PUBLICATION

Efficient gene transfer into zebrafish skeletal muscle by intramuscular injection of plasmid DNA

Authors
Tan, J.H. and Chan, W.K.
ID
ZDB-PUB-970918-6
Date
1997
Source
Molecular marine biology and biotechnology   6(2): 98-109 (Journal)
Registered Authors
Chan, Woon-Khiong
Keywords
none
MeSH Terms
  • Animals
  • Chloramphenicol O-Acetyltransferase/genetics
  • Cytomegalovirus/genetics
  • Gene Expression
  • Gene Transfer Techniques*
  • Genes, Reporter
  • Genetic Vectors
  • Immediate-Early Proteins/genetics
  • Injections, Intramuscular
  • Luciferases/genetics
  • Metallothionein/genetics
  • Muscle, Skeletal*
  • Plasmids*
  • Promoter Regions, Genetic
  • Salmon/genetics
  • Zebrafish/genetics*
  • beta-Galactosidase/genetics
PubMed
9200836
Abstract
The ability of zebrafish skeletal muscles to internalize and express plasmid DNA was demonstrated using pCMVCAT1, a chloramphenicol acetyltransferase (CAT) construct driven by the human cytomegalovirus immediate early (CMV-IE) promoter. We found that CAT activity was correlated to the amount of plasmid DNA injected, with maximal expression at 5 micrograms of pCMVCAT1. CAT activity was also shown to increase steadily over the first seven days after injection, with high levels of CAT expression persisting up to one year. Intramuscular injection of CAT constructs driven by other viral promoters also resulted in high levels of CAT activity. Histochemical localization using a CMV beta-galactosidase construct confirmed that only myofibers at the site of injection expressed beta-galactosidase enzyme. The persistence and strong expression of injected plasmid constructs suggest that zebrafish may be a simple and readily accessible system for direct muscle injection studies.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping