PUBLICATION

Electroporation of DNA, RNA, and morpholinos into zebrafish embryos

Authors
Cerda, G.A., Thomas, J.E., Allende, M.L., Karlstrom, R.O., and Palma, V.
ID
ZDB-PUB-060724-3
Date
2006
Source
Methods (San Diego, Calif.)   39(3): 207-211 (Journal)
Registered Authors
Allende, Miguel L., Karlstrom, Rolf
Keywords
Electroporation, Lissamine, Morpholino, Zebrafish, GFP
MeSH Terms
  • Animals
  • DNA*
  • Electroporation/instrumentation
  • Electroporation/methods*
  • Embryo, Nonmammalian/chemistry
  • Green Fluorescent Proteins/analysis
  • Oligonucleotides, Antisense*
  • RNA*
  • Zebrafish/embryology
  • Zebrafish/genetics*
  • Zebrafish Proteins/analysis
  • Zebrafish Proteins/genetics
PubMed
16837210 Full text @ Methods
Abstract
The combination of accessible embryology and forward genetic techniques has made zebrafish a powerful model system for the study of vertebrate development. One limitation of genetic analysis is that the study of gene function is usually limited to the first developmental event affected by a gene. In vivo electroporation has recently matured as a method for studying gene function at different developmental time points and in specific regions of the organism. The focal application of current allows macromolecules to be efficiently introduced into a targeted region at any time in the life cycle. Here we describe a rapid protocol by which DNA, RNA and morpholinos can all be precisely electroporated into zebrafish in a temporally and spatially controlled manner. This versatile technique allows gene function to be determined by both gain and loss of function analyses in specific regions at specific times. This is the first report that describes the electroporation of three different molecules into embryonic and larval zebrafish cells.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping