Whole-Genome Sequencing Reveals Rare Off-Target Mutations in MC1R -Edited Pigs Generated by Using CRISPR-Cas9 and Somatic Cell Nuclear Transfer.
Zhenyang LiJin LanXuan ShiTong LuXiaoli HuXiaohong LiuYaosheng ChenZuyong HePublished in: The CRISPR journal (2024)
The clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 system has been widely used to create animal models for biomedical and agricultural use owing to its low cost and easy handling. However, the occurrence of erroneous cleavage (off-targeting) may raise certain concerns for the practical application of the CRISPR-Cas9 system. In this study, we created a melanocortin 1 receptor ( MC1R )-edited pig model through somatic cell nuclear transfer (SCNT) by using porcine kidney cells modified by the CRISPR-Cas9 system. We then carried out whole-genome sequencing of two MC1R -edited pigs and two cloned wild-type siblings, together with the donor cells, to assess the genome-wide presence of single-nucleotide variants and small insertions and deletions (indels) and found only one candidate off-target indel in both MC1R -edited pigs. In summary, our study indicates that the minimal off-targeting effect induced by CRISPR-Cas9 may not be a major concern in gene-edited pigs created by SCNT.
Keyphrases
- crispr cas
- genome editing
- copy number
- genome wide
- induced apoptosis
- low cost
- single cell
- cell cycle arrest
- wild type
- cancer therapy
- cell therapy
- oxidative stress
- dna methylation
- climate change
- gene expression
- endoplasmic reticulum stress
- stem cells
- drug delivery
- heavy metals
- mesenchymal stem cells
- bone marrow
- autism spectrum disorder
- transcription factor
- genome wide identification