Generation of a Zebrafish Knock-In Model Recapitulating Childhood ETV6: RUNX1-Positive B-Cell Precursor Acute Lymphoblastic Leukemia

Veronika Zapilko, Sanni Moisio, Mataleena Parikka, Merja Heinäniemi, Olli Lohi

Tutkimustuotos: ArtikkeliTieteellinenvertaisarvioitu

10 Lataukset (Pure)

Abstrakti

Approximately 25% of children with B-cell precursor acute lymphoblastic leukemia (pB-ALL) harbor the t(12;21)(p13;q22) translocation, leading to the ETV6::RUNX1 (E::R) fusion gene. This translocation occurs in utero, but the disease is much less common than the prevalence of the fusion in newborns, suggesting that secondary mutations are required for overt leukemia. The role of these secondary mutations remains unclear and may contribute to treatment resistance and disease recurrence. We developed a zebrafish model for E::R leukemia using CRISPR/Cas9 to introduce the human RUNX1 gene into zebrafish etv6 intron 5, resulting in E::R fusion gene expression controlled by the endogenous etv6 promoter. As seen by GFP fluorescence at a single-cell level, the model correctly expressed the fusion protein in the right places in zebrafish embryos. The E::R fusion expression induced an expansion of the progenitor cell pool and led to a low 2% frequency of leukemia. The introduction of targeted pax5 and cdkn2a/b gene mutations, mimicking secondary mutations, in the E::R line significantly increased the incidence in leukemia. Transcriptomics revealed that the E::R;pax5mut leukemias exclusively represented B-lineage disease. This novel E::R zebrafish model faithfully recapitulates human disease and offers a valuable tool for a more detailed analysis of disease biology in this subtype.

AlkuperäiskieliEnglanti
Artikkeli5821
JulkaisuCancers
Vuosikerta15
Numero24
DOI - pysyväislinkit
TilaJulkaistu - 13 jouluk. 2023
OKM-julkaisutyyppiA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä

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