Greer Eric Lieberman, Blanco Mario Andres, Gu Lei, Sendinc Erdem, Liu Jianzhao, Aristizábal-Corrales David, Hsu Chih-Hung, Aravind L, He Chuan, Shi Yang
Division of Newborn Medicine, Children's Hospital Boston, 300 Longwood Avenue, Boston, MA 02115, USA; Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Division of Newborn Medicine, Children's Hospital Boston, 300 Longwood Avenue, Boston, MA 02115, USA; Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Cell. 2015 May 7;161(4):868-78. doi: 10.1016/j.cell.2015.04.005. Epub 2015 Apr 30.
In mammalian cells, DNA methylation on the fifth position of cytosine (5mC) plays an important role as an epigenetic mark. However, DNA methylation was considered to be absent in C. elegans because of the lack of detectable 5mC, as well as homologs of the cytosine DNA methyltransferases. Here, using multiple approaches, we demonstrate the presence of adenine N(6)-methylation (6mA) in C. elegans DNA. We further demonstrate that this modification increases trans-generationally in a paradigm of epigenetic inheritance. Importantly, we identify a DNA demethylase, NMAD-1, and a potential DNA methyltransferase, DAMT-1, which regulate 6mA levels and crosstalk between methylations of histone H3K4 and adenines and control the epigenetic inheritance of phenotypes associated with the loss of the H3K4me2 demethylase spr-5. Together, these data identify a DNA modification in C. elegans and raise the exciting possibility that 6mA may be a carrier of heritable epigenetic information in eukaryotes.
在哺乳动物细胞中,胞嘧啶第五位的DNA甲基化(5mC)作为一种表观遗传标记发挥着重要作用。然而,由于缺乏可检测到的5mC以及胞嘧啶DNA甲基转移酶的同源物,秀丽隐杆线虫中被认为不存在DNA甲基化。在此,我们使用多种方法证明了秀丽隐杆线虫DNA中存在腺嘌呤N(6)-甲基化(6mA)。我们进一步证明,这种修饰在表观遗传遗传模式中会跨代增加。重要的是,我们鉴定出一种DNA去甲基化酶NMAD-1和一种潜在的DNA甲基转移酶DAMT-1,它们调节6mA水平以及组蛋白H3K4甲基化与腺嘌呤甲基化之间的串扰,并控制与H3K4me2去甲基化酶spr-5缺失相关的表型的表观遗传遗传。这些数据共同确定了秀丽隐杆线虫中的一种DNA修饰,并提出了令人兴奋的可能性,即6mA可能是真核生物中可遗传表观遗传信息的载体。