NPAT links cyclin E–Cdk2 to the regulation of replication-dependent histone gene transcription

  1. Jiyong Zhao1,4,5,
  2. Brian K. Kennedy1,
  3. Brandon D. Lawrence2,
  4. David A. Barbie1,
  5. A. Gregory Matera3,
  6. Jonathan A. Fletcher2, and
  7. Ed Harlow1
  1. 1Massachusetts General Hospital Cancer Center, Charlestown, Massachusetts 02129, USA; 2Brigham and Women's Hospital, Department of Pathology, Boston, Massachusetts 02115, USA; 3Case Western Reserve University, Department of Genetics, Cleveland, Ohio 44106, USA

Abstract

In eukaryotic cells, histone gene expression is one of the major events that mark entry into S phase. While this process is tightly linked to cell cycle position, how it is regulated by the cell cycle machinery is not known. Here we show that NPAT, a substrate of the cyclin E–Cdk2 complex, is associated with human replication-dependent histone gene clusters on both chromosomes 1 and 6 in S phase. We demonstrate that NPAT activates histone gene transcription and that this activation is dependent on the promoter elements (SSCSs) previously proposed to mediate cell cycle–dependent transcription. Cyclin E is also associated with the histone gene loci, and cyclin E–Cdk2 stimulates the NPAT-mediated activation of histone gene transcription. Thus, our results both show that NPAT is involved in a key S phase event and provide a link between the cell cycle machinery and activation of histone gene transcription.

Keywords

Footnotes

  • 4 Present address: Center for Cancer Biology, University of Rochester Medical Center, Rochester, NY 14642, USA

  • 5 Corresponding author.

  • E-MAIL jiyong_zhao{at}urmc.rochester.edu; FAX (716) 273-1450.

  • Article and publication are at www.genesdev.org/cgi/doi/10.1101/gad.827700.

    • Received June 15, 2000.
    • Accepted July 28, 2000.
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