Literature DB >> 33602898

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

Yoshiro Morimoto1,2, Shinji Ono3,4, Shintaro Yoshida1,2, Hiroyuki Mishima5, Akira Kinoshita5, Takeshi Tanaka6, Yoshihiro Komohara7, Naohiro Kurotaki8, Tatsuya Kishino9, Yuji Okazaki10, Hiroki Ozawa1,2, Koh-Ichiro Yoshiura11, Akira Imamura1,2.   

Abstract

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.

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Year:  2021        PMID: 33602898      PMCID: PMC7892873          DOI: 10.1038/s41398-021-01258-1

Source DB:  PubMed          Journal:  Transl Psychiatry        ISSN: 2158-3188            Impact factor:   6.222


  67 in total

1.  Rare variants are common in schizophrenia.

Authors:  Jacob Gratten
Journal:  Nat Neurosci       Date:  2016-10-26       Impact factor: 24.884

Review 2.  Social motivation in schizophrenia: How research on basic reward processes informs and limits our understanding.

Authors:  Daniel Fulford; Tim Campellone; David E Gard
Journal:  Clin Psychol Rev       Date:  2018-05-28

3.  Acetylation by Tip60 is required for selective histone variant exchange at DNA lesions.

Authors:  Thomas Kusch; Laurence Florens; W Hayes Macdonald; Selene K Swanson; Robert L Glaser; John R Yates; Susan M Abmayr; Michael P Washburn; Jerry L Workman
Journal:  Science       Date:  2004-11-04       Impact factor: 47.728

4.  EP400 Deposits H3.3 into Promoters and Enhancers during Gene Activation.

Authors:  Suman K Pradhan; Trent Su; Linda Yen; Karine Jacquet; Chengyang Huang; Jacques Côté; Siavash K Kurdistani; Michael F Carey
Journal:  Mol Cell       Date:  2015-12-06       Impact factor: 17.970

5.  The unfoldomics decade: an update on intrinsically disordered proteins.

Authors:  A Keith Dunker; Christopher J Oldfield; Jingwei Meng; Pedro Romero; Jack Y Yang; Jessica Walton Chen; Vladimir Vacic; Zoran Obradovic; Vladimir N Uversky
Journal:  BMC Genomics       Date:  2008-09-16       Impact factor: 3.969

6.  The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease.

Authors:  Loukas Moutsianas; Vineeta Agarwala; Christian Fuchsberger; Jason Flannick; Manuel A Rivas; Kyle J Gaulton; Patrick K Albers; Gil McVean; Michael Boehnke; David Altshuler; Mark I McCarthy
Journal:  PLoS Genet       Date:  2015-04-23       Impact factor: 5.917

7.  Human genetic variation database, a reference database of genetic variations in the Japanese population.

Authors:  Koichiro Higasa; Noriko Miyake; Jun Yoshimura; Kohji Okamura; Tetsuya Niihori; Hirotomo Saitsu; Koichiro Doi; Masakazu Shimizu; Kazuhiko Nakabayashi; Yoko Aoki; Yoshinori Tsurusaki; Shinichi Morishita; Takahisa Kawaguchi; Osuke Migita; Keiko Nakayama; Mitsuko Nakashima; Jun Mitsui; Maiko Narahara; Keiko Hayashi; Ryo Funayama; Daisuke Yamaguchi; Hiroyuki Ishiura; Wen-Ya Ko; Kenichiro Hata; Takeshi Nagashima; Ryo Yamada; Yoichi Matsubara; Akihiro Umezawa; Shoji Tsuji; Naomichi Matsumoto; Fumihiko Matsuda
Journal:  J Hum Genet       Date:  2016-02-25       Impact factor: 3.172

8.  ImageJ2: ImageJ for the next generation of scientific image data.

Authors:  Curtis T Rueden; Johannes Schindelin; Mark C Hiner; Barry E DeZonia; Alison E Walter; Ellen T Arena; Kevin W Eliceiri
Journal:  BMC Bioinformatics       Date:  2017-11-29       Impact factor: 3.169

9.  Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

Authors:  Tarjinder Singh; Mitja I Kurki; David Curtis; Shaun M Purcell; Lucy Crooks; Jeremy McRae; Jaana Suvisaari; Himanshu Chheda; Douglas Blackwood; Gerome Breen; Olli Pietiläinen; Sebastian S Gerety; Muhammad Ayub; Moira Blyth; Trevor Cole; David Collier; Eve L Coomber; Nick Craddock; Mark J Daly; John Danesh; Marta DiForti; Alison Foster; Nelson B Freimer; Daniel Geschwind; Mandy Johnstone; Shelagh Joss; Georg Kirov; Jarmo Körkkö; Outi Kuismin; Peter Holmans; Christina M Hultman; Conrad Iyegbe; Jouko Lönnqvist; Minna Männikkö; Steve A McCarroll; Peter McGuffin; Andrew M McIntosh; Andrew McQuillin; Jukka S Moilanen; Carmel Moore; Robin M Murray; Ruth Newbury-Ecob; Willem Ouwehand; Tiina Paunio; Elena Prigmore; Elliott Rees; David Roberts; Jennifer Sambrook; Pamela Sklar; David St Clair; Juha Veijola; James T R Walters; Hywel Williams; Patrick F Sullivan; Matthew E Hurles; Michael C O'Donovan; Aarno Palotie; Michael J Owen; Jeffrey C Barrett
Journal:  Nat Neurosci       Date:  2016-03-14       Impact factor: 24.884

10.  A culture system to study oligodendrocyte myelination processes using engineered nanofibers.

Authors:  Seonok Lee; Michelle K Leach; Stephanie A Redmond; S Y Christin Chong; Synthia H Mellon; Samuel J Tuck; Zhang-Qi Feng; Joseph M Corey; Jonah R Chan
Journal:  Nat Methods       Date:  2012-07-15       Impact factor: 28.547

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