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果蝇zeste基因同源物2(EZH 2)的多梳蛋白家族蛋白是一种癌基因,可影响骨髓瘤细胞生长及突变型ras表型。

The polycomb group protein enhancer of zeste homolog 2 (EZH 2) is an oncogene that influences myeloma cell growth and the mutant ras phenotype.

作者信息

Croonquist Paula A, Van Ness Brian

机构信息

The Graduate Program in Molecular, Cellular, Developmental Biology, and Genetics, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

Oncogene. 2005 Sep 15;24(41):6269-80. doi: 10.1038/sj.onc.1208771.

DOI:10.1038/sj.onc.1208771
PMID:16007202
Abstract

Three distinct proliferative signals for multiple myeloma (MM) cell lines induce enhancer of zeste homolog 2 (ezh 2) transcript expression. EZH 2 is a polycomb group protein that mediates repression of gene transcription at the chromatin level through its methyltransferase activity. Normal bone marrow plasma cells do not express ezh2; however, gene expression is induced and correlates with tumor burden during progression of this disease. We therefore investigated how EZH 2 expression is deregulated in MM cell lines and determined the consequence of this activity on proliferation and transformation. We found that EZH 2 protein expression is induced by interleukin 6 (IL-6) in growth factor-dependent cell lines and is constitutive in IL-6-independent cell lines. Furthermore, EZH 2 expression correlates with proliferation and B-cell terminal differentiation. Significantly, EZH 2 protein inhibition by short interference RNA treatment results in MM cell growth arrest. Conversely, EZH 2 ectopic overexpression induces growth factor independence. We found that the growth factor-independent proliferative phenotype in MM cell lines harboring a mutant N- or K-ras gene requires EZH 2 activity. Finally, this is the first report to demonstrate that EZH 2 has oncogenic activity in vivo, and that cell transformation and tumor formation require histone methyltransferase activity.

摘要

针对多发性骨髓瘤(MM)细胞系的三种不同增殖信号可诱导zeste同源物2增强子(EZH2)转录本表达。EZH2是一种多梳蛋白家族蛋白,通过其甲基转移酶活性在染色质水平介导基因转录的抑制。正常骨髓浆细胞不表达EZH2;然而,在该疾病进展过程中基因表达被诱导且与肿瘤负荷相关。因此,我们研究了MM细胞系中EZH2表达是如何失调的,并确定了这种活性对增殖和转化的影响。我们发现,在依赖生长因子的细胞系中,EZH2蛋白表达由白细胞介素6(IL-6)诱导,而在不依赖IL-6的细胞系中是组成性表达。此外,EZH2表达与增殖和B细胞终末分化相关。重要的是,通过短干扰RNA处理抑制EZH2蛋白会导致MM细胞生长停滞。相反,EZH2异位过表达会诱导生长因子非依赖性。我们发现,在携带突变型N-或K-ras基因的MM细胞系中,不依赖生长因子的增殖表型需要EZH2活性。最后,这是第一份证明EZH2在体内具有致癌活性,且细胞转化和肿瘤形成需要组蛋白甲基转移酶活性的报告。

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