A Transcriptomic Dataset of Embryonic Murine Telencephalon of Fmr1-Deficient Mice

Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by mutations in the fragile X messenger ribonucleoprotein 1 (FMR1) gene. FXS patients exhibit autistic behaviors and abnormal brain structures, with notable sex differences. However, the mechanisms by which Fmr1 deficiency leads to these sex differences during brain development remain unclear. In this study, we performed bulk RNA sequencing on telencephalon samples of Fmr1-knockout mice of both sexes at embryonic day (E) 14.5, i.e., at the peak of neurogenesis. Clustering analysis revealed gene expression differences influenced by Fmr1 gene dosage and sex. We found that majority of the transcripts were shared between male and female sample groups, while a smaller number were unique to each sex. Our dataset underscores the importance of studying brain development during the embryonic period to detect sex-dependent genetic factors which contribute to neurodevelopmental disorders.

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Publication Details

Journal
Scientific Data
Published
2025-06-02
DOI
https://doi.org/10.1038/s41597-025-05104-7
Citations
2
Primary Topic
Genetics and Neurodevelopmental Disorders
Type
article
Field-Weighted Citation Impact
3.63

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article

A Transcriptomic Dataset of Embryonic Murine Telencephalon of Fmr1-Deficient Mice

Mikio Hoshino, Atsushi Toyoda, Takako Kikkawa, Sara Ebrahimiazar et al.
2 citations
Scientific Data
Genetics and Neurodevelopmental Disorders
3.63
article

A Transcriptomic Dataset of Embryonic Murine Telencephalon of Fmr1-Deficient Mice

Mikio Hoshino, Atsushi Toyoda, Takako Kikkawa, Sara Ebrahimiazar, Satoshi Miyashita, Yohei Minakuchi, Noriko Osumi, Shyu Manabe
article en
2 citations

Abstract

Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by mutations in the fragile X messenger ribonucleoprotein 1 (FMR1) gene. FXS patients exhibit autistic behaviors and abnormal brain structures, with notable sex differences. However, the mechanisms by which Fmr1 deficiency leads to these sex differences during brain development remain unclear. In this study, we performed bulk RNA sequencing on telencephalon samples of Fmr1-knockout mice of both sexes at embryonic day (E) 14.5, i.e., at the peak of neurogenesis. Clustering analysis revealed gene expression differences influenced by Fmr1 gene dosage and sex. We found that majority of the transcripts were shared between male and female sample groups, while a smaller number were unique to each sex. Our dataset underscores the importance of studying brain development during the embryonic period to detect sex-dependent genetic factors which contribute to neurodevelopmental disorders.

Scientific DataVol. 12(1)
National Institute of Genetics (JP), Tohoku University (JP), National Center of Neurology and Psychiatry (JP)
Japan Agency for Medical Research and Development, Mochida Memorial Foundation for Medical and Pharmaceutical Research, Japan Society for the Promotion of Science, Frontier Research Institute for Interdisciplinary Sciences, Tohoku University
Zero hunger
Openalex Percentile: Top 8%
Genetics and Neurodevelopmental Disorders
3.63
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A Transcriptomic Dataset of Embryonic Murine Telencephalon of Fmr1-Deficient Mice — Mikio Hoshino, Atsushi Toyoda, et al. · Scientific Data (2025) | TGRS Research Map | TGRS