PUBLICATION

A minimally invasive fin scratching protocol for fast genotyping and early selection of zebrafish embryos

Authors
Venditti, M., Pedalino, C., Rosello, M., Fasano, G., Serafini, M., Revenu, C., Del Bene, F., Tartaglia, M., Lauri, A.
ID
ZDB-PUB-230101-3
Date
2022
Source
Scientific Reports   12: 2259722597 (Journal)
Registered Authors
Del Bene, Filippo, Revenu, Celine, Rosello, Marion
Keywords
none
MeSH Terms
  • Animals
  • Biopsy
  • Genetic Engineering*
  • Genotype
  • Humans
  • Models, Animal
  • Zebrafish*/genetics
PubMed
36585409 Full text @ Sci. Rep.
Abstract
Current genetic modification and phenotyping methods in teleost fish allow detailed investigation of vertebrate mechanisms of development, modeling of specific aspects of human diseases and efficient testing of drugs at an organ/organismal level in an unparalleled fast and large-scale mode. Fish-based experimental approaches have boosted the in vivo verification and implementation of scientific advances, offering the quality guaranteed by animal models that ultimately benefit human health, and are not yet fully replaceable by even the most sophisticated in vitro alternatives. Thanks to highly efficient and constantly advancing genetic engineering as well as non-invasive phenotyping methods, the small zebrafish is quickly becoming a popular alternative to large animals' experimentation. This approach is commonly associated to invasive procedures and increased burden. Here, we present a rapid and minimally invasive method to obtain sufficient genomic material from single zebrafish embryos by simple and precise tail fin scratching that can be robustly used for at least two rounds of genotyping already from embryos within 48 h of development. The described protocol betters currently available methods (such as fin clipping), by minimizing the relative animal distress associated with biopsy at later or adult stages. It allows early selection of embryos with desired genotypes for strategizing culturing or genotype-phenotype correlation experiments, resulting in a net reduction of "surplus" animals used for mutant line generation.
Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping