Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects - PubMed (original) (raw)

. 2017 Jan 5;100(1):160-168.

doi: 10.1016/j.ajhg.2016.11.019. Epub 2016 Dec 29.

Niki T Loges 2, Isabella Aprea 2, Kaman Wu 3, Zeineb Bakey 3, Eric G Haarman 4, Johannes M A Daniels 5, Erik A Sistermans 6, Natalija Bogunovic 7, Gerard W Dougherty 2, Inga M Höben 2, Jörg Große-Onnebrink 2, Anja Matter 2, Heike Olbrich 2, Claudius Werner 2, Gerard Pals 6, Miriam Schmidts 8, Heymut Omran 2, Dimitra Micha 9

Affiliations

Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects

Tamara Paff et al. Am J Hum Genet. 2017.

Abstract

Defects in motile cilia and sperm flagella cause primary ciliary dyskinesia (PCD), characterized by chronic airway disease, infertility, and left-right body axis disturbance. Here we report maternally inherited and de novo mutations in PIH1D3 in four men affected with PCD. PIH1D3 is located on the X chromosome and is involved in the preassembly of both outer (ODA) and inner (IDA) dynein arms of cilia and sperm flagella. Loss-of-function mutations in PIH1D3 lead to absent ODAs and reduced to absent IDAs, causing ciliary and flagellar immotility. Further, PIH1D3 interacts and co-precipitates with cytoplasmic ODA/IDA assembly factors DNAAF2 and DNAAF4. This result has clinical and genetic counseling implications for genetically unsolved male case subjects with a classic PCD phenotype that lack additional phenotypes such as intellectual disability or retinitis pigmentosa.

Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.

PubMed Disclaimer

Figures

Figure 1

Figure 1

Results of the Mutational Analyses in PIH1D3, Pedigrees of the PCD-Affected Families PCD-10 and OP-1899, and Clinical Features of OP-1899 II1 (A) Hemizygous loss-of-function mutations in PIH1D3 located on the X chromosome were identified in two families. Pedigree of PCD-affected families PCD-10 and OP-1899. PCD-affected siblings are shaded black and the unaffected sibling is shaded white. (B) The chest X-ray radiograph as well as two computed tomography scans show situs inversus totalis, chronic airway disease with bronchiectasis in the middle lobe, and mucus plugging in OP-1899 II1. (C) Exon-intron structure of PIH1D3. The exon-intron structure of PIH1D3 with untranslated (light gray) and translated (black) regions and the PIH1 domain (dark gray).

Figure 2

Figure 2

Loss-of-Function PIH1D3 Mutations Result in Absence of Outer and Inner Dynein Arms in Respiratory Epithelial Cells (A) The analysis of transmission electron microscopy cross-sections from respiratory cilia from OP-1899 II1, PCD-10 I1, and PCD-10 II2 showed a normal 9+2 architecture with absence of outer dynein and inner dynein arms. Scale bars represent 200 nm. (B–D) Respiratory epithelial cells from control (B) and PCD-affected individuals OP-1899 II1 (C) and PCD-10 II2 (D) were double-labeled with antibodies directed against outer dynein arm heavy chain DNAH5 (green) and the N-DRC component GAS8 (red). Both proteins colocalize along the cilia in cells from the unaffected controls (B, yellow). In contrast, in mutant cells, DNAH5 was absent from or severely reduced in ciliary axonemes (C and D). The green staining in the nuclei observed in (C) is most probably background. (E–G) Cells were double-labeled with antibodies directed against acetylated tubulin (green) and the inner dynein arm light chain DNALI1 (red). In unaffected control cilia, both proteins colocalize along the ciliary axonemes (E, yellow). In contrast, in cells of individuals carrying PIH1D3 mutations, DNALI1 was absent from or severely reduced in the ciliary axonemes (F and G). The red staining at the ciliary base is an artifact caused by the polyclonal rabbit antibody. Nuclei were stained with Hoechst33342 (blue). Scale bars represent 10 μm.

Figure 3

Figure 3

PIH1D3 Mutant Sperm Flagella Are Deficient for the Outer Dynein Arm Intermediate Chains DNAI1 and DNAI2 Sperms were double-labeled with antibodies directed against acetylated tubulin (green) and DNAI1 or DNAI2 (both in red). DNAI1 and DNAI2 colocalize with acetylated tubulin along the flagellum in sperms from unaffected controls (yellow) (A and C). In contrast, in PIH1D3 mutant sperm tails, DNAI1 (B) and DNAI2 (D) were absent from flagellar axonemes. Nuclei were stained with Hoechst33342 (blue). Scale bars represent 10 μm.

Figure 4

Figure 4

Identification of PIH1D3 Interacting Genes (A) Y2H assays show strong interaction of PIH1D3 with DNAAF2 and DNAAF4. Lamin-C-pBD- Gal4-pAD was used as a negative control and Gal4-pBD - Gal4-pAD as a positive control. (B) Confirmation of PIH1D3 interactors from the Y2H screen by co-IP from HEK293T cells. Co-expressions of tagged versions of PIH1D3 and either DNAAF2 or DNAAF4 revealed protein-protein interactions with DNAAF2 and DNAAF4 (left, western-blot anti-Flag; right, western blot anti-HA).

References

    1. Fliegauf M., Benzing T., Omran H. When cilia go bad: cilia defects and ciliopathies. Nat. Rev. Mol. Cell Biol. 2007;8:880–893. - PubMed
    1. Satir P. Studies on cilia. 3. Further studies on the cilium tip and a “sliding filament” model of ciliary motility. J. Cell Biol. 1968;39:77–94. - PMC - PubMed
    1. Summers K.E., Gibbons I.R. Adenosine triphosphate-induced sliding of tubules in trypsin-treated flagella of sea-urchin sperm. Proc. Natl. Acad. Sci. USA. 1971;68:3092–3096. - PMC - PubMed
    1. Satir P., Heuser T., Sale W.S. A structural basis for how motile cilia beat. Bioscience. 2014;64:1073–1083. - PMC - PubMed
    1. Wilson K.S., Gonzalez O., Dutcher S.K., Bayly P.V. Dynein-deficient flagella respond to increased viscosity with contrasting changes in power and recovery strokes. Cytoskeleton (Hoboken) 2015;72:477–490. - PMC - PubMed

MeSH terms

Substances

LinkOut - more resources