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Cell cycle regulated transcription of heterochromatin in mammals vs. fission yeast: Functional conservation or coincidence?

Junjie Lu and David Gilbert

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Although it is tempting to speculate that the transcription-dependent heterochromatin assembly pathway found in fission yeast may operate in higher mammals, transcription of heterochromatin has been difficult to substantiate in mammalian cells. We recently demonstrated that transcription from the mouse pericentric heterochromatin major (γ) satellite repeats is under cell cycle control being sharply down regulated at the metaphase to anaphase transition and resuming in late G1-phase dependent upon passage through the restriction point. The highest rates of transcription were in early S-phase and again in mitosis with different RNA products detected at each of these times.1 Importantly, differences in the percentage of cells in G1-phase can account for past discrepancies in the detection of major satellite transcripts and suggest that pericentric heterochromatin transcription takes place in all proliferating mammalian cells. A similar cell-cycle regulation of heterochromatin transcription has now been shown in fission yeast,2,3 providing further support for a conserved mechanism. However, there are still fundamental differences between these two systems that preclude the identification of a functional or mechanistic link.

Authors

Junjie Lu

Florida State University

David Gilbert

NIH/NIMH

This is an open-access article

 Download PDF

If the document does not open, please right-click on the link (control-click on a Macintosh) and select the option to save the file to disk.