PUBLICATION

pIGLET: Safe harbor landing sites for reproducible and efficient transgenesis in zebrafish

Authors
Lalonde, R.L., Wells, H.H., Kemmler, C.L., Nieuwenhuize, S., Lerma, R., Burger, A., Mosimann, C.
ID
ZDB-PUB-240606-6
Date
2024
Source
Science advances   10: eadn6603eadn6603 (Journal)
Registered Authors
Burger, Alexa, Kemmler, Cassie L., Mosimann, Christian, Nieuwenhuize, Susan
Keywords
none
MeSH Terms
  • Animals
  • Animals, Genetically Modified*
  • Attachment Sites, Microbiological/genetics
  • Gene Transfer Techniques*
  • Integrases/genetics
  • Integrases/metabolism
  • Transgenes*
  • Zebrafish*/genetics
PubMed
38838146 Full text @ Sci Adv
Abstract
Standard zebrafish transgenesis involves random transgene integration with resource-intensive screening. While phiC31 integrase-based attP/attB recombination has streamlined transgenesis in mice and Drosophila, validated attP-based landing sites for universal applications are lacking in zebrafish. Here, we developed phiC31 Integrase Genomic Loci Engineered for Transgenesis (pIGLET) as transgenesis approach, with two attP landing sites pIGLET14a and pIGLET24b from well-validated Tol2 transgenes. Both sites facilitate diverse transgenesis applications including reporters and Cre/loxP transgenes. The pIGLET14a and pIGLET24b landing sites consistently yield 25 to 50% germline transmission, substantially reducing the resources needed for transgenic line generation. Transgenesis into these sites enables reproducible expression patterns in F0 zebrafish embryos for enhancer discovery and testing of gene regulatory variants. Together, our new landing sites streamline targeted, reproducible zebrafish transgenesis as a robust platform for various applications while minimizing the workload for generating transgenic lines.
Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping