Identification and functional characterization of rare mutations of the neuroligin-2 gene (NLGN2) associated with schizophrenia

Chicheng Sun, Min Chih Cheng, Rosie Qin, Ding Lieh Liao, Tzu Ting Chen, Farn Jong Koong, Gong Chen, Chia Hsiang Chen

Research output: Contribution to journalArticle

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Abstract

Schizophrenia is a severe chronic mental disorder with a high genetic component in its etiology. Several lines of study have suggested that synaptic dysfunction may underlie the pathogenesis of schizophrenia. Neuroligin proteins function as cell-adhesion molecules at post-synaptic membrane and play critical roles in synaptogenesis and synaptic maturation. In this study, we systemically sequenced all the exons and promoter region of neuroligin-2 (NLGN2) gene in a sample of 584 schizophrenia patients and 549 control subjects from Taiwan. In total, we identified 19 genetic variants, including six rare missense mutations such as R215H (one patient), V510M (two patients), R621H (one patient), A637T (two patients), P800L (one patient and one control) and A819S (one patient and one control). In silico analysis predicted that two patient-specific missense mutations, R215H and R621H, had damaging effect, whereas the other missense mutations were benign. Importantly, functional analysis with immunocytochemistry and electrophysiological recordings identified the R215H mutant as a loss-of-function mutant in inducing GABAergic synaptogenesis. Mechanistically, the synaptogenic deficiency of R215H mutant was due to its retention inside the endoplasmic reticulum and inability to be transported to cell membrane. Our study suggests that defects in GABAergic synapse formation in the brain may be an important contributing factor for the onset of schizophrenia. In the family study of this mutation, we found his elder brother also carried this mutation but did not have psychiatric symptoms, indicating that this mutation has incomplete penetrance, and thus the clinical relevance of this mutation should be interpreted with caution.

Original languageEnglish (US)
Article numberddr208
Pages (from-to)3042-3051
Number of pages10
JournalHuman Molecular Genetics
Volume20
Issue number15
DOIs
StatePublished - Aug 1 2011

Fingerprint

Schizophrenia
Mutation
Genes
Missense Mutation
Synaptic Membranes
neuroligin 2
Penetrance
Cell Adhesion Molecules
Taiwan
Genetic Promoter Regions
Mental Disorders
Endoplasmic Reticulum
Computer Simulation
Synapses
Psychiatry
Siblings
Exons
Immunohistochemistry
Cell Membrane
Brain

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

Cite this

Sun, C., Cheng, M. C., Qin, R., Liao, D. L., Chen, T. T., Koong, F. J., ... Chen, C. H. (2011). Identification and functional characterization of rare mutations of the neuroligin-2 gene (NLGN2) associated with schizophrenia. Human Molecular Genetics, 20(15), 3042-3051. [ddr208]. https://doi.org/10.1093/hmg/ddr208
Sun, Chicheng ; Cheng, Min Chih ; Qin, Rosie ; Liao, Ding Lieh ; Chen, Tzu Ting ; Koong, Farn Jong ; Chen, Gong ; Chen, Chia Hsiang. / Identification and functional characterization of rare mutations of the neuroligin-2 gene (NLGN2) associated with schizophrenia. In: Human Molecular Genetics. 2011 ; Vol. 20, No. 15. pp. 3042-3051.
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Identification and functional characterization of rare mutations of the neuroligin-2 gene (NLGN2) associated with schizophrenia. / Sun, Chicheng; Cheng, Min Chih; Qin, Rosie; Liao, Ding Lieh; Chen, Tzu Ting; Koong, Farn Jong; Chen, Gong; Chen, Chia Hsiang.

In: Human Molecular Genetics, Vol. 20, No. 15, ddr208, 01.08.2011, p. 3042-3051.

Research output: Contribution to journalArticle

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AU - Sun, Chicheng

AU - Cheng, Min Chih

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AU - Liao, Ding Lieh

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AU - Koong, Farn Jong

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