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Targeted mutagenesis in the olive flounder (Paralichthys olivaceus) using the CRISPR/Cas9 system with electroporation
Wang, Ling1,2,3; Tan, Xungang1,2; Wu, Zhihao1,2; Wang, Lijuan1,2; Jiao, Shuang1,2; Zou, Yuxia1,2; Ji, Guanglei4,5; You, Feng1,2
2021-01-20
发表期刊BIOLOGIA
ISSN0006-3088
页码8
通讯作者Tan, Xungang([email protected]) ; You, Feng([email protected])
摘要As a new breeding technology, genome editing becomes a powerful tool owing to its high efficiency of gene targeting. In CRISPR/Cas9 system, how to efficiently transfer gRNA and Cas9 mRNA into embryos is an important step. Though microinjection is the most common method for operating on fish embryos, it is not easy to inject the RNA into pelagic and telolecithal eggs with hard egg chorion, such as the olive flounder (Paralichthys olivaceus) eggs. Therefore, an efficient and simple technology is urgently needed for this kind of study. In the present study, we used the electroporation method to introduce foreign gene into the flounder eggs. The results showed that the proper electroporation condition was 3 pulses for 1 millisecond (ms), 50 ms interval, at 25 V with high survival rate. Under this condition, the effect of CRISPR/Cas9 system on genome editing by using two different genes, myomaker and gonadal soma derived factor (gsdf) was investigated. Around 12% and 7% of the electroporated embryos for myomaker and gsdf hatched, respectively. The mutation sites including insert and deletion mutations at the candidate sites were visible for both targeted genes in the hatched larvae. The checked frame-shift and start codon deletion mutations would lead to complete destruction of these genes' structure. Above results implied that CRISPR/Cas9 system could work well in marine fish with pelagic eggs by using electroporation, and genome editing could be achieved on a large scale which may be useful for study of gene function in marine fish.
关键词Genome editing CRISPR/Cas9 system Electroporation Myomaker and gsdf Olive flounder (Paralichthys olivaceus)
DOI10.2478/s11756-020-00677-7
收录类别SCI
语种英语
资助项目National Key R&D Program of China[2018YFD0900202]; National Sciences of Foundation of China[31672636]; National Sciences of Foundation of China[31772834]
WOS研究方向Life Sciences & Biomedicine - Other Topics
WOS类目Biology
WOS记录号WOS:000609070200004
出版者SPRINGER
引用统计
被引频次:6[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.qdio.ac.cn/handle/337002/170064
专题实验海洋生物学重点实验室
通讯作者Tan, Xungang; You, Feng
作者单位1.Chinese Acad Sci, Ctr Ocean Megasci, Inst Oceanol, CAS Key Lab Expt Marine Biol, 7 Nanhai Rd, Qingdao 266071, Peoples R China
2.Pilot Natl Lab Marine Sci & Technol Qingdao, Lab Marine Biol & Biotechnol, Qingdao 266237, Peoples R China
3.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
4.Weihai Fisheries Technol Promot Stn, Weihai, Peoples R China
5.Shenghang Aquat Sci & Technol Co Ltd, Weihai, Peoples R China
第一作者单位中国科学院海洋大科学研究中心
通讯作者单位中国科学院海洋大科学研究中心
推荐引用方式
GB/T 7714
Wang, Ling,Tan, Xungang,Wu, Zhihao,et al. Targeted mutagenesis in the olive flounder (Paralichthys olivaceus) using the CRISPR/Cas9 system with electroporation[J]. BIOLOGIA,2021:8.
APA Wang, Ling.,Tan, Xungang.,Wu, Zhihao.,Wang, Lijuan.,Jiao, Shuang.,...&You, Feng.(2021).Targeted mutagenesis in the olive flounder (Paralichthys olivaceus) using the CRISPR/Cas9 system with electroporation.BIOLOGIA,8.
MLA Wang, Ling,et al."Targeted mutagenesis in the olive flounder (Paralichthys olivaceus) using the CRISPR/Cas9 system with electroporation".BIOLOGIA (2021):8.
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