Genome mutation after the introduction of the gene editing by electroporation of Cas9 protein (GEEP) system into bovine putative zygotes

• Published in: In vitro cellular & developmental biology. Animal Vol. 55; no. 8; pp. 598 - 603
• Main Authors: Namula, Zhao, Wittayarat, Manita, Hirata, Maki, Hirano, Takayuki, Nguyen, Nhien Thi, Le, Quynh Anh, Fahrudin, Mokhamad, Tanihara, Fuminori, Otoi, Takeshige
• Format: Journal Article
• Language: English
• Published: New York Springer Science & Business Media LLC 01-09-2019; Springer US; Society for In Vitro Biology
• Subjects: Animal Genetics and Genomics; Animals; Biomedical and Life Sciences; BIOTECHNOLOGY; Blastocyst - metabolism; Blastocysts; Cattle; Cell Biology; Cell Culture; CRISPR; CRISPR-Associated Protein 9 - metabolism; Deoxyribonucleic acid; Developmental Biology; DNA; Efficiency; Electric potential; Electroporation; Electroporation - methods; Embryo, Mammalian - metabolism; Embryos; Gene Editing; Genetic modification; Genome; Genome editing; Genomes; Life Sciences; MSTN gene; Mutants; Mutation; Mutation - genetics; Mutation Rate; Mutation rates; Nucleotide sequence; Stem Cells; Strength; Voltage; Zygote - metabolism; Zygotes; In vitro fertilization; Electroporation; MSTN gene; Bovine; CRISPR/Cas9
• ISSN: 1071-2690; 1543-706X
• DOI: 10.1007/s11626-019-00385-w

The present study was designed to investigate the effects of voltage strength on embryonic developmental rate and mutation efficiency in bovine putative zygotes during electroporation with the CRISPR/Cas9 system to target the MSTN gene at different time points after insemination. Results showed that there was no significant interaction between electroporation time and voltage strength on the embryonic cleavage and blastocyst formation rates. However, increasing the voltage strength to 20 V/mm to electroporate the zygotes at 10 h after the start of insemination yielded significantly lower blastocyst formation rates (P < 0.05) than those of the 10-V/mm electroporated zygotes. Mutation efficiency was then assessed in individual blastocysts by DNA sequence analysis of the target sites in the MSTN gene. A positive correlation between mutation rate and voltage strength was observed. The mutation efficiency in mutant blastocysts was significantly higher in the zygotes electroporated with 20 V/mm at 10 h after the start of insemination (P < 0.05) than in the zygotes electroporated at 15 h, irrespective of the voltage strength. We also noted that a certain number of blastocysts from zygotes that were electroporated with more than 15 V/mm at 10 h (4.8-16.7%) and 20 V/mm at 15 h (4.8%) were biallelic mutants. Our results suggest that the voltage strength during electroporation as well as electroporation time certainly have effects on the embryonic developmental rate and mutation efficiency in bovine putative zygotes.