www.sciencemag.org] webcite

    Science

  2. [http://www.dfci.harvard.edu] webcite

    Dana-Farber Cancer Institute

  3. Unusual proliferation arrest and transcriptional control properties of a newly discovered E2F family member, E2F-6.

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