| Literature DB >> 22850114 |
Christina R Majer1, Lei Jin, Margaret Porter Scott, Sarah K Knutson, Kevin W Kuntz, Heike Keilhack, Jesse J Smith, Mikel P Moyer, Victoria M Richon, Robert A Copeland, Tim J Wigle.
Abstract
Heterozygous point mutations at Y641 and A677 in the EZH2 SET domain are prevalent in about 10-24% of Non-Hodgkin lymphomas (NHL). Previous studies indicate that these are gain-of-function mutations leading to the hypertrimethylation of H3K27. These EZH2 mutations may drive the proliferation of lymphoma and make EZH2 a molecular target for patients harboring these mutations. Here, another EZH2 SET domain point mutation, A687V, occurring in about 1-2% of lymphoma patients, is also shown to be a gain-of-function mutation that greatly enhances its ability to perform dimethylation relative to wild-type EZH2 and is equally proficient at catalyzing trimethylation. We propose that A687V EZH2 also leads to hypertrimethylation of H3K27 and may thus be a driver mutation in NHL.Entities:
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Year: 2012 PMID: 22850114 DOI: 10.1016/j.febslet.2012.07.066
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124