| Literature DB >> 29910000 |
Xiang-Ping Yao1, Xuewen Cheng2, Chong Wang1, Miao Zhao1, Xin-Xin Guo1, Hui-Zhen Su1, Lu-Lu Lai1, Xiao-Huan Zou1, Xue-Jiao Chen3, Yuying Zhao4, En-Lin Dong1, Ying-Qian Lu1, Shuang Wu1, Xiaojuan Li5, Gaofeng Fan5, Hongjie Yu6, Jianfeng Xu6, Ning Wang7, Zhi-Qi Xiong8, Wan-Jin Chen9.
Abstract
Primary familial brain calcification (PFBC) is a genetically heterogeneous disorder characterized by bilateral calcifications in the basal ganglia and other brain regions. The genetic basis of this disorder remains unknown in a significant portion of familial cases. Here, we reported a recessive causal gene, MYORG, for PFBC. Compound heterozygous or homozygous mutations of MYORG co-segregated completely with PFBC in six families, with logarithm of odds (LOD) score of 4.91 at the zero recombination fraction. In mice, Myorg mRNA was expressed specifically in S100β-positive astrocytes, and knockout of Myorg induced the formation of brain calcification at 9 months of age. Our findings provide strong evidence that loss-of-function mutations of MYORG cause brain calcification in humans and mice.Entities:
Keywords: MYORG; PFBC; astrocyte; brain calcification; glycosidase
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Year: 2018 PMID: 29910000 DOI: 10.1016/j.neuron.2018.05.037
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173