Department of Computer Science and Applied Mathematics, Weizmann Institute of Science, Rehovot 76100, Israel.
Cell. 2011 May 27;145(5):773-86. doi: 10.1016/j.cell.2011.04.024.
Mammalian CpG islands are key epigenomic elements that were first characterized experimentally as genomic fractions with low levels of DNA methylation. Currently, CpG islands are defined based on their genomic sequences alone. Here, we develop evolutionary models to show that several distinct evolutionary processes generate and maintain CpG islands. One central evolutionary regime resulting in enriched CpG content is driven by low levels of DNA methylation and consequentially low rates of CpG deamination. Another major force forming CpG islands is biased gene conversion that stabilizes constitutively methylated CpG islands by balancing rapid deamination with CpG fixation. Importantly, evolutionary analysis and population genetics data suggest that selection for high CpG content is not a significant factor contributing to conservation of CpGs in differentially methylated regions. The heterogeneous, but not selective, origins of CpG islands have direct implications for the understanding of DNA methylation patterns in healthy and diseased cells.
哺乳动物 CpG 岛是关键的表观基因组元件,最初是作为 DNA 甲基化水平较低的基因组部分进行实验鉴定的。目前,CpG 岛是根据其基因组序列单独定义的。在这里,我们开发了进化模型来表明,几个不同的进化过程会产生和维持 CpG 岛。一个导致 CpG 含量丰富的核心进化机制是由低水平的 DNA 甲基化和由此导致的低 CpG 脱氨酶速率驱动的。另一个形成 CpG 岛的主要力量是偏向性基因转换,它通过平衡快速脱氨和 CpG 固定来稳定组成型甲基化的 CpG 岛。重要的是,进化分析和群体遗传学数据表明,高 CpG 含量的选择并不是导致差异甲基化区域中 CpG 保留的重要因素。CpG 岛的异质性而非选择性起源对理解健康和患病细胞中的 DNA 甲基化模式具有直接意义。