Li Liping, Zang Liqun, Zhang Feiran, Chen Junchen, Shen Hui, Shu Liqi, Liang Feng, Feng Chunyue, Chen Deng, Tao Huikang, Xu Tianlei, Li Ziyi, Kang Yunhee, Wu Hao, Tang Lichun, Zhang Pumin, Jin Peng, Shu Qiang, Li Xuekun
Institute of Genetics, College of Life Sciences, Zhejiang University, Hangzhou 310058, China.
The Children's Hospital, School of Medicine, Zhejiang University, Hangzhou 310052, China.
Hum Mol Genet. 2017 Jul 1;26(13):2398-2411. doi: 10.1093/hmg/ddx128.
Fat mass and obesity-associated gene (FTO) is a member of the Fe (II)- and oxoglutarate-dependent AlkB dioxygenase family and is linked to both obesity and intellectual disability. The role of FTO in neurodevelopment and neurogenesis, however, remains largely unknown. Here we show that FTO is expressed in adult neural stem cells and neurons and displays dynamic expression during postnatal neurodevelopment. The loss of FTO leads to decreased brain size and body weight. We find that FTO deficiency could reduce the proliferation and neuronal differentiation of adult neural stem cells in vivo, which leads to impaired learning and memory. Given the role of FTO as a demethylase of N6-methyladenosine (m6A), we went on to perform genome-wide m6A profiling and observed dynamic m6A modification during postnatal neurodevelopment. The loss of FTO led to the altered expression of several key components of the brain derived neurotrophic factor pathway that were marked by m6A. These results together suggest FTO plays important roles in neurogenesis, as well as in learning and memory.
脂肪量和肥胖相关基因(FTO)是依赖于Fe(II)和α-酮戊二酸的AlkB双加氧酶家族的成员,与肥胖和智力残疾都有关联。然而,FTO在神经发育和神经发生中的作用在很大程度上仍不清楚。在这里,我们表明FTO在成体神经干细胞和神经元中表达,并在出生后神经发育过程中表现出动态表达。FTO的缺失导致脑尺寸和体重减小。我们发现FTO缺陷会降低体内成体神经干细胞的增殖和神经元分化,从而导致学习和记忆受损。鉴于FTO作为N6-甲基腺苷(m6A)去甲基化酶的作用,我们接着进行了全基因组m6A分析,并观察到出生后神经发育过程中动态的m6A修饰。FTO的缺失导致脑源性神经营养因子途径的几个关键成分的表达改变,这些成分以m6A为标记。这些结果共同表明FTO在神经发生以及学习和记忆中发挥重要作用。