Coordinated activities of wild-type plus mutant EZH2 drive tumor-associated hypertrimethylation of lysine 27 on histone H3 (H3K27) in human B-cell lymphomas
Epizyme (United States) · University of California, San Francisco
Abstract
EZH2, the catalytic subunit of the PRC2 complex, catalyzes the mono- through trimethylation of lysine 27 on histone H3 (H3K27). Histone H3K27 trimethylation is a mechanism for suppressing transcription of specific genes that are proximal to the site of histone modification. Point mutations of the EZH2 gene (Tyr641) have been reported to be linked to subsets of human B-cell lymphoma. The mutant allele is always found associated with a wild-type allele (heterozygous) in disease cells, and the mutations were reported to ablate the enzymatic activity of the PRC2 complex for methylating an unmodified peptide substrate. Here we demonstrate that the WT enzyme displays greatest catalytic efficiency (k(cat)/K) for the…
Citation impact
- FWCI
- 19.87
- Percentile
- 100%
- References
- 35
Authors
7- CJChristopher J. SneeringerCorresponding
Epizyme (United States)
- MPMargaret Porter Scott
University of California, San Francisco, Epizyme (United States)
- KWKevin W. Kuntz
University of California, San Francisco, Epizyme (United States)
- SKSarah K. Knutson
University of California, San Francisco, Epizyme (United States)
- RMRoy M. Pollock
University of California, San Francisco, Epizyme (United States)
Topics & keywords
- Histone H3
- EZH2
- PRC2
- Histone
- Biology
- Methylation
- Lysine
- Mutant