Behavioral abnormalities observed in Zfhx2-deficient mice.

Zfhx2 (also known as zfh-5) encodes a transcription factor containing three homeobox domains and 18 Zn-finger motifs. We have reported that Zfhx2 mRNA is expressed mainly in differentiating neurons in the mouse brain and its expression level is negatively regulated by the antisense transcripts of Zf...

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Autores principales: Yuriko Komine, Keizo Takao, Tsuyoshi Miyakawa, Tetsuo Yamamori
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Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2012
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Acceso en línea:https://doaj.org/article/c7c59388361e49b7a8b1a77df2c7955d
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spelling oai:doaj.org-article:c7c59388361e49b7a8b1a77df2c7955d2021-11-18T08:03:03ZBehavioral abnormalities observed in Zfhx2-deficient mice.1932-620310.1371/journal.pone.0053114https://doaj.org/article/c7c59388361e49b7a8b1a77df2c7955d2012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23300874/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Zfhx2 (also known as zfh-5) encodes a transcription factor containing three homeobox domains and 18 Zn-finger motifs. We have reported that Zfhx2 mRNA is expressed mainly in differentiating neurons in the mouse brain and its expression level is negatively regulated by the antisense transcripts of Zfhx2. Although the expression profile of Zfhx2 suggests that ZFHX2 might have a role in a particular step of neuronal differentiation, the specific function of the gene has not been determined. We generated a Zfhx2-deficient mouse line and performed a comprehensive battery of behavioral tests to elucidate the function of ZFHX2. Homozygous Zfhx2-deficient mice showed several behavioral abnormalities, namely, hyperactivity, enhanced depression-like behaviors, and an aberrantly altered anxiety-like phenotype. These behavioral phenotypes suggest that ZFHX2 might play roles in controlling emotional aspects through the function of monoaminergic neurons where ZFHX2 is expressed. Moreover, considering their phenotypes, the Zfhx2-deficient mice may provide a novel model of human psychiatric disorders.Yuriko KomineKeizo TakaoTsuyoshi MiyakawaTetsuo YamamoriPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 12, p e53114 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Yuriko Komine
Keizo Takao
Tsuyoshi Miyakawa
Tetsuo Yamamori
Behavioral abnormalities observed in Zfhx2-deficient mice.
description Zfhx2 (also known as zfh-5) encodes a transcription factor containing three homeobox domains and 18 Zn-finger motifs. We have reported that Zfhx2 mRNA is expressed mainly in differentiating neurons in the mouse brain and its expression level is negatively regulated by the antisense transcripts of Zfhx2. Although the expression profile of Zfhx2 suggests that ZFHX2 might have a role in a particular step of neuronal differentiation, the specific function of the gene has not been determined. We generated a Zfhx2-deficient mouse line and performed a comprehensive battery of behavioral tests to elucidate the function of ZFHX2. Homozygous Zfhx2-deficient mice showed several behavioral abnormalities, namely, hyperactivity, enhanced depression-like behaviors, and an aberrantly altered anxiety-like phenotype. These behavioral phenotypes suggest that ZFHX2 might play roles in controlling emotional aspects through the function of monoaminergic neurons where ZFHX2 is expressed. Moreover, considering their phenotypes, the Zfhx2-deficient mice may provide a novel model of human psychiatric disorders.
format article
author Yuriko Komine
Keizo Takao
Tsuyoshi Miyakawa
Tetsuo Yamamori
author_facet Yuriko Komine
Keizo Takao
Tsuyoshi Miyakawa
Tetsuo Yamamori
author_sort Yuriko Komine
title Behavioral abnormalities observed in Zfhx2-deficient mice.
title_short Behavioral abnormalities observed in Zfhx2-deficient mice.
title_full Behavioral abnormalities observed in Zfhx2-deficient mice.
title_fullStr Behavioral abnormalities observed in Zfhx2-deficient mice.
title_full_unstemmed Behavioral abnormalities observed in Zfhx2-deficient mice.
title_sort behavioral abnormalities observed in zfhx2-deficient mice.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/c7c59388361e49b7a8b1a77df2c7955d
work_keys_str_mv AT yurikokomine behavioralabnormalitiesobservedinzfhx2deficientmice
AT keizotakao behavioralabnormalitiesobservedinzfhx2deficientmice
AT tsuyoshimiyakawa behavioralabnormalitiesobservedinzfhx2deficientmice
AT tetsuoyamamori behavioralabnormalitiesobservedinzfhx2deficientmice
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