| Literature DB >> 33033216 |
Francisca M Real1,2, Stefan A Haas3, Paolo Franchini4, Peiwen Xiong4, Oleg Simakov5, Heiner Kuhl6, Robert Schöpflin1,2, David Heller3, M-Hossein Moeinzadeh3, Verena Heinrich3, Thomas Krannich3, Annkatrin Bressin3, Michaela F Hartmann7, Stefan A Wudy7, Dina K N Dechmann8,9, Alicia Hurtado10,11, Francisco J Barrionuevo10,11, Magdalena Schindler1,2, Izabela Harabula1, Marco Osterwalder12,13, Michael Hiller14,15,16, Lars Wittler17, Axel Visel12,18,19, Bernd Timmermann1, Axel Meyer4, Martin Vingron3, Rafael Jiménez10,11, Stefan Mundlos20,2,21, Darío G Lupiáñez20,2,21,22.
Abstract
Linking genomic variation to phenotypical traits remains a major challenge in evolutionary genetics. In this study, we use phylogenomic strategies to investigate a distinctive trait among mammals: the development of masculinizing ovotestes in female moles. By combining a chromosome-scale genome assembly of the Iberian mole, Talpa occidentalis, with transcriptomic, epigenetic, and chromatin interaction datasets, we identify rearrangements altering the regulatory landscape of genes with distinct gonadal expression patterns. These include a tandem triplication involving CYP17A1, a gene controlling androgen synthesis, and an intrachromosomal inversion involving the pro-testicular growth factor gene FGF9, which is heterochronically expressed in mole ovotestes. Transgenic mice with a knock-in mole CYP17A1 enhancer or overexpressing FGF9 showed phenotypes recapitulating mole sexual features. Our results highlight how integrative genomic approaches can reveal the phenotypic impact of noncoding sequence changes.Entities:
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Year: 2020 PMID: 33033216 PMCID: PMC8243244 DOI: 10.1126/science.aaz2582
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728