HomeInVivo Biosystems BlogGene EditingInsertion of two loxP sites to produce a knockout (KO) of an embryonic lethal gene

Insertion of two loxP sites to produce a knockout (KO) of an embryonic lethal gene

A client wanted a knockout (KO) of an embryonic lethal gene. We could not make this line using our standard methods. Instead, we inserted two loxP sites. One in the first intron of the gene and the second in the 3’utr. After we confirmed this line by PCR and sequencing, we injected this line with a ubiquitously expressing Cre Recombinase plasmid.

We found while the uninjected animals could reproduce, the Cre injected animals did not (Figure A). We tested recombination by PCR and found that only the Cre injected progeny showed recombination of the loxP sites (Figure B).

This line could be used to study KO of this gene in adulthood or in specific tissues, something that was not previously possible due to the embryonic lethality caused by the KO of this gene.

About the Author: Trisha Brock

x Dr. Brock is the Director of Genomics R&D at NemaMetrix. She has been creating and studying transgenic C. elegans for 17 years including training at Washington State University, University of Utah, and Harvard. At NemaMetrix, she is leading our efforts to understand the genetics of Epilepsy using gene editing in model organisms.
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