Protein Tyrosine Phosphatase Studies in Zebrafish

Daniëlle T.J. Woutersen, Jisca Majolée, Jeroen den Hertog*

*Corresponding author for this work

    Research output: Chapter in Book/Report/Conference proceedingChapterAcademicpeer-review

    Abstract

    The zebrafish is an ideal model for functional analysis of genes at the molecular, protein, cell, organ, and organism levels. We have used zebrafish to analyze the function of members of the protein tyrosine phosphatase (PTP) superfamily for more than two decades. The molecular genetic toolbox has significantly improved over the years. Currently, generating mutant lines that lack the function of a PTP gene is relatively straightforward by CRISPR/Cas9 technology-mediated generation of insertions or deletions in the target gene. In addition, generating point mutations using CRISPR/Cas9 technology and homology-directed repair (HDR) is feasible, albeit the success rate could be higher. Here, we describe the methods, including the tips and tricks, that we have used to generate knock-out and knock-in zebrafish lines in PTP genes successfully.

    Original languageEnglish
    Title of host publicationMethods in Molecular Biology
    PublisherHumana Press Inc.
    Chapter6
    Pages93-110
    Number of pages18
    ISBN (Electronic)978-1-0716-3569-8
    ISBN (Print)978-1-0716-3568-1
    DOIs
    Publication statusPublished - 2024

    Publication series

    NameMethods in Molecular Biology
    Volume2743
    ISSN (Print)1064-3745
    ISSN (Electronic)1940-6029

    Keywords

    • CRISPR/Cas9
    • Genome editing
    • Protein tyrosine phosphatases
    • PTEN
    • PTP
    • SHP2
    • Zebrafish

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