4.8 Article

Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification

Journal

NEURON
Volume 98, Issue 6, Pages 1116-+

Publisher

CELL PRESS
DOI: 10.1016/j.neuron.2018.05.037

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Funding

  1. National Natural Science Foundation of China (NSFC) [81322017, 81771230, U1505222, 31771139]
  2. CAS grant [QYZDJ-SSW-SMC010]
  3. MOST grant [2016YFA0501002]
  4. National Key Clinical Specialty Discipline Construction Program
  5. Key Clinical Specialty Discipline Construction Program of Fujian
  6. Joint Funds for the Innovation of Science and Technology of Fujian Province [2017Y9094]

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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.

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