Technische Universität Dortmund, Fakultät für Chemie und Chemische Biologie, Otto-Hahn-Strasse 4a, 44227, Dortmund, Germany.
Chembiochem. 2016 Jun 2;17(11):975-80. doi: 10.1002/cbic.201600072. Epub 2016 Apr 20.
Epigenetic modification of the cytosine 5-position is an important regulator of gene expression with essential roles in genome stability, development, and disease. In addition to 5-methylcytosine (mC), the oxidized mC derivatives 5-hydroxymethyl-, 5-formyl-, and 5-carboxylcytosine (hmC, fC, and caC) have recently been discovered. These are intermediates of an active demethylation pathway but might also represent new epigenetic marks with individual biological roles. This increase in chemical complexity of DNA-encoded information has created a pressing need for new approaches that allow reading and editing of this information. Transcription-activator-like effectors (TALEs) are DNA-binding domains with programmable sequence selectivity that enable the direct reading of epigenetic cytosine modifications but can also guide enzymatic editing domains to genomic loci of choice. Here, we review recent advances in employing TALEs for these applications.
DNA 胞嘧啶 5-位的表观遗传修饰是基因表达的重要调控因子,在基因组稳定性、发育和疾病中发挥着重要作用。除了 5-甲基胞嘧啶(mC)外,最近还发现了 mC 的氧化衍生物 5-羟甲基胞嘧啶(hmC)、5-甲酰基胞嘧啶(fC)和 5-羧基胞嘧啶(caC)。这些是一种活跃的去甲基化途径的中间产物,但也可能代表具有独特生物学功能的新的表观遗传标记。这种 DNA 编码信息化学复杂性的增加,迫切需要新的方法来读取和编辑这些信息。转录激活因子样效应物(TALEs)是具有可编程序列选择性的 DNA 结合结构域,可直接读取表观遗传胞嘧啶修饰,也可指导酶编辑结构域到所需的基因组位点。在这里,我们综述了最近利用 TALEs 进行这些应用的进展。