Document Type
Article
Language
eng
Format of Original
13 p.
Publication Date
7-1-2014
Publisher
Oxford University Press
Source Publication
Human Molecular Genetics
Source ISSN
0964-6906
Abstract
Primary ciliary dyskinesia (PCD) is an inherited chronic respiratory obstructive disease with randomized body laterality and infertility, resulting from cilia and sperm dysmotility. PCD is characterized by clinical variability and extensive genetic heterogeneity, associated with different cilia ultrastructural defects and mutations identified in >20 genes. Next generation sequencing (NGS) technologies therefore present a promising approach for genetic diagnosis which is not yet in routine use. We developed a targeted panel-based NGS pipeline to identify mutations by sequencing of selected candidate genes in 70 genetically undefined PCD patients. This detected loss-of-function RSPH1 mutations in four individuals with isolated central pair (CP) agenesis and normal body laterality, from two unrelated families. Ultrastructural analysis in RSPH1-mutated cilia revealed transposition of peripheral outer microtubules into the ‘empty’ CP space, accompanied by a distinctive intermittent loss of the central pair microtubules. We find that mutations in RSPH1, RSPH4A and RSPH9, which all encode homologs of components of the ‘head’ structure of ciliary radial spoke complexes identified in Chlamydomonas, cause clinical phenotypes that appear to be indistinguishable except at the gene level. By high-resolution immunofluorescence we identified a loss of RSPH4A and RSPH9 along with RSPH1 from RSPH1-mutated cilia, suggesting RSPH1 mutations may result in loss of the entire spoke head structure. CP loss is seen in up to 28% of PCD cases, in whom laterality determination specified by CP-less embryonic node cilia remains undisturbed. We propose this defect could arise from instability or agenesis of the ciliary central microtubules due to loss of their normal radial spoke head tethering.
Creative Commons License
This work is licensed under a Creative Commons Attribution 3.0 License.
Recommended Citation
Onoufriadis, Alexandros; Shoemark, Amelia; Schmidts, Miriam; Patel, Mitali; Jimenez, Gina; Liu, Hui; Thomas, Biju; Dixon, Mellisa; Hirst, Robert A.; Rutman, Andrew; Burgoyne, Thomas; Williams, Christopher; Scully, Juliet; Bolard, Florence; Lafitte, Jean-Jacques; Beales, Philip L.; Hogg, Claire; Yang, Pinfen; Chung, Eddie M.K.; Emes, Richard D.; O’Callaghan, Christopher; 10K, UK; Bouvagnet, Patrice; and Mitchison, Hannah M., "Targeted NGS Gene Panel Identifies Mutations in RSPH1 Causing Primary Ciliary Dyskinesia and a Common Mechanism for Ciliary Central Pair Agenesis Due to Radial Spoke Defects" (2014). Biological Sciences Faculty Research and Publications. 375.
https://epublications.marquette.edu/bio_fac/375
Comments
Published version. Human Molecular Genetics, Vol. 23, No. 13 (2014): 3362-3374. DOI. © 2014 The Authors. Used with permission.