Department of Molecular and Cellular Biology, University of California, Davis, Davis, CA 95616, USA.
Mol Cell. 2012 Mar 30;45(6):814-25. doi: 10.1016/j.molcel.2012.01.017. Epub 2012 Mar 1.
CpG islands (CGIs) function as promoters for approximately 60% of human genes. Most of these elements remain protected from CpG methylation, a prevalent epigenetic modification associated with transcriptional silencing. Here, we report that methylation-resistant CGI promoters are characterized by significant strand asymmetry in the distribution of guanines and cytosines (GC skew) immediately downstream from their transcription start sites. Using innovative genomics methodologies, we show that transcription through regions of GC skew leads to the formation of long R loop structures. Furthermore, we show that GC skew and R loop formation potential is correlated with and predictive of the unmethylated state of CGIs. Finally, we provide evidence that R loop formation protects from DNMT3B1, the primary de novo DNA methyltransferase in early development. Altogether, these results suggest that protection from DNA methylation is a built-in characteristic of the DNA sequence of CGI promoters that is revealed by the cotranscriptional formation of R loop structures.
CpG 岛(CGIs)作为大约 60%的人类基因的启动子发挥作用。这些元件中的大多数仍然受到 CpG 甲基化的保护,CpG 甲基化是一种与转录沉默相关的普遍表观遗传修饰。在这里,我们报告说,抗甲基化 CGI 启动子的特征是在其转录起始位点下游的碱基对(GC 倾斜)分布上存在显著的链不对称性。使用创新的基因组学方法,我们表明,通过 GC 倾斜区域的转录导致长 R 环结构的形成。此外,我们表明,GC 倾斜和 R 环形成潜力与 CGIs 的非甲基化状态相关,并具有预测性。最后,我们提供的证据表明,R 环形成可以防止 DNA 甲基转移酶 3B1(早期发育中的主要从头 DNA 甲基转移酶)的作用。总之,这些结果表明,对 DNA 甲基化的保护是 CGI 启动子 DNA 序列的固有特征,这种特征是通过 R 环结构的共转录形成而显现出来的。