PUBLICATION

Fast, precise and cloning-free knock-in of reporter sequences in vivo with high efficiency

Authors
Zhang, Y., Marshall-Phelps, K., Almeida, R.G.
ID
ZDB-PUB-230614-32
Date
2023
Source
Development (Cambridge, England)   150(12): (Journal)
Registered Authors
Almeida, Rafael
Keywords
HDR, Knock-in, Neuron, Synaptobrevin, Vamp, Zebrafish
MeSH Terms
  • Animals
  • CRISPR-Cas Systems*/genetics
  • Gene Editing
  • Gene Knock-In Techniques
  • Genome
  • Zebrafish*/genetics
PubMed
37309812 Full text @ Development
Abstract
Targeted knock-in of fluorescent reporters enables powerful gene and protein analyses in a physiological context. However, precise integration of long sequences remains challenging in vivo. Here, we demonstrate cloning-free and precise reporter knock-in into zebrafish genes, using PCR-generated templates for homology-directed repair with short homology arms (PCR tagging). Our novel knock-in reporter lines of vesicle-associated membrane protein (vamp) zebrafish homologues reveal subcellular complexity in this protein family. Our approach enables fast and efficient reporter integration in the zebrafish genome (in 10-40% of injected embryos) and rapid generation of stable germline-transmitting lines.
Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping