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首页> 外文期刊>The Journal of biological chemistry >The Nuclear Envelope Protein Emerin Binds Directly to Histone Deacetylase 3 (HDAC3) and Activates HDAC3 Activity
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The Nuclear Envelope Protein Emerin Binds Directly to Histone Deacetylase 3 (HDAC3) and Activates HDAC3 Activity

机译:核包膜蛋白emerin直接与组蛋白脱乙酰酶3(HDAC3)结合并激活HDAC3活性

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Organization of the genome is critical for maintaining cell-specific gene expression, ensuring proper cell function. It is well established that the nuclear lamina preferentially associates with repressed chromatin. However, the molecular mechanisms underlying repressive chromatin formation and maintenance at the nuclear lamina remain poorly understood. Here we show that emerin binds directly to HDAC3, the catalytic subunit of the nuclear co-repressor (NCoR) complex, and recruits HDAC3 to the nuclear periphery. Emerin binding stimulated the catalytic activity of HDAC3, and emerin-null cells exhibit increased H4K5 acetylation, which is the preferred target of the NCoR complex. Emerin-null cells exhibit an epigenetic signature similar to that seen in HDAC3-null cells. Emerin-null cells also had significantly less HDAC3 at the nuclear lamina. Collectively, these data support a model whereby emerin facilitates repressive chromatin formation at the nuclear periphery by increasing the catalytic activity of HDAC3.
机译:组织基因组对于维持细胞特异性基因表达至关重要,确保适当的细胞功能。很好地确定,核薄膜优先与压抑的染色质缔解者联系起来。然而,在核薄片上抑制染色质形成和维护的分子机制仍然明确。在这里,我们表明Emerin直接与HDAC3,核心抑制剂(NCOR)复合物的催化亚基结合,并向核周边招募HDAC3。 Emerin结合刺激了HDAC3的催化活性,并且肌键细胞表现出增加的H4K5乙酰化,这是Ncor络合物的优选靶标。 Emerin-Null细胞表现出类似于HDAC3-NULL细胞中的表观遗传签名。核薄片在核薄片中的HDAC3也具有显着较低的HDAC3。总的来说,这些数据支持一种模型,即通过增加HDAC3的催化活性来促进在核外周处的压抑染色质形成。

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