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小鼠aprt基因启动子中的Sp1位点对于防止CpG岛甲基化是必需的。

Sp1 sites in the mouse aprt gene promoter are required to prevent methylation of the CpG island.

作者信息

Macleod D, Charlton J, Mullins J, Bird A P

机构信息

Institute of Cell and Molecular Biology, University of Edinburgh, Scotland.

出版信息

Genes Dev. 1994 Oct 1;8(19):2282-92. doi: 10.1101/gad.8.19.2282.

Abstract

In an attempt to find the mechanism by which CpG islands remain free of methylation we have undertaken a detailed examination of the mouse adenine phosphoribosyltransferase (aprt) gene. This housekeeping gene has a CpG island that extends over the gene promoter and includes the first two exons. We show that the island is free of methylation at all CpGs, whereas the flanks are methyated. Detailed patterns of methylation beyond the boundaries of the CpG island vary between cells. In vivo footprinting across the island region shows that three GC boxes clustered at the 5' edge of the CpG island are occupied, most probably by Sp1. No other footprints are detected within the island region. Deletion or mutagenesis of the Sp1 sites causes de novo methylation of the CpG island in a transgenic mouse assay. Thus, the peripherally located Sp1 sites are necessary to keep the aprt island methylation free.

摘要

为了找到CpG岛保持无甲基化状态的机制,我们对小鼠腺嘌呤磷酸核糖转移酶(aprt)基因进行了详细研究。这个管家基因有一个CpG岛,该岛延伸至基因启动子区域并包含前两个外显子。我们发现该岛的所有CpG位点均无甲基化,而其侧翼区域则发生甲基化。CpG岛边界之外的详细甲基化模式在不同细胞间存在差异。对整个岛区域进行的体内足迹分析表明,聚集在CpG岛5'边缘的三个GC框被占据,最有可能是被Sp1占据。在岛区域内未检测到其他足迹。在转基因小鼠实验中,Sp1位点的缺失或诱变会导致CpG岛发生从头甲基化。因此,位于周边的Sp1位点对于保持aprt岛无甲基化是必需的。

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