TY - JOUR
T1 - Comprehensive Experimental System for a Promising Model Organism Candidate for Marine Teleosts
AU - Sakaguchi, Keishi
AU - Yoneda, Michio
AU - Sakai, Noriyoshi
AU - Nakashima, Kanako
AU - Kitano, Hajime
AU - Matsuyama, Michiya
N1 - Funding Information:
This work was supported by JSPS KAKENHI Grant Number 15K14805 (KS). We would like to thank Dr. Minori Shinya, Department of Business and Commerce, Keio University, for technical advice on microinjection manipulation. We wish to thank Jonathon Pines for providing us with pVenus-N1 (Addgene plasmid #61854), David Grunwald for pCS2TAL3-DD (Addgene plasmid #37275), Elly Tanaka for T7-TPase (Addgene plasmid #51818) and Professor K. Kawakami for pT2AL200R150G. We would like to thank to Dr. Naoki Nagano and the staff of the Fisheries Research Institute of Karatsu for their generous support during the experiments. We would also like to thank Ms. Yuka Sakaguchi for assistance with seed production, rearing and genotyping analysis and Enago (www.enago.jp) for the English language review.
PY - 2019/12/1
Y1 - 2019/12/1
N2 - A comprehensive experimental system for Japanese anchovy, a promising candidate model organism for marine teleosts, was established. Through the design of a rearing/spawning facility that controls the photoperiod and water temperature, one-cell eggs were continuously obtained shortly after spawning throughout the rearing period. The stages of eggs are indispensable for microinjection experiments, and we developed an efficient and robust microinjection system for the Japanese anchovy. Embryos injected with GFP mRNA showed strong whole-body GFP fluorescence and the survival rates of injected- and non-injected embryos were not significantly different, 87.5% (28 in 32 embryos) and 90.0% (45 in 50 embryos), respectively. We verified that the Tol2 transposon system, which mediates gene transfer in vertebrates, worked efficiently in the Japanese anchovy using the transient transgenesis protocol, with GFP or DsRed as the reporter gene. Finally, we confirmed that genome-editing technologies, namely Transcription Activator-Like Effector Nucleases (TALEN) and Clustered Regulatory Interspaced Short Palindromic Repeats (CRISPR)/Cas9, were applicable to the Japanese anchovy. In practice, specific gene-disrupted fishes were generated in the F 1 generation. These results demonstrated the establishment of a basic, yet comprehensive, experimental system, which could be employed to undertake experiments using the Japanese anchovy as a model organism for marine teleost fish.
AB - A comprehensive experimental system for Japanese anchovy, a promising candidate model organism for marine teleosts, was established. Through the design of a rearing/spawning facility that controls the photoperiod and water temperature, one-cell eggs were continuously obtained shortly after spawning throughout the rearing period. The stages of eggs are indispensable for microinjection experiments, and we developed an efficient and robust microinjection system for the Japanese anchovy. Embryos injected with GFP mRNA showed strong whole-body GFP fluorescence and the survival rates of injected- and non-injected embryos were not significantly different, 87.5% (28 in 32 embryos) and 90.0% (45 in 50 embryos), respectively. We verified that the Tol2 transposon system, which mediates gene transfer in vertebrates, worked efficiently in the Japanese anchovy using the transient transgenesis protocol, with GFP or DsRed as the reporter gene. Finally, we confirmed that genome-editing technologies, namely Transcription Activator-Like Effector Nucleases (TALEN) and Clustered Regulatory Interspaced Short Palindromic Repeats (CRISPR)/Cas9, were applicable to the Japanese anchovy. In practice, specific gene-disrupted fishes were generated in the F 1 generation. These results demonstrated the establishment of a basic, yet comprehensive, experimental system, which could be employed to undertake experiments using the Japanese anchovy as a model organism for marine teleost fish.
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U2 - 10.1038/s41598-019-41468-8
DO - 10.1038/s41598-019-41468-8
M3 - Article
C2 - 30894668
AN - SCOPUS:85063290134
SN - 2045-2322
VL - 9
JO - Scientific reports
JF - Scientific reports
IS - 1
M1 - 4948
ER -