A unique missense variant in the E1A-binding protein P400 gene is implicated in schizophrenia by whole-exome sequencing and mutant mouse models

Genetic and epidemiological evidence has suggested that genetic factors are important in schizophrenia, although its pathophysiology is poorly understood. This study used whole-exome sequencing to investigate potential novel schizophrenia-causing genes in a Japanese family containing several members...

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Veröffentlicht in:Translational psychiatry 2021-02, Vol.11 (1), p.132-132, Article 132
Hauptverfasser: Morimoto, Yoshiro, Ono, Shinji, Yoshida, Shintaro, Mishima, Hiroyuki, Kinoshita, Akira, Tanaka, Takeshi, Komohara, Yoshihiro, Kurotaki, Naohiro, Kishino, Tatsuya, Okazaki, Yuji, Ozawa, Hiroki, Yoshiura, Koh-ichiro, Imamura, Akira
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Sprache:eng
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Zusammenfassung:Genetic and epidemiological evidence has suggested that genetic factors are important in schizophrenia, although its pathophysiology is poorly understood. This study used whole-exome sequencing to investigate potential novel schizophrenia-causing genes in a Japanese family containing several members affected by severe or treatment-resistant schizophrenia. A missense variant, chr12:132064747C>T (rs200626129, P2805L), in the E1A-binding protein P400 (EP400) gene completely segregated with schizophrenia in this family. Furthermore, numerous other EP400 mutations were identified in the targeted sequencing of a schizophrenia patient cohort. We also created two lines of Ep400 gene-edited mice, which had anxiety-like behaviours and reduced axon diameters. Our findings suggest that rs200626129 in EP400 is likely to cause schizophrenia in this Japanese family, and may lead to a better understanding and treatment of schizophrenia.
ISSN:2158-3188
2158-3188
DOI:10.1038/s41398-021-01258-1