Extraordinary variability in gene activation and repression programs during gonadal sex differentiation across vertebrates

Front Cell Dev Biol. 2024 Jan 23:12:1328365. doi: 10.3389/fcell.2024.1328365. eCollection 2024.

Abstract

Genes involved in gonadal sex differentiation have been traditionally thought to be fairly conserved across vertebrates, but this has been lately questioned. Here, we performed the first comparative analysis of gonadal transcriptomes across vertebrates, from fish to mammals. Our results unambiguously show an extraordinary overall variability in gene activation and repression programs without a phylogenetic pattern. During sex differentiation, genes such as dmrt1, sox9, amh, cyp19a and foxl2 were consistently either male- or female-enriched across species while many genes with the greatest expression change within each sex were not. We also found that downregulation in the opposite sex, which had only been quantified in the mouse model, was also prominent in the rest of vertebrates. Finally, we report 16 novel conserved markers (e.g., fshr and dazl) and 11 signaling pathways. We propose viewing vertebrate gonadal sex differentiation as a hierarchical network, with conserved hub genes such as sox9 and amh alongside less connected and less conserved nodes. This proposed framework implies that evolutionary pressures may impact genes based on their level of connectivity.

Keywords: gene activation; gene expression networks; gene repression; gonadal development; sex determination; sex differentiation; sex markers; transcriptomics.

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. NS-B was supported by a Spanish Ministry of Science (SMS) predoctoral scholarship (BES-2017–079744). Research was supported by SMS grant no. PID 2019-108888RB-I00 to FP. Also with funding from the Spanish government through the ‘Severo Ochoa Centre of Excellence’ accreditation (CEX 2019-000928-S). MS was supported by the Deutsche Forschungsgemeinschaft (SCHA 408/10-1).