Demethylation of H3K27 Regulates Polycomb Recruitment and H2A Ubiquitination
The Wistar Institute · Institució Catalana de Recerca i Estudis Avançats · +2 more institutions
Abstract
Methylation of histone H3 lysine 27 (H3K27) is a posttranslational modification that is highly correlated with genomic silencing. Here we show that human UTX, a member of the Jumonji C family of proteins, is a di- and trimethyl H3K27 demethylase. UTX occupies the promoters of HOX gene clusters and regulates their transcriptional output by modulating the recruitment of polycomb repressive complex 1 and the monoubiquitination of histone H2A. Moreover, UTX associates with mixed-lineage leukemia (MLL) 2/3 complexes, and during retinoic acid signaling events, the recruitment of the UTX complex to HOX genes results in H3K27 demethylation and a concomitant methylation of H3K4. Our results suggest a concerted…
Citation impact
- FWCI
- 25.83
- Percentile
- 100%
- References
- 27
Authors
8- MGMin Gyu Lee
The Wistar Institute, Institució Catalana de Recerca i Estudis Avançats, Howard Hughes Medical Institute, New York University
- RVRaffaella Villa
The Wistar Institute, Institució Catalana de Recerca i Estudis Avançats, Howard Hughes Medical Institute, New York University
- PTPatrick Trojer
The Wistar Institute, Institució Catalana de Recerca i Estudis Avançats, Howard Hughes Medical Institute, New York University
- JNJessica Norman
The Wistar Institute, Institució Catalana de Recerca i Estudis Avançats, Howard Hughes Medical Institute, New York University
- KYKai-Ping Yan
The Wistar Institute, Institució Catalana de Recerca i Estudis Avançats, Howard Hughes Medical Institute, New York University
Topics & keywords
- Demethylase
- Histone H3
- Histone
- Biology
- Hox gene
- Demethylation
- Histone methylation
- Polycomb-group proteins