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Please use this identifier to cite or link to this item:
http://ir.nhri.org.tw/handle/3990099045/5864
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| Title: | Identification and functional characterization of rare mutations of the neuroligin-2 gene (NLGN2) associated with schizophrenia |
| Authors: | Sun, CC;Cheng, MC;Qin, R;Liao, DL;Chen, TT;Koong, FJ;Chen, G;Chen, CH |
| Contributors: | Division of Mental Health and Addiction Medicine |
| 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. |
| Date: | 2011-08 |
| Relation: | Human Molecular Genetics. 2011 Aug;20(15):3042-3051. |
| Link to: | http://dx.doi.org/10.1093/hmg/ddr208 |
| JIF/Ranking 2023: | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0964-6906&DestApp=IC2JCR |
| Cited Times(WOS): | https://www.webofscience.com/wos/woscc/full-record/WOS:000292560000013 |
| Cited Times(Scopus): | http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=79960146777 |
| Appears in Collections: | [陳嘉祥(2009-2013)] 期刊論文
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| PB2011071806.pdf | | 405Kb | Adobe PDF | 463 | View/Open |
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