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Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder caused by cilia and sperm dysmotility. About 12% of cases show perturbed 9+2 microtubule cilia structure and inner dynein arm (IDA) loss, historically termed ‘radial spoke defect’. We sequenced CCDC39 and CCDC40 in 54 ‘radial spoke defect’ families, as these are the two genes identified so far to cause this defect. We discovered biallelic mutations in a remarkable 69% (37/54) of families, including identification of 25 (19 novel) mutant alleles (12 in CCDC39 and 13 in CCDC40). All the mutations were nonsense, splice and frameshift predicting early protein truncation, which suggests this defect is caused by ‘null’ alleles conferring complete protein loss. Most families (73%; 27/37) had homozygous mutations, including families from outbred populations. A major putative hotspot mutation was identified, CCDC40 c.248delC, as well as several other possible hotspot mutations. Together, these findings highlight the key role of CCDC39 and CCDC40 in PCD with axonemal disorganisation and IDA loss, and these genes represent major candidates for genetic testing in families affected by this ciliary phenotype. We show that radial spoke structures are largely intact in these patients and propose this ciliary ultrastructural abnormality be referred to as ‘IDA and nexin-dynein regulatory complex (N-DRC) defect’, rather than ‘radial spoke defect’.
Primary ciliary dyskinesia (PCD) is a recessively inherited disorder which arises from cilia/sperm dysmotility that is associated with a number of different axonemal ultrastructural abnormalities. The symptoms of deficient mucociliary clearance are usually obvious from birth, and patients have recurrent respiratory tract infections leading to irreversible lung damage (bronchiectasis). They also manifest with otitis media, chronic sinusitis, and subfertility. Internal organ laterality is randomised with about half of patients having situs inversus, an association reflecting dysmotility of nodal cilia during embryonic development.
Motile flagella and cilia are related organelles found on the surface of cells evolutionarily conserved across 1.6 billion years from the flagella of the green alga Chlamydomonas to the ciliated respiratory and embryonic node cells of vertebrates (Pazour, 2004). In humans, motile cilia have a common microtubule-based ultrastructure (axoneme), comprising 9 peripheral microtubule doublets either surrounding (in ‘9+2’ motile respiratory and fallopian tube cilia, and sperm flagella) or lacking (in ‘9+0’ motile nodal cilia) a central microtubule pair (Becker-Heck et al., 2012; Fliegauf et al., 2007), and linked to a variety of microtubule-associated proteins. These include the inner and outer dynein arm motor complexes, which project from the peripheral microtubule doublets; the radial spokes, which provide a radial scaffold between the central pair and peripheral microtubules and facilitate signal transduction from the centre out to the dynein arms to govern ciliary beat and waveform (Becker-Heck et al., 2012); and nexin-dynein regulatory complexes (N-DRC), which attach between adjacent peripheral doublets to facilitate inner dynein arm attachment and regulate dynein activity (Heuser et al., 2009). This complex superstructure creates the rigid organisation along the entire length of the axoneme which is required for motor ATPase signalling to generate a uniquely coordinated and self-propagating beat (Mitchison and Mitchison, 2010).
PCD is genetically heterogeneous with 18 identified genes causing non-syndromic disease. The range of genetic defects cause a small number of defective ciliary ultrastructural subtypes by current imaging resolution, and no correlations have been defined between ultrastructural defects and the course of disease (Kispert et al., 2003). Mutations in genes that cause axonemal outer dynein arm (ODA) defects (DNAH5, DNAI1, DNAI2, DNAL1, TXNDC3 and CCDC114) are the genetic basis of the majority of PCD cases (Olbrich et al., 2002; Pennarun et al., 1999; Loges et al., 2008; Mazor et al., 2011; Duriez et al., 2007; Bartoloni et al., 2002; Onoufriadis et al., 2012; Knowles et al., 2012a). Mutations in genes encoding components of the radial spoke head (RSPH4A and RSPH9) cause defects involving the central pair microtubules (Castleman et al., 2009). Mutations in genes encoding cytoplasmic or dual location proteins involved in the assembly and transport of dynein arm components into the axoneme from the cell body (DNAAF1/LRRC50, DNAAF2/KTU, DNAAF3/PF22, CCDC103, HEATR2 and LRRC6) cause inner and outer dynein arm defects (Loges et al., 2009; Duquesnoy et al., 2009; Omran et al., 2008; Mitchison et al., 2012; Panizzi et al., 2012; Horani et al., 2012; Kott et al., 2012). Lastly, two genes associated with PCD give rise to no discernible ultrastructural defects of the axoneme (DNAH11) or defects of the central microtubule pair C2b projection that are too subtle to be easily detected (HYDIN) (Bartoloni et al., 2002; Knowles et al., 2012b; Olbrich et al., 2012).
Mutations in two genes, CCDC39 (MIM# 613798) (Merveille et al., 2011) and CCDC40 (MIM# 613799) (Becker-Heck et al., 2011), have recently been shown in PCD patients that have a defect of the cilia axoneme, involving loss of the inner dynein arms accompanied by a variably expressed disorganisation of the 9+2 microtubule arrangement. Recent transmission electron microscopy (TEM) surveys of several different PCD cohorts estimated that at least ~12% of all PCD cases have this defect (Chilvers et al., 2003; Shoemark et al., 2012; Papon et al., 2010). The nine peripheral microtubules are retained but are mislocalised, often becoming more centralised, while the central microtubule pair may be variously lost (9+0), eccentrically positioned towards the periphery (9+2), or increased in number with a supernumerary central pair present (9+4); and the inner dynein arm structures are reduced or absent. Furthermore, in axonemes with this defect abnormal and/or absent N-DRC complexes have been recorded (Schneeberger et al., 1980; Konradova et al., 1982) and radial spokes (Sturgess et al., 1979; Antonelli et al., 1981). This ultrastructural defect has historically often been referred to as ‘radial spoke defect’. The reasons for the various disarrangements are unclear, but since a range of microtubule disorganisations may be seen within a single TEM sample of respiratory epithelia from a patient, it is even possible that a variety of changes may occur along the length of the axoneme. These perturbations of structure create a characteristic ciliary motility defect with a beating pattern of mixed appearance, where stiff cilia displaying a reduced amplitude (70%) and cilia that are fully immotile (30%) are both visible (Chilvers et al., 2003; Merveille et al., 2011; Becker-Heck et al., 2011). The partially retained motility may be explained by activity of the outer dynein arm motors, but cilia waveform is misregulated and the mean ciliary beat frequency is reduced (Chilvers et al., 2003).
The CCDC39 and CCDC40 genes encode structurally related coiled-coil domain-containing proteins of unknown function that are localised to the axoneme (Merveille et al., 2011; Becker-Heck et al., 2011; Becker-Heck et al., 2012). The loss of IDAs and N-DRCs from ciliary axonemes of CCDC39 and CCDC40 patients has been previously confirmed using antibodies to DNALI1 and the N-DRC component GAS11/8 respectively (Merveille et al., 2011; Becker-Heck et al., 2011), and it is proposed that CCDC39 and CCDC40 proteins interact with N-DRC components and play a role in inner dynein arm attachment. Neither protein has yet been identified in proteomic studies of N-DRC composition (Lin 2011); thus, rather than being integral N-DRC proteins, they may be otherwise involved in N-DRC assembly, microtubule attachment, or protein interactions. The role of the CCDC39 and CCDC40 proteins in the structure and function of radial spokes is not known, and radial spokes in cilia from ‘radial spoke defect’ patients have never been examined at the molecular level using antibody staining techniques.
In this study, we applied a combination of candidate gene Sanger sequencing and next-generation whole exome sequencing to identify the genetic cause of PCD in a large cohort of ‘radial spoke defect’ patients with cilia dysmotility associated with axonemal microtubule disorganisation and absence of IDAs. We also used antibody and immunofluorescence techniques to investigate radial spoke perturbations in nasal ciliated cells in patients with CCDC39/40 mutations.
A total of 54 unrelated PCD families were involved in the screen. Parallel mutational analysis on a collection of 17 families from UCL-ICH (labelled in the text by ‘PCD’ prefix), 4 from Belgium/UHM (University Hospital Muenster) (‘OP’ and ‘KUL’ prefix) and 33 from UNC (‘UNC’ prefix) was performed using genomic DNA samples obtained from peripheral blood cells. All families agreed under informed consent to participate in this study in accordance with protocols approved by the ethical committees of the Institute of Child Health/Great Ormond Street Hospital and University College London Hospital NHS Trust, and those of collaborating institutions.
The transcripts referred to are CCDC39 NM_181426.1 and CCDC40 NM_017950.2. Sanger sequencing was performed by amplifying and sequencing the coding exons and flanking intronic sequences of CCDC39 and CCDC40 (primer sequence available on request). Sequence alignments for variant identification were made using Sequencher software (Gene Codes Corporation). Whole exome sequencing was performed for most samples by capturing the exons using the Agilent SureSelect All Exon Human V3 (50 Mb) kit. TruSeq Pair End Cluster kit V3 was used for cluster generation and 100 bp. paired-end reads were generated on an Illumina HiSeq 2000 analyser using Illumina TruSeq V3 SBS sequencing chemistry. The BWA alignment tool (Li and Durbin, 2010) was used to map sequence reads back to the genome (human reference hg19) then the GATK tool suite (McKenna et al., 2010) was used to process the alignments and identify variations. The SNP-Effects (http://snpeff.sourceforge.net/) and ANNOVAR (Wang et al., 2010) programs were used to annotate variations. The details of the whole exome sequencing are presented in Supp. Table S1.
In one case (PCD22) exome sequencing was performed as part of the Wellcome Trust Sanger Institute UK10K Project as described previously (Olbrich et al., 2012; Onoufriadis et al., 2012). Exome variant analysis was achieved by filtering of the total variant list according to consistent autosomal recessive inheritance pattern, novelty in comparison to human polymorphism databases including the 1000 Genomes (1000 Genomes Project Consortium, 2010) and NHLBI Exome Sequencing projects (http://evs.gs.washington.edu/EVS) and dbSNP v135, and finally for their functional significance. This analysis required the presence of at least one homozygous or two heterozygous changes occurring with an estimated frequency <0.01, and all the patients included in this study had clear-cut biallelic variants in the CCDC39 and CCDC40 genes that were identified via excellent coverage in all cases, without any other obvious causal candidates indicated. Sanger sequencing was used to confirm all the identified variants from exome sequencing and to verify the segregation pattern of each change in other unaffected family members, identified by both methods.
Nucleotide numbering reflects cDNA numbering with +1 corresponding to the A of the ATG translation initiation codon in the reference sequence, according to journal guidelines (www.hgvs.org/mutnomen). The initiation codon is codon 1.
Respiratory epithelial cells were obtained using a cytology brush or rhinoprobe from the inferior turbinate of participants and immediately analysed for cilia beat frequency and beat pattern under light microscopy as described (Chilvers et al., 2003). Samples were fixed in glutaraldehyde and an ultrastructural defect of the cilia was confirmed by electron microscopy (Rutland et al., 1982).
The effect of the CCDC40 splice mutation in patient 114 II:1 was confirmed by Immunofluorescence analysis. Respiratory epithelial cells obtained by nasal brush biopsy were suspended in cell culture medium. Samples were spread onto glass slides, air dried and stored at −80°C until use. Cells were fixed with 4% PFA for 4 minutes at room temperature, washed 5X with PBS and then permeabilized with 0.5% TritonX100 for 10 minutes. After 5 more washes with PBS cells were incubated with 5% bovine serum albumin (Sigma) in PBS for 1 hour. The cells were then incubated with primary antibodies overnight at room temperature using the following dilutions: CCDC39 antibody 1:100 (rabbit polyclonal Sigma); RSPH4A 1:100 (rabbit polyclonal Sigma); ROPN1L 1:200 (rabbit polyclonal Sigma) monoclonal mouse anti-acetylated and gamma tubulin 1:500 (Sigma) over night at room temperature. After 5 washes with PBS cells were incubated with secondary anti-rabbit antibody (Alexa Fluor 488 Molecular Probes Invitrogen) and secondary anti-mouse antibody (Alexa Fluor 594 Molecular Probes Invitrogen). DNA was stained using DAPI (Invitrogen). Cells were finally washed 5X with PBS, mounted in Vectashield (Vector Laboratories) and confocal images were taken using a Zeiss LSM 710.
Conserved domains were predicted using SMART (Letunic et al., 2012) and CDD (Marchler-Bauer et al., 2011), and coiled-coil protein folds predicted using Paircoil2 (McDonnell et al., 2006) with minimum window size of 28 amino acids. Protein homologies and network predictions were identified using PSI-BLAST (Altschul et al., 1997) to search the nr database and STRING 9.0 (Szklarczyk et al., 2011).
The entire coding region and flanking intronic sequences of the CCDC39 and CCDC40 genes were sequenced in a cohort of 59 patients from 54 PCD families that displayed ciliary dysmotility and a similar axonemal ultrastructural phenotype to that associated with CCDC39 and CCDC40 mutations (Merveille et al., 2011; Becker-Heck et al., 2011). The patients were all diagnosed based on having a classic PCD phenotype, including recurrent respiratory tract infections, pneumonia, rhinosinusitis, otitis media usually requiring repeated grommet insertion, and age-dependent bronchiectasis, where chest CT data was available. Most patients showed symptoms in the neonatal period, with respiratory distress, as well as recurrent airway infections. In addition, patients showed abnormal cilia ultrastructure and motility at the electron and light microscopic levels respectively, as described below.
Combined whole exome sequencing and Sanger sequencing analysis in the 54 families identified a total of 25 different putative mutations, 12 in CCDC39 and 13 in CCDC40 that affected a total of 47 patients in 37 families (Table 1). All the changes consisted of frameshift, nonsense and essential splice site mutations, the latter all affecting the 100% conserved splicing consensus intronic nucleotides. None of the identified variants are present in dbSNP (Sherry et al., 2001), or the 1000 Genomes Project (1000 Genomes Project Consortium, 2010) and NHLBI ESP Exome Variant Server (http://evs.gs.washington.edu/EVS/) exome repositories, nor where they detected in 180 exomes available via the UK10K project (uk10k.org). Genotyping of all available members of the affected families carrying CCDC39/40 mutations showed that all the identified variants segregated correctly in association with disease status, having an autosomal recessive inheritance pattern. Of the 37 families carrying CCDC39/40 mutations, segregation was possible for 26 families, the other 11 families being represented by single affected patients (Figs. 1A, B and Supp. Fig. S1). Thus, in this study just 17/54 families did not carry CCDC39 and CCDC40 variants, so these two genes accounted for 69% (37/54) of families.
The clinical details for the affected families are shown in Supp. Table S2. In all patients with either CCDC39 or CCDC40 mutations, TEM of respiratory bronchial epithelial cells showed similar microtubule disorganisation comprising disorganisation of the peripheral microtubule doublets, absent or shifted central pairs. In all samples there was a documented reduction or complete loss of the inner dynein arms. Therefore, the CCDC39 and CCDC40 mutations cause defects that are indistinguishable by TEM.
A detailed clinical review was performed for six CCDC39 and three CCDC40 patients under the care of the Royal Brompton Hospital London that were part of the UCL-ICH cohort, then compared to findings on the UNC cohort of 20 patients. Their nasal nitric oxide levels were low in both cohorts at 45-79 ppb and 6-34 nl/min respectively, as expected for PCD patients where the normal mean level is 639 ppb (range 422-890) (Shoemark and Wilson, 2009). TEM of at least 30 cilia cross sections was examined in UCL-ICH patients which revealed disarrangement of the outer microtubular doublets in 43% (CCDC39) and 36% (CCDC40) of cilia cross sections, mainly involving translocation of peripheral microtubular doublets and acentric microtubular central pairs (Fig. 1Cb–d). Other less prominent features included additional central microtubules or absence of the central pair structures (Fig. 1Cc–e). Inner dynein arms were absent from 69% (CCDC39) and 90% (CCDC40) of cilia cross sections (Fig 1Cb–e). The outer dynein arm was apparent throughout. In one subject with CCDC40 mutations a fallopian tube biopsy revealed similar abnormalities (Fig. 1Ce). The UNC study found similar results in TEM of at least 30 cilia cross-sections from CCDC39/40 patients, with 26% of cilia on average showing microtubule disorganisation and 92% showing IDAs lost on average, and outer dynein arms present in all. High speed video analysis of ciliated nasal brush biopsies of UCL-ICH patients with CCDC39 mutations showed the majority of cilia to be static at 37°C (~ 75%), and also at 25°C in UNC CCDC39/40 patients. In patches where movement was present, the CCDC39 mutant cilia beat pattern was typically stiff, rigid and ineffective (Supp. Movie. S1, S2). This was indistinguishable from CCDC40 (Supp. Movie S3). A control sample is shown in Supp. Movie S4. In cilia which demonstrated motility there were a wide range of ciliary beat frequencies (range 3.3-13.0 Hz). Mean 37°C CBF was 8.1Hz in CCDC39 patients and 9.2Hz in CCDC40 patients, where the normal range is 11-16 Hz. In UNC CCDC39/40 patients the mean 25°C CBF was reduced to 4.3Hz from the normal mean value of 7.3Hz. In three CCDC39 and one CCDC40 patients, sperm dysmotility was also recorded (data not shown).
We used a number of protein modelling tools to identify the location of CCDC39 and CCDC40 mutations identified in this study, and those previously published, in relation to putative protein functional domains. CCDC39 has 941 residues and 10 predicted coiled-coils, in agreement with previous structural modelling (Merveille et al., 2011), and CCDC40 has 1142 residues and 8 predicted coiled-coils (Fig. 2A, B). Both proteins contain two large Structural Maintenance of Chromosomes (SMC) conserved domains which, as previously discussed, are found in several ciliary proteins and likely play a role in microtubule-based ciliary transport processes (Merveille et al., 2011). A conserved BRE1 domain (Kim et al., 2005) was identified in CCDC40, but the significance is not clear. STRING predicted interactions between CCDC39 and protein phosphatase 1 F-actin cytoskeleton targeting subunit (phostensin), an actin filament-binding protein that can modulate actin dynamics that has not been connected with cilia functions (Lai et al., 2009); and between CCDC40 and MCTP1, a membrane protein with putative calcium mediated signalling functions (Shin et al., 2005).
Of the 25 mutations reported here, 19 are novel to this study. Fig. 2 shows the location of the identified mutations in both genes and encoded CCDC39 and CCDC40 proteins. All the identified mutations predict premature protein truncation via nonsense (5/12 and 5/13 for CCDC39 and CCDC40 respectively) and frameshift effects, the latter either arising from small indels within the coding sequence (5/12 and 6/13 respectively), or from single base substitutions of the essential splice site residues at the immediate exon-intron boundaries (2/12 and 2/13, respectively). All these variants are likely to give rise to null alleles via nonsense-mediated decay, indicating that the inner dynein arm and microtubule disorganisation phenotype arises from complete loss of these proteins and consequent loss-of-function. This supports the published evidence that mutations in CCDC39 and CCDC40 have a similar functional effect in being highly deleterious (Merveille et al., 2011; Becker-Heck et al., 2011). No particular clustering of mutations is evident since in both proteins the changes that we have identified, and previously published mutations, are evenly distributed across the gene and protein structure. This suggests that protein termination at any point leads to the same deleterious dysfunction.
This study identified six mutations that have already been reported: a CCDC39 splice site mutation c.357+1G>C (Merveille et al., 2011) and the CCDC40 frameshift mutations c.248delC and c.3129delC; and nonsense mutations c.2440C>T, c.961C>T and c.1345C>T (Becker-Heck et al., 2011; Nakhleh et al., 2012). All of these mutations are only present in patients from families of Northern European descent, except for CCDC39 c.357+1G>C which was reported in 1 Turkish and 3 Northern European families previously. In addition, two mutations that are novel to this study were shared amongst different families within our cohort: a CCDC39 frameshift mutation c.526_527delCT was common to both a UK and a Zimbabwean origin family, and a CCDC40 splice site mutation c.2712-1G>T was shared in two UK and one US families.
We found that the CCDC40 frameshift mutation c.248delC is extremely common, and is restricted to families of N. European origin spread worldwide, suggesting an ancient shared ancestry and past Founder effect mutation occurrence. c.248delC accounts for 34/56 N.European ancestry disease chromosomes in CCDC40 disease, a remarkable 63% (Table 1). It is not known whether the other smaller putative ‘hotspot’ mutations may also represent Caucasian N. European-origin Founder effect mutations, or whether they are functionally significant changes that have occurred separately many times in different countries. Despite the fact that only five out of the total 37 CCDC39/40 families carrying mutations were consanguineous, there was an overall predominance of homozygous changes amongst the families, with 27/37 (73%) of CCDC39/40 families carrying homozygous changes due to identical alleles being inherited from both parents. The Turkish-origin in one family for CCDC39 c.357+1G>C (Merveille et al., 2011) and Zimbabwean origin in one family for CCDC39 c.526_527delCT indicates a more complex evolution of these common mutations than a N. European Founder effect, and the possibility of Non-Founder mutation hotspots. However, firm conclusions are precluded by the small family numbers. It should be noted that although the family UCL210 carrying a homozygous nonsense mutation in CCDC40, c.2245G>T, was not aware of familial consanguinity, they orginate from a small Punjabi-speaking isolate located in Afghanistan likely to have underlying ancestral endogamy and consanguinity.
The ciliary ultrastructure of patients with CCDC39 and CCDC40 mutations has been referred to as ‘radial spoke defect’, and several reports have suggested that radial spokes are defective (Sturgess et al., 1979; Antonelli et al., 1981; Merveille et al., 2011; Becker-Heck et al., 2011). We sought to investigate radial spoke structures in the patients at the molecular level, by high-resolution immunofluorescence analysis of nasal epithelial cells. In one CCDC40 mutation patient 114 II:1, we confirmed an absence of the CCDC39 protein along the length of the axoneme in all cilia analysed in this patient (Figs. 3A, B). These findings are consistent with published information reporting the loss of CCDC39 from axonemes of CCDC40 mutant cilia. However, both RSPH4A which is a radial spoke ‘head’ component (Yang et al., 2006) and ROPN1L/RSP11 which is a radial spoke ‘stalk’ component (Yang et al., 2006; O’Toole et al., 2012) were present in axonemes from the patient as well as controls, with no differences in protein levels observable (Figs. 3C, D and Supp. Fig. S2). This shows for the first time that components of the radial spoke structures are present in axonemes of patients that have long been typically referred to as ‘radial spoke defect’. These data do not however prove that these radial spoke proteins are properly localized in the cilia superstructure, thus they may be present but not functioning correctly.
This study shows that CCDC39 and CCDC40 mutations are the major cause of PCD in patients with the previously termed ‘radial spoke defect’, which is characterised by a ciliary axonemal loss of inner dynein arms and axonemal disorganisation. We report the identification of 25 different allelic mutations in CCDC39 and CCDC40 affecting a total of 46 PCD patients in 37 families. Nineteen of the mutations are novel to this study, while six are shared with patients in three previously published reports (Merveille et al., 2011; Becker-Heck et al., 2011; Nakhleh et al., 2012). A report of additional mutations not referred to here was also published during preparation of this manuscript (Blanchon et al., 2012). In our cohort, two of the novel mutations are found in more than one family across different population origins. Therefore in our patients and also in those reported elsewhere, there are putative common or ‘hotspot’ mutations for both genes; specifically c.357+1G>C and c.526_527delCT in CCDC39, and c.248delC, c.3129delC, c.2440C>T, c.961C>T, c.1345C>T and c.2712-1G>T in CCDC40. The c.248delC mutation is very common, affecting 18/28 CCDC40 families (64%) in this study, in particular US-origin families. The total number of different alleles in CCDC39/40 is smaller than might be expected from the outbred populations we have analysed. This collective evidence is rather unusual for PCD disease and supports the idea that critical regions or important functional residues within the two proteins may be repeatedly vulnerable to mutation arising separately within different populations, probably combined with some localised Founder effects.
Mutations in either gene give rise to the same ciliary and clinical phenotypes, and ciliary defects that are indistinguishable using current methodologies of TEM and high-speed video microscopy. Our TEM and cilia dysmotility findings are consistent with published findings for CCDC39 and CCDC40 mutation (Merveille et al., 2011; Becker-Heck et al., 2011). Therefore, mutations in these genes give rise to analogous defects, which is consistent with similarities in their protein architecture, axonemal localisation, and putative biological role(s). The large number of patients within the ‘radial spoke defect’ subtype of PCD that carry mutations in CCDC39/40 is striking given the extensive underlying genetic heterogeneity in PCD.
Notably, all CCDC39/40 mutations give rise to null alleles, due to nonsense, frameshift or conserved splice site effects. This suggests that complete loss of protein is required to give the characteristic ultrastructural defects, and individuals carrying ‘milder’ effect alleles would likely not express a PCD-like disease phenotype, although this might affect disease severity of other airway diseases. This is in direct contrast with other ciliopathy disorders (affecting non-motile primary cilia) where missense mutations predominantly confer disease, and it is reported that two null alleles are never seen in patients because they affect development so severely that they are incompatible with embryonic survival (Dagoneau et al., 2009; Beales et al., 2007; Davis et al., 2011; Schmidts et al., 2012). An intriguing alternative hypothesis is that CCDC39/CCDC40 missense mutations are not observed because they may be more deleterious than loss of function mutations, rather than less deleterious, and are thus selected against in the surviving clinical patient population. This model is also plausible, for example, if CCDC39/CCDC40 were to orchestrate cilia assembly in multiprotein complexes, such that loss of function mutations could be better tolerated than gain-of-function missense mutations.
Combining our data with that of the three previous reports, a total of 26 mutations in CCDC39 and 21 mutations in CCDC40 have been identified, all encoding predicted null alleles. In N-DRC Chlamydomonas null-mutant strains, loss of any one of the N-DRC components gives rise to complete loss of the entire N-DRC structure (Piperno et al., 1994). CCDC39 and CCDC40 mutation patients also lack at least some of the N-DRC structure, and this also appears to be associated with mutations causing complete loss of protein.
The predicted loss-of-function reported for all CCDC39 and CCDC40 mutations correlates with the widespread distribution of mutations across both genes, without any evidence of clustering. We expect that all mutations identified in these two genes would make the protein subject to nonsense mediated decay; however, both proteins contain multiple functionally important domains that are highly evolutionarily conserved across species and likely critical to function. The possible role of the BRE1 domain in CCDC40 is less clear, but the large SMC domains in both proteins are thought to be involved in microtubule transporting (Merveille et al., 2011). Both proteins have multiple coiled-coil domains, which leads to a compositional bias of charged and hydrophobic residues containing many lysine, leucine and glutamic acid residues which are generally located at the ‘surface’ of the coiled-coil domains involved in conferring solubility and interaction properties. The 10 nonsense mutations identified in this study mostly affect glutamic acid or arginine residues, mostly in coiled-coil domains; however, their codon composition makes these residues prone to nonsense mutations, rather than indicating specific functional importance at those residues. Coiled-coil domains are found in many different proteins with diverse functions (Strauss and Keller, 2008), including structural and motor proteins. They are also associated with signal transduction functions, and assembly/disassembly of protein complexes, which may relate to the inner dynein arm-N-DRC-radial spoke complexes of cilia. If the stability provided by multiple coiled-coils is mutated, this may result in reduced efficiency or loss of protein function. Alternatively, some motor proteins have intrinsic instability in the coiled-coil domains to allow the relaxing of tertiary structure and movement of the motor proteins, which could be important in the cilia.
In contrast with N-DRC components, components of the radial spokes, such as the spoke ‘head’ protein RSPH4A and spoke ‘stalk’ protein ROPN1L, are present in CCDC40 mutant axonemes. This provides the first evidence that the ultrastructural defect in patients with CCDC39 /CCDC40 mutations, commonly referred to as ‘radial spoke defect’, may not reflect a loss of spokes, but proves supporting evidence that they may remain largely intact. We have not been able to exclude the possibility that radial spoke components may be present, but mislocalised, misattached, incomplete or non-functional for other reasons. However, we can conclude that this defect may be more accurately referred to as ‘IDA and N-DRC defect’, rather than ‘radial spoke defect’.
It is not yet clear how this ciliary ultrastructural defect arises, because little is known about the formation and co-assembly of the human inner dynein arms, radial spokes and N-DRC structures, which are all attached in close proximity at the peripheral doublets. These components are all positioned at regular periodicity along the entire axoneme length, and form a sophisticated regulatory network governing dynein activity that is key to cilia motility. The loss of IDAs and N-DRC complexes together in CCDC39 and CCDC40 mutant axonemes is consistent with the role that the N-DRC plays in tethering of IDA components, as shown in Chlamydomonas. The resultant disorganisation of the peripheral microtubules and the resultant instability of the central pair apparatus, indicates that these structures are critical for integrity and motility of the axoneme. Studies of Chlamydomonas motility mutant strains suggest the N-DRC has a number of roles apart from binding of the inner dynein arms to the peripheral microtubules, which includes mediating signalling from the central pair-radial spoke complex to the dynein arms, and influencing dynein-controlled axonemal bending (Piperno et al., 1994; Lin et al., 2011; Lin et al., 2011). Thus, a deficiency in these regulatory mechanisms could also explain the defect. In contrast, even though the radial spokes are located close to the IDA-N-DRC components of axonemes, they may not be directly involved in the dysmotility in CCDC39 and CCDC40 mutation patients, but are bystanders that are perturbed secondarily to microtubule disorganisation.
The IDA-N-DRC defect accounts for at least 12% of PCD cases, and the great majority of these are caused by mutations in CCDC39 and CCDC40 (69% in this study). Mutations in these genes may have an specially increased prevalence within the isolated and consanguineous Afghanistan-Punjabi and UK-based Pakistani populations. The high prevalence of these two genes, together, as causative for this subtype of PCD, makes these results significant for clinical application, including the development of prenatal and carrier genetic tests in at-risk families, and for development of genetic therapeutic strategies.
We would like to thank all the PCD patients and families, Michele Manion and the U.S. PCD Foundation, Fiona Copeland and the U.K. PCD Family Support Group. We thank Angelina Heer, Carmen Kopp, Denise Nergenau and Karin Sutter for excellent technical assistance. This work was supported by the Kindness for Kids Foundation, grants from the European Community (SYS-CILIA) and donation from the “Schröder-Stiftung” for HO. We thank Drs. John Carson, Milan Hazucha, Hilda Metjian, Stephanie Davis, Ms. Susan Minnix, Ms. Kimberly Burns, Peter Noone, Christine Olson, and Lu Huang from UNC Chapel Hill; Consortium PIs, Drs. Sharon Dell, Carlos Milla and Ken Olivier, and all the coordinators for the “Genetics Disorders of Mucociliary Clearance Consortium (GDMCC) that is part of the Rare Disease Clinical Research Network (http://rarediseasenetwork.epi.usf.edu/gdmcc/index.htm). We thank Robert Mueller, Yannick Crow, Astrid Weber, Maggie Meeks, Rahul Chodhari and R. Mark Gardiner for patient recruitment and their involvement in the project. We thank Mellisa Dixon and Sarah Donovan for electron and light microscopy at Royal Brompton Hospital. MRK, MWL, TWF, SDS, MR and MAZ are supported by National Institute of Health research grant 5 U54 HL096458-06, funded by the Office of the Director, and supported by ORDR and NHLBI, NIH. MRK and MAZ are supported by National Institute of Health grant 5 R01HL071798. This work was supported in part by grant ULI TR000083 from the National Center of Research Resources. This publication was made possible by grant 5 U54 HL096458-06 from National Center for Research Resources (NCRR), a component of National Institute of Health (NIH). Its contents are solely the responsibility of the authors and do not necessarily represent the official view of NCRR or NIH. We thank all the participants of the UK10K RARE group, as listed in the Supporting Information file, that is part of the UK10K Consortium (uk10k.org.uk) in particular Matthew Hurles, Saeed Al Turki and Philip Beales. Funding for UK10K was provided by the Wellcome Trust under award WT091310. DA, MS, AO, EMKC and HMM are funded by Action Medical Research and Newlife Foundation. DA is supported by The Henry Smith Charity.
The authors have no conflicts of interest to declare.
Supporting Information for this preprint is available from the Human Mutation editorial office upon request (humu/at/wiley.com)