| Literature DB >> 35546631 |
Anne S Bassett1,2,3, Ryan K C Yuen4,5, Bahareh A Mojarad6, Worrawat Engchuan6,7, Brett Trost6,7, Ian Backstrom6, Yue Yin6, Bhooma Thiruvahindrapuram6,7, Linda Pallotto6, Aleksandra Mitina6, Mahreen Khan6,8, Giovanna Pellecchia6,7, Bushra Haque6,8, Keyi Guo6, Tracy Heung9,10, Gregory Costain6,8,11, Stephen W Scherer6,7,8,12, Christian R Marshall13, Christopher E Pearson6,8.
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.Entities:
Year: 2022 PMID: 35546631 DOI: 10.1038/s41380-022-01575-x
Source DB: PubMed Journal: Mol Psychiatry ISSN: 1359-4184 Impact factor: 15.992