PUBLICATION

Mutation Knock-in Methods Using Single-Stranded DNA and Gene Editing Tools in Zebrafish

Authors
Prykhozhij, S.V., Berman, J.N.
ID
ZDB-PUB-230906-69
Date
2024
Source
Methods in molecular biology (Clifton, N.J.)   2707: 279303279-303 (Chapter)
Registered Authors
Berman, Jason, Prykhozhij, Sergey
Keywords
CRISPR/Cas9, Disease model, Knock-in, Long ssDNA, Point mutation, Zebrafish, ssODN
MeSH Terms
  • Animals
  • DNA, Single-Stranded*/genetics
  • Gene Editing
  • Mutation
  • Nucleotides
  • Point Mutation
  • Zebrafish*/genetics
PubMed
37668920 Full text @ Meth. Mol. Biol.
Abstract
Introduction or knock-in of precise genomic modifications remains one of the most important applications of CRISPR/Cas9 in all model systems including zebrafish. The most widely used type of donor template containing the desired modification is single-stranded DNA (ssDNA), either in the form of single-stranded oligodeoxynucleotides (ssODN) (<150 nucleotides (nt)) or as long ssDNA (lssDNA) molecules (up to about 2000 nt). Despite the challenges posed by DNA repair after DNA double-strand breaks, knock-in of precise mutations is relatively straightforward in zebrafish. Knock-in efficiency can be enhanced by careful donor template design, using lssDNA as template or tethering the donor template DNA to the Cas9-guide RNA complex. Other point mutation methods such as base editing and prime editing are starting to be applied in zebrafish and many other model systems. However, these methods may not always be sufficiently accessible or may have limited capacity to perform all desired mutation knock-ins which are possible with ssDNA-based knock-in methods. Thus, it is likely that there will be complementarity in the technologies used for generating precise mutants. Here, we review and describe a suite of CRISPR/Cas9 knock-in procedures utilizing ssDNA as the donor template in zebrafish, point out the potential challenges and suggest possible approaches for their solution ultimately leading to successful generation of precise mutant lines.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping