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The effect of Dnaaf5 gene dosage on primary ciliary dyskinesia phenotypes.
Horani, Amjad; Gupta, Deepesh Kumar; Xu, Jian; Xu, Huihui; Carmen Puga-Molina, Lis Del; Santi, Celia M; Ramagiri, Sruthi; Brennan, Steven K; Pan, Jiehong; Koenitzer, Jeffrey R; Huang, Tao; Hyland, Rachael M; Gunsten, Sean P; Tzeng, Shin-Cheng; Strahle, Jennifer M; Mill, Pleasantine; Mahjoub, Moe R; Dutcher, Susan K; Brody, Steven L.
Afiliação
  • Horani A; Department of Pediatrics.
  • Gupta DK; Department of Cell Biology and Physiology.
  • Xu J; Department of Pediatrics.
  • Xu H; Department of Medicine.
  • Carmen Puga-Molina LD; Department of Pediatrics.
  • Santi CM; Department of Obstetrics and Gynecology, and.
  • Ramagiri S; Department of Obstetrics and Gynecology, and.
  • Brennan SK; Department of Neurosurgery, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Pan J; Department of Pediatrics.
  • Koenitzer JR; Department of Medicine.
  • Huang T; Department of Medicine.
  • Hyland RM; Department of Medicine.
  • Gunsten SP; Department of Pediatrics.
  • Tzeng SC; Department of Medicine.
  • Strahle JM; Donald Danforth Plant Science Center, St. Louis, Missouri, USA.
  • Mill P; Department of Neurosurgery, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Mahjoub MR; MRC Human Genetics Unit, University of Edinburgh, Edinburgh, United Kingdom.
  • Dutcher SK; Department of Cell Biology and Physiology.
  • Brody SL; Department of Medicine.
JCI Insight ; 8(11)2023 06 08.
Article em En | MEDLINE | ID: mdl-37104040
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 partially 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. Transcriptional analysis of mouse and human mutant cells showed increased expression of genes coding for axonemal proteins. 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Kartagener Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: JCI Insight Ano de publicação: 2023 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Kartagener Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: JCI Insight Ano de publicação: 2023 Tipo de documento: Article País de publicação: Estados Unidos