ZFIN ID: ZDB-PUB-010424-2
Enhanced expression and stable transmission of transgenes flanked by inverted terminal repeats from adeno-associated virus in zebrafish
Hsiao, C.D., Hsieh, F.J., and Tsai, H.J.
Date: 2001
Source: Developmental dynamics : an official publication of the American Association of Anatomists   220(4): 323-336 (Journal)
Registered Authors: Hsiao, Chung-Der, Tsai, Huai-Jen
Keywords: actin promoter; adeno-associated virus; green fluorescent protein; germline transmission; inverted terminal repeats; transgenic zebrafish; uniform expression
MeSH Terms:
  • Actins/genetics
  • Animals
  • Animals, Genetically Modified*
  • Blotting, Southern
  • Dependovirus/genetics*
  • Female
  • Genetic Techniques*
  • Green Fluorescent Proteins
  • Luminescent Proteins/metabolism
  • Male
  • Models, Genetic
  • Muscle, Skeletal/metabolism
  • Plasmids/metabolism
  • Polymerase Chain Reaction
  • Promoter Regions, Genetic
  • Repetitive Sequences, Nucleic Acid
  • Time Factors
  • Tissue Distribution
  • Transgenes*
  • Zebrafish
PubMed: 11307166 Full text @ Dev. Dyn.
ABSTRACT
Mosaic expression of transgenes in the F0 generation severely hinders the study of transient expression in transgenic fish. To avoid mosaicism, enhanced green fluorescent protein (EGFP) gene cassettes were constructed and introduced into one-celled zebrafish embryos. These EGFP gene cassettes were flanked by inverted terminal repeats (ITRs) from adeno-associated virus (AAV) and driven by zebrafish alpha-actin (palpha-actin-EGFP-ITR) or medaka beta-actin promoters (pbeta-actin-EGFP-ITR). EGFP was expressed specifically and uniformly in the skeletal muscle of 56% +/- 8% of the palpha-actin-EGFP-ITR-injected survivors and in the entire body of 1.3% +/- 0.8% of the pbeta-actin-EGFP-ITR-injected survivors. Uniform transient expression never occurred in zebrafish embryos injected with EGFP genes that were not flanked by AAV-ITRs. In the F0 generation, uniformly distributed EGFP could mimic the stable expression in transgenic lines early in development. We established five transgenic lines derived from palpha-actin-EGFP-ITR-injected embryos crossed with wild-type fish and 11 transgenic lines derived from pbeta-actin-EGFP-ITR-injected embryos crossed with wild-type fish. None of these transgenic lines failed to express the transgene, a result confirmed by polymerase chain reaction analysis. Stable mendelian transmission of the transgenes was achieved in both alpha-actin and beta-actin transgenic lines without changing the patterns of expression and integration. Progeny inheritance test and Southern blot analysis results strongly suggest that transgenes flanked by AAV-ITRs were integrated randomly into the genome at a single locus with a concatamerized multiplier. Thus, incorporating AAV-ITRs into transgenes results in uniform gene expression in the F0 generation and stable transmission of transgenes in zebrafish.
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