Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification

被引:145
作者
Yao, Xiang-Ping [1 ,2 ]
Cheng, Xuewen [3 ,4 ]
Wang, Chong [1 ,2 ]
Zhao, Miao [1 ,2 ]
Guo, Xin-Xin [1 ,2 ]
Su, Hui-Zhen [1 ,2 ]
Lai, Lu-Lu [1 ,2 ]
Zou, Xiao-Huan [1 ,2 ]
Chen, Xue-Jiao [5 ]
Zhao, Yuying [6 ,7 ]
Dong, En-Lin [1 ,2 ]
Lu, Ying-Qian [1 ,2 ]
Wu, Shuang [1 ,2 ]
Li, Xiaojuan [8 ]
Fan, Gaofeng [8 ]
Yu, Hongjie [9 ]
Xu, Jianfeng [9 ]
Wang, Ning [1 ,2 ,10 ]
Xiong, Zhi-Qi [3 ,4 ]
Chen, Wan-Jin [1 ,2 ,10 ]
机构
[1] Fujian Med Univ, Affiliated Hosp 1, Dept Neurol, Fuzhou 350005, Fujian, Peoples R China
[2] Fujian Med Univ, Affiliated Hosp 1, Inst Neurol, Fuzhou 350005, Fujian, Peoples R China
[3] Chinese Acad Sci, Inst Neurosci, Shanghai 200031, Peoples R China
[4] Chinese Acad Sci, State Key Lab Neurosci, CAS Ctr Excellence Brain Sci & Intelligence Techn, Shanghai Inst Biol Sci, Shanghai 200031, Peoples R China
[5] Fujian Med Univ, Zhangzhou Affiliated Hosp, Dept Neurol, Zhangzhou 363000, Peoples R China
[6] Shandong Univ, Qilu Hosp, Lab Neuromuscular Disorders, Jinan 250012, Shandong, Peoples R China
[7] Shandong Univ, Qilu Hosp, Dept Neurol, Jinan 250012, Shandong, Peoples R China
[8] ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
[9] NorthShore Univ HealthSyst, Program Personalized Canc Care, Evanston, IL 60201 USA
[10] Fujian Med Univ, Fujian Key Lab Mol Neurol, Fuzhou 350005, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
BASAL GANGLIA CALCIFICATION; ONE-STEP GENERATION; CEREBRAL CALCIFICATION; MICE; DISEASE; GENE; PATHOGENESIS; CALCINOSIS; PERICYTES; SPECTRUM;
D O I
10.1016/j.neuron.2018.05.037
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 S100b-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.
引用
收藏
页码:1116 / +
页数:13
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