PUBLICATION
ift140-Deficient Zebrafish as a Model for Kidney Cystogenesis and an F0-Based Screen for Genetic Modifiers of Kidney Cysts
- Authors
- Zhu, P., Lavin, A., Xu, X., Lin, X.
- ID
- ZDB-PUB-250910-2
- Date
- 2025
- Source
- Journal of the American Society of Nephrology : JASN : (Journal)
- Registered Authors
- Lin, Xueying, Xu, Xiaolei, Zhu, Ping
- Keywords
- none
- MeSH Terms
- none
- PubMed
- 40924493 Full text @ J. Am. Soc. Nephrol.
Citation
Zhu, P., Lavin, A., Xu, X., Lin, X. (2025) ift140-Deficient Zebrafish as a Model for Kidney Cystogenesis and an F0-Based Screen for Genetic Modifiers of Kidney Cysts. Journal of the American Society of Nephrology : JASN. :.
Abstract
Background Genetic modifiers are believed to play an important role in the onset and severity of polycystic kidney disease (PKD), but identifying these modifiers has been challenging due to the lack of effective methodologies.
Methods We generated zebrafish mutants of IFT140, a skeletal ciliopathy gene and newly identified autosomal dominant PKD (ADPKD) gene, to examine skeletal development and kidney cyst formation in larval and juvenile mutants. Additionally, we utilized ift140 crispants, generated through efficient microhomology-mediated end joining (MMEJ)-based genome editing, to compare phenotypes with mutants and conduct a pilot genetic modifier screen.
Results ift140 mutants developed kidney cysts and bone defects similar to those seen in mammalian models. ift140 crispants recapitulated mutant phenotypes while bypassing the early lethality of the mutants, enabling the analysis of kidney cyst formation in adult fish. In addition to cilia defects, we identified non-ciliary phenotypes, including disrupted cell polarity and aberrant cytoplasmic microtubule stabilization in kidney epithelial cells, as potential contributors to ift140-associated cystogenesis. The ability to detect ift140-associated kidney cysts with ease allowed us to develop an F0-based genetic screen to identify potential protective modifiers. A pilot screen of sixteen genes previously implicated in dysregulated signaling pathways in ADPKD revealed both known and novel modifiers, including mtor and ulk1a. We further found that inhibition of mtor and ulk1a reversed both cilia-related and non-cilia-related abnormalities in the kidney.
Conclusions By establishing a zebrafish model of ift140-associated cystic kidney disease, we recapitulated ift140's ciliary role and uncovered a non-ciliary function in kidney cystogenesis. Importantly, we demonstrated the feasibility of using ift140 mosaic crispants to evaluate cystogenesis in adult fish and to perform F0-based screening for identifying genetic modifiers of kidney cysts.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping