State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
J Am Chem Soc. 2012 Oct 31;134(43):17963-71. doi: 10.1021/ja3064149. Epub 2012 Oct 17.
The direct nucleic acid repair dioxygenase FTO is an enzyme that demethylates N(6)-methyladenosine (m(6)A) residues in mRNA in vitro and inside cells. FTO is the first RNA demethylase discovered that also serves a major regulatory function in mammals. Together with structure-based virtual screening and biochemical analyses, we report the first identification of several small-molecule inhibitors of human FTO demethylase. The most potent compound, the natural product rhein, which is neither a structural mimic of 2-oxoglutarate nor a chelator of metal ion, competitively binds to the FTO active site in vitro. Rhein also exhibits good inhibitory activity on m(6)A demethylation inside cells. These studies shed light on the development of powerful probes and new therapies for use in RNA biology and drug discovery.
直接核酸修复双加氧酶 FTO 是一种酶,能够在体外和细胞内将 mRNA 中的 N(6)-甲基腺苷(m(6)A)残基去甲基化。FTO 是第一个被发现的同时在哺乳动物中具有主要调节功能的 RNA 去甲基酶。通过基于结构的虚拟筛选和生化分析,我们首次鉴定出几种人 FTO 去甲基酶的小分子抑制剂。最有效的化合物是天然产物大黄酸,它既不是 2-氧戊二酸的结构类似物,也不是金属离子的螯合剂,能够在体外竞争性地结合 FTO 活性位点。大黄酸在细胞内也表现出良好的 m(6)A 去甲基化抑制活性。这些研究为 RNA 生物学和药物发现中使用的强大探针和新疗法的开发提供了线索。