The rewiring of a terminal selector regulatory cascade generates convergent neuronal laterality

Neuronal identity is established and maintained by “terminal-selector” transcription factors, yet how these networks evolve remains unclear. We examined the specification of the chemosensory ASE and thermosensory AFD neurons in the nematode Pristionchus pacificus , a species that expresses the terminal-selector, Ppa- CHE-1, in both sensory neurons. To determine if the ASE neurons exhibits left-right laterality, we used HCR-FISH and transgenic reporters to discover 8 ASE left-right-specific and 3 AFD-specific receptor-type guanylyl-cyclases. Late embryos exhibit a multipotential state in which AFD precursors transiently co-express ASEL, ASER and AFD markers. A forward genetic screen for defects in ASER asymmetry identified a Ppa- DIE-1 homolog, whereas the maintenance of AFD neuronal identity requires another terminal-selector, Ppa- TTX-1, and CNG channels, Ppa- TAX-2/TAX-4. Defects in miRNA-processing convert ASEL to ASER fate while mutations in conserved regions in the 3′ UTR of the cog-1 homolog reveal multiple miRNA binding sites that toggle between left/right ASE versus AFD identities. Together, these results demonstrate that P. pacificus deploys a convergent, likely miRNA-mediated regulatory repertoire to generate left/right neuronal asymmetry and highlight changes in the Ppa-cog-1 3’ UTR as a key locus for rewiring selector networks.