Polysialylation in a DISC1 Mutant Mouse
Schizophrenia is a serious psychiatric disorder that affects the social life of patients. Psychiatric disorders are caused by a complex combination of genetic (G) and environmental (E) factors. Polysialylation represents a unique posttranslational modification of a protein, and such changes in neura...
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Published in | International journal of molecular sciences Vol. 23; no. 9; p. 5207 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Abstract | Schizophrenia is a serious psychiatric disorder that affects the social life of patients. Psychiatric disorders are caused by a complex combination of genetic (G) and environmental (E) factors. Polysialylation represents a unique posttranslational modification of a protein, and such changes in neural cell adhesion molecules (NCAMs) have been reported in postmortem brains from patients with psychiatric disorders. To understand the G × E effect on polysialylated NCAM expression, in this study, we performed precise measurements of polySia and NCAM using a disrupted-in-schizophrenia 1 (DISC1)-mutant mouse (G), a mouse model of schizophrenia, under acute stress conditions (E). This is the first study to reveal a lower number and smaller length of polySia in the suprachiasmatic nucleus of DISC1 mutants relative to those in wild-type (WT) mice. In addition, an analysis of polySia and NCAM responses to acute stress in five brain regions (olfactory bulb, prefrontal cortex, suprachiasmatic nucleus, amygdala, and hippocampus) revealed that the pattern of changes in these responses in WT mice and DISC1 mutants differed by region. These differences could indicate the vulnerability of DISC1 mutants to stress. |
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AbstractList | Schizophrenia is a serious psychiatric disorder that affects the social life of patients. Psychiatric disorders are caused by a complex combination of genetic (G) and environmental (E) factors. Polysialylation represents a unique posttranslational modification of a protein, and such changes in neural cell adhesion molecules (NCAMs) have been reported in postmortem brains from patients with psychiatric disorders. To understand the G × E effect on polysialylated NCAM expression, in this study, we performed precise measurements of polySia and NCAM using a disrupted-in-schizophrenia 1 (DISC1)-mutant mouse (G), a mouse model of schizophrenia, under acute stress conditions (E). This is the first study to reveal a lower number and smaller length of polySia in the suprachiasmatic nucleus of DISC1 mutants relative to those in wild-type (WT) mice. In addition, an analysis of polySia and NCAM responses to acute stress in five brain regions (olfactory bulb, prefrontal cortex, suprachiasmatic nucleus, amygdala, and hippocampus) revealed that the pattern of changes in these responses in WT mice and DISC1 mutants differed by region. These differences could indicate the vulnerability of DISC1 mutants to stress. |
Author | Sato, Chihiro Abe, Chikara Wu, Di Kitajima, Ken Takahashi, Yuka Hane, Masaya |
AuthorAffiliation | 1 Bioscience and Biotechnology Center, Nagoya University, Chikusa, Nagoya 464-8601, Japan; takahashi.yuka@i.mbox.nagoya-u.ac.jp (Y.T.); abe.c.nucoop@gmail.com (C.A.); mhane@agr.nagoya-u.ac.jp (M.H.); diwu@agr.nagoya-u.ac.jp (D.W.); kitajima@agr.nagoya-u.ac.jp (K.K.) 3 Integrated Glyco-Biomedical Research Center (iGMED), Institute for Glyco-core Research (iGCORE), Nagoya University, Chikusa, Nagoya 464-8601, Japan 2 Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa, Nagoya 464-8601, Japan |
AuthorAffiliation_xml | – name: 1 Bioscience and Biotechnology Center, Nagoya University, Chikusa, Nagoya 464-8601, Japan; takahashi.yuka@i.mbox.nagoya-u.ac.jp (Y.T.); abe.c.nucoop@gmail.com (C.A.); mhane@agr.nagoya-u.ac.jp (M.H.); diwu@agr.nagoya-u.ac.jp (D.W.); kitajima@agr.nagoya-u.ac.jp (K.K.) – name: 2 Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa, Nagoya 464-8601, Japan – name: 3 Integrated Glyco-Biomedical Research Center (iGMED), Institute for Glyco-core Research (iGCORE), Nagoya University, Chikusa, Nagoya 464-8601, Japan |
Author_xml | – sequence: 1 givenname: Yuka surname: Takahashi fullname: Takahashi, Yuka organization: Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa, Nagoya 464-8601, Japan – sequence: 2 givenname: Chikara surname: Abe fullname: Abe, Chikara organization: Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa, Nagoya 464-8601, Japan – sequence: 3 givenname: Masaya orcidid: 0000-0001-6830-2900 surname: Hane fullname: Hane, Masaya organization: Integrated Glyco-Biomedical Research Center (iGMED), Institute for Glyco-core Research (iGCORE), Nagoya University, Chikusa, Nagoya 464-8601, Japan – sequence: 4 givenname: Di surname: Wu fullname: Wu, Di organization: Integrated Glyco-Biomedical Research Center (iGMED), Institute for Glyco-core Research (iGCORE), Nagoya University, Chikusa, Nagoya 464-8601, Japan – sequence: 5 givenname: Ken surname: Kitajima fullname: Kitajima, Ken organization: Integrated Glyco-Biomedical Research Center (iGMED), Institute for Glyco-core Research (iGCORE), Nagoya University, Chikusa, Nagoya 464-8601, Japan – sequence: 6 givenname: Chihiro orcidid: 0000-0002-2075-6185 surname: Sato fullname: Sato, Chihiro organization: Integrated Glyco-Biomedical Research Center (iGMED), Institute for Glyco-core Research (iGCORE), Nagoya University, Chikusa, Nagoya 464-8601, Japan |
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Keywords | tail suspension test environmental factor genetic factor NCAM acute stress polysialic acid mental disorder schizophrenia DISC1 polysialyltransferase |
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Snippet | Schizophrenia is a serious psychiatric disorder that affects the social life of patients. Psychiatric disorders are caused by a complex combination of genetic... |
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SubjectTerms | Amygdala Bipolar disorder Brain Cell adhesion Cell adhesion molecules DISC1 Disc1 protein environmental factor genetic factor Mental disorders Mutants Mutation NCAM Neural cell adhesion molecule Olfactory bulb polysialic acid Polysialylation Prefrontal cortex Rodents Schizophrenia Suprachiasmatic nucleus |
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Title | Polysialylation in a DISC1 Mutant Mouse |
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