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Genome-wide tandem repeat expansions contribute to schizophrenia risk.

Authors :
Mojarad BA
Engchuan W
Trost B
Backstrom I
Yin Y
Thiruvahindrapuram B
Pallotto L
Mitina A
Khan M
Pellecchia G
Haque B
Guo K
Heung T
Costain G
Scherer SW
Marshall CR
Pearson CE
Bassett AS
Yuen RKC
Source :
Molecular psychiatry [Mol Psychiatry] 2022 Sep; Vol. 27 (9), pp. 3692-3698. Date of Electronic Publication: 2022 May 12.
Publication Year :
2022

Abstract

Tandem repeat expansions (TREs) can cause neurological diseases but their impact in schizophrenia is unclear. Here we analyzed genome sequences of adults with schizophrenia and found that they have a higher burden of TREs that are near exons and rare in the general population, compared with non-psychiatric controls. These TREs are disproportionately found at loci known to be associated with schizophrenia from genome-wide association studies, in individuals with clinically-relevant genetic variants at other schizophrenia loci, and in families where multiple individuals have schizophrenia. We showed that rare TREs in schizophrenia may impact synaptic functions by disrupting the splicing process of their associated genes in a loss-of-function manner. Our findings support the involvement of genome-wide rare TREs in the polygenic nature of schizophrenia.<br /> (© 2022. The Author(s).)

Details

Language :
English
ISSN :
1476-5578
Volume :
27
Issue :
9
Database :
MEDLINE
Journal :
Molecular psychiatry
Publication Type :
Academic Journal
Accession number :
35546631
Full Text :
https://doi.org/10.1038/s41380-022-01575-x