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Genome mutation after the introduction of the gene editing by electroporation of Cas9 protein (GEEP) system into bovine putative zygotes.
Namula, Zhao; Wittayarat, Manita; Hirata, Maki; Hirano, Takayuki; Nguyen, Nhien Thi; Le, Quynh Anh; Fahrudin, Mokhamad; Tanihara, Fuminori; Otoi, Takeshige.
Afiliação
  • Namula Z; Faculty of Veterinary Science, Guangdong Ocean University, Zhanjiang, China.
  • Wittayarat M; Faculty of Veterinary Science, Prince of Songkla University, Songkhla, Thailand.
  • Hirata M; Faculty of Veterinary Science, Guangdong Ocean University, Zhanjiang, China.
  • Hirano T; Laboratory of Animal Reproduction, Faculty of Bioscience and Bioindustry, Tokushima University, 2272-1 Ishii, Myozai-gun, Tokushima, 779-3233, Japan.
  • Nguyen NT; Laboratory of Animal Reproduction, Faculty of Bioscience and Bioindustry, Tokushima University, 2272-1 Ishii, Myozai-gun, Tokushima, 779-3233, Japan.
  • Le QA; Laboratory of Animal Reproduction, Faculty of Bioscience and Bioindustry, Tokushima University, 2272-1 Ishii, Myozai-gun, Tokushima, 779-3233, Japan.
  • Fahrudin M; Laboratory of Animal Reproduction, Faculty of Bioscience and Bioindustry, Tokushima University, 2272-1 Ishii, Myozai-gun, Tokushima, 779-3233, Japan.
  • Tanihara F; Faculty of Veterinary Science, Bogor Agricultural University, Bogor, Indonesia.
  • Otoi T; Faculty of Veterinary Science, Guangdong Ocean University, Zhanjiang, China. tanihara@tokushima-u.ac.jp.
In Vitro Cell Dev Biol Anim ; 55(8): 598-603, 2019 Sep.
Article em En | MEDLINE | ID: mdl-31297696
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Zigoto / Genoma / Eletroporação / Edição de Genes / Proteína 9 Associada à CRISPR / Mutação Limite: Animals Idioma: En Revista: In Vitro Cell Dev Biol Anim Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Zigoto / Genoma / Eletroporação / Edição de Genes / Proteína 9 Associada à CRISPR / Mutação Limite: Animals Idioma: En Revista: In Vitro Cell Dev Biol Anim Ano de publicação: 2019 Tipo de documento: Article