World Aquaculture Singapore 2022

November 29 - December 2, 2022

Singapore

GENOME EDITING TO PRODUCE MONOSEX AND STERILE FISH FOR AQUACULTURE

John T. Buchanan, Takeshi Umazume, Alan Tinch, and Xavier Lauth

Center for Aquaculture Technologies
8445 Camino Santa Fe Suite 104, San Diego, California, USA
jbuchanan@aquatechcenter.com

 



The ability to produce sterile progeny from broodstock for aquaculture has significant benefits to productivity and environmental sustainability.  In addition, to responsibly introduce fish which harness the power of genome editing into commercial production systems, the farmed fish should be sterile. We describe the development of a strategy to generate, breed and mass-produce infertile fish. Our solutions rely on precise genetic modifications to create broodstock lines that can be incorporated into breeding programs. These approaches have been validated in tilapia but are transferrable to multiple species of fish. We expect that adoption of these technologies will result in broad economic and environmental benefits for aquaculture.

Our strategy for mass producing sterile fish is designed to produce monosex, sterile populations. In addition to the benefit of sterility, this allows the benefit of sexually dimorphic performance traits. We investigated gene mutations in two evolutionarily conserved pathways, one governing sex differentiation and the other sexual competency. We created edits in genes necessary for spermiogenesis and steroid hormone synthesis causing male sterility and masculinization, respectively. Double gene edit combinations for these genes produced all-male sterile populations. Likewise, we created variants in genes whose inactivation disrupted oogenesis. We further disrupted genes causing genetic males to sex reverse into females. Double gene edit combinations for these genes produced all-female, sterile populations. 

Propagation of the double KO broodstock lines was achieved via germ cell transplantation from a juvenile edited donor into a germ cell free wild-type recipient embryo. In the resulting recipients, the induced edits had no effect as the genes targeted are not expressed in germ cells. With this approach, we generated fertile broodstock that successfully mass-produced sterile, monosex populations.