Literature DB >> 29910000

Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification.

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.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  MYORG; PFBC; astrocyte; brain calcification; glycosidase

Mesh:

Substances:

Year:  2018        PMID: 29910000     DOI: 10.1016/j.neuron.2018.05.037

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  26 in total

1.  Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian family.

Authors:  Eliana Marisa Ramos; Alessandro Roca; Noravit Chumchim; Deepika Reddy Dokuru; Victoria Van Berlo; Giovanna De Michele; Maria Lieto; Enrico Tedeschi; Giuseppe De Michele; Giovanni Coppola
Journal:  Neurogenetics       Date:  2019-03-21       Impact factor: 2.660

Review 2.  MYORG Mutations: a Major Cause of Recessive Primary Familial Brain Calcification.

Authors:  Max Bauer; Dolev Rahat; Elad Zisman; Yuval Tabach; Alexander Lossos; Vardiella Meiner; David Arkadir
Journal:  Curr Neurol Neurosci Rep       Date:  2019-08-23       Impact factor: 5.081

3.  A mutation map for human glycoside hydrolase genes.

Authors:  Lars Hansen; Diab M Husein; Birthe Gericke; Torben Hansen; Oluf Pedersen; Mitali A Tambe; Hudson H Freeze; Hassan Y Naim; Bernard Henrissat; Hans H Wandall; Henrik Clausen; Eric P Bennett
Journal:  Glycobiology       Date:  2020-07-16       Impact factor: 4.313

4.  The primary familial brain calcification-associated protein MYORG is an α-galactosidase with restricted substrate specificity.

Authors:  Richard W Meek; Jacob Brockerman; Osei B Fordwour; Wesley F Zandberg; Gideon J Davies; David J Vocadlo
Journal:  PLoS Biol       Date:  2022-09-21       Impact factor: 9.593

5.  In silico functional and structural characterization of hepatitis B virus PreS/S-gene in Iranian patients infected with chronic hepatitis B virus genotype D.

Authors:  Nastaran Khodadad; Seyed Saeed Seyedian; Afagh Moattari; Somayeh Biparva Haghighi; Roya Pirmoradi; Samaneh Abbasi; Manoochehr Makvandi
Journal:  Heliyon       Date:  2020-07-15

6.  Interplay between primary familial brain calcification-associated SLC20A2 and XPR1 phosphate transporters requires inositol polyphosphates for control of cellular phosphate homeostasis.

Authors:  Uriel López-Sánchez; Sandrine Tury; Gaël Nicolas; Miranda S Wilson; Snejana Jurici; Xavier Ayrignac; Valérie Courgnaud; Adolfo Saiardi; Marc Sitbon; Jean-Luc Battini
Journal:  J Biol Chem       Date:  2020-05-11       Impact factor: 5.157

7.  Brain Calcification in a Young Adult with Abnormal Copper Metabolism.

Authors:  Yanbing Hou; Junyu Lin; Huifang Shang
Journal:  Mov Disord Clin Pract       Date:  2021-02-02

Review 8.  Molecular Genetics and Modifier Genes in Pseudoxanthoma Elasticum, a Heritable Multisystem Ectopic Mineralization Disorder.

Authors:  Hongbin Luo; Masoomeh Faghankhani; Yi Cao; Jouni Uitto; Qiaoli Li
Journal:  J Invest Dermatol       Date:  2020-12-17       Impact factor: 8.551

9.  Astrocyte-microglial association and matrix composition are common events in the natural history of primary familial brain calcification.

Authors:  Khayrun Nahar; Thibaud Lebouvier; Maarja Andaloussi Mäe; Anne Konzer; Jonas Bergquist; Yvette Zarb; Bengt Johansson; Christer Betsholtz; Michael Vanlandewijck
Journal:  Brain Pathol       Date:  2019-10-10       Impact factor: 6.508

10.  Severe brain calcification and migraine headache caused by SLC20A2 and PDGFRB heterozygous mutations in a five-year-old Chinese girl.

Authors:  Hao Sun; Zhijian Cao; Ruixi Gao; Yulei Li; Rui Chen; Shiyue Du; Tingbin Ma; Junhan Wang; Xuan Xu; Jing Yu Liu
Journal:  Mol Genet Genomic Med       Date:  2021-04-01       Impact factor: 2.183

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.