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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
Nat Genet. Author manuscript; available in PMC 2012 December 1.
Published in final edited form as:
PMCID: PMC3371652

CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms


Cilia are essential for fertilization, respiratory clearance, cerebrospinal fluid circulation, and to establish laterality1. Cilia motility defects cause Primary Ciliary Dyskinesia (PCD, MIM 242650), a disorder affecting 1:15-30,000 births. Cilia motility requires the assembly of multisubunit dynein arms that drive cilia bending2. Despite progress in understanding the genetic basis of PCD, mutations remain to be identified for several PCD linked loci3. Here we show that the zebrafish cilia paralysis mutant schmalhanstn222 (smh) mutant encodes the coiled-coil domain containing 103 protein (Ccdc103), a foxj1a regulated gene. Screening 146 unrelated PCD families identified patients in six families with reduced outer dynein arms, carrying mutations in CCDC103. Dynein arm assembly in smh mutant zebrafish was rescued by wild-type but not mutant human CCDC103. Chlamydomonas Ccdc103 functions as a tightly bound, axoneme-associated protein. The results identify Ccdc103 as a novel dynein arm attachment factor that when mutated causes Primary Ciliary Dyskinesia.

Zebrafish schmalhans (smhtn222) mutants4 exhibit curved body axis, randomized left-right asymmetry, and pronephric kidney cysts (figure 1A-B and Supplementary Table 1), characteristic features of ciliopathy5. Electron microscopy of smhtn222 cilia revealed that compared to wildtype cilia (figure 1C), schmalhans mutant cilia completely lacked inner and outer dynein arms (figure 1D and Supplementary figure 1), while cilia length was not altered (Supplementary figure 2). High-speed microvideo and linescan analysis of wildtype zebrafish pronephric cilia (figure 1E; Supplementary Movie 1) or olfactory placode multicilia (Supplementary figure 3; Supplementary Movie 2) revealed rhythmic cilia motility. However, consistent with dynein arm defects, schmalhans mutant cilia were completely paralyzed in the pronephros (figure 1F; Supplementary Movie 3), the olfactory placode (Supplementary figure 3 B,D; Supplementary Movie 4), and in the spinal canal (Supplementary movies 5 and 6). The schmalhans tn222 mutation was mapped to a ~2Mb region of Chromosome 3 and subsequently fine mapped to a 0.43Mb region containing 8 genes (Supplementary figure 4 and Supplementary Tables 2 and 3). Sequencing candidate genes in this interval revealed a C>T mutation at nucleotide 79 in exon 1 of zgc:100838 (ccdc103), generating a predicted Q>Stop at amino acid 27 of the 247 amino acid protein (Dr-Q27Stop) (Figure 1G,H). Embryo injection of myc-tagged wild-type ccdc103 mRNA rescued axis curvature, left-right asymmetry defects, and kidney cyst phenotypes, and also restored cilia motility in smh mutants (figure 1I,J; Supplementary Movie 7 and data not shown), confirming that ccdc103 was the schmalhans mutant gene. Mutant Ccdc103 mRNA carrying the Q27Stop smh mutation not only failed to rescue but also increased the frequency of axis curvature defects, suggesting it may act as a dominant-negative (figure 1K). Antisense morpholino knockdown of ccdc103 induced curved body axes, left-right asymmetry defects, hydrocephalus, and kidney cysts (Supplementary figure 5 A,B and Supplementary Table 4), and caused cilia paralysis (Supplementary Movie 8), phenocopying schmalhans. Together, these data identify ccdc103 as an essential gene for dynein arm assembly and cilia motility.

Figure 1
The schmalhans mutation causes cilia paralysis and absent dynein arms

Whole genome linkage analysis in a group of four consanguineous Pakistani PCD families from a UK-based genetic isolate6 with absent inner and outer dynein arms revealed a novel PCD locus on chromosome 17q12-q22 containing the human ccdc103 ortholog, CCDC103. The maximum HLOD score was 4.8 with an α value (proportion of linked families) of 1. The critical genetic interval spanned 14 cM (16 Mb) between SNP markers rs1859212 and rs2045418 (Supplementary figure 6). Screening affected individuals of the Pakistani PCD families as well as nine other Pakistani patients with identified linkage to CCDC103 and 132 unrelated PCD families (54% ODA defects; 47% functional or other structural PCD defects) for mutations in CCDC103 identified ten PCD patients carrying DNA exchanges in the CCDC103 (NM_213607) coding sequence (figure 2, Supplementary figure 7,8). We found homozygous loss-of-function mutations in three chromosome 17-linked Pakistani families (UCL120, OP-1192 and OP-1193) with six affected individuals (c.383_384insG) predicting a frame shift and premature termination of translation (p.Gly128fs25*) (figure 2, Supplementary figure 7). The three families originate from nearby regions in Pakistan making it very likely that the mutations result from a common founder (ancestor). The consanguineous parents of family UCL120 and OP-1193 were heterozygous for this truncating mutation (figure 2), consistent with autosomal recessive inheritance and homozygosity by descent. In two other chromosome 17-linked Pakistani families (Supplementary figure 8; UCL143 and OP-1194) and a German family (Supplementary figure 8; OP-32), we identified in all four affected individuals (OP-31II1, OP-31II2, UCL-143II1; OP-1194II1) a homozygous transversion (c.A461C) that converts a histidine to a proline at amino acid 154 (p.His154Pro) that co-segregated with the disease phenotype (Supplementary figure 8). Multiple sequence alignment (Supplementary figure 9) showed that the p.His154Pro exchange occurred in a region flanking a highly conserved domain of Ccdc103. Polyphen-2 software analysis generated a protein damage score of 0.972 for this mutation, highly suggestive of pathogenic significance. The c.A461C variant was absent in 180 Caucasian controls as well as in the dbSNP, 1000 Genomes Project and NHLBI-ESP human polymorphism databases. Eight other UK-Pakistani families compatible with linkage to the CCDC103 locus (Supplementary figure 6 for UCL130, UCL145) did not carry mutations in CCDC103 coding sequences. In one other family, an affected child carried a heterozygous transversion (c.G31C) predicting an alanine to proline change (p.Ala11Pro) with no mutation on the other allele.

Figure 2
Pedigrees of families carrying CCDC103 loss of function mutations

All six affected individuals carrying recessive truncating CCDC103 mutations exhibited typical clinical findings for PCD (Supplementary Table 5) comprising recurrent upper and lower airway infections, sinusitis and documented lung damage (bronchiectasis), and two affected displayed dextrocardia and one situs inversus. In four other PCD affected individuals we identified homozygous amino-acid exchange p.His154Pro. Two patients had situs inversus totalis, one had situs inversus abdominalis, one dextrocardia and one exhibited normal organ situs. Our findings indicate that CCDC103 mutations cause PCD and randomization of left/right body asymmetry resembling findings in smh mutant zebrafish.

To test the pathogenic significance of the identified CCDC103 variants (figure 3A), we assayed their function in zebrafish smh mRNA rescue experiments. Injection of myc-tagged wildtype human CCDC103 mRNA completely rescued the smh mutant phenotype (Figure 3B,C). mRNA encoding the CCDC103 Hs-Ala11Pro variant also completely rescued the smh mutant phenotype (Figure 3B,C) confirming that the heterozygous p.Ala11Pro variant observed in one PCD individual represents a rare, nonpathogenic polymorphism. mRNAs encoding the p.His154Pro and p.Gly128fs25* variants failed to fully rescue the smh axis curvature or cilia motility phenotypes, indicating that these mutations are pathogenic (Figure 3B,C; Supplementary Table 6,7). Notably, expression of CCDC103 p.His154Pro partially rescued the smh body axis curvature; 13 of 27 Hs-His154Pro mRNA-injected, homozygous mutants by genotype displayed a mild “bent” phenotype and lacked full curvature (Figure 3B, Supplementary Table 6), indicating that the Hs-His154Pro variant may represent a hypomorphic mutation. Wildtype epitope-tagged CCDC103 protein migrated as a monomer and dimer in denaturing SDS gels with a major band at approximately 56 KD and a minor band at 27.6 KD (Figure 3D), the predicted size of the CCDC103 monomer. While the mRNA encoding the rescuing CCDC103 p.Ala11Pro protein (M2; figure 3D) was expressed similarly to wildtype, mutant CCDC103 proteins that failed to rescue smh embryos were unstable in vivo and did not generate significant amounts of protein (p.His154Pro; M1 and p.Gly128fs25*; M3, figure 3D) even when injected at ten-fold higher doses (350 pg; data not shown). Consistent with its ability to rescue smh mutant phenotypes, wild-type human CCDC103 mRNA also restored dynein arms to genotypically mutant axonemes (figure 3E).

Figure 3
Functional assay of human CCDC103 mutant alleles in smh embryos

Defects in ODA composition in human axonemes were analysed by immunofluorescence microscopy of respiratory cells. Cells of patient OP-1192II1 carrying the homozygous p.Gly128fs25* loss-of-function mutation demonstrated partial loss of ODA complexes along the ciliary axonemes (Figure 4A–C) with some proximally localized type 1 ODA complexcomponents DNAH5 and DNAI2 still present in the ciliary axonemes. In contrast, DNAH5 and DNAI2 were absent from the distal ciliary axonemes with DNAH5 accumulating in the perinuclear and apical cytoplasm (figure 4A). This is consistent with absence of distally localized type-2 ODA complexes, which we confirmed by absence of DNAH9 from the ciliary axonemes in mutant cilia (figure 4C). This defect is very similar to findings obtained in patients carrying mutations in the dynein arm assembly factor KTU7. In addition we analyzed respiratory cells from the PCD patient OP-1194II1 carrying the homozygous hypomorphic p.His154Pro variant. The mutant cells displayed a normal localization of DNAH5, DNAI2 and DNAH9 (data not shown). Interestingly, both patients showed normal localization of the IDA component DNALI1 (data not shown), thus at least parts of IDA components can be assembled in the ciliary axoneme. TEM analysis of all three affected individuals of the UCL-120 family harboring the homozygous CCDC103 p.Gly128fs25* loss-of-function mutation showed either loss or strong reduction in outer dynein arms (shown for UCL-120II2 and UCL-120II3; figure 4D), similar to the smh mutant phenotype (figure 1D). Variation in the degree of the ODA defects in the three affected UCL-120 siblings (figure 4D) may reflect the position (proximal vs. distal) of the cilia cross section since some proximal ODA components can persist in CCDC103 p.Gly128fs25* mutant cilia (figure 4A,B). The effects of CCDC103 mutations were further analysed by high-speed videomicroscopy of respiratory cells obtained by nasal brushing biopsy. Normal respiratory cell cilia beat vigorously and coordinately (Supplementary Movie 9). Consistent with severe outer dynein arm defects observed by EM (figure 4D), patients carrying the homozygous p.Gly128fs25* mutation (OP-1193 II1) exhibited complete cilia paralysis (Supplementary Movie 10). Patients carrying the homozygous p.His154Pro mutation exhibited either reduced cilia beat amplitude (patient OP-32II1; Supplementary Movie 11) or loss of beat coordination and cilia paralysis (patient OP-32II2; Supplementary Movie 12; compare with control Supplementary Movie 13), consistent with the variable reduction in EM ODA arm structure in these patients which ranged from apparently normal to complete ODA/IDA loss (patient UCL-143II1; Supplementary figure 10). The less severe phenotype seen in affected children of family OP-32 is consistent with our CCDC103 functional assays in zebrafish that identified the p.His154Pro exchange as a hypomorphic mutation. The variable phenotype observed within the UCL-120 family and among affected children of different families harboring identical mutations (UCL-143; OP-32) may suggest modulation of the phenotype by genetic modifiers frequently observed in ciliopathies8.

Figure 4
Localization of DNAH5, DNAI2 and DNAH9 in respiratory epithelial cells from a PCD patient carrying the CCDC103 loss-of-function mutation

ccdc103 mRNA was highly expressed in all zebrafish cells bearing motile cilia (Supplementary figure 11) and was not expressed in foxj1a-deficient embryos (Supplementary figure 11), indicating that ccdc103 expression is controlled coordinately with foxj1 motile cilia target genes9. Ccdc103 protein was expressed both in the cytoplasm and axonemes of zebrafish olfactory placode cells (figure 5A); Ccdc103 staining was not observed in smh morpholino knockdown embryos (Supplementary figure 12). To gain insight into the function of Ccdc103 in dynein arm assembly we examined the Chlamydomonas ccdc103 ortholog, Pr46b (Supplementary figure 9). Like zebrafish Ccdc103, Pr46b protein was present in both flagella and cytoplasmic extracts and migrated as apparent monomers and dimers on SDS gels (figure 5B,C), similar to protein expressed in zebrafish embryos (figure 3G). In isolated flagella, Ccdc103/Pr46b was tightly associated with axonemes even after 0.6 M NaCl extraction (figure 5B). Fractionation of Chlamydomonas cytoplasm (Figure 5C) identified Ccdc103/Pr46b in high molecular weight complexes (440 KD - 2 MD) that co-purified with outer arm dynein light chain LC2, as well as in lower molecular weight complexes (<440,000 Da). Analysis of human CCDC103 expression in respiratory epithelial cells confirmed that CCDC103 is present as apparent monomers and dimers (Supplementary figure 13 B,C). The remarkable stability of putative dimeric forms of Ccdc103 protein in heat-denatured, SDS gel samples prompted us to further examine the properties of recombinant Ccdc103/Pr46b protein. Circular dichroism spectroscopic analysis of Ccdc103/Pr46b revealed a high alpha helical content, and thermal titration (temperature range 4–85° C) showed that Ccdc103 was remarkably thermo-stable since it was not fully denatured even at 85° C (figure 5D). Furthermore, the helical content of ccdc103/Pr46b was not diminished by addition of 1% SDS and heating at 100° C for 2.5 minutes (Supplementary figure 14). Gel filtration of purified Ccdc103/Pr46b protein revealed peaks corresponding to a mixture of monomeric and dimeric forms of Ccdc103/Pr46b (figure 5E, Supplementary figure 15), confirming that Ccdc103 can homodimerize. Thus, the stability of Ccdc103 dimers during SDS gel electrophoresis is due to the extraordinary thermal tolerance of the protein. We noted previously that over-expression of smh mutant Q27Stop Ccdc103 protein containing part of the N-terminal coiled-coil domain could have dominant effects in zebrafish embryos and induce ciliopathy phenotypes (figure 1K). To test whether smh mutant Ccdc103 might exert these effects by interfering with wild-type Ccdc103 dimer formation, full-length myc-tagged Ccdc103 and smh N-terminal Q27Stop mRNAs were co-expressed in zebrafish embryos. Increasing amounts of N-terminal Q27Stop Ccdc103 reduced the Ccdc103 dimer : monomer ratio (figure 5F), linking Ccdc103 function to homodimer formation. Finally, Ccdc103/Pr46b protein remained stably associated with axonemes in mutants lacking other dynein arm components including ODA docking complex proteins (Supplementary figure 16). This, along with its stable association with axonemes in high salt (figure 5B) distinquishes Ccdc103 from the docking complex proteins1012 and indicates it is a core factor for dynein arm binding to cilia microtubules. Taken together, our findings demonstrate an essential role for Ccdc103 as a novel coiled-coil containing, foxj1a-regulated dynein arm anchoring factor required for cilia motility. Although the patient families examined in this work showed typical recessive PCD, ciliopathy induced by over expression of the ccdc103/schmalhans mutant protein raises the possibility that dominant mutations could also contribute PCD. Future studies should reveal how Ccdc103 assembles with other ODA proteins1012 to ultimately anchor dynein motor complexes to cilia microtubules.

Figure 5
Ccdc103 homodimers assemble with dynein light chain 2 in the cytoplasm and bind tightly to cilia axonemes


Zebrafish maintenance, embryo generation, and staging

Wild-type (WT) zebrafish of AB, TUAB, TL, and hybrid strains were maintained as previously described13. Embryos were obtained from natural matings, kept at 28.5°C in E3 solution with or without 0.003% 1-Phenyl-2-thiourea (PTU, Sigma) to suppress pigmentation, and staged according to morphology and/or age, as indicated14.

Positional cloning of the mutant locus

A genomic DNA panel was isolated from 1200 homozygous mutant zebrafish embryos of a heterozygous mating, along with genomic DNA from siblings, using Lysis buffer (10mM Tris-Cl, pH 8.3, 50 mM KCl, 0.3% Tween20, 0.3% Nonidet P40, 0.5 μg/μl Proteinase K). SSRP analysis was conducted by PCR amplification of markers followed by 6% polyacrylamide gel electrophoresis and staining with SYBR gold in 0.5xTBE. Zebrafish SNPs were identified using Ensembl browser, then PCR amplified and sequenced (Massachusetts General Hospital DNA Core).

Cloning of ccdc103

Total RNA was isolated from 48-hour WT zebrafish embryos with TRIzol Reagent (Invitrogen), and used to produce cDNA via Superscript First-Strand Synthesis (Invitrogen). Using zf-ccdc103 RT primers (Supplementary Table 2), zebrafish ccdc103 was PCR-amplified with Platinum Pfx DNA Polymerase (Invitrogen) to incorporate Gateway cloning sites. The complete coding sequence was cloned into pDONR221 (Invitrogen), then pCS2+ vector15 modified for Gateway cloning and verified by sequencing. N-terminal tagged ccdc103 constructs were made by subcloning into Gateway-myc-pCS2+ (gift from Dr. N. Lawson, U. Mass, Worcester). Human CCDC103 was cloned in the same manner, except it was PCR-amplified from Open Biosystems clone 5455678 (Genbank BC041060) using h-CCDC103 RT primers (Supplementary Table 2). The zebrafish ccdc103 full-length wild-type gene coding sequence reported in this paper corresponds to the existing GenBank record NM_001002753.

For genotyping embryos, genomic DNA was isolated as described above with Lysis buffer, then a 436 bp fragment spanning the mutation point was PCR amplified with smh genotyping primers (Supplementary Table 2). The fragment was digested with BfaI (New England Biolabs, NEB), a restriction site introduced by the smh mutation. Mutant DNA was cut into fragments of 351 and 85 bp, which were separated by agarose gel electrophoresis. When necessary, these results were verified by DNA sequencing.

In situ hybridization

Sense and antisense probes for ccdc103 were made from a pCRII construct of 1329 bp containing some 3' UTR sequence made by TOPO-TA cloning (Invitrogen) after amplification from cDNA with zf-ccdc103 in situ primers (Supplementary Table 2). Probes were synthesized with digoxigenin NTPs (Roche) after template linearization with BamHI (sense) or XbaI (anti-sense) before RNA synthesis with T7 or SP6 RNA polymerases, respectively. Embryos were fixed at the indicated stages and processed essentially as previously-described16. Antisense probes for cardiac myosin light chain 2 (myl7)17, preproinsulin (ins)18, foxa319, and pitx220, were prepared as described previously.

RNA and morpholino injections

Capped sense RNA encoding Ccdc103 was synthesized with SP6 RNA polymerase (Ambion mMessage mMachine) after linearization of pCS2-ccdc103 with NotI. RNA was purified using G-50 Sephadex Quick Spin Columns (Roche) and diluted to the indicated concentrations with tissue culture grade distilled water. Microinjections were performed on 1–4 cell embryos using a Nanoliter 2000 (World Precision Instruments, Inc.)

A translation-blocking morpholino oligonucleotide (MO), MOAUG (Supplementary Table 2; Gene-Tools, LLC) targeted to the 5’-UTR, and a splice-blocking MO, MOSPL (Supplementary Table 2; Gene-Tools, LLC) targeted to the exon 2/intron 2 boundary were resuspended in DEPC treated water to stock concentrations of 20 μg/μl then further diluted to the given concentrations with DEPC water prior to injection.

foxj1a morpholino injections were performed using a cocktail of splice-and translation-blocking oligonucleotides, as previously described21.

Protein expression and antibody production


Full-length zebrafish Ccdc103 coding region was subcloned and expressed using the Champion pET160 Gateway Expression System (Invitrogen). The protein was purified from cell insoluble fractions after resuspension in 3M NaSCN, then purified using His-Trap HP affinity columns (GE Healthcare) with imidazole gradient elution. Purified protein was dialyzed overnight into PBS, and sent to Rockland Immunochemicals for guinea pig polyclonal antibody production. Antibody was purified separately from serum of two animals by affinity purification on a Ccdc103 column prepared using AminoLink Plus Immobilization Kit (Thermo Scientific).


The 70–267 residue region of Chlamydomonas Ccdc103/Pr46b was obtained by PCR from EST clone AV626473 and subcloned into pMal-c2 vector (NEB). The complete fusion protein was used for production of rabbit antibody CT285 (Covance Immunology Services, Denver, PA). Specific antibody was obtained by blot purification against recombinant Ccdc103/Pr46b (residues 70–267).

Western blotting

Western blotting on embryo extracts was performed as previously described22 using Rabbit anti-c-myc at 1:10000 and Goat anti-rabbit-HRP at 1:5000, or 1:2000 mouse anti-alpha tubulin and 1:4000 goat anti-mouse-HRP.

Immunofluorescence Analysis


Embryos were fixed with Dent's fixative (20%DMSO/80%Methanol) overnight, then washed in phosphate buffered saline plus 0.1%Tween20 (PBST) before incubation in blocking solution (5% Goat serum/5mg/ml bovine serum albumin/2%DMSO). Prior to blocking embryos for anti-zCcdc103 staining, they were incubated in 6M urea/0.1M glycine at 4C for 10 minutes. After blocking, primary antibodies were added in block solution overnight at 4C. Guinea pig anti-zCcdc103 was used at 1:100 dilution, while mouse anti-acetylated tubulin (Sigma) was used at 1:1000. Embryos were washed with PBST then secondary antibodies were added in block solution for 2 hours at room temperature. CY3-conjugated anti-guinea pig secondary antibodies (Jackson ImmunoResearch Laboratories, Inc.) were used at 1:200, while Alex488 or Alexa546 anti-mouse antibodies (Invitrogen) were used at 1:1000. After washing in PBST, embryos were analyzed by confocal microscopy (Zeiss LSM 5 Pascal) using a 63X oil immersion lens. Confocal stacks were deconvolved using Huygens Universal software and rotated to desired position prior to acquiring single frame images.


Respiratory epithelial cells were obtained by nasal brush biopsy (Engelbrecht Medicine and Laboratory Technology, Germany) and suspended in cell culture medium. Samples were spread onto glass slides, air dried and stored at −80°C until use. Cells were treated with 4% paraformaldehyde, 0.2% Triton-X 100 and 1% skim milk prior to incubation with primary (at least 3 hours at room temperature or overnight at 4°C) and secondary antibodies (30 minutes at room temperature) . Controls were performed omitting the primary antibodies. Monoclonal anti-DNALI1 antibody and monoclonal anti-DNAH5 were reported previously7,23. Polyclonal rabbit anti-α/β-tubulin was used from Cell Signaling Technology (USA). Highly cross-adsorbed secondary antibodies (Alexa Fluor 488, Alexa Fluor 546) were obtained from Molecular Probes (Invitrogen). DNA was stained with Hoechst 33342 (Sigma). Confocal images were taken on a Zeiss LSM 510 I-UV.

Patients and families

Signed and informed consent was obtained from patients fulfilling diagnostic criteria of PCD3 and family members using protocols approved by the Institutional Ethics Review Board at the University of Freiburg, University College London Hospital NHS Trust, and collaborating institutions. We studied DNA from a total of 144 PCD patients originating from 141 unrelated families.

Human linkage analysis

For whole genome linkage analysis, family samples were analysed using the Illumina SNP-based Linkage IVb Panel consisting of 6,008 evenly spaced SNPs with an average density of 0.64 cM. Standard parametric multipoint linkage analysis was carried out using MERLIN 1.0.1 software assuming autosomal recessive inheritance, a disease allele frequency of 0.007 and a disease penetrance of 0.9.

Transmission electron microscopy

Zebrafish embryos were prepared for TEM by previously published protocols24. Human biopsies were prepared for TEM as previously reported25.

High-speed video analyses of ciliary beat

Human cells

Ciliary beat was assessed with the SAVA system. Trans nasal brush biopsies were rinsed in cell culture medium and immediately viewed with an Olympus IMT-2 inverted phase-contrast microscope equipped with a Redlake ES-310 Turbo monochrome high-speed video camera (Redlake, San Diego, USA) and a 40x objective. Digital image sampling was performed at 125 frames per second and 640x480 pixel resolution. The ciliary beat pattern was evaluated by slow motion playback (30 fps).


Movies of olfactory, pronephric duct, and spinal canal cilia from 52 hpf embryos were captured at 240 frames per second using a 40X water immersion lens on Nikon Eclipse E800 with DragonFly Express high-speed camera (Point Grey Research, Inc.) and processed as described26 for viewing at 15 fps.

Chlamydomonas Strains

Strains used in this study were obtained from the Chlamydomonas Center and grown as described27.

Chlamydomonas fractionation

Cells were harvested by centrifugation, deflagellated using dibucaine and flagella isolated by standard methods28. Cell bodies were disrupted using an Emusiflex-C3 cell disruptor, clarified by centrifugation and concentrated using an Amicon Ultra 4 ultrafiltration unit (10,000 Da cutoff). Extract was fractionated in a Superose 6 10/300 GL column equilibrated with 20 mM Tris.Cl pH8.0, 0.5 mM EDTA, 5 mM MgSO4, 150 mM NaCl. The column was calibrated with blue dextran (>2×106 Da) and ferritin (440,000 Da), and 0.5 ml fractions were collected. Samples were electrophoresed in 10% SDS polyacrylamide gels and either stained with Coomassie blue or blotted to nitrocellulose and probed with antibody CT285. Immunoreactive bands were detected by chemiluminescence using an ImageQuant LAS4000 digital imaging system.

Recombinant Protein Analysis

Soluble recombinant His10-tagged Ccdc103/Pr46b was purified by nickel chromatography. After removal of the tag by cleavage with Factor Xa, protein was analyzed by gel filtration using Superose 6 and Superdex 200 columns. Circular dichroism spectroscopy was performed using a Jasco J-715 spectropolarimeter.

Supplementary Material


We wish to thank the patients and their families for their participation, and acknowledge support from the PCD Family Support Group (UK) and the German patient support group “Kartagener Syndrom und Primaere Ciliaere Dyskinesie e.V.”. We thank Professor R. Mark Gardiner and Dr Eduardo Moya for their help and involvement in the study. We thank Robert Hirst, Andrew Rutman for electron microscopy. We thank Angelina Heer, Christian Warmt, Denise Nergenau, Ramila S. Patel-King and Li Luo for excellent technical assistance. This work was funded by NIH grants DK053093 (I.A.D), GM051293 (S.M.K.), NRSA fellowship grant F32DK083868 (J.R.P), an American Heart Association Established Investigator Award to A.F.S.; DFG grants (DFG Om 6/4, GRK1109, SFB592), EU-grant SYSCILIA, and kindness for kids grant to H.O. The Medical Research Council UK, the Wellcome Trust and the Fondation Milena Carvajal Pro-Kartagener.


Accession numbers

The zebrafish ccdc103 full-length wild-type gene coding sequence corresponds to GenBank record NM_001002753. Human CCDC103: NM_213607. Chlamydomonas: AV626473.

Author Contributions. Genetic mapping and Ccdc103/CCDC103 characterization in zebrafish were conducted by J.R.P., Y.L., C.A-T., A.G. N.H., A.K.Z., R.B., F.O., A.F.S., N.P. and I.A.D. Studies with patient samples were conducted by A.B.-H.,D.A., N.T.L., E.S., M.S., H.O., C.W., K.H., R.C., C.C., E.M.K.C, R.R., H.M.M. and H.O. Chlamydomonas studies were performed by S.K.. The manuscript was prepared by J.R.P., A.B.-H., S.K., H.O. and I.A.D.

The authors state that they have no competing financial interests.


Polyphen-2 software analysis:


dbSNP human polymorphism database:

1000 Genomes Project human polymorphism database:

NHLBI-ESP human polymorphism database:

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