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  Co-option of the transcription factor SALL1 in mole ovotestis formation

Schindler, M., Osterwalder, M., Harabula, I., Wittler, L., Tzika, A. C., Dechmann, D., et al. (2022). Co-option of the transcription factor SALL1 in mole ovotestis formation. bioRxiv, 514220. doi:10.1101/2022.10.28.514220.

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Schindler et al_2022.pdf (Preprint), 29MB
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Schindler, Magdalena1, Autor           
Osterwalder, Marco, Autor
Harabula, Izabela , Autor
Wittler, Lars2, Autor           
Tzika, Athanasia C., Autor
Dechmann, Dina, Autor
Vingron, Martin3, Autor           
Visel, Axel , Autor
Haas, Stefan4, Autor           
Real, Francisca M.1, Autor           
Affiliations:
1Gene Regulation and Evolution (Francisca Martinez Real), Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_3430951              
2Dept. of Developmental Genetics (Head: Bernhard G. Herrmann), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433548              
3Transcriptional Regulation (Martin Vingron), Dept. of Computational Molecular Biology (Head: Martin Vingron), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1479639              
4Dept. of Computational Molecular Biology (Head: Martin Vingron), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433547              

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 Zusammenfassung: Changes in gene expression represent an important source for phenotypical innovation. Yet, how such changes emerge and impact the evolution of traits remains elusive. Here, we explore the molecular mechanisms associated with the development of masculinizing ovotestes in female moles. By performing comparative analyses of epigenetic and transcriptional data in mole and mouse, we identified SALL1 as a co-opted gene for the formation of testicular tissue in mole ovotestes. Chromosome conformation capture analyses highlight a striking conservation of the 3D organization at the SALL1 locus, but a prominent evolutionary turnover of enhancer elements. Interspecies reporter assays support the capability of mole-specific enhancers to activate transcription in urogenital tissues. Through overexpression experiments in transgenic mice, we further demonstrate the capability of SALL1 to induce the ectopic gene expression programs that are a signature of mole ovotestes. Our results highlight the co-option of gene expression, through changes in enhancer activity, as a prominent mechanism for the evolution of traits.

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Sprache(n): eng - English
 Datum: 2022-10-28
 Publikationsstatus: Online veröffentlicht
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 Identifikatoren: DOI: 10.1101/2022.10.28.514220
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Titel: bioRxiv
Genre der Quelle: Webseite
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Seiten: - Band / Heft: - Artikelnummer: 514220 Start- / Endseite: - Identifikator: -