Gene Expression Profile of the Neonatal Female Mouse Brain After Administration of Testosterone Propionate
Abstract
Introduction Clinical care decisions for peripubertal adolescents with gender dysphoria (GD) should be made carefully. Furthermore, the identification of biomarkers is very important for rapid and accurate diagnosis of GD in young people. Aim The aim of this study was to investigate gene expression profiles during masculinization of the neonatal female mouse brain by testosterone and to identify biomarkers related to GD. Methods Microarray analysis was performed using RNAs extracted from the brains of neonatal mice treated by intraperitoneal injection of testosterone propionate during the sexual determination period. Sequence motif enrichment analysis for sex hormone receptor responsive elements was performed for the flanking regions of genes that showed significant expression changes following administration of testosterone propionate. Main outcome measures We revealed a gene set with marked changes in expression during brain masculinization of neonatal female mice following administration of testosterone propionate. Results We identified 334 genes that showed differential expression in the masculinized neonatal female brain after testosterone propionate treatment. Interestingly, most of these genes are not reported to be expressed in a sexually dimorphic manner. Moreover, sequence motif enrichment analysis suggested that masculinization of the neonatal female brain by testosterone was controlled more by estrogen receptors than androgen receptors. Conclusions Differences in…
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The single moderate dose and timing of testosterone used in this study has been shown to masculinize a female rodent brain.
“This dose and timing was chosen because it has been shown to masculinize a female rodent brain”
From Excess Neonatal Testosterone Causes Male-Specific Social and Fear Memory Deficits in Wild-Type Mice (2025) · cites this paper as Nakachi et al., 2015
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Allen Brain Atlas: an integrated spatio-temporal portal for exploring the central nervous system
Sunkin, S. M., Ng, L., Lau, C., Dolbeare, T., Gilbert, T. L., Thompson, C. L., Hawrylycz, M., & Dang, C. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks1042 · Cited by 796 · see citing works
Rametti, G., Carrillo, B., Gómez-Gil, E., Junque, C., Segovia, S., Gomez, Á., & Guillamon, A. (2011) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2010.05.006 · Cited by 187 · see citing works
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Excess Neonatal Testosterone Causes Male-Specific Social and Fear Memory Deficits in Wild-Type Mice
Quiñones-Labernik, P., Blocklinger, K. L., Bruce, M. R., Hagan, E., Preuschl, D., Tesar, C., & Ferri, S. L. (2025) · eneuro · doi:10.1523/eneuro.0020-25.2025 · Cited by 4 · see citing works
- Authors
- Nakachi, Y., Iseki, M., Yokoo, T., Mizuno, Y., & Okazaki, Y.
- Affiliations
- Saitama Medical University (JP)
- Corresponding author
- Nakachi, Yutaka
- Okazaki, Yasushi
- Venue
- The Journal of Sexual Medicine
- Publisher
- Oxford University Press (OUP)
- Published
- 2015-04-01
- Volume
- 12
- Issue
- 4
- Pages
- 887-896
- ISSN
- 1743-6095 (ISSN-L)
- 1743-6109
- OpenAlex
- W2100372788
- Cited by
- 4
- References
- 2
- Citations by year
- 2026: 1 · 2025: 1 · 2018: 1 · 2016: 1
- FWCI
- 0.29
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- The Journal of Sexual Medicine (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Kawano Masanori Memorial Public Interest Incorporated Foundation
- Ministry of Education, Culture, Sports, Science and Technology
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Social Sciences › Psychology › Social Psychology › LGBTQ Health, Identity, and Policy
- Keywords
- gender dysphoria, brain masculinization, testosterone propionate, gene expression profiling, estrogen receptor, androgen receptor, biomarkers, sexual differentiation of the brain, differential gene expression
- MeSH terms
- Animals, Animals, Newborn, Female, Mice, Inbred C57BL, Sexual Dysfunction, Physiological, Biomarkers, Gene Expression, Testosterone Propionate, Mice, Transcriptome
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