bioRxivCell Biology
The effect of Dnaaf5 gene dosage on primary ciliary dyskinesia phenotypes
A. Horani, D. K. Gupta, J. Xu, H. Xu, L. D. C. Puga-Molina, C. Santi, S. Ramagiri, S. K. Brennen, J. Pan, T. Huang, R. M. Hyland, S. Gunsten, S.-C. Tzeng, J. M. Strahle, P. Mill, M. R. Mahjoub, S. K. Dutcher, S. L. Brody
Abstract
DNAAF5 is a dynein motor assembly factor associated with the autosomal heterogenic recessive condition of motile cilia, primary ciliary dyskinesia (PCD). The effects of allele heterozygosity on motile cilia function are unknown. We used CRISPR-Cas9 genome editing in mice to recreate a human missense variant identified in patients with mild PCD and a second, frameshift null deletion in Dnaaf5. Litters with Dnaaf5 heteroallelic variants showed distinct missense and null gene dosage effects. Homozygosity for the null Dnaaf5 alleles was embryonic lethal. Compound heterozygous animals with the missense and null alleles showed severe disease manifesting as hydrocephalus and early lethality. However, animals homozygous for the missense mutation had improved survival, with partial preserved cilia function and motor assembly observed by ultrastructure analysis. Notably, the same variant alleles exhibited divergent cilia function across different multiciliated tissues. Proteomic analysis of isolated airway cilia from mutant mice revealed reduction in some axonemal regulatory and structural proteins not previously reported in DNAAF5 variants. While transcriptional analysis of mouse and human mutant cells showed increased expression of genes coding for axonemal proteins. Together, these findings suggest allele-specific and tissue-specific molecular requirements for cilia motor assembly that may affect disease phenotypes and clinical trajectory in motile ciliopathies. Brief SummaryA mouse model of human DNAAF5 primary ciliary dyskinesia variants reveals gene dosage effects of mutant alleles and tissue-specific molecular requirements for cilia motor assembly.
- organism: mouse
- assay: proteomics
- research focus: cell type annotation
- research focus: differential expression
- approach: genetic perturbation / CRISPR
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