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

ABSTRACT: This SuperSeries is composed of the SubSeries listed below.

ORGANISM(S): Mus musculus Talpa occidentalis

PROVIDER: GSE219025 | GEO | 2022/11/29

REPOSITORIES: GEO

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Co-option of the transcription factor SALL1 in mole ovotestis formation [4C]

Project description: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.

2022-11-22 | GSE218437 | GEO

Co-option of the transcription factor SALL1 in mole ovotestis formation [ChIP-seq]

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Co-option of the transcription factor SALL1 in mole ovotestis formation [RNA-seq]

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

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

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Co-option of the transcription factor SALL1 in mole ovotestis formation [RNA-seq]

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Induction of kidney-related gene programs through co-option of SALL1 in mole ovotestes.

Project description:Changes in gene expression represent an important source of phenotypic 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 integrative analyses of epigenetic and transcriptional data in mole and mouse, we identified the co-option of SALL1 expression in mole ovotestes formation. Chromosome conformation capture analyses highlight a striking conservation of the 3D organization at the SALL1 locus, but an evolutionary divergence of enhancer activity. 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 kidney-related gene programs, which are a signature of mole ovotestes. Our results highlight the co-option of gene expression, through changes in enhancer activity, as a plausible mechanism for the evolution of traits.

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