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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Dates
Type | When |
---|---|
Created | 22 years, 11 months ago (Sept. 3, 2002, 12:44 p.m.) |
Deposited | 3 years, 9 months ago (Nov. 15, 2021, 11:13 a.m.) |
Indexed | 1 month, 3 weeks ago (July 2, 2025, 1:51 p.m.) |
Issued | 22 years, 11 months ago (Sept. 1, 2002) |
Published | 22 years, 11 months ago (Sept. 1, 2002) |
Published Online | 22 years, 11 months ago (Sept. 1, 2002) |
Published Print | 22 years, 11 months ago (Sept. 1, 2002) |
@article{Rice_2002, title={Mitotic-specific methylation of histone H4 Lys 20 follows increased PR-Set7 expression and its localization to mitotic chromosomes}, volume={16}, ISSN={1549-5477}, url={http://dx.doi.org/10.1101/gad.1014902}, DOI={10.1101/gad.1014902}, number={17}, journal={Genes & Development}, publisher={Cold Spring Harbor Laboratory}, author={Rice, Judd C. and Nishioka, Kenichi and Sarma, Kavitha and Steward, Ruth and Reinberg, Danny and Allis, C. David}, year={2002}, month=sep, pages={2225–2230} }