Gene Regulatory Networks of Epidermal and Neural Fate Choice in a Chordate

• Published in: Molecular biology and evolution 2022, Vol.39 (4)
• Main Authors: Leon, Anthony, Subirana, Lucie, Magre, Kevin, Cases, Ildefonso, Tena, Juan J., Irimia, Manuel, Gomez-Skarmeta, Jose Luis, Escriva, Hector, Bertrand, Stéphanie
• Format: Article
• Language: English
• Subjects: Animals; Cell fate; Central nervous system; Cephalochordata; Development Biology; Discoveries; DNA binding proteins; Ectoderm; Embryogenesis; Embryology and Organogenesis; Embryonic development; Embryonic growth stage; Epidermis; Epidermis - metabolism; Explants; Ganglia; Gene Expression Regulation, Developmental; Gene Regulatory Networks; Genes; Genetic transcription; Lancelets; Life Sciences; Nervous System - metabolism; Neurobiology; Neurons; Neurons and Cognition; Pluripotency; Transcription factors; Transcription Factors - genetics; Transcription Factors - metabolism; Vertebrates
• ISSN: 0737-4038; 1537-1719
• DOI: 10.1093/molbev/msac055

Abstract Neurons are a highly specialized cell type only found in metazoans. They can be scattered throughout the body or grouped together, forming ganglia or nerve cords. During embryogenesis, centralized nervous systems develop from the ectoderm, which also forms the epidermis. How pluripotent ectodermal cells are directed toward neural or epidermal fates, and to which extent this process is shared among different animal lineages, are still open questions. Here, by using micromere explants, we were able to define in silico the putative gene regulatory networks (GRNs) underlying the first steps of the epidermis and the central nervous system formation in the cephalochordate amphioxus. We propose that although the signal triggering neural induction in amphioxus (i.e., Nodal) is different from vertebrates, the main transcription factors implicated in this process are conserved. Moreover, our data reveal that transcription factors of the neural program seem to not only activate neural genes but also to potentially have direct inputs into the epidermal GRN, suggesting that the Nodal signal might also contribute to neural fate commitment by repressing the epidermal program. Our functional data on whole embryos support this result and highlight the complex interactions among the transcription factors activated by the signaling pathways that drive ectodermal cell fate choice in chordates.