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Exome Sequencing Identifies TENM4 as a Novel Candidate Gene for Schizophrenia in the SCZD2 Locus at 11q14-21

Authors :
Chao-Biao Xue
Zhou-Heng Xu
Jun Zhu
Yu Wu
Xi-Hang Zhuang
Qu-Liang Chen
Cai-Ru Wu
Jin-Tao Hu
Hou-Shi Zhou
Wei-Hang Xie
Xin Yi
Shan-Shan Yu
Zhi-Yu Peng
Huan-Ming Yang
Xiao-Hong Hong
Jian-Huan Chen
Source :
Frontiers in Genetics, Vol 9 (2019)
Publication Year :
2019
Publisher :
Frontiers Media S.A., 2019.

Abstract

Schizophrenia is a complex psychiatric disorder with high genetic heterogeneity, however, the contribution of rare mutations to the disease etiology remains to be further elucidated. We herein performed exome sequencing in a Han Chinese schizophrenia family and identified a missense mutation (c.6724C>T, p.R2242C) in the teneurin transmembrane protein 4 (TENM4) gene in the SCZD2 locus, a region previously linked to schizophrenia at 11q14-21. The mutation was confirmed to co-segregate with the schizophrenia phenotype in the family. Subsequent investigation of TENM4 exons 31, 32, and 33 adjacent to the p.R2242C mutation revealed two additional missense mutations in 120 sporadic schizophrenic patients. Residues mutated in these mutations, which are predicted to be deleterious to protein function, were highly conserved among vertebrates. These rare mutations were not detected in 1000 Genomes, NHLBI Exome Sequencing Project databases, or our in-house 1136 non-schizophrenic control exomes. Analysis of RNA-Seq data showed that TENM4 is expressed in the brain with high abundance and specificity. In line with the important role of TENM4 in central nervous system development, our findings suggested that increased rare variants in TENM4 could be associated with schizophrenia, and thus TENM4 could be a novel candidate gene for schizophrenia in the SCZD2 locus.

Details

Language :
English
ISSN :
16648021
Volume :
9
Database :
Directory of Open Access Journals
Journal :
Frontiers in Genetics
Publication Type :
Academic Journal
Accession number :
edsdoj.0b3c25449eab4993bc071f5ea57f31b2
Document Type :
article
Full Text :
https://doi.org/10.3389/fgene.2018.00725