Germ cell–specific expression of Venus by Tol2‐mediated transgenesis in endangered endemic cyprinid Honmoroko (Gnathopogon caerulescens)

• Published in: Journal of fish biology Vol. 99; no. 4; pp. 1341 - 1347
• Main Authors: Higaki, Shogo, Nishie, Tomomi, Todo, Takaaki, Teshima, Reiko, Kusumi, Kenichiro, Mitsumori, Risa, Tooyama, Ikuo, Fujioka, Yasuhiro, Kawasaki, Toshihiro, Sakai, Noriyoshi, Takada, Tatsuyuki
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.10.2021; Wiley Subscription Services, Inc
• Subjects: Animals; Biological fertilization; Cell culture; Cyprinidae - genetics; Endangered species; Endemic animals; endemic fish; Female; Fertilization; Fish; Fish conservation; Fish eggs; Fluorescence; Fluorescence in situ hybridization; Freshwater fishes; Gametocytes; Gene expression; Gene transfer; Gene Transfer Techniques; germ cell; Germ cells; Gnathopogon caerulescens; Gonads; Juveniles; Lakes; Larvae; Male; mRNA; Oocytes; Oogonia; piwil1; Promoters; Proteins; Spermatogenesis; Spermatogonia; Tol2; transgenic; Transgenic fish; Transposase; Transposons; Zebrafish; Zebrafish - genetics; transgenic; Tol2; germ cell; piwil1; endemic fish
• ISSN: 0022-1112; 1095-8649
• DOI: 10.1111/jfb.14840

Fishes expressing a fluorescent protein in germ cells are useful to perform germ cell transfer experiments for conservation study. Nonetheless, no such fish has been generated in endangered endemic fishes. In this study, we tried to produce a fish expressing Venus fluorescent protein in germ cells using Honmoroko (Gnathopogon caerulescens), which is one of the threatened small cyprinid endemic to the ancient Lake Biwa in Japan. To achieve germ cell‐specific expression of Venus, we used piwil1 (formally known as ziwi) promoter and Tol2 transposon system. Following the co‐injection of the piwil1‐Venus expression vector and the Tol2 transposase mRNA into fertilized eggs, presumptive transgenic fish were reared. At 7 months of post‐fertilization, about 19% (10/52) of the examined larvae showed Venus fluorescence in their gonad specifically. Immunohistological staining and in vitro spermatogenesis using gonads of the juvenile founder fish revealed that Venus expression was detected in spermatogonia and spermatocyte in male, and oogonia and stage I and II oocytes in female. These results indicate that the Tol2 transposon and zebrafish piwil1 promoter enabled gene transfer and germ cell‐specific expression of Venus in G. caerulescens. In addition, in vitro culture of juvenile spermatogonia enables the rapid validation of temporal expression of transgene during spermatogenesis.