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Structural alterations in the amygdala and impaired social incentive learning in a mouse model of a genetic variant associated with neurodevelopmental disorders

Copy number variants (CNVs) are robustly associated with psychiatric disorders and their dimensions and changes in brain structures and behavior. However, as CNVs contain many genes, the precise gene-phenotype relationship remains unclear. Although various volumetric alterations in the brains of 22q...

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Autores principales: Hiramoto, Takeshi, Sumiyoshi, Akira, Kato, Risa, Yamauchi, Takahira, Kang, Gina, Matsumura, Bailey, Stevens, Lucas J., Ryoke, Rie, Nonaka, Hiroi, Machida, Akihiro, Nomoto, Kensaku, Mogi, Kazutaka, Kikusui, Takefumi, Kawashima, Ryuta, Hiroi, Noboru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350205/
https://www.ncbi.nlm.nih.gov/pubmed/37461714
http://dx.doi.org/10.21203/rs.3.rs-3070199/v1
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author Hiramoto, Takeshi
Sumiyoshi, Akira
Kato, Risa
Yamauchi, Takahira
Kang, Gina
Matsumura, Bailey
Stevens, Lucas J.
Ryoke, Rie
Nonaka, Hiroi
Machida, Akihiro
Nomoto, Kensaku
Mogi, Kazutaka
Kikusui, Takefumi
Kawashima, Ryuta
Hiroi, Noboru
author_facet Hiramoto, Takeshi
Sumiyoshi, Akira
Kato, Risa
Yamauchi, Takahira
Kang, Gina
Matsumura, Bailey
Stevens, Lucas J.
Ryoke, Rie
Nonaka, Hiroi
Machida, Akihiro
Nomoto, Kensaku
Mogi, Kazutaka
Kikusui, Takefumi
Kawashima, Ryuta
Hiroi, Noboru
author_sort Hiramoto, Takeshi
collection PubMed
description Copy number variants (CNVs) are robustly associated with psychiatric disorders and their dimensions and changes in brain structures and behavior. However, as CNVs contain many genes, the precise gene-phenotype relationship remains unclear. Although various volumetric alterations in the brains of 22q11.2 CNV carriers have been identified in humans and mouse models, it is unknown how the genes in the 22q11.2 region individually contribute to structural alterations and associated mental illnesses and their dimensions. Our previous studies have identified Tbx1, a T-box family transcription factor encoded in 22q11.2 CNV, as a driver gene for social interaction and communication, spatial and working memory, and cognitive flexibility. However, it remains unclear how TBX1 impacts the volumes of various brain regions and their functionally linked behavioral dimensions. In this study, we used volumetric magnetic resonance imaging analysis to comprehensively evaluate brain region volumes in congenic Tbx1 heterozygous mice. Our data show that the volumes of anterior and posterior portions of the amygdaloid complex and its surrounding cortical regions were reduced in Tbx1 heterozygous mice. Moreover, we examined the behavioral consequences of an altered volume of the amygdala. Tbx1 heterozygous mice were impaired for their ability to detect the incentive value of a social partner in a task that depends on the amygdala. Our findings identify the structural basis for a specific social dimension associated with loss-of-function variants of TBX1 and 22q11.2 CNV.
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spelling pubmed-103502052023-07-17 Structural alterations in the amygdala and impaired social incentive learning in a mouse model of a genetic variant associated with neurodevelopmental disorders Hiramoto, Takeshi Sumiyoshi, Akira Kato, Risa Yamauchi, Takahira Kang, Gina Matsumura, Bailey Stevens, Lucas J. Ryoke, Rie Nonaka, Hiroi Machida, Akihiro Nomoto, Kensaku Mogi, Kazutaka Kikusui, Takefumi Kawashima, Ryuta Hiroi, Noboru Res Sq Article Copy number variants (CNVs) are robustly associated with psychiatric disorders and their dimensions and changes in brain structures and behavior. However, as CNVs contain many genes, the precise gene-phenotype relationship remains unclear. Although various volumetric alterations in the brains of 22q11.2 CNV carriers have been identified in humans and mouse models, it is unknown how the genes in the 22q11.2 region individually contribute to structural alterations and associated mental illnesses and their dimensions. Our previous studies have identified Tbx1, a T-box family transcription factor encoded in 22q11.2 CNV, as a driver gene for social interaction and communication, spatial and working memory, and cognitive flexibility. However, it remains unclear how TBX1 impacts the volumes of various brain regions and their functionally linked behavioral dimensions. In this study, we used volumetric magnetic resonance imaging analysis to comprehensively evaluate brain region volumes in congenic Tbx1 heterozygous mice. Our data show that the volumes of anterior and posterior portions of the amygdaloid complex and its surrounding cortical regions were reduced in Tbx1 heterozygous mice. Moreover, we examined the behavioral consequences of an altered volume of the amygdala. Tbx1 heterozygous mice were impaired for their ability to detect the incentive value of a social partner in a task that depends on the amygdala. Our findings identify the structural basis for a specific social dimension associated with loss-of-function variants of TBX1 and 22q11.2 CNV. American Journal Experts 2023-06-30 /pmc/articles/PMC10350205/ /pubmed/37461714 http://dx.doi.org/10.21203/rs.3.rs-3070199/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Hiramoto, Takeshi
Sumiyoshi, Akira
Kato, Risa
Yamauchi, Takahira
Kang, Gina
Matsumura, Bailey
Stevens, Lucas J.
Ryoke, Rie
Nonaka, Hiroi
Machida, Akihiro
Nomoto, Kensaku
Mogi, Kazutaka
Kikusui, Takefumi
Kawashima, Ryuta
Hiroi, Noboru
Structural alterations in the amygdala and impaired social incentive learning in a mouse model of a genetic variant associated with neurodevelopmental disorders
title Structural alterations in the amygdala and impaired social incentive learning in a mouse model of a genetic variant associated with neurodevelopmental disorders
title_full Structural alterations in the amygdala and impaired social incentive learning in a mouse model of a genetic variant associated with neurodevelopmental disorders
title_fullStr Structural alterations in the amygdala and impaired social incentive learning in a mouse model of a genetic variant associated with neurodevelopmental disorders
title_full_unstemmed Structural alterations in the amygdala and impaired social incentive learning in a mouse model of a genetic variant associated with neurodevelopmental disorders
title_short Structural alterations in the amygdala and impaired social incentive learning in a mouse model of a genetic variant associated with neurodevelopmental disorders
title_sort structural alterations in the amygdala and impaired social incentive learning in a mouse model of a genetic variant associated with neurodevelopmental disorders
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350205/
https://www.ncbi.nlm.nih.gov/pubmed/37461714
http://dx.doi.org/10.21203/rs.3.rs-3070199/v1
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