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Emergence of sex-specific transcriptomes in a sexually dimorphic brain nucleus

We present the transcriptomic changes underlying the development of an extreme neuroanatomical sex difference. The robust nucleus of the arcopallium (RA) is a key component of the songbird vocal motor system. In zebra finch, the RA is initially monomorphic and then atrophies in females but grows up...

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Autores principales: Friedrich, Samantha R., Nevue, Alexander A., Andrade, Abraão L.P., Velho, Tarciso A.F., Mello, Claudio V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9385264/
https://www.ncbi.nlm.nih.gov/pubmed/35926465
http://dx.doi.org/10.1016/j.celrep.2022.111152
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author Friedrich, Samantha R.
Nevue, Alexander A.
Andrade, Abraão L.P.
Velho, Tarciso A.F.
Mello, Claudio V.
author_facet Friedrich, Samantha R.
Nevue, Alexander A.
Andrade, Abraão L.P.
Velho, Tarciso A.F.
Mello, Claudio V.
author_sort Friedrich, Samantha R.
collection PubMed
description We present the transcriptomic changes underlying the development of an extreme neuroanatomical sex difference. The robust nucleus of the arcopallium (RA) is a key component of the songbird vocal motor system. In zebra finch, the RA is initially monomorphic and then atrophies in females but grows up to 7-fold larger in males. Mirroring this divergence, we show here that sex-differential gene expression in the RA expands from hundreds of predominantly sex chromosome Z genes in early development to thousands of predominantly autosomal genes by the time sexual dimorphism asymptotes. Male-specific developmental processes include cell and axonal growth, synapse assembly and activity, and energy metabolism; female-specific processes include cell polarity and differentiation, transcriptional repression, and steroid hormone and immune signaling. Transcription factor binding site analyses support female-biased activation of pro-apoptotic regulatory networks. The extensive and sex-specific transcriptomic reorganization of RA provides insights into potential drivers of sexually dimorphic neurodevelopment.
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spelling pubmed-93852642022-08-17 Emergence of sex-specific transcriptomes in a sexually dimorphic brain nucleus Friedrich, Samantha R. Nevue, Alexander A. Andrade, Abraão L.P. Velho, Tarciso A.F. Mello, Claudio V. Cell Rep Article We present the transcriptomic changes underlying the development of an extreme neuroanatomical sex difference. The robust nucleus of the arcopallium (RA) is a key component of the songbird vocal motor system. In zebra finch, the RA is initially monomorphic and then atrophies in females but grows up to 7-fold larger in males. Mirroring this divergence, we show here that sex-differential gene expression in the RA expands from hundreds of predominantly sex chromosome Z genes in early development to thousands of predominantly autosomal genes by the time sexual dimorphism asymptotes. Male-specific developmental processes include cell and axonal growth, synapse assembly and activity, and energy metabolism; female-specific processes include cell polarity and differentiation, transcriptional repression, and steroid hormone and immune signaling. Transcription factor binding site analyses support female-biased activation of pro-apoptotic regulatory networks. The extensive and sex-specific transcriptomic reorganization of RA provides insights into potential drivers of sexually dimorphic neurodevelopment. 2022-08-02 /pmc/articles/PMC9385264/ /pubmed/35926465 http://dx.doi.org/10.1016/j.celrep.2022.111152 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Friedrich, Samantha R.
Nevue, Alexander A.
Andrade, Abraão L.P.
Velho, Tarciso A.F.
Mello, Claudio V.
Emergence of sex-specific transcriptomes in a sexually dimorphic brain nucleus
title Emergence of sex-specific transcriptomes in a sexually dimorphic brain nucleus
title_full Emergence of sex-specific transcriptomes in a sexually dimorphic brain nucleus
title_fullStr Emergence of sex-specific transcriptomes in a sexually dimorphic brain nucleus
title_full_unstemmed Emergence of sex-specific transcriptomes in a sexually dimorphic brain nucleus
title_short Emergence of sex-specific transcriptomes in a sexually dimorphic brain nucleus
title_sort emergence of sex-specific transcriptomes in a sexually dimorphic brain nucleus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9385264/
https://www.ncbi.nlm.nih.gov/pubmed/35926465
http://dx.doi.org/10.1016/j.celrep.2022.111152
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