Background Mutations in microtubule-regulating genes are associated with disorders of neuronal migration and microcephaly. Regulation of centriole length has been shown to underlie the pathogenesis of certain ciliopathy phenotypes. Using a next-generation sequencing approach, we identified mutations in a novel centriolar disease gene in a kindred with an embryonic lethal ciliopathy phenotype and in a patient with primary microcephaly.
Methods and results Whole exome sequencing data from a non-consanguineous Caucasian kindred exhibiting mid-gestation lethality and ciliopathic malformations revealed two novel non-synonymous variants in CENPF, a microtubule-regulating gene. All four affected fetuses showed segregation for two mutated alleles [IVS5-2A>C, predicted to abolish the consensus splice-acceptor site from exon 6; c.1744G>T, p.E582X]. In a second unrelated patient exhibiting microcephaly, we identified two CENPF mutations [c.1744G>T, p.E582X; c.8692 C>T, p.R2898X] by whole exome sequencing. We found that CENP-F colocalised with Ninein at the subdistal appendages of the mother centriole in mouse inner medullary collecting duct cells. Intraflagellar transport protein-88 (IFT-88) colocalised with CENP-F along the ciliary axonemes of renal epithelial cells in age-matched control human fetuses but did not in truncated cilia of mutant CENPF kidneys. Pairwise co-immunoprecipitation assays of mitotic and serum-starved HEKT293 cells confirmed that IFT88 precipitates with endogenous CENP-F.
Conclusions Our data identify CENPF as a new centriolar disease gene implicated in severe human ciliopathy and microcephaly related phenotypes. CENP-F has a novel putative function in ciliogenesis and cortical neurogenesis.
- Clinical genetics
- Molecular genetics
This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Centrioles are microtubule (MT)-derived structures that play an essential role in centrosome and cilia formation.1 Mutations in centrosomal and MT-regulating genes have been described in cancer, disorders of neuronal migration2 ,3 and microcephaly (MCPH) including Majewski osteodysplastic primordial dwarfism type II.4 ,5 Disrupted processes include abnormalities of centriole duplication, centrosome maturation and spindle pole formation6 with defective asymmetric divisions of neuronal progenitors and failure of cortical neurogenesis.7 ,8
Following mitosis, the distal appendages of the mother centriole become the transition fibres of the ciliary basal body.9 Transition fibres promote ciliogenesis by recruiting intraflagellar transport (IFT) proteins which traffic tubulin subunits and other proteins to the ciliary tip.10 Mutations in genes regulating centriole length have recently been described in ciliopathic disorders characterised by heterotaxia, retinal degeneration, skeletal dysplasia, renal disease and cerebral anomalies including microcephaly.11–13 These findings support emerging evidence that certain centriolar protein complexes have dual roles in spindle orientation and ciliogenesis.8 ,14
In the current study, we identify CENPF, the MT-regulating gene, as a new centriolar disease gene implicated in severe human ciliopathy and MCPH-related phenotypes. Our data suggests a novel putative function for CENP-F in ciliogenesis as well as cortical neurogenesis.
In order to determine the genetic basis of a novel congenital malformation disorder and MCPH, we employed a next-generation sequencing approach using whole exome sequencing combined with genome-wide linkage analysis.
Approval for research involving human subjects was obtained from the Institute of Child Health research ethics board, University College London, and the Scottish multicentre research ethics committee.
For genome-wide SNP mapping, the GeneChip Human Mapping 500 k Array from Affymetrix was used. Genotypes from DNA of the three affected and two unaffected children in the index kindred in addition to the parents were generated. Genotypes were examined with the use of a multipoint parametric linkage analysis, and haplotype reconstruction performed with GENEHUNTER V.2.1 through stepwise use of a sliding window with sets of 110 SNPs and the program, ALLEGRO, in order to identify regions of homozygosity as described using a disease allele frequency of 0.0001 and Caucasian marker allele frequencies.
Targeted capture was performed on genomic DNA from one affected and one unaffected sibling of the index kindred with the EZ Exome Library (Roche Nimblegen, V.1) and sequenced on a single lane of a Solexa/Illumina Genome Analyser II. Reads were aligned to the human reference genome (GRC37 release, downloaded from the ENSEMBL database). Three different software programs were used for sequence evaluation: Maq, BWA and Novoalign. The coverage along the genome was calculated using BEDtools (GenomeCoverageBed function), without omitting zero values. Variant calling was undertaken using UnifiedGenotyper.15 The final output was then converted to variant call format. On average, we obtained about 43 million single short reads per lane with 91.8% of reads correctly mapped to the genome. The median sequencing depth per coding nucleotide was 23, with 90% of the targeted exons covered at least once. Variants from all samples were annotated and prioritised to identify pathogenic mutations as previously described.16 Variants annotated in dbSNP132 and the 1000 Genomes project or in our in-house databases with an allele frequency above 0.5% were removed. An autosomal recessive inheritance model was applied for gene identification in both kindreds, with known ciliopathy and MCPH genes manually analysed using the Integrative Genomics Viewer (http://www.broadinstitute.org/igv/). Candidate pathogenic variants were validated and assessed for familial segregation by Sanger sequencing.
Mutations were analysed by Sanger sequencing. CENPF primer pairs are described in online supplementary table S1.
NIH 3T3 fibroblasts, mouse inner medullary collecting duct (mIMCD3) and retinal pigmentary epithelial (RPE) cells were seeded onto glass coverslips and grown in Dulbecco’s modified eagle medium (DMEM) with 10% fetal bovine serum (FBS) and penicillin/streptomycin, until they reached 70% confluency, after which the medium was replaced with DMEM without serum overnight. Cells were stained with antibodies against CENP-F (1:200, ab 90, Abcam; sheep anti-CENP-F, 1:500, courtesy of Stephen Taylor, University of Manchester, rabbit anti-CENP-F,1:500, courtesy of Tim Yen, University of Pennsylvania), anti-IFT88 (1:800, 13967-1-AP Proteintech), anti-KIF3B (1:50, ab42494, Abcam), anti-α-acetylated-tubulin (1:800, T6793-clone 6-11B-1,Sigma-Aldrich), anti-γ-tubulin (1:500, T6557, Sigma-Aldrich), anti-GT335 (1:800, Novus Biologicals), anti-Ninein (1:200, ab 4447 Abcam), as previously described.17 Alexa-488, Alexa-594 and Alexa-647 conjugated secondary antibodies were obtained from Invitrogen. Confocal imaging was performed using a Zeiss LSM-710 system with an upright DM6000 compound microscope, and the images were processed with Zen software suite.
Kidneys from 22-week-old control fetuses (phenotypically normal without karyotypical abnormality and normal kidney histology) and fetuses with CENPF mutations were fixed in 4% paraformaldehyde (PFA), dehydrated, embedded in paraffin and sectioned at 20 μm. Sections were stained with H&E. For immunofluorescent studies, microwave antigen retrieval and immunostaining were carried out as previously described.18 Confocal imaging was performed using a Zeiss LSM-710 system with an upright DM6000 compound microscope, and images were processed with Zen software suite. Z stacks were acquired at 0.5 μm intervals and converted to single planes by maximum projection with FiJi software.
For immunogold labelling of RPE cells, the cells were serum-starved at 70% confluency for 3 days and then fixed in 0.25% glutaraldehyde +4% formaldehyde in 0.1 M cacodylate buffer, pH 7.4, and processed for embedment in LR White. Ultrathin sections (70 nm) were labelled with primary antibody, followed by secondary antibody conjugated to 12 nm gold particles.
HEKT293, NIH 3T3 fibroblasts and RPE cells were plated onto tissue culture 100 mm dishes with 10 mL of DMEM medium containing 10% FBS and 1% penicillin/streptomycin. Cells were lysed after 48 h in a radio-immunoprecipitation assay buffer and were incubated with a monoclonal antibody to CENP-F (ab90, Abcam, 1:100) for 24 h at 4°C. After incubation, the lysates containing the Ag-Ab complexes were resolved by SDS-PAGE. Protein interactions were assessed by immunoblotting with affinity-purified polyclonal anti-IFT88 and anti-KIF3B antibodies (1:100). Enhanced chemiluminescence was used to detect specific proteins using secondary rabbit and mouse-conjugated horseradish peroxidase antibodies (dilution 1:2000).
Gel filtration studies
Gel filtration was performed as previously described.19
Wild-type zebrafish, from AB×Tupfel long fin and transgenic cardiac myosin light chain (cmlc2); GFP—zebrafish were staged and housed as previously described.20 Groups of 25–50 stage-matched embryos were collected at 8-somite and 18-somite stages, 24, 48, 72 and 120 h postfertilisation (hpf). For cenpf knockdown, antisense morpholino oligonucleotides (MO) (GeneTools) were designed against the 25 bps upstream of transcript start codon of cenpf and against the splice junction of the intron 3–exon 4 boundary (see online supplementary table S2). For controls, a standard control MO (5′-CCT CTT ACC TCA GTT ACA ATT TAT A 3′) was injected into wild-type embryos. Specificity of splice MO was confirmed by RT-PCR (see online supplementary figure S1). RNA was extracted from 25 morphants and 25 controls at 48 hpf using the TRIzol (Invitrogen) method. First-strand cDNA was synthesised using random hexamers (Sigma-Aldrich) and Omniscript transcriptase (QIAGEN), according to the manufacturer's instructions. Fertilised eggs were injected with MO (2 ng/embryo) at the 1-cell to 2-cell stage and allowed to develop at 28.5°C to the desired stages. For rescue experiments, full-length human CENPF plasmids were linearised with Not1 and mRNA synthesised using Ambion mMessage mMachine SP6 kit. Wild-type mRNA (75 pg) was injected into the cytosol of one-cell-stage embryos with cenpf MO. For whole-mount in situ hybridisation (WISH) studies, groups of 25–50 stage-matched embryos were collected at 18-somite stages and were fixed in 4% PFA/phosphate buffered saline overnight at 4°C. WISH for southpaw mRNA expression was undertaken with standard protocols.
Statistical analyses were performed in GraphPad Prism V.5 (GraphPad Prism Software, USA). Numbers were reported as median values and comparison was made using the two-sample Wilcoxon rank sum test for non-parametric data. Where numbers are reported as mean values, comparison was made using the Student t test for parametric data. p<0.05 was considered statistically significant.
Mutations in human CENPF cause a novel congenital malformation syndrome and MCPH
We identified a non-consanguineous Caucasian kindred with four affected fetuses exhibiting mid-gestation lethality and dysmorphic craniofacial features (figure 1A, B; table 1). Autopsy findings revealed ciliopathy features, such as cerebellar vermis hypoplasia, corpus callosum agenesis, cleft palate, duodenal atresia and bilateral renal hypoplasia.
A search of several validated dysmorphology databases including the London Dysmorphology Database failed to show phenotypical identity with any known syndrome. Genome-wide SNP analysis using high-density SNP arrays (Affymetrix 500 k Marshfield V.2) was undertaken on all except one family member (CIL 1.1). Linkage analysis using GENEHUNTER V.2 lr5 (multipoint) revealed 10 regions with a maximum positive HLOD of 1.32. Linked intervals were identified on chromosome 1 (2 intervals), 2, 6, 7, 8, 13, 19 and 20. One of the intervals on chromosome 1 and the interval on Chromosome 19 were the largest and contained the most homozygous markers covering a total of 839 genes (see online supplementary figure S2).21 Using Identity by Descent Finder, significant regions of homozygosity were not present, consistent with declared non-consanguinity. Given that the linked regions were large, spanning up to 15 Mb on 19p13.3, whole exome capture and consecutive massive parallel deep sequencing of one affected and one unaffected offspring was employed as a strategy to identify the underlying genetic aetiology of this novel phenotype. Variants were prioritised for analysis on the basis of novel coding non-synonymous SNPs, splice variants, truncating variants and InDels (see online supplementary table S3). A further variant filtering strategy based on an autosomal recessive mode of inheritance, as suggested by the pedigree, identified two novel homozygous and 40 novel compound heterozygous mutations in 20 genes that were unique to the affected offspring. Only one of the 22 candidate genes was present in a linked interval located on chromosome 1. Two novel non-synonymous variants in the CENPF gene (NM_016343.3), involving a heterozygous IVS5-2A>C nucleotide change, which was predicted to abolish the consensus splice-acceptor site from exon 6, and a second heterozygous c.1744G>T nucleotide change in exon 12 were identified (figure 2A, B). Sanger sequencing of both variants confirmed segregation with affected offspring and revealed that each parent carried a single variant (see online supplementary figure S3A). The variant was detected neither in the 200 ethnically-matched control alleles nor in the 200 control in-house exomes. The protein-truncating non sense variant, c.1744G>T, p.E582*, was predicted to be disease-causing in the Mutation Taster programme (score 6.0). The expected damaging effect provides strong support for its likely pathogenic effect. Furthermore, the mutated amino acid sequence is conserved among vertebrates (see online supplementary figure S3B). The canonical splice-site variant (IVS5-2A>C) disrupts the exon 6 acceptor splice site probably ablating exon 6 and leading to a 97 amino acid in-frame deletion affecting the MT-binding domain at the N-terminus of the protein. Another possible consequence of this mutation is that a cryptic splice site might be recruited downstream with resulting frameshift and the introduction of a premature stop codon (p.Lys191fs*). Non-sense-mediated decay would probably lead to loss of function. As all four affected fetuses died in utero, there was no RNA available to determine the effect of the canonical splice-site variant (IVS5-2A>C). Human CENPF consists of 20 coding exons that encode at least two protein-coding transcripts (see online supplementary table S4). Neither mutation is present in the second protein-coding transcript which overlaps its sequence with amino acids 2610–2774. The longest coding transcript of CENPF encodes a 350 kDa protein consisting of 3114 amino acid residues and mainly coiled coil domains. Other domains include MT binding domains at both the N and C termini, in addition to Nudel (Nde) binding, activating transcription factor-4 (ATF4)-binding and Nup133-binding domains (figure 2C).
Nde-1, the protein product of the centrosomal gene, mutated in microcephaly, has previously been shown to interact with CENP-F.22–26 We, therefore, investigated, by whole exome sequencing, a large cohort of patients (n=1000) with microcephaly (MCPH) for CENPF mutations, where no deleterious or potentially pathogenic variants were identified in known MCPH genes (CEP135, ASPM, WDR62, MCPH1, CEP152, STIL, CEP63 and CENPJ). We identified two CENPF mutated alleles [c.1744G>T, p.E582*, c.8692 C>T, p.R2898*] in a patient with MCPH associated with mild to moderate learning difficulties (occipital head circumference (OFC) at birth: 29.5 cm, below 0.4th centile; adult OFC 45.5 cm, below 0.4th centile, figures 1C, D and 2A, B; see online supplementary figure S4). The other body systems were unaffected and overall growth was normal. Of note, MCPH was evident by mid-gestation in affected fetuses of Family 1 (figure 1D). The protein-truncating non sense variant, c.8692 C>T, p.R2898* was predicted to be disease-causing in the Mutation Taster programme (score 6.0). The expected damaging effect provides strong support for its likely pathogenic effect. The mutation c.1744G>T, p.E582* was shared between the two kindreds. Western blot analysis of protein lysates from CENPF mutant MCPH fibroblasts revealed a much greater reduction in CENP-F protein levels compared with wild-type controls (see online supplementary figure S5). The presence of residual protein could be explained by incomplete nonsense-mediated decay. Truncation of the residual protein as a result of the p.R2898* mutation is possible but the estimated difference in molecular weight of 23.7 kDa (estimated by loss of 216 amino acids) was difficult to resolve by SDS-PAGE gel electrophoresis owing to the high molecular weight of CENP-F (see online supplementary figure S9).
Mutational screening did not identify mutations in CENPF in 12 consanguineous patients with Meckel Grüber syndrome (MKS) who had compatible clinical features, potential autozygous regions and did not have a mutation in known MKS genes and in three patients with isolated nephronophthisis (NPHP) who showed homozygosity by descent at the CENPF locus out of a cohort of 150 families with NPHP or Joubert syndrome (JBTS). We also conducted mutational screening of 96 unrelated patients with Bardet Biedl syndrome (BBS) who were not preselected based on known BBS mutations. We did not detect recessive CENPF mutations in any of the MKS, NPHP, JBTS or BBS families, and because of the small sample size, we were unable to conclude that the heterozygous mutations in CENPF detected in BBS pedigrees act as phenotypical modifiers as has been described for other ciliopathy disease genes (see online supplementary table S5).
CENP-F is localised to the subdistal appendages of the mother centriole
The findings of mid-gestation fetal lethality together with abnormal craniofacial, cerebellar, palate, foregut and renal development, and the known role of Hedgehog signalling in organogenesis,27 suggested that these features may represent a ciliopathy disorder. Immunofluorescence microscopy of ciliated NIH 3T3 fibroblasts revealed a basal body localisation for CENP-F (figure 3A). Furthermore, CENP-F colocalised with Ninein at the subdistal appendages of the mother centriole of mIMCD3 cells (figure 3B). Transmission electron microscopy following immunogold labelling of CENP-F in serum-starved human RPE cells confirmed a centriolar localisation for CENP-F at the subdistal appendages and the distal end of the mother centriole (figure 3C).
Zebrafish cenpf knockdown results in ciliopathy phenotypes
To understand the functional relevance of CENP-F in relation to its localisation at the basal body, we performed knockdown experiments using both translation-blocking and splice-blocking antisense MO against zebrafish cenpf which shares 60% homology with its human orthologue (see online supplementary table S2). Compared with controls, a significantly reduced number of cenpf morphants survived (p<0.008, online supplementary figure S1). Morphological analysis of surviving zebrafish embryos at 24 hpf, revealed axis curvature defects and at 48 hpf, cenpf morphants exhibited abnormal heart looping compared with controls (figure 4A). At 72 hpf, hydrocephalus was observed in cenpf morphants, and at 120 hpf, all surviving cenpf morphants exhibited pronephric cysts (figure 4A). Coinjection of cenpf MO with human wild-type CENPF RNA rescued significantly the axis curvature defects (p<0.001) and pronephric cysts in cenpf morphants (p<0.001; figure 4B, online supplementary figure S6 and table S5). The occurrence of these morphological findings support a role for CENP-F in zebrafish ciliary function.28
Cilia-driven fluid flow within zebrafish Kupffer's vesicle (KV), or across the mouse ventral node, has been shown to underlie a conserved symmetry-breaking event that establishes a left–right (LR) pattern.29 To corroborate our findings of early lethality and abnormal heart looping in embryos surviving to 48 hpf, we next determined whether LR patterning defects are evident in cenpf morphants. At mid-somite stages, normal LR patterning can be defined by southpaw mRNA expression in the left lateral plate mesoderm.29 In cenpf morphants, right-sided (top right panel), bilateral (bottom left panel) and absent (bottom right panel) expression of southpaw mRNA was observed compared with left-sided expression in control embryos (figure 4C and also see online supplementary figure S7). To determine whether the laterality defects are caused by defects in KV cilia, we next analysed cilia formation in 8-somite-stage (ss) control and cenpf morphants. Following labelling of KV ciliary axonemes with anti-α-acetylated tubulin antibody in stage-matched embryos at 8-somites (figure 4D), analysis of cenpf morphants revealed that the length of KV cilia were shorter compared with controls (p<0.0001; figure 4E) and the number of KV cilia was significantly less in cenpf morphants compared with controls (p<0.001; figure 4F).
Following our observations that cenpf morphants show defective KV ciliogenesis, we next determined whether defective ciliogenesis was a feature of mutant CENPF renal epithelia. Immunofluorescence labelling of ciliary axonemes with anti-α-acetylated tubulin antibody in kidney sections of autopsy tissue from age-matched control fetuses were longer compared with those in renal epithelia of fetuses carrying the identified CENPF mutations (figure 4G). While renal epithelial cilia were noted to be present on some but not all cells, morphologically, the cilia that were present were stumpy with a terminally distended appearance (figure 4G).
CENP-F colocalises with IFT88 along the ciliary axoneme and precipitates with endogenous IFT88 and other IFT-B components
Previous work has demonstrated that during mitosis, CENP-F localises to the spindle poles in a process that relies on cytoplasmic dynein-1.22–24 ,30 Similar findings for IFT88 have recently been reported,19 suggesting that ciliary proteins may have specific roles in mitosis.19 ,31 Consequently, we tested the hypothesis that CENP-F might interact with IFT88. To test this, we showed that CENP-F colocalised with IFT88 and KIF3B at the centrosome of asynchronous NIH 3T3 fibroblasts (figure 5A, B) and along the ciliary axonemes of ATDC5 cells (chondrocytes) (figure 5C) Furthermore, in human autopsy samples, IFT88 colocalised with ciliary axonemes of renal epithelial cells of control fetuses (figure 5D). However, IFT88 did not localise to ciliary axonemes and centrioles in mutant CENPF kidneys (figure 5E). These data prompted us to test a possible functional relationship between CENP-F and IFT88. Pairwise co-immunoprecipitation assays of mitotic and serum-starved HEKT293 cells confirmed that IFT88 precipitates with endogenous CENP-F (figure 5F). In unsynchronised HeLa cells, endogenous CENP-F co-fractionated with other IFT-B components such as IFT52 and IFT20 in addition to motors, such as cytoplasmic dynein-1 and Kif3a (figure 5G). Therefore, this data suggest that CENP-F interacts with proteins involved in cilia formation and function.
Together with our findings that CENPF mutations result in a microcephalic phenotype and recent evidence for a role for IFT88 and Pericentrin in mitotic spindle orientation,8 ,19 we hypothesised that CENP-F may also interact with proteins implicated in the cortical polarity pathway which could account for defective cortical neurogenesis. This hypothesis was supported by co-immunoprecipitation assays suggesting an interaction between CENP-F and the NuMA/p150 Glued dynactin/Par 3 protein complex, proteins implicated in asymmetric cell division32 (see online supplementary figure S8).
Mutations in CENPF link the kinetochore complex to human ciliopathy and MCPH phenotypes
Our discovery of a novel severe human ciliopathy-related phenotype attributed to mutations in a kinetochore protein, supports recent evidence for a dual role for ciliary proteins in spindle orientation and ciliogenesis.19 CENP-F was first characterised in cancer cell lines as a component of the outer kinetochore and as a binding partner of the retinoblastoma (Rb) protein.33–35 CENP -F is dynamically expressed throughout the cell cycle. It binds to the nuclear envelope at the transition between G2 and M phase of the cell cycle. In early prophase until anaphase onset, it is found at the kinetochore where it stabilises the attachment of MTs to the centromere. In early anaphase, CENP-F is found at the spindle mid-zone, while in late anaphase, it migrates with cytoplasmic dynein-1 and recruits the spindle checkpoint regulatory complex to the spindle poles.22 In early G0, it undergoes proteasome degradation.36 Depletion of CENP-F in vitro results in mitotic delay, with failure of kinetochore assembly and misalignment of chromosomes in a subset of mitotic cells.37 ,38 Studies in murine embryonic stem cells and in avian myocyte lines suggest primary roles for this protein complex in differentiation, but the exact mechanism is unknown.39 Several studies have highlighted an additional role for CENP-F in the regulation of cell shape and vesicle transport.23 ,40–42 Given the overlap of features in fetuses with CENPF mutations with human ciliopathy phenotypes, we hypothesised that CENP-F may play a role in cilia formation and function. The finding that CENP-F colocalises with IFT88 along the ciliary axoneme, and the existence of CENPF-IFT88 protein complexes is further supported by the co-migration of CENP-F with other IFT-B components. Furthermore, the absence of IFT88-stained ciliary axonemes and mislocalisation of IFT88 within renal tubular epithelia of CENPF-mutant kidneys proposes a putative role for CENP-F-dependent IFT88-ciliary targeting.
We attribute, for the first time, that mutations in the CENPF gene play a causal role in human congenital malformation syndromes. All four affected fetuses of the index kindred had compound heterozygous mutations in CENPF. Further supporting the pathogenicity of these mutations was the finding that one of these mutations also occurred in the context of MCPH in a second unrelated kindred. Phenotypical disparity is not a unique finding to mutations in the CENPF gene. Divergent phenotypes have been previously described in several disorders associated with mutations in genes encoding centrosomal proteins. For example, for mutations in the CEP290 gene, 90 mutations have been reported exclusively in only one phenotype, while 14 others have segregated with two diseases, and eight have been associated with three or more phenotypes.43 In most cases, these phenotypes are partially overlapping, although few mutations were observed to lead to strongly divergent disorders, such as Leber's Congenital Amaurosis (LCA) and MKS. It is interesting that mutations causing JBTS tend to cluster in the second half of the CEP290 gene, whereas mutations segregating with LCA, Senior Löken Syndrome and MKS are homogeneously distributed throughout the gene.44 ,45 Of note, domains within the CEP290 protein share significant similarity with CENP-F, with several putative coiled-coil domains, a region with homology to structural maintenance of chromosomes segregation ATPases, a bipartite nuclear localisation signal and six RepA/Rep+ protein kinase inducible domain motifs and an ATF4-binding domain.46
In the current study, we sought to explain the divergent phenotypes by an analysis for potential modifier alleles in genes known to be associated with ciliopathy phenotypes, but did not find any variants which were predicted to change the amino acid sequence. A plausible explanation could be perhaps that the more severe phenotype in the embryonic lethal disorder was associated with a lack of a protein product necessary for ciliary function. Because residual CENP-F protein was observed in the fibroblasts of our MCPH patient, a dosage-dependent mechanism could be proposed in which complete loss of function of both CENPF alleles would lead to an embryonic lethal ciliopathy phenotype, whereas residual CENP-F activity would be sufficient for normal ciliary targeting of IFT88 and, perhaps, a less severe phenotype.
Genes involved in centrosome maturation and spindle-pole formation have been implicated in MCPH phenotypes.6 As CENP-F migrates with cytoplasmic dynein-1 and recruits the spindle checkpoint regulatory complex to the spindle poles in late anaphase,22 the findings of CENPF mutations in a MCPH phenotype is therefore not unexpected. MCPH phenotypes have been ascribed to defective asymmetric divisions of neuronal progenitors and failure of correct neural cell fate specification.6 ,8 Our data supports a role for CENP-F in asymmetric cell divisions through its putative interactions with p150-dynactin, NuMA and Par3, proteins which have been implicated in this pathway.32 Future investigations using conditional Cenpf-deleted transgenic mice will be needed to dissect the role of CENP-F in cortical neurogenesis.
We thank Kerra Pearce and Justyna Porwisz of UCL Genomics for genotyping support. We thank T Giddings at MCDB University of Colorado, Boulder, for immunogold analysis, X Zhu for full-length CENPF plasmid, M Tada at University College London for southpaw plasmid, T Yen (University of Pennsylvania) and Stephen Taylor (University of Manchester) for Cenp-F antibody and C Roberts for valuable technical assistance. We thank John Sayer at Newcastle University for immunofluorescence studies. We thank Catherine King, Applications Specialist for shRNA library advice, at Scientific Support Services, UCL. We thank Marc Gouw, Instituto Gulbenkian de Ciência for computational genomics input. We thank G Pazour for the gift of GFP-IFT88 LLC-PK1 cell line. We also thank the histology services at GOSH/ICH-UCL for tissue processing. Lisa Schaffer, Jill Mokry, David Chitayat, Muriel Holder, Jennifer Vincelli, Karen Chong, Peter Jacky are graciously acknowledged for provision of DNA samples for CENPF sequencing. P J Scambler is thanked for hosting AW's fellowship.
Contributors AMW, MW and PLB designed the study with substantial contributions from FL and ES for bioinformatics analysis. CB, EC, AB helped with pilot exome pipeline analysis. SC-S, RA and GO helped with immunofluorescence studies. GO and PC sequenced MCPH family for CENPF variants. AC provided technical expertise with co-immunoprecipitation assays and genetic analysis. HS and CD identified the study families. HS and RK helped with linkage analysis. DMB and PMM shared critical reagents. AB and SD helped with microscopy, biochemical assays, cell rescue experiments and intellectual contributions to the manuscript. ED and NK sequenced BBS cohorts, CAJ and KS sequenced MKS cohorts and FH and EO sequenced NPHP cohorts for CENPF mutations. PC and AJ provided sequencing and western blot data on MCPH patient. AMW designed the study, performed exome capture, analysis, mutation segregation, microscopy, biochemical assays, cell, zebrafish and fetal kidney experiments and wrote the manuscript.
Funding This work was supported by a Medical Research Council Clinical Research Training fellowship to AW (G0802138/1), the March of Dimes Foundation (1-FY07-422) and Guggenheim Foundation (MW), the Wellcome Trust (PLB) and ICH-UCL Biomedical Research Centre to GOSgene. FH is an Investigator of the Howard Hughes Medical institute and is supported by the NIH (DK-06308).
Competing interests None.
Patient consent Obtained.
Ethics approval Great Ormond Street Hospital NHS Foundation Trust and The Scottish multicentre research ethics committee.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement We are happy to share our data with any principal investigators in the field.