| Literature DB >> 28115522 |
Ruoyu Chen1, Qiao Zhang1, Xiaoya Duan1, Philippe York2, Guo-Dong Chen3, Pengcheng Yin4, Haijun Zhu1, Meichen Xu4, Peilin Chen1, Qihan Wu1, Dali Li1, Jacques Samarut5, Guoliang Xu3, Pumin Zhang2, Xiaohua Cao4, Jiwen Li6, Jiemin Wong7,8.
Abstract
UHRF2 has been implicated as a novel regulator for both DNA methylation (5mC) and hydroxymethylation (5hmC), but its physiological function and role in DNA methylation/hydroxymethylation are unknown. Here we show that in mice, UHRF2 is more abundantly expressed in the brain and a few other tissues. Uhrf2 knock-out mice are viable and fertile and exhibit no gross defect. Although there is no significant change of DNA methylation, the Uhrf2 null mice exhibit a reduction of 5hmC in the brain, including the cortex and hippocampus. Furthermore, the Uhrf2 null mice exhibit a partial impairment in spatial memory acquisition and retention. Consistent with the phenotype, gene expression profiling uncovers a role for UHRF2 in regulating neuron-related gene expression. Finally, we provide evidence that UHRF2 binds 5hmC in cells but does not appear to affect the TET1 enzymatic activity. Together, our study supports UHRF2 as a bona fide 5hmC reader and further demonstrates a role for 5hmC in neuronal function.Entities:
Keywords: DNA demethylation; DNA methylation; dioxygenase; epigenetics; mouse genetics; neurobiology; protein-DNA interaction
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Year: 2017 PMID: 28115522 PMCID: PMC5377770 DOI: 10.1074/jbc.M116.754580
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157