Unknown

Dataset Information

0

Programmable Base Editing of the Sheep Genome Revealed No Genome-Wide Off-Target Mutations.


ABSTRACT: Since its emergence, CRISPR/Cas9-mediated base editors (BEs) with cytosine deaminase activity have been used to precisely and efficiently introduce single-base mutations in genomes, including those of human cells, mice, and crop species. Most production traits in livestock are induced by point mutations, and genome editing using BEs without homology-directed repair of double-strand breaks can directly alter single nucleotides. The p.96R > C variant of Suppressor cytokine signaling 2 (SOCS2) has profound effects on body weight, body size, and milk production in sheep. In the present study, we successfully obtained lambs with defined point mutations resulting in a p.96R > C substitution in SOCS2 by the co-injection of BE3 mRNA and a single guide RNA (sgRNA) into sheep zygotes. The observed efficiency of the single nucleotide exchange in newborn animals was as high as 25%. Observations of body size and body weight in the edited group showed that gene modification contributes to enhanced growth traits in sheep. Moreover, targeted deep sequencing and unbiased family trio-based whole genome sequencing revealed undetectable off-target mutations in the edited animals. This study demonstrates the potential for the application of BE-mediated point mutations in large animals for the improvement of production traits in livestock species.

SUBMITTER: Zhou S 

PROVIDER: S-EPMC6428697 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

altmetric image

Publications


Since its emergence, CRISPR/Cas9-mediated base editors (BEs) with cytosine deaminase activity have been used to precisely and efficiently introduce single-base mutations in genomes, including those of human cells, mice, and crop species. Most production traits in livestock are induced by point mutations, and genome editing using BEs without homology-directed repair of double-strand breaks can directly alter single nucleotides. The p.96R > C variant of Suppressor cytokine signaling 2 (SOCS2) has  ...[more]

Similar Datasets

| S-EPMC5524635 | biostudies-literature
| S-EPMC6194229 | biostudies-literature
| S-EPMC4873371 | biostudies-literature
| S-EPMC8376083 | biostudies-literature
| S-EPMC6419479 | biostudies-literature
| S-EPMC6956565 | biostudies-literature
2021-03-12 | GSE164477 | GEO
2022-09-20 | GSE155734 | GEO
| S-EPMC11289083 | biostudies-literature
| S-EPMC9458445 | biostudies-literature