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肌细胞生成素募集组蛋白伴侣来促进染色质转录(FACT),以促进肌肉特异性基因的核小体解体。

Myogenin recruits the histone chaperone facilitates chromatin transcription (FACT) to promote nucleosome disassembly at muscle-specific genes.

机构信息

Department of Biochemistry and Molecular Biology and Simmons Cancer Institute, Southern Illinois University, School of Medicine, Carbondale, Illinois 62901.

Department of Biochemistry and Molecular Biology, University of Arkansas for Medical Science, Little Rock, Arkansas 72205.

出版信息

J Biol Chem. 2013 Mar 15;288(11):7676-7687. doi: 10.1074/jbc.M112.426718. Epub 2013 Jan 30.

Abstract

Facilitates chromatin transcription (FACT) functions to reorganize nucleosomes by acting as a histone chaperone that destabilizes and restores nucleosomal structure. The FACT complex is composed of two subunits: SSRP1 and SPT16. We have discovered that myogenin interacts with the FACT complex. Transfection of FACT subunits with myogenin is highly stimulatory for endogenous muscle gene expression in 10T1/2 cells. We have also found that FACT subunits do not associate with differentiation-specific genes while C2C12 cells are proliferating but are recruited to muscle-specific genes as differentiation initiates and then dissociate as differentiation proceeds. The recruitment is dependent on myogenin, as knockdowns of myogenin show no recruitment of the FACT complex. These data suggest that FACT is involved in the early steps of gene activation through its histone chaperone activities that serve to open the chromatin structure and facilitate transcription. Consistent with this hypothesis, we find that nucleosomes are depleted at muscle-specific promoters upon differentiation and that this activity is dependent on the presence of FACT. Our results show that the FACT complex promotes myogenin-dependent transcription and suggest that FACT plays an important role in the establishment of the appropriate transcription profile in a differentiated muscle cell.

摘要

促进染色质转录 (FACT) 功能,通过作为组蛋白伴侣来重新组织核小体,使核小体结构不稳定并恢复。FACT 复合物由两个亚基组成:SSRPl 和 SPT16。我们发现肌细胞生成素与 FACT 复合物相互作用。肌细胞生成素与 FACT 亚基的转染对 10T1/2 细胞中内源性肌肉基因表达有高度的刺激作用。我们还发现,FACT 亚基在 C2C12 细胞增殖时不会与分化特异性基因相关联,但在分化开始时被招募到肌肉特异性基因上,然后随着分化的进行而解离。这种招募依赖于肌细胞生成素,因为肌细胞生成素的敲低显示 FACT 复合物没有招募。这些数据表明,FACT 通过其组蛋白伴侣活性参与基因激活的早期步骤,从而打开染色质结构并促进转录。与这一假设一致,我们发现分化时肌肉特异性启动子上的核小体减少,并且这种活性依赖于 FACT 的存在。我们的结果表明,FACT 复合物促进肌细胞生成素依赖性转录,并表明 FACT 在分化的肌肉细胞中建立适当的转录谱方面发挥重要作用。

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