| Literature DB >> 22431509 |
Camille Simon1, Jalila Chagraoui, Jana Krosl, Patrick Gendron, Brian Wilhelm, Sébastien Lemieux, Geneviève Boucher, Pierre Chagnon, Simon Drouin, Raphaëlle Lambert, Claude Rondeau, Annie Bilodeau, Sylvie Lavallée, Martin Sauvageau, Josée Hébert, Guy Sauvageau.
Abstract
In this study, we show the high frequency of spontaneous γδ T-cell leukemia (T-ALL) occurrence in mice with biallelic deletion of enhancer of zeste homolog 2 (Ezh2). Tumor cells show little residual H3K27 trimethylation marks compared with controls. EZH2 is a component of the PRC2 Polycomb group protein complex, which is associated with DNA methyltransferases. Using next-generation sequencing, we identify alteration in gene expression levels of EZH2 and acquired mutations in PRC2-associated genes (DNMT3A and JARID2) in human adult T-ALL. Together, these studies document that deregulation of EZH2 and associated genes leads to the development of mouse, and likely human, T-ALL.Entities:
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Year: 2012 PMID: 22431509 PMCID: PMC3323876 DOI: 10.1101/gad.186411.111
Source DB: PubMed Journal: Genes Dev ISSN: 0890-9369 Impact factor: 11.361