AP-4 loss in CRISPR-edited zebrafish affects early embryo development. (January 2023)

• Record Type: Journal Article
• Authors: Pembridge, Olivia G.; Wallace, Natalie S.; Clements, Thomas P.; Jackson, Lauren P.
• Is Part Of: Advances in biological regulation. Volume 87(2023)
• Publication Date: 2023-01
• Subjects: Membrane trafficking -- Coat proteins -- CRISPR -- Gene editing -- Zebrafish; Cellular control mechanisms -- Periodicals; Biological control systems -- Periodicals; Molecular biology -- Periodicals; Periodicals; 571.74
• DOI: 10.1016/j.jbior.2022.100945
• Languages: English
• ISSNs: 2212-4926

Abstract

Abstract: Mutations in the heterotetrametric adaptor protein 4 (AP-4; ε/β4/μ4/σ4 subunits) membrane trafficking coat complex lead to complex neurological disorders characterized by spastic paraplegia, microcephaly, and intellectual disabilities. Understanding molecular mechanisms underlying these disorders continues to emerge with recent identification of an essential autophagy protein, ATG9A, as an AP-4 cargo. Significant progress has been made uncovering AP-4 function in cell culture and patient-derived cell lines, and ATG9A trafficking by AP-4 is considered a potential target for gene therapy approaches. In contrast, understanding how AP-4 trafficking affects development and function at the organismal level has long been hindered by loss of conserved AP-4 genes in key model systems ( S. cerevisiae, C. elegans, D. melanogaster ). However, zebrafish ( Danio rerio ) have retained AP-4 and can serve as an important model system for studying both the nervous system and overall development. We undertook gene editing in zebrafish using a CRISPR-ExoCas9 knockout system to determine how loss of single AP-4, or its accessory protein tepsin, genes affect embryo development 24 h post-fertilization (hpf). Single gene-edited embryos display abnormal head morphology and neural necrosis. We further conducted the first exploration of how AP-4 single gene knockouts in zebrafish embryos affect expression levels and patterns of two autophagy genes, atg9a and map1lc3b . This work suggests zebrafish may be further adapted and developed as a tool to uncover AP-4 function in membrane trafficking and autophagy in the context of a model organism.