Mutation of vsx genes in zebrafish highlights the robustness of the retinal specification network

Abstract

early function in progenitors' specification, and a later requirement for bipolar-cells fate determination. Despite their conserved expression patterns, it is currently unclear to which extent Vsx functions are also conserved across vertebrates, as mutant models are available only in mammals. To gain insight into vsx function in teleosts, we have generated vsx1 and vsx2 CRISPR/Cas9 double knockouts (vsxKO) in zebrafish. Our electrophysiological and histological analyses indicate severe visual impairment and bipolar cells depletion in vsxKO larvae, with retinal precursors being rerouted toward photoreceptor or Muller glia fates. Surprisingly, neural retina is properly specified and maintained in mutant embryos, which do not display microphthalmia. We show that although important cis-regulatory remodelling occurs in vsxKO retinas during early specification, this has little impact at a transcriptomic level. Our observations point to genetic redundancy as an important mechanism sustaining the integrity of the retinal specification network, and to Vsx genes regulatory weight varying substantially among vertebrate species.Consejo Superior de Investigaciones Cientificas 2020AEP014 Juan R Martinez-Morales; Spanish Ministry of Science, Innovation and Universities BFU2017-86339P Juan R Martinez-Morales; Spanish Ministry of Science, Innovation and Universities CEX2020-001088-M Juan R Martinez-Morales; Spanish Ministry of Science, Innovation and Universities PID2020-112566GB-I00 Juan R Martinez-Morales; Spanish Ministry of Science, Innovation and Universities RED2018-102553-T Juan R Martinez-Morales