Aquaculture Europe 2021

October 4 - 7, 2021

Funchal, Madeira

Add To Calendar 07/10/2021 15:10:0007/10/2021 15:30:00Europe/LisbonAquaculture Europe 2021GENOME EDITING TO PRODUCE MONOSEX AND STERILE FISH FOR AQUACULTUREFunchal-HotelThe European Aquaculture Societywebmaster@aquaeas.orgfalseDD/MM/YYYYaaVZHLXMfzTRLzDrHmAi181982

GENOME EDITING TO PRODUCE MONOSEX AND STERILE FISH FOR AQUACULTURE

John Buchanan, Spencer Herbert, Takeshi Umazume, and Xavier Lauth

 Center for Aquaculture Technologies, 8395 Camino Santa Fe Suite E, San Diego, California, USA
jbuchanan@aquatechcenter.com

 



Introduction

The ability to produce sterile progeny from broodstock for aquacul ture has significant benefits to culture productivity and environmental sustainability.  We describe the development of strategies 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 were 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.

Methods and Results

 One strategy for mass producing sterile fish is designed to produce monosex, sterile populations in culture . In addition to  the benefit of sterile fish, t his  allows the benefit of sexually dimorphic performance traits in culture. We first investigated gene mutations in two evolutionarily conserved pathways, one governing sex differentiation and the other sex 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 caused females to develop atrophic ovaries arrested at a previtellogenic stage or string-like ovaries lacking oocytes. 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 mutant 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 mas- produce d sterile, monosex populations.