Skip to main content

Advertisement

Log in

High Efficiency Production of germ-line Transgenic Japanese Medaka (Oryzias latipes) by Electroporation with Direct Current-shifted Radio Frequency Pulses

  • Published:
Transgenic Research Aims and scope Submit manuscript

Abstract

Although there have been several studies showing the production of transgenic fish through electroporation techniques, success rates have been low and few studies show germ-line integration and expression. When electroporation has been successful, the device used is no longer commercially available. The goal of this experiment was to find an alternative efficient method of generating transgenic Japanese medaka (Oryzias latipes) using a commercially available electroporation device. The Gene Pulser II and RF module (Bio-Rad Laboratories, USA), along with two reporter gene constructs, were used. In contrast to other electroporation devices, which are based on a single pulse with exponential decay or square wave technology, the Gene Pulser II incorporates a direct current (DC)-shifted radio frequency (RF) signal. With this technique, over 1000 embryos can be electroporated in less than 30 min. The plasmid pCMV-SPORT-β-gal (Invitrogen, USA) was used in the supercoiled form to optimize parameters for gene transfer into single-celled embryos, and resulted in up to 100% somatic gene transfer. Similar conditions were used to generate fish transgenic for both the pCMV-EGFP plasmid (Clontech, USA) and a cytomegalovirus (CMV) driven phytase-EGFP construct. The conditions used were a voltage of 25 V, a percent modulation of 100%, a radio frequency of 35 kHz, a burst duration of 10 ms, 3 bursts, and a burst interval of 1.0 s. Seventy percent of the embryos electroporated with the pCMV-EGFP construct survived to sexual maturity, and of those, 85% were capable of passing the transgene on to their offspring. Transgenic second generation back-crossed (BC2) fry were subjected to Southern blot analysis, which confirmed germ-line integration, and observation for green fluorescence protein, which confirmed protein expression. DC-shifted RF pulses are effective and efficient in the production of transgenic medaka, and germ-line integration and expression can be achieved without linearization of the transgene vector.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Blacklidge KH and Bidwell CA (1993) Laboratory fish egg incubator. Prog Fish Cult 55: 204–206.

    Google Scholar 

  • Buono RJ and Linser PJ (1991) Transgenic zebrafish by electroporation. Bio-Rad US/EG Bull 1354: 1–3.

    Google Scholar 

  • Chang DC (1989) Cell poration and cell fusion using an oscillating electric field. Biophys J 56: 641–652.

    Google Scholar 

  • Chou C-Y, Hong L-S and Tsai H-J (2001) Uniform GFP-expression in transgenic medaka (Oryzias latipes) at the F0 generation. Transgenic Res 10: 303–315.

    Google Scholar 

  • Fletcher GL and Davies PL (1991) Transgenic fish for aquaculture. Genet Eng 13: 331–370.

    Google Scholar 

  • Ginsburg AS (1963) Sperm-egg association and its relationship to the activation of the egg in salmonid fishes. J Embryol Exp Morph 11: 13–33.

    Google Scholar 

  • Hamada K, Tamaki K, Sasado Y, Watai Y, Kani S, Wakamatsu Y, et al. (1998) Usefulness of the medaka β-actin promoter investigated using a mutant GFP reporter gene in transgenic medaka (Oryzias latipes). Mol Mar Biol Biotechnol 7: 173–180.

    Google Scholar 

  • Inoue K, Yamashita S, Hata J-I, Kabeno S, Asada S, Nagahisa E, et al. (1990) Electroporation as a new technique for producing transgenic fish. Cell Diff Dev 29: 123–128.

    Google Scholar 

  • Iyengar A, Müller F and Maclean N (1996) Regulation and expression of transgenes in fish - a review. Transgenic Res 5: 147–166.

    Google Scholar 

  • Jowett T (1986) Preparation of nucleic acids. In: Roberts DB, ID (ed), Drosophila: A Practical Approach. (pp. 275–286) IRL Press, Oxford.

    Google Scholar 

  • Khoo H-W, Ang L-H, Lim H-B, and Wong K-Y (1992) Sperm cells as vectors for introducing foreign DNA into zebrafish. Aquaculture 107: 1–19.

    Google Scholar 

  • Lin S, Gaiano N, Culp P, Burns JC, Friedmann T, Yee JK, et al. (1994) Integration and germ-line transmission of a pseudotyped retroviral vector in zebrafish. Science 265: 666–669.

    Google Scholar 

  • Linney E, Hardison NL, Lonze BE, Lyons L and DiNapoli L (1999) Transgene expression in zebrafish: a comparison of retroviralvector and DNA-injection approaches. Dev Biol 213: 207–216.

    Google Scholar 

  • Ma C, Fan L, Ganassin R, Bols N and Collodi P (2001) Production of zebrafish germ-line chimeras from embryo cell cultures. Proc Natl Acad Sci USA 98: 2461–2466.

    Google Scholar 

  • Maniatis T, Fritsch EF and Sambook J (1982) Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY.

    Google Scholar 

  • Muir WM and Hostetler HA (2001) Transgenic fish: production, testing, and risk assessment. In: Renaville R and Burny A (eds), Biotechnology in Animal Husbandry. (pp. 261–281) Kluwer Academic Press, Dordrecht.

    Google Scholar 

  • Müller F, Lele Z, Váradi L, Menczel L and Orbán L (1993) Efficient transient expression system based on square pulse electroporation and in vivo luciferase assay of fertilized fish eggs. FEBS Lett 324: 27–32.

    Google Scholar 

  • Murakami Y, Motohashi K, Yano K, Ikebukuro K, Yokoyama K, Tamiya E, et al. (1994) Micromachined electroporation system for transgenic fish. J Biotechnol 34: 35–42.

    Google Scholar 

  • Neumann E, Schaefer-Ridder M, Wang Y and Hofschneider PH (1982) Gene transfer into mouse lyoma cells by electroporation in high electric fields. EMBO J 1: 841–845.

    Google Scholar 

  • Ozato K, Kondoh H, Inohara H, Iwamatsu T, Wakamatsu Y and Okada TS (1986) Production of transgenic fish: introduction and expression of chicken β-crystallin gene in medaka embryos. Cell Differen 19: 237–244.

    Google Scholar 

  • Ozato K, Inoue K and Wakamatsu Y (1989) Transgenic fish: biological and technical problems. Zool Sci 6: 445–457.

    Google Scholar 

  • Patil JG, Wong V and Khoo HW (1994) Assessment of PMTL construct for detection in vivo of luciferase expression and fate of the transgene in the zebrafish, Brachydanio-rerio. Zool Sci 11: 63–68.

    Google Scholar 

  • Sarmasik A, Warr G, and Chen TT (2002) Production of transgenic medaka with increased resistance to bacterial pathogens. Mar Biotechnol 4(3): 310–322.

    Google Scholar 

  • Sheela SG, Pandian TJ and Mathavan S (1999) Electroporatic transfer, stable integration, expression and transmission of ZpβypGH and ZpβrtGH in Indian catfish, Heteropneustes fossilis (Bloch). Aquacult Res 30: 233–248.

    Google Scholar 

  • Shigekawa K and Dower WJ (1988) Electroporation of eukaryotes and prokaryotes: a general approach to the introduction of macromolecules into cells. Biotechniques 6: 742–751.

    Google Scholar 

  • Sin FYT (1997) Transgenic fish. Rev Fish Biol Fish 7: 417–441.

    Google Scholar 

  • Sin FYT, Bartley AL, Walker SP, Sin IL, Symonds JE, Hawke L, et al. (1993) Gene transfer in chinook salmon (Oncorhynchus tshawytscha) by electroporating sperm in the presence of pRSVlacZ DNA. Aquaculture 117: 57–69.

    Google Scholar 

  • Steel RGD and Torrie JH (1980) Principles and Procedure of Statistics: A Biometrical Approach. McGraw-Hill, Inc., New York, NY.

    Google Scholar 

  • Strauss WM (1997) Hybridization with radioactive probes. In: Ausubel FM, Brent R, Kingston RE, Moore DD, Seidman JG, Smith JA and Struhl K (eds), Current Protocols in Molecular Biology. (pp. 6.3.1–6.3.6) John Wiley and Sons, New York.

    Google Scholar 

  • Stuart GW, McMurray JV and Westerfield M (1988) Replication, integration and stable germ-line transmission of foreign sequences injected into early zebrafish embryos. Development 103: 403–412.

    Google Scholar 

  • Symonds JE, Walker SP, Sin FYT and Sin I (1994) Development of a mass gene transfer method in chinook salmon: optimization of gene transfer by electroporated sperm. Mol Mar Biol Biotechnol 3: 104–111.

    Google Scholar 

  • Tsai H-J (2000) Electroporated sperm mediation of a gene transfer system for finfish and shellfish. Mol Reprod Dev 56: 281–284.

    Google Scholar 

  • Tsai H-J, Wang SH, Inoue K, Takagi S, Kimura M, Wakamatsu Y, et al. (1995) Initiation of the transgenic lacZ gene expression in medaka (Oryzias latipes) embryos. Mol Mar Biol Biotechnol 4: 1–9.

    Google Scholar 

  • Tseng FS, Tsai HJ, Liao IC and Song YL (2000) Introducing foreign DNA into tiger shrimp (Penawus monodon) by electroporation. Theriogenology 54: 1421–1432.

    Google Scholar 

  • Venugopal T, Pandian TJ, Mathavan S and Sarangi N (1998) Gene transfer in Indian major carps by electroporation. Curr Sci 74: 636–638.

    Google Scholar 

  • Zhao X, Zhang PJ and Wong TK (1993) Application of baekonization: a new approach to produce transgenic fish.Mol Mar Biol Biotech 2: 63–69.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to William M. Muir.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hostetler, H.A., Peck, S.L. & Muir, W.M. High Efficiency Production of germ-line Transgenic Japanese Medaka (Oryzias latipes) by Electroporation with Direct Current-shifted Radio Frequency Pulses. Transgenic Res 12, 413–424 (2003). https://doi.org/10.1023/A:1024248300592

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1024248300592

Navigation