Author/Authors :
Averina, O.A Institute of functional genomics - Lomonosov Moscow State University, Moscow, Russia , Vysokikh, M.Y Belozersky Institute of Physico-Chemical Biology - Lomonosov Moscow State University, Moscow, Russia , Permyakov, O.A Institute of functional genomics - Lomonosov Moscow State University, Moscow, Russia , Sergiev, P.V Institute of functional genomics - Lomonosov Moscow State University, Moscow, Russia
Abstract :
The generation of transgenic model organisms (primarily mice) is an integral part of modern fun-
damental and applied research. Simple techniques based on the biology of these laboratory rodents can often
increase efficiency when generating genome-edited mouse strains. In this study, we share our three years of
experience in the optimization of mouse genome editing based on microinjection of CRISPR/Cas9 components
into ca. 10,000 zygotes. We tested a number of techniques meant to improve efficiency in generating knockout
mice, such as optimization of the superovulation method and choosing the optimal mouse strains to be used as
zygote donors and foster mothers. The presented results might be useful to laboratories aiming to quickly and
efficiently create new mouse strains with tailored genome editing.
Keywords :
mouse foster mothers , mouse zygote donors , superovulation , transgenic mice , genome editing