Tissue-specific in vivo transformation of plasmid DNA in Neotropical tadpoles using electroporation

PLoS One. 2023 Aug 17;18(8):e0289361. doi: 10.1371/journal.pone.0289361. eCollection 2023.

Abstract

Electroporation is an increasingly common technique used for exogenous gene expression in live animals, but protocols are largely limited to traditional laboratory organisms. The goal of this protocol is to test in vivo electroporation techniques in a diverse array of tadpole species. We explore electroporation efficiency in tissue-specific cells of five species from across three families of tropical frogs: poison frogs (Dendrobatidae), cryptic forest/poison frogs (Aromobatidae), and glassfrogs (Centrolenidae). These species are well known for their diverse social behaviors and intriguing physiologies that coordinate chemical defenses, aposematism, and/or tissue transparency. Specifically, we examine the effects of electrical pulse and injection parameters on species- and tissue-specific transfection of plasmid DNA in tadpoles. After electroporation of a plasmid encoding green fluorescent protein (GFP), we found strong GFP fluorescence within brain and muscle cells that increased with the amount of DNA injected and electrical pulse number. We discuss species-related challenges, troubleshooting, and outline ideas for improvement. Extending in vivo electroporation to non-model amphibian species could provide new opportunities for exploring topics in genetics, behavior, and organismal biology.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anura / genetics
  • DNA
  • Electroporation Therapies*
  • Electroporation*
  • Green Fluorescent Proteins / genetics
  • Plasmids / genetics
  • Transfection

Substances

  • DNA
  • Green Fluorescent Proteins

Grants and funding

This work is supported by a grant from the National Science Foundation (www.nsf.org; IOS-1827333). and New York Stem Cell Foundation (https://nyscf.org/; NYSCF-R-NI58) to LAO. During analyses and drafting, JD was supported by a Gerstner Scholars Fellowship provided by the Gerstner Family Foundation and the Richard Gilder Graduate School at the American Museum of Natural History (https://gerstner.org/; www.amnh.org/research/richard-gilder-graduate-school/). DS is supported by a NSF Graduate Research Fellowship (www.nsf.org; DGE-1656518). LAO is a New York Stem Cell Investigator. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.