Redefining mouse transgenesis with CRISPR/Cas9 genome editing technology.
Genome biology, 19(1): 27 PMID 29490686 DOI 10.1186/s13059-018-1409-1
Abstract
The generation of genetically modified alleles in mice using conventional transgenesis technologies is a long and inefficient process. A new study shows that the in situ delivery of CRISPR/Cas9 reagents into pregnant mice results in a high efficiency of editing, and enables the rapid generation of both simple and complex alleles.