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Polysialylation in a DISC1 Mutant Mouse
by
Sato, Chihiro
, Abe, Chikara
, Wu, Di
, Kitajima, Ken
, Takahashi, Yuka
, Hane, Masaya
in
Amygdala
/ Animals
/ Bipolar disorder
/ Brain
/ Brain - metabolism
/ Humans
/ Mental disorders
/ Mice
/ Mutation
/ Nerve Tissue Proteins - genetics
/ Nerve Tissue Proteins - metabolism
/ Neural Cell Adhesion Molecules - genetics
/ Neural Cell Adhesion Molecules - metabolism
/ Prefrontal Cortex - metabolism
/ Rodents
/ Schizophrenia - genetics
/ Schizophrenia - metabolism
/ Sialyltransferases - metabolism
2022
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Polysialylation in a DISC1 Mutant Mouse
by
Sato, Chihiro
, Abe, Chikara
, Wu, Di
, Kitajima, Ken
, Takahashi, Yuka
, Hane, Masaya
in
Amygdala
/ Animals
/ Bipolar disorder
/ Brain
/ Brain - metabolism
/ Humans
/ Mental disorders
/ Mice
/ Mutation
/ Nerve Tissue Proteins - genetics
/ Nerve Tissue Proteins - metabolism
/ Neural Cell Adhesion Molecules - genetics
/ Neural Cell Adhesion Molecules - metabolism
/ Prefrontal Cortex - metabolism
/ Rodents
/ Schizophrenia - genetics
/ Schizophrenia - metabolism
/ Sialyltransferases - metabolism
2022
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Polysialylation in a DISC1 Mutant Mouse
by
Sato, Chihiro
, Abe, Chikara
, Wu, Di
, Kitajima, Ken
, Takahashi, Yuka
, Hane, Masaya
in
Amygdala
/ Animals
/ Bipolar disorder
/ Brain
/ Brain - metabolism
/ Humans
/ Mental disorders
/ Mice
/ Mutation
/ Nerve Tissue Proteins - genetics
/ Nerve Tissue Proteins - metabolism
/ Neural Cell Adhesion Molecules - genetics
/ Neural Cell Adhesion Molecules - metabolism
/ Prefrontal Cortex - metabolism
/ Rodents
/ Schizophrenia - genetics
/ Schizophrenia - metabolism
/ Sialyltransferases - metabolism
2022
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Journal Article
Polysialylation in a DISC1 Mutant Mouse
2022
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Overview
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.
Publisher
MDPI AG,MDPI
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