Kapoor Avnish, Agius Fernanda, Zhu Jian-Kang
Institute for Integrative Genome Biology, Department of Botany and Plant Sciences, University of California, Riverside, Riverside, CA 92521, USA.
FEBS Lett. 2005 Oct 31;579(26):5889-98. doi: 10.1016/j.febslet.2005.08.039. Epub 2005 Aug 31.
DNA methylation is important for stable transcriptional gene silencing. DNA methyltransferases for de novo as well as maintenance methylation have been well characterized. However, enzymes responsible for active DNA demethylation have been elusive and several reported mechanisms of active demethylation have been controversial. There has been a critical need for genetic analysis in order to firmly establish an in vivo role for putative DNA demethylases. Mutations in the bifunctional DNA glycosylase/lyase ROS1 in Arabidopsis cause DNA hypermethylation and transcriptional silencing of specific genes. Recombinant ROS1 protein has DNA glycosylase/lyase activity on methylated but not unmethylated DNA substrates. Therefore, there is now strong genetic evidence supporting a base excision repair mechanism for active DNA demethylation. DNA demethylases may be critical factors for genome wide hypomethylation seen in cancers and possibly important for epigenetic reprogramming during somatic cell cloning and stem cell function.
DNA甲基化对于稳定的转录基因沉默很重要。用于从头甲基化以及维持甲基化的DNA甲基转移酶已得到充分表征。然而,负责活性DNA去甲基化的酶一直难以捉摸,并且几种已报道的活性去甲基化机制一直存在争议。迫切需要进行遗传分析,以便牢固确立推定的DNA去甲基化酶在体内的作用。拟南芥中双功能DNA糖基化酶/裂解酶ROS1的突变会导致特定基因的DNA超甲基化和转录沉默。重组ROS1蛋白对甲基化而非未甲基化的DNA底物具有DNA糖基化酶/裂解酶活性。因此,现在有强有力的遗传学证据支持活性DNA去甲基化的碱基切除修复机制。DNA去甲基化酶可能是癌症中全基因组低甲基化的关键因素,并且可能对体细胞克隆和干细胞功能过程中的表观遗传重编程很重要。