Journal Article

Adenine base-editing-mediated exon skipping induces gene knockout in cultured pig cells

Jia-sheng, Pan, Xiang-xing, Zhu, Xiao-li, Zhang, Lin, Tao, Zi-xiao, Qu, Qiu-yan, Huang, Jia-hong, Lu, Shuai-peng, Yang, Dong-sheng, Tang, Feng, Juan, Liu, Lian, Jian-cong, Wen, Zi-sheng, Lin, Ai-fen, Yan, Ye-cheng, Yang

2022

Overview

Gene-knockout pigs have important applications in agriculture and medicine. Compared with CRISPR/Cas9, Adenine base editor (ABE) convert single A·T pairs to G·C pairs in the genome without generating DNA double-strand breaks, and this method has higher accuracy and biosafety in pig genetic modification. However, the application of ABE in pig gene knockout is limited by protospacer-adjacent motif sequences and the base-editing window. Alternative mRNA splicing is an important mechanism underlying the formation of proteins with diverse functions in eukaryotes. Spliceosome recognizes the conservative sequences of splice donors and acceptors in a precursor mRNA. Mutations in these conservative sequences induce exon skipping, leading to proteins with novel functions or to gene inactivation due to frameshift mutations. In this study, adenine base-editing-mediated exon skipping was used to expand the application of ABE in the generation of gene knockout pigs. We first constructed a modified “all-in-one” ABE vector suitable for porcine somatic cell transfection that contained an ABE for single-base editing and an sgRNA expression cassette. The “all-in-one” ABE vector induced efficient sgRNA-dependent A-to-G conversions in porcine cells during single base-editing of multiple endogenous gene loci. Subsequently, an ABE system was designed for single adenine editing of the conservative splice acceptor site (AG sequence at the 3′ end of the intron 5) and splice donor site (GT sequence at the 5′ end of the intron 6) in the porcine gene GHR; this method achieved highly efficient A-to-G conversion at the cellular level. Then, porcine single-cell colonies carrying a biallelic A-to-G conversion in the splice acceptor site in the intron 5 of GHR were generated. RT-PCR indicated exon 6 skipped at the mRNA level. Western blotting revealed GHR protein loss, and gene sequencing showed no sgRNA-dependent off-target effects. These results demonstrate accurate adenine base-editing-mediated exon skipping and gene knockout in porcine cells. This is the first proof-of-concept study of adenine base-editing-mediated exon skipping for gene regulation in pigs, and this work provides a new strategy for accurate and safe genetic modification of pigs for agricultural and medical applications.

• Publisher: Springer Nature B.V
• Subject: Adenine / Alternative splicing / Conversion / CRISPR / DNA damage / Editing / Eukaryotes / Exon skipping / Frameshift mutation / Gene regulation / Gene sequencing / Genetic modification / Genomes / Hogs / Inactivation / mRNA / Mutation / Polymerase chain reaction / Proteins / Splicing / Swine / Transfection / Western blotting