Cree Simone L, Fredericks Rayleen, Miller Allison, Pearce F Grant, Filichev Vyacheslav, Fee Conan, Kennedy Martin A
Department of Pathology, University of Otago, Christchurch, New Zealand.
Department of Chemical and Process Engineering, University of Canterbury, Christchurch, New Zealand.
FEBS Lett. 2016 Sep;590(17):2870-83. doi: 10.1002/1873-3468.12331. Epub 2016 Aug 11.
The DNA methyltransferase enzymes (DNMTs) catalyzing cytosine methylation do so at specific locations of the genome, although with some level of redundancy. The de novo methyltransferases DNMT3A and 3B play a vital role in methylating the genome of the developing embryo in regions devoid of methylation marks. The ability of DNMTs to colocalize at sites of DNA damage is suggestive that recognition of mispaired bases and unusual structures is inherent to the function of these proteins. We provide evidence for G-quadruplex formation within imprinted gene promoters, and report high-affinity binding of recombinant human DNMTs to such DNA G-quadruplexes in vitro. These observations suggest a potential interaction of G-quadruplexes with the DNA methylation machinery, which may be of epigenetic and biological significance.
DNA甲基转移酶(DNMTs)催化胞嘧啶甲基化,尽管存在一定程度的冗余,但它们是在基因组的特定位置进行催化的。从头甲基转移酶DNMT3A和3B在缺乏甲基化标记的区域对发育中胚胎的基因组进行甲基化过程中起着至关重要的作用。DNMTs在DNA损伤位点共定位的能力表明,识别错配碱基和异常结构是这些蛋白质功能所固有的。我们提供了印迹基因启动子内形成G-四链体的证据,并报告了重组人DNMTs在体外与这种DNA G-四链体的高亲和力结合。这些观察结果表明G-四链体与DNA甲基化机制之间可能存在相互作用,这可能具有表观遗传学和生物学意义。