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5'区域特定位点的去甲基化对于小鼠α FcγR基因的表达至关重要。

Unmethylation of specific sites in the 5' region is critical for the expression of murine alpha Fc gamma R gene.

作者信息

Bonnerot C, Amigorena S, Fridman W H, Even J, Daëron M

机构信息

Laboratoire d'Immunologie Cellulaire et Clinique, INSERM Unité 255, Institut Curie, Paris, France.

出版信息

J Immunol. 1990 Jan 1;144(1):323-8.

PMID:1688573
Abstract

Three subtypes of murine low-affinity receptors for IgG (Fc gamma RII) have been identified. One is encoded by the alpha Fc gamma R gene, two are encoded by the beta Fc gamma R gene. In the present work, we examined whether DNA methylation might control expression of the alpha Fc gamma R gene. We found that, in DNA from a panel of Fc gamma R(+) and (-) cell lines, two MspI sites of the alpha Fc gamma R gene were selectively unmethylated only in the two cell lines containing alpha transcripts. These sites, separated by a distance of 1.2 kb, are located in the 5' region of the gene. All other MspI sites were methylated in all cell lines. Furthermore, 5-azacytidine induced the demethylation and the expression of the alpha Fc gamma R gene in the Fc gamma R(-) thymoma BW5147. Both alpha Fc gamma R gene transcripts and corresponding protein products became detectable in 5-azacytidine-treated cells. The alpha Fc gamma R gene was also demethylated and expressed in mouse spleen cells cultured with human rIL-2. We conclude that a correlation links the unmethylation and the expression of the alpha Fc gamma R gene in murine cell lines as well as in nontransformed lymphoid cells responding to a physiological stimulus.

摘要

已鉴定出小鼠IgG低亲和力受体(FcγRII)的三种亚型。一种由αFcγR基因编码,两种由βFcγR基因编码。在本研究中,我们检测了DNA甲基化是否可能控制αFcγR基因的表达。我们发现,在一组FcγR(+)和(-)细胞系的DNA中,αFcγR基因的两个MspI位点仅在含有α转录本的两个细胞系中选择性地未甲基化。这两个位点相距1.2 kb,位于基因的5'区域。所有其他MspI位点在所有细胞系中均被甲基化。此外,5-氮杂胞苷诱导FcγR(-)胸腺瘤BW5147中αFcγR基因的去甲基化和表达。在5-氮杂胞苷处理的细胞中可检测到αFcγR基因转录本和相应的蛋白质产物。在用人类重组白细胞介素-2培养的小鼠脾细胞中,αFcγR基因也发生了去甲基化并表达。我们得出结论,在小鼠细胞系以及对生理刺激有反应的未转化淋巴细胞中,αFcγR基因的去甲基化与表达之间存在相关性。

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