F Radtke, M Hug, O Georgiev, K Matsuo, W Schaffner
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引用次数: 33
摘要
CpG 位点的胞嘧啶甲基化通常与哺乳动物基因的活性呈负相关。许多转录因子的 DNA 结合位点含有一个或多个 CpG 二核苷酸,当该位点被甲基化时,它们就不能再有效地结合 DNA。锌指因子 Sp1 是一个明显的例外,即使其结合位点被甲基化,它也能结合 DNA 并激活转录。在这里,我们发现另外两个锌指因子 MTF-1 和 Krox-20 也能与 CpG 甲基化位点结合。MTF-1通过与一些金属反应元件(MRE)结合来调控金属硫蛋白基因的转录,而Krox-20则在后脑分割过程中调控Hox基因。然而,对 MTF-1/MRE 结合的精细分析表明,并非每个结合位点都能容忍甲基化:小鼠金属硫蛋白 I 基因中亲和力最高的位点 MREd 不受甲基化影响,而另外两个在不同位置上具有 CpGs 的 MRE 位点则因甲基化而部分或完全丧失功能。甲基化敏感和不敏感因子/结合位点都可能决定基因的发育表达模式。
Differential sensitivity of zinc finger transcription factors MTF-1, Sp1 and Krox-20 to CpG methylation of their binding sites.
Cytosine methylation at CpG sites is often negatively correlated with mammalian gene activity. Many transcription factors whose DNA binding site contains one or more CpG dinucleotides are no longer able to efficiently bind DNA when the site is methylated. A notable exception is the zinc finger factor Sp1 which binds DNA and activates transcription even when its binding site is methylated. Here we show that two other zinc finger factors, MTF-1 and Krox-20, can also bind to CpG methylated sites. MTF-1 regulates metallothionein gene transcription by binding to a number of metal responsive elements (MREs), and Krox-20 regulates Hox genes during hindbrain segmentation. However, a refined analysis of MTF-1/MRE binding shows that methylation is not tolerated at every binding site: the highest affinity site in the mouse metallothionein I gene, MREd, is unaffected by methylation, while two other MRE sites with CpGs at different positions are rendered partially or completely nonfunctional by methylation. Both methylation sensitive and insensitive factors/binding sites are likely to determine the developmental expression pattern of a gene.