|Home | About | Journals | Submit | Contact Us | Français|
Mutations of the Ectodysplasin-A (EDA) gene are generally associated with the syndrome hypohidrotic ectodermal dysplasia (MIM 305100), but they can also manifest as selective, non-syndromic tooth agenesis (MIM300606). We have performed an in vitro functional analysis of six selective tooth agenesis-causing EDA mutations (one novel and five known) that are located in the C-terminal tumor necrosis factor homology domain of the protein. Our study reveals that expression, receptor binding or signaling capability of the mutant EDA1 proteins is only impaired in contrast to syndrome-causing mutations, which we have previously shown to abolish EDA1 expression, receptor binding or signaling. Our results support a model in which the development of the human dentition, especially of anterior teeth, requires the highest level of EDA-receptor signaling, whereas other ectodermal appendages, including posterior teeth, have less stringent requirements and form normally in response to EDA mutations with reduced activity.
Tooth development is largely under genetic control and all familial cases, as well as the majority of sporadic cases of congenital tooth agenesis are likely to be caused by sequence variations in one of the many genes that are involved in tooth development.1 Classically, a distinction has been made between non-syndromic and syndromic tooth agenesis. hypohidrotic ectodermal dysplasia (HED) is such a syndrome that features hypoplasia of most epithelial appendages including variable numbers of missing teeth, sparse hair and hypoplastic or aplastic sweat glands leading to hypohidrosis with potentially life-threatening hyperthermia. Non-syndromic tooth agenesis, on the other hand, has been defined as affecting predominantly the dentition and involving primarily the tooth-specific genes.2, 3, 4
The distinction between syndromic and non-syndromic tooth agenesis is becoming less apparent as genetic knowledge advances. Mutations in the Muscle Segment Homeobox 1 gene (MSX1), for example, not only cause selective tooth agenesis, but are also involved in orofacial cleft syndromes.5 Not only do the more ‘tooth-specific' genes contribute to non-dental problems but also the reverse is observed: Several reports describe isolated tooth agenesis in families with mutations in Ectodysplasin-A (EDA),6, 7, 8, 9, 10, 11, 12 a gene that is usually responsible for the HED syndrome.13
The EDA gene occupies a 425-kb segment of the long arm of the X-chromosome (Xq12-13.1) 14 and encodes a protein that belongs to the tumor necrosis factor (TNF) superfamily of ligands. In total, eight isoforms of the EDA transcript can be created by differential splicing of the 12 exons. The longest splice form encodes a 391 amino acid protein with a transmembrane domain, a furin cleavage site, a collagen type repeat area in the middle and a C-terminal TNF-like structure.15, 16, 17 On proteolytic processing at the furin consensus site, the C-terminal portion of the protein containing the collagen domain and the TNF homology domain is released as a soluble, trimeric ligand.18 Only the following two splice isoforms of EDA contain the receptor-binding TNF homology domain: EDA1, which binds the EDA-receptor EDAR, and EDA2, a two amino acid shorter variant that binds exclusively to a receptor called XEDAR.19 The TNF homology domains of both EDA1 and EDA2 have been crystallized as homotrimers, but further multimerization through interactions of the collagen domain seem to be functionally important.
Both the receptors, EDAR and XEDAR, activate the NF-κB pathway, but only the EDA1/EDAR interaction seems relevant for the development of ectodermal appendages. Indeed, mutations in EDA1 as well as in EDAR can cause an HED syndrome that is phenotypically indistinguishable except for the different inheritance pattern, X-linked and autosomal, respectively.20 In addition, XEDAR mutations have not yet been identified in HED or any other condition, and XEDAR-deficient mice are normal and display none of the phenotypes characteristic of ectodermal dysplasia.21
Almost a hundred different EDA gene mutations have been identified in patients with the HED syndrome. These mutations range from exon deletions and frameshifts to conservative replacements of single amino acids and may be located in any of the three main functional domains of the EDA protein, furin cleavage site, the collagen-like multimerization domain or the TNF homology domain. Phenotypically, the HED syndrome is diverse with a broad range of intra- and interfamilial variation in severity. However, despite the great number of different EDA mutations that have been studied so far, no genotype/phenotype correlations have been uncovered.
Previous investigations of the impact of EDA missense mutations on different aspects of protein function have shown that proteolytic processing, glycosylation, multimerization, and solubility or solely receptor binding can be affected by the different mutations.8, 18, 22 Ultimately, most of the mutations could be predicted to lead to an elimination of receptor signaling; only one mutation was shown to possess residual receptor-binding activity. Interestingly, this mutation was found in an HED family whose main complaint was tooth agenesis.8 Here, we describe an additional family with X-linked recessive, non-syndromic tooth agenesis that can be linked to an EDA mutation and present a functional analysis of this EDA mutation in comparison with other tooth agenesis and HED-causing mutations in the TNF homology domain of EDA.
The family participated in our IRB-approved tooth agenesis study. All adults consented to participate in this study; in the case of minors, parental consent and child assent in >12-year-olds were obtained. A pedigree was established showing that only males were affected. Phenotype evaluation was performed using an HED-specific questionnaire, interviews and panoramic radiographs of the dentition and/or dental records.
Blood samples or buccal swabs were collected for DNA extraction. A candidate gene approach was chosen with the X-chromosomal EDA gene as the first target. In total, eight exons of the EDA gene were PCR amplified and sequenced with automated fluorescent dideoxy technology.
A T-to-C transition in the last exon of the EDA gene of the affected index male was found to create an HhaI restriction site. All other participating members of the family as well as 65 unrelated females and 14 unrelated males were tested for the presence of this restriction site. Primers 5′CACGCCTTCACATGGCACT3′ and 5′CGGCTGCAACACCAATACAC3′ were used for amplification of the exon.
Mammalian expression vectors for secreted Flag-tagged forms of EDA1 and EDA2 with the tooth agenesis-causing mutations V365A, Q358E, D316G, T338M or M364T were generated as described earlier for other EDA mutants, including S374R.8 Briefly, these constructs code for the signal peptide of hemagglutinin, the Flag sequence (DYKDDDDK), a linker (GPGQVQLQVD) and the TNF homology domain of EDA1 (amino acids 245–391) or EDA2 (amino acids 245–389). Other EDA constructs used in this study and expression vectors for human EDAR-Fc and human XEDAR-Fc have been described earlier.8
Vectors encoding soluble, wild-type (wt) or mutant Flag-tagged EDA1 or EDA2 protein, or EDAR:Fc were transfected into 293T cells, and the cells were maintained in serum-free OptiMEM (Invitrogen Corporation, Carlsbad, CA USA) for 7 days. The concentration of Flag-tagged EDA proteins in cell supernatants was estimated by comparative anti-Flag Western blot using serial dilutions of each protein and known amounts of purified Flag-TRAIL.
293T cells were transfected with wild-type or mutant Flag-EDA1, and supernatant and cells were harvested separately. The cell pellets were lysed by sonication in a known volume of SDS-PAGE sample buffer. Two-fold serial dilutions of cell extracts and the corresponding supernatants were evaluated for relative EDA protein content by densitometry of slot blots developed with anti-Flag. The percentage of secretion was calculated as (EDA amount in supernatant) divided by (EDA amount in cells + supernatant) × 100.
The binding of wild-type and mutant EDA1 and EDA2 to EDAR and XEDAR was monitored by ELISA as described earlier.8, 23 Briefly, ELISA plates were coated with a mouse anti-human monoclonal antibody (100μl at a concentration of 5μg/ml in 50m of Na carbonate (pH 9)), blocked, incubated with 100μl of EDAR:Fc or XEDAR:Fc (Alexis, Lausen, Switzerland) at a concentration of 0.5μg/ml, followed by two-fold dilutions of quantified Flag-EDA. Bound ligands were revealed with biotinylated anti-Flag antibody (0.5μg/ml, Sigma-Aldrich, Buchs, Switzerland), horseradish peroxidase-conjugated streptavidin (1/4000, Jackson Immunoresearch, Newmarket, UK) and orthophenylene diamine reagent, and read at 492nm.
Fas-deficient Jurkat-JOM2 cells expressing the EDAR:Fas fusion protein were generated essentially as described earlier for BCMA:Fas.24 For this purpose, the retroviral vector pMSCVpuro encoding the extracellular domain of human EDAR (amino acids 1–183), amino acids VD and the transmembrane, and intracellular domains of human Fas (amino acids 169–335) was used. About 40 clones were tested for their sensitivity to Fc-EDA1,25 and one of the sensitive clones (Jurkat-2199 clone 23) was selected for further experimentation. In these cells, the binding of EDA1 to EDAR:Fas induces cell death through the Fas signaling pathway. Cytotoxicity assays with Flag-EDA1 wt or mutants were performed in the presence or absence of 2μg/ml of cross-linking anti-Flag M2 monoclonal antibody (Sigma) as described earlier.26, 27
The pedigree of this Caucasian tooth agenesis family shows a typical X-linked recessive pattern of inheritance, affecting only males (Figure 1a). Figure 1b gives an overview of the dental phenotype of the affected participants. In all cases, two to six primary or permanent incisors are missing, with the exception of maxillary central incisors. First or second premolars and second molars of the permanent dentition may be missing as well. Carrier female family members report full dentition without shape or size abnormality.
As the pedigree pattern was strongly suggestive of an X-linked condition and the EDA gene on Xq12-13.1 is associated with a syndrome that includes tooth agenesis, a candidate gene approach was pursued and led to the detection of a T → C transition at nucleotide 1336 of the deduced cDNA sequence. The nucleotide replacement produces a conservative change of the surface-expressed Valine 365 to Alanine (Figure 2a and b). The T → C nucleotide change also introduces an HhaI restriction site into the last exon of the EDA gene, which allowed the testing of all 26 available family members for the V365A mutation by restriction fragment length polymorphism. A perfect segregation of the T-to-C transition with the phenotype became apparent: Affected males have a single mutant copy, carrier females have one mutant and one wild-type copy, and unaffected probands have only wild-type copy(s) (Figure 1a).
A common polymorphism at this site of the EDA gene was excluded by testing 79 controls with a total of 144 X-chromosomes (65 females, 14 males) for the T-to-C transition at nucleotide 1336. None of these unrelated controls showed the mutation. We conclude that the V365A substitution is the likely cause for the tooth agenesis in this family.
To evaluate the phenotype further, participating family members were asked to complete a detailed two-page questionnaire (summarized in Table 1). The only symptoms reminiscent of HED seem to be a tendency for fine, curly hair, early balding (in their middle to late twenties) and thin skin. Heat intolerance is reported not only by some of the affected males but also by unaffected family members. The condition has been observed for four generations in this family but was never diagnosed as ectodermal dysplasia because of the uncharacteristically mild systemic features that are not significantly different from random variability in the general population. We conclude that this family's features fit the designation, X-linked Hypodontia MIM300606.
The V365A mutation and the five other mutations8, 9, 10, 11, 12 that cause selective tooth agenesis are located in the COOH-terminal quarter of the TNF-like receptor-binding domain (Figure 2a), and cluster close to the interface of two adjacent monomers where receptor binding is predicted to occur23 (Figure 2b).
All six mutations were tested for expression, glycosylation, cellular export, quantitative receptor binding and signaling ability as described earlier for the S374R mutation.8 Figure 3a shows normalized amounts of wild-type and mutant EDA1 and EDA2, with the tooth agenesis-causing mutations V365A, Q358E, S374R, D316G, T338M and M364T, or the HED-causing mutations Y343C and H252L. The two bands in each lane represent the glycosylated and the unglycosylated polypeptides of each construct, as shown by peptide-N glycanase F digestion (Figure 3b). Although all nine protein constructs are expressed, glycosylated and exported out of the cells, there are a few marked differences. In mutant Q358E, the glycosylated band is consistently overrepresented when compared with the lower non-glycosylated band. This may indicate a solubility problem of the unglycosylated form, causing it to be retained in the cell. Indeed, <10% of the tooth agenesis-causing mutant Q358E is recovered from cell supernatants. Secretion problems are not detectable in the other mutants, with the exception of the HED-causing Y343C variant, which is also mostly retained in the transfected cells, consistent with our previous report8 (Figure 2d).
The relative amounts of Flag-tagged wt and mutant proteins were carefully determined to exclude the fact that the small differences in receptor-binding activity are due to a difference in ligand concentration (Figure 3c). Indeed, the quantitative ELISA (Figure 4a, upper panel) shows that the binding of all hypodontia-causing EDA1 proteins to the receptor EDAR is variably reduced compared with wt, but not abolished. In contrast, EDA1 carrying either of the two HED-causing mutations Y343C and H252L lose all receptor-binding capability, consistent with the results that we obtained earlier by testing HED-causing mutants.8 The affinity of the corresponding EDA2 proteins to XEDAR is only slightly reduced, if reduced at all, for five of the six tooth agenesis-causing mutants (Figure 4a, lower panel).
We next investigated the ability of EDA1 wt and mutant constructs to trigger a surrogate, multimerization-dependent signaling pathway in Jurkat T cells engineered to express an EDAR:Fas fusion receptor. In this system, a functional EDA1 ligand can induce cell death through the Fas pathway; however, this requires earlier cross-linking of the EDA1 ligand with anti-Flag antibodies in analogy to the cross-linking of FasL, which is required for signaling in the original FasL/Fas pathway.26 Figure 4b shows that cross-linked wt EDA1 can induce cell death in this assay. The Q358E mutant is the only one showing appreciable yet reduced activity in this assay. Surprisingly, V365A and M364T are mostly inefficient in the cell death-induction assay, indicating that the signaling capacity of the mutated proteins is impaired even though cellular production, export and receptor binding are readily detectable. S374R and T338M have hardly any activity in the EDAR-Fas signaling assay, in line with their severely reduced receptor-binding capacity. Our assays would predict the D316G mutation to have the most severe effect, and according to the published phenotype data, this seems to be the case.9
The development of teeth depends on a highly coordinated interaction of multiple signaling events between ectodermal and underlying mesenchymal cells, similar to the development of other skin appendages such as hair follicles, nails and glands. A multitude of genes are known to be expressed in the developing tooth, but so far only four of them have been associated with selective, non-syndromic tooth agenesis in humans (1) The Paired Box 9 gene (PAX9) is strongly expressed in developing teeth. Heterozygous mutations in PAX9 cause predominantly molar tooth agenesis. (2) MSX1, a homeobox protein, can cause a slightly different phenotype with more premolar involvement. It may also contribute to Witkop28 and cleft lip/palate syndromes. (3) Axis Inhibitor 2 (AXIN2) is a signaling molecule in the ‘wingless-type MMTV integration site family' (WNT) pathway that starts operating very early in tooth placode formation. Autosomal dominant mutations in exon 7 of AXIN2 have been shown to cause not only a severe mixed pattern of tooth agenesis but also intestinal polyposis and predisposition to colon cancer. (4) The EDA gene, known to be affected in most patients with the HED syndrome, is also implicated in selective tooth agenesis. The hypodontia phenotype in EDA-associated isolated tooth agenesis seems to favor the lack of incisors, but other teeth are involved as well.
However, these four genes are responsible for tooth agenesis in only a fraction of all observed hypodontia cases. Many more genes remain to be discovered; and so far, only a few functional analyses of tooth agenesis-causing mutations are available to explain the pathogenesis of congenital hypodontia.
Most of the known EDA mutations affect a variety of ectodermal appendages such as hair, teeth and glands. Absent or severely decreased sweating can lead to hyperthermia and death during minor febrile infections in childhood. Other problems caused by glandular hypoplasia are constipation, respiratory infections, insufficient production of saliva and lacrimal fluid, earwax impaction, frequent middle-ear infections, and underdeveloped mammillae and lactation difficulties in affected females. Hair and eyebrows are sparse or missing. Some affected males lack all teeth, and some only a few, but on an average 22 permanent teeth are missing, not counting third molars.29 Shape abnormalities include smaller size, peg shape, reduced cusp number and root abnormalities. The facial features may be slightly dysmorphic with frontal bossing and depressed nasal bridge.
The HED often manifests with variability among affected males of the same family. Carrier females generally show a much milder phenotype with only one or two teeth missing, slightly smaller teeth, sparse hair or no symptoms at all. Mutations in all portions of the gene can cause ectodermal dysplasia, with no apparent correlation between the location of the mutation and severity of the phenotype.
The V365A mutation reported here is located in the C-terminal TNF-like portion of the protein, as are most of the other tooth agenesis-causing mutations, including the three newly-described ones (A259E, R289C and R334H).30 However, this position is not required for the milder effect of these mutations. One selective tooth agenesis-causing EDA mutation, G165A, is located at the end of the collagen-like domain;31 two others (R65G6 and E67V12) are located at the extracellular end of the EDA transmembrane sequence. The R65G and E67V replacements may reduce the expression or translocation, and therefore the dosage of otherwise normal ligands. In HED patients, this area is less frequently affected, and the predominance of frameshift and nonsense mutations suggests that the importance of mutations occurring in this part lies more in the abolishment of the rest of the protein than in a local dysfunctional effect. On the other hand, amino acid changes in this least conserved region of EDA are responsible for major adaptive changes in stickleback evolution32 and may have some other important function.
In our previous functional analysis of HED causing EDA mutations,8 we noticed that the only mutation with residual receptor-binding activity, S374R, came from a family with a predominantly missing teeth phenotype. However, we could not determine whether this was a coincidence or a truly tissue-specific phenomenon. Our current results strongly suggest that there is indeed a tissue-specific effect, in that residual EDA/EDAR activity can prevent the hypoplasia of most ectodermal appendages, except for the development of incisors and a few other teeth. In other words, the development of teeth, especially of incisors and premolars, requires the highest dosage of EDA signaling. However, the mutations associated with tooth agenesis are remarkably dissimilar in the effects they produce in assays with recombinant EDA. The adjacent mutations V365A and M364T are well expressed and show modestly lower binding to EDAR, which translates into a major impairment at activating a cross-linking-dependent surrogate signaling pathway.
For S374R, we reproduce the weak binding of the EDA1 isoform to EDAR,8 but see little, if any, activity in the bioassay. We also observe a much reduced but detectable binding of the EDA2 isoform of this mutant to XEDAR. The mutant proteins T338M and D316G share similar functional properties such as S374R with D316G performing worst in the EDAR-binding assay and D316G family members presenting with anodontia or severe oligodontia. Mutation Q358E has different effects. Binding to XEDAR and EDAR is little affected, and it retains significant capacity to activate multimerization-dependent signal transduction. However, the 90% reduced secretion level may explain the observed phenotype.
Altogether, we propose that EDA mutations associated with selective tooth agenesis share the property to retain some receptor signaling activity, but to be impaired either in receptor binding, and/or in their expression level and/or in their ability to induce efficient signaling downstream of the receptor. The phenotype strongly suggests that the threshold for EDA signaling in tooth development must be higher than in other EDA-dependent structures. Tooth shape abnormalities seem to be less frequent in EDA-caused selective tooth agenesis, possibly reflecting different requirements for the level of EDA/ EDAR activity in shape formation. There are other examples in which different levels of residual gene function can lead to sometimes dramatically different clinical phenotypes, which are as follows: More severe mutations in the X-chromosomal NEMO gene, which operates downstream in the EDA/EDAR signaling pathway, lead to incontinentia pigmenti in females and prenatal lethality in males. Milder mutations present as HED with severe immunodeficiency in surviving males.33
The finding that tooth development requires more EDA pathway signaling than other ectodermal appendages is supported by two observations made in EDA-deficient animals treated with a recombinant form of EDA1 endowed with cross-placental transfer properties by fusion to the Fc portion of IgG1 (Fc-EDA1). When Fc-EDA1 was administered to pregnant EDA-deficient (Tabby) mice, most Tabby-related defects were permanently rescued in offspring, except for tooth number and a special type of murine hair.25 In the second experiment, recombinant EDA preparations were injected postnatally into dog pups with the HED syndrome. It was recognized that the development of permanent teeth required a relatively higher or repeated dosage of recombinant EDA-A1.34 These findings also point to the exciting possibility that the isolated tooth agenesis of permanent teeth caused by EDA mutations may be preventable in humans. Health care professionals should be aware of the possibility that patients with agenesis of incisors and various other anterior teeth may carry a mutation in the EDA gene without showing other classical ectodermal dysplasia symptoms.
The authors declare no conflict of interest.
We thank the tooth agenesis family for their cooperation, Joseph F Maher, MD, for advice with the EDA questionnaire, and Sarah C Pollan White, DDS, for orthodontic evaluations. This work was supported by National Institute of Health Grant U24-PEI6472 to RDS and by Swiss National Science Foundation Grant 3100A0–122553 to PS.