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Cited by 233

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Mitotic-specific methylation of histone H4 Lys 20 follows increased PR-Set7 expression and its localization to mitotic chromosomes

Open access
Rice, Judd C., Nishioka, Kenichi, Sarma, Kavitha, Steward, Ruth, Reinberg, Danny, Allis, C. David·2002·Genes & Development

Abstract

We describe distinct patterns of histone methylation during human cell cycle progression. Histone H4 methyltransferase activity was found to be cell cycle-regulated, consistent with increased H4 Lys 20 methylation at mitosis. This increase closely followed the cell cycle-regulated expression of the H4 Lys 20 methyltransferase, PR-Set7. Localization of PR-Set7 to mitotic chromosomes and subsequent increase in H4 Lys 20 methylation were inversely correlated to transient H4 Lys 16 acetylation in early S-phase. These data suggest that H4 Lys 20 methylation by PR-Set7 during mitosis acts to antagonize H4 Lys 16 acetylation and to establish a mechanism by which this mark is epigenetically transmitted.

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Metadata

Authors
Rice, J. C., Nishioka, K., Sarma, K., Steward, R., Reinberg, D., & Allis, C. D.
Venue
Genes & Development
Published
2002-09-01
Volume
16
Issue
17
Pages
2225-2230
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W2111494715
Cited by
233
References
2
Type
posted content
Language
en
Open access
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CoChat. (2026). Citation check: Mitotic-specific methylation of histone H4 Lys 20 follows increased PR-Set7 expression and its localization to mitotic chromosomes. https://app.cochat.ai/papers/10.1101/gad.1014902
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Rice, J. C., Nishioka, K., Sarma, K., Steward, R., Reinberg, D., & Allis, C. D. (2002). Mitotic-specific methylation of histone H4 Lys 20 follows increased PR-Set7 expression and its localization to mitotic chromosomes. Genes & Development. https://doi.org/10.1101/gad.1014902

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