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Nat Genet ; 42(8): 665-7, 2010 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-20601954

RESUMEN

In myelodysplastic syndromes (MDS), deletions of chromosome 7 or 7q are common and correlate with a poor prognosis. The relevant genes on chromosome 7 are unknown. We report here that EZH2, located at 7q36.1, is frequently targeted in MDS. Analysis of EZH2 deletions, missense and frameshift mutations strongly suggests that EZH2 is a tumor suppressor. As EZH2 functions as a histone methyltransferase, abnormal histone modification may contribute to epigenetic deregulation in MDS.


Asunto(s)
Mutación , Síndromes Mielodisplásicos/genética , Proteínas de Unión al ADN , Proteína Potenciadora del Homólogo Zeste 2 , Genes Supresores de Tumor , Histona Metiltransferasas , N-Metiltransferasa de Histona-Lisina , Humanos , Complejo Represivo Polycomb 2 , Factores de Transcripción
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