NPAT links cyclin E–Cdk2 to the regulation of replication-dependent histone gene transcription
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.
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Footnotes
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↵4 Present address: Center for Cancer Biology, University of Rochester Medical Center, Rochester, NY 14642, USA
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↵5 Corresponding author.
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E-MAIL jiyong_zhao@urmc.rochester.edu; FAX (716) 273-1450.
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Article and publication are at www.genesdev.org/cgi/doi/10.1101/gad.827700.
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- Received June 15, 2000.
- Accepted July 28, 2000.
- Cold Spring Harbor Laboratory Press