Chen Ruoyu, Zhang Qiao, Duan Xiaoya, York Philippe, Chen Guo-Dong, Yin Pengcheng, Zhu Haijun, Xu Meichen, Chen Peilin, Wu Qihan, Li Dali, Samarut Jacques, Xu Guoliang, Zhang Pumin, Cao Xiaohua, Li Jiwen, Wong Jiemin
From the Shanghai Key Laboratory of Regulatory Biology, Institute of Biomedical Sciences and School of Life Sciences, East China Normal University, Shanghai 200241, China.
the Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas 77030.
J Biol Chem. 2017 Mar 17;292(11):4533-4543. doi: 10.1074/jbc.M116.754580. Epub 2017 Jan 23.
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. knock-out mice are viable and fertile and exhibit no gross defect. Although there is no significant change of DNA methylation, the null mice exhibit a reduction of 5hmC in the brain, including the cortex and hippocampus. Furthermore, the 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 5hmC reader and further demonstrates a role for 5hmC in neuronal function.
UHRF2被认为是DNA甲基化(5mC)和羟甲基化(5hmC)的一种新型调节因子,但其在DNA甲基化/羟甲基化中的生理功能和作用尚不清楚。在此我们表明,在小鼠中,UHRF2在大脑和其他一些组织中表达更为丰富。基因敲除小鼠存活且可育,未表现出明显缺陷。虽然DNA甲基化没有显著变化,但基因敲除小鼠大脑(包括皮层和海马体)中的5hmC减少。此外,基因敲除小鼠在空间记忆获取和保持方面表现出部分损伤。与该表型一致,基因表达谱分析揭示了UHRF2在调节神经元相关基因表达中的作用。最后,我们提供证据表明UHRF2在细胞中与5hmC结合,但似乎不影响TET1酶活性。总之,我们的研究支持UHRF2作为一种5hmC识别蛋白,并进一步证明了5hmC在神经元功能中的作用。