The authors have no conflict of interest
A Missense Mutation in the Mouse Col2a1 Gene Causes Spondyloepiphyseal Dysplasia Congenita, Hearing Loss, and Retinoschisis†
Article first published online: 1 SEP 2003
Copyright © 2003 ASBMR
Journal of Bone and Mineral Research
Volume 18, Issue 9, pages 1612–1621, September 2003
How to Cite
Donahue, L. R., Chang, B., Mohan, S., Miyakoshi, N., Wergedal, J. E., Baylink, D. J., Hawes, N. L., Rosen, C. J., Ward-Bailey, P., Zheng, Q. Y., Bronson, R. T., Johnson, K. R. and Davisson, M. T. (2003), A Missense Mutation in the Mouse Col2a1 Gene Causes Spondyloepiphyseal Dysplasia Congenita, Hearing Loss, and Retinoschisis. J Bone Miner Res, 18: 1612–1621. doi: 10.1359/jbmr.2003.18.9.1612
- Issue published online: 2 DEC 2009
- Article first published online: 1 SEP 2003
- Manuscript Accepted: 26 MAR 2003
- Manuscript Revised: 18 FEB 2003
- Manuscript Received: 25 NOV 2002
- bone density
A missense mutation in the mouse Col2a1 gene has been discovered, resulting in a mouse phenotype with similarities to human spondyloepiphyseal dysplasia (SED) congenita. In addition, SED patients have been identified with a similar molecular mutation in human COL2A1. This mouse model offers a useful tool for molecular and biological studies of bone development and pathology.
Introduction: A new mouse autosomal recessive mutation has been discovered and named spondyloepiphyseal dysplasia congenita (gene symbol sedc).
Materials and Methods: Homozygous sedc mice can be identified at birth by their small size and shortened trunk. Adults have shortened noses, dysplastic vertebrae, femora, and tibias, plus retinoschisis and hearing loss. The mutation was mapped to Chr15, and Col2a1 was identified as a candidate gene.
Results: Sequence analyses revealed that the affected gene is Col2a1, which has a missense mutation at exon 48 causing an amino acid change of arginine to cysteine at position 1417. Two human patients with spondyloepiphyseal dysplasia (SED) congenita have been reported with the same amino acid substitution at position 789 in the human COL2A1 gene.
Conclusions: Thus, sedc/sedc mice provide a valuable model of human SED congenita with molecular and phenotypic homology. Further biochemical analyses, molecular modeling, and cell culture studies using sedc/sedc mice could provide insight into mechanisms of skeletal development dependent on Col2a1 and its role in fibril formation and cartilage template organization.
Osteochondrodysplasias comprise a large group of conditions that present with a variety of clinical skeletal phenotypes from severe, lethal abnormalities to less severe short stature. More than 100 types of human osteochondrodysplasias have been identified that involve joint abnormalities, impaired growth of long bones, and often have effects in eyes and ears.(1) The chondrodysplasias, a subgroup of the osteochondrodysplasias, have abnormalities in the growth of long bone and spine.(2) The basis for further classification of the chondrodysplasias is the region of long bone most affected; hence subclasses include epiphyseal, metaphyseal, and diaphyseal dysplasias.(2) If the vertebrae are also affected, the subclass for the condition is spondyloepiphyseal dysplasia.(2) Chondrodysplasias are relatively rare in the human population and may appear to be sporadic, or they may have a recognized pattern of inheritance that is dominant or recessive, with autosomal or X-linked transmission.(1) Molecular analyses of gene mutations responsible for these human dysplasias have shown that different mutations in the same gene may result in the same or a slightly different phenotype, and that locus heterogeneity exists, whereby indistinguishable phenotypes are caused by mutations in different genes.(1,3–7) Because a large number of chondrodysplasias have been identified both in humans and mice, the genetic and phenotypic analyses of these disorders continue to provide insight into complex pathways of skeletal development.
At least five different types of collagen-I, II, IX, X, and XI-are associated with cartilage abnormalities in humans and in mice. Among collagens, type II is the most abundant protein in articular cartilage and has been shown to be involved in many forms of chondrodysplasias and the associated cartilage degeneration.(1) The mouse type II collagen gene, Col2a1, is highly conserved with its human homolog, COL2A1, in exon/intron structure, intron lengths, intronic transcription factor binding sites, and regulatory elements.(8–10) The type II collagen gene in both species encodes the a-chains of type II collagen, a homotrimer of three identical a-chains.(1) Mutations in this gene limit formation of the triple helical assembly of cartilage, and several studies in humans have shown that the severity of the clinical phenotype corresponds to the number of altered collagen fragments left unfolded and to their altered mobility.(11,12) Human patients heterozygous for mutations in the COL2A1 gene have been diagnosed with many types of skeletal dysplasias including achondrogenesis type II, hypochondrogenesis, spondyloepiphyseal dysplasia congenita, Kniest syndrome, Stickler syndrome, and Wagner syndrome.(13) Each human clinical phenotype has similarities and differences, and each is associated with a different molecular defect in the COL2A1 gene, including deletions, insertions, splicing mutations, and point mutations.(14,15)COL2A1 is specifically transcribed in a limited number of human tissues including articular cartilage, the vitreous of the eye, and the nucleus pulposi of the spine, but the specific combination of affected sites coupled with the variability in severity of effect results in a variety of clinical syndromes.(16)
We have discovered a naturally occurring missense mutation in the mouse Col2a1 gene at exon 48 that results in a cysteine substitution for an arginine. This mouse mutation in the Col2a1 gene is molecularly similar to that found in the homologous human COL2A1 gene in two patients with chondrodysplastic features, given the subclassification of spondyloepiphyseal dysplasia congenita (14,15). Mice homozygous for this mutation in Col2a1 have shortened axial and appendicular skeletons with abnormal growth plates in the vertebrae and long bones, undefined nucleus pulposi, plus retinoschisis, and impaired hearing. Because the mouse phenotype resembles the human clinical phenotype, we have named the new mouse mutant allele spondyloepiphyseal dysplasia congenita (sedc). This new mutation offers a viable and valuable model of human cartilage disease for mechanistic studies.
MATERIALS AND METHODS
The sedc phenotype was discovered in the Mouse Mutant Resource at The Jackson Laboratory in 1997, when a male mouse with spinning behavior was observed. Homozygous sedc mice often can be identified at birth by their head bobbing behavior. With age, the bodies of sedc/sedc mice are shorter and squarer than normal littermates, and reduced in weight. Both sexes are fertile, and females have normal litter size and number. Genotyping on chromosome (Chr) 15 showed that the sedc mutation arose on the C57BL/6J chromosome in a mixed background comprised of C57BL/6J, C3H/HeJ, and AKR/J strains. The sedc mutation is currently maintained on the original mixed background by crossing a homozygous male or female to a heterozygote of the opposite sex.
Mice for this work were produced in our colony and maintained under 14:10-h light:dark cycles; autoclaved diet National Institutes of Health-31 (6% fat, 18% protein, Ca:P 1:1, vitamin and mineral fortified; PMI, Richmond, IN, USA) and HCl acidified water (pH 2.8–3.2) were provided ad libitum. Mice were housed in groups of four or five within 51-in2 polycarbonate boxes on sterilized shavings of Northern White Pine as bedding. Serum was harvested and skeletal preparations were made at necropsy. All procedures were approved by The Jackson Laboratory's Institutional Animal Care and Use Committee and performed in accordance with National Institutes of Health guidelines for the care and use of animals in research.
Mapping of the sedc mutation
The sedc mutation was mapped in the Mouse Mutant Resource at The Jackson Laboratory using F2 mice from an intercross of F1 hybrids from matings of homozygous sedc/sedc mice with mice of the wild-derived strain CAST/Ei. DNA was isolated from frozen spleens of sixty affected F2 mice using phenol/chloroform extraction and typed for polymorphic markers throughout the genome using standard polymerase chain reaction (PCR) methodology.(17) Gene order and recombination frequencies were calculated with the Map Manager computer program.(18) Linkage data for individual F2 mice have been deposited in the Mouse Genome Database, accession number MGD J:68217.
Gene identification/genomic sequencing
To test the Col2a1 gene as a candidate, we designed four pairs of PCR primers based on mRNA sequence from GenBank accession number M65161 (Table 1). For direct sequencing, the PCR reaction was scaled up to 30 μl; amplification was done during 36 cycles with a 15-s denaturing step at 94°C, a 2-minute annealing step at 60°C, and a 2-minute extension step at 72°C. PCR products were purified from agarose gels using a Qiagen kit (Qiagen Co., Valencia, CA, USA). Sequencing reactions were carried out with automated fluorescence tag sequencing. Genomic DNA was prepared from spleens of 3-week-old mice according to standard procedures. Total RNA was isolated from retinas of newborn mice by TRIzol LS Reagent (GIBCO BRL, Web Scientific, Crewe, Cheshire, UK) and the SuperScript preamplification system (GIBCO BRL) was used to make first strand cDNA. For BstF5I digestion, we designed another pair of primers to amplify genomic DNA to confirm the mutation: Col2a48F 5′-TTGGTCCCTCTGGCAAAG-3′ and Col2a48R 5′-AACAGGGCCTGTTTCTCCTG-3′. Amplification was done during 36 cycles with a 15-s denaturing step at 94°C, a 1-minute annealing step at 51°C, and a 1-minute extension step at 72°C. BstF5I digestion was carried out directly in a 10-μl volume by adding 8 μl of PCR products, 1 μl of 10× buffer (SE Buffer 5), and 2–5 U of BstF5I (SibEnzyme, Academtown, Russia).
Images were obtained using a Faxitron MX20 cabinet X-ray (Faxitron X-Ray Corp., Wheeling, IL, USA) with 1–5× magnification capabilities. Kodak Min-R 2000 mammography film (Eastman Kodak Co., Windsor, CO, USA) was used for maximum resolution.
The skeletal indices (length, height, width) of the right femur, right tibia, and L6 vertebrae were measured with a dial caliper (Mitutoyo, Kanagawa, Japan) to 0.01 mm. Craniofacial measurements were taken with a digital caliper (Stoelting, Wood Dale, IL, USA) from skulls prepared by incomplete maceration in potassium hydroxide, stained with alizarin red, and stored in undiluted glycerin.(19)
Histology and dynamic histomorphometry
Mutant and control mice at 4 months and 1 year of age were deeply anesthetized with tribromoethanol and killed by intracardial perfusion of Bouin's fixative following flushing of the vasculature with physiological saline. Longitudinal and cross-sections of the lumbar spine (L2-L5) and distal femur were stained with hematoxylin and eosin (H&E). For the evaluation of the femoral growth plate, femurs from 2- and 6-week-old mice were decalcified in 14% EDTA solution for 10 days at 4°C and embedded in paraffin. Five-micrometer-thick sections in the mid-frontal plane were obtained and were stained with toluidine blue.
For dynamic histomorphometry, 6- to 16-week-old mice (5–11 per group) were labeled with tetracycline (20 mg/kg) and then declomycine (20 mg/kg) with a 6-day interval. Tissues were harvested 1 day after the declomycine label. The calvaria, lumbar spine, and both femora and tibias were removed and fixed with 10% cold neutral buffered formalin. All histomorphometric parameters were measured with the OsteoMeasure system equipped with a digitizing tablet (OsteoMetrics, Atlanta, GA, USA) and a color video camera (Sony, Tokyo, Japan). Measurements were made at a total magnification of ×600 (×20 microscope objective and ×30 camera magnification). The cancellous bone area (tissue volume [TV]) at secondary spongiosa was measured in a standardized sampling site 250 μm distal to the growth plate-metaphyseal junction to exclude primary spongiosa.
Nomenclature and symbols used in bone histomorphometry are the same as those described in the report of the American Society for Bone and Mineral Research Committee.(20) The following histomorphometric parameters were measured: longitudinal growth rate (LGR, μm/day), the distance between the fluorescent labels at the metaphysis divided by the fluorescent period; percent cancellous bone volume (BV/TV, %), the percentage of cancellous bone volume to TV; trabecular thickness (Tb.Th, μm), the BV/TV divided by one-half the bone surface (BS); percent osteoid surface (OS/BS, %), the percentage osteoid surface to BS; mineral apposition rate (MAR, μm/day), the mean of the width of the double labels divided by the interlabel time; volume referent bone formation rate (BFR/TV,%/year), MAR × (1/2 × single-labeled surface + double-labeled surface)/TV × 365 × 100%; percent eroded surface (ES/BS, %), percentage eroded surface to BS; percent osteoclast surface (Oc.S/BS, %), percentage osteoclast surface to BS; and osteoclast number (N.Oc/TV, /mm2). We identified osteoclasts as multinucleated cells on eroded surfaces.
Assessment of hearing
Hearing was assessed by auditory-evoked brainstem response (ABR) thresholds with equipment from Intelligent Hearing Systems (HIS, Miami, FL, USA) using previously described methods and equipment.(21) Subdermal needle electrodes are inserted at the vertex and ventrolaterally to both ears of anesthetized mice. Specific auditory stimuli (broad-band click and pure-tone pips of 8, 16, and 32 kHz) from high-frequency transducers are delivered binaurally through plastic tubes to the ear canals. Evoked brainstem responses are amplified and averaged, and their wave patterns displayed on a computer screen. Auditory thresholds are obtained for each stimulus by varying the sound pressure level (SPL) to identify the lowest level at which an ABR pattern can be recognized.
Data are presented as means ± SE. Statistical analyses were performed with StatView 4.5 (Abacus Concepts, Berkeley, CA, USA) software for Macintosh. Results for each measured parameter were analyzed by three-way ANOVA with gender, time, and genotype as the variables. Results were considered significantly different at p < 0.05.
sedc maps to Chr 15 and is a mutation of Col2a1
The sedc mutation was mapped to mouse Chr15 between D15Mit74 and D15Mit44 in a region homologous with human Chr 12q12–13; no recombination between sedc and D15Mit41was detected in 60 sedc/sedc mice. Because homozygotes exhibited a skeletal phenotype consistent with a collagen mutation (see below), and because D15Mit41 is within the Col2a1 gene,(22) we determined Col2a to be a likely candidate gene.
Sequence analysis of the Col2a1 gene showed that the sedc/sedc mutation is caused by a missense mutation in exon 48 that changes codon 1417 CGC to TGC, resulting in an arginine to a cysteine (Arg1417Cys) change (Fig. 1). This mutation resulted in the creation of a new BstF5I restriction site (Fig. 1) that enabled us to genotype the sedc mutation by PCR/restriction fragment length polymorphism (RFLP). To confirm the presence of the missense codon in the sedc Col2a1 gene, we re-examined 46 DNAs (15 affected and 31 unaffected mice) from our linkage analysis for the BstF5I RFLP. We amplified a Col2a48F/Col2a48R 92-bp genomic fragment that contains one BstF5I site in the sedc allele and none in the normal allele (Fig. 1). Digestion of the PCR amplified products with BstF5I from wild-type, heterozygous, and homozygous sedc DNA revealed the predicted RFLP pattern (wild-type—one band of 92 bp; heterozygous sedc—three bands of 92, 72, and 20 bp; homozygous sedc—two bands of 72 and 20 bp). This analysis showed that there was absolute concordance between the sedc/sedc phenotype and the missense mutation (χ2 = 46, p < 0.001). The RFLP pattern thus provides a tool for verification of the presence or absence of the sedc allele in genetic analyses.
To determine whether the sequence alteration at codon 1417 was specific for the Col2a1 gene of the sedc/sedc mice, we analyzed the corresponding genomic DNA region in 12 different inbred mouse strains by RFLP analysis and found that none of the 12 had the BstF5I site present. BLAST results from the nuclear acid database for nucleotide C at position 4249 or from the protein database for amino acid R at position 1417 of the Col2a1 gene indicated that the nucleotide C or amino acid R is conserved across all species examined including Mus musculus, Rattus norvegicus, Homo sapiens, Equus caballus, Canis familiaris, Gallus gallus, Gallus gallus, Oryctolagus cuniculus, Danio rerio, and Cynops pyrrhogaster. These results further argue that the C to T transition at position 4249 of the Col2a1 gene is the mutation underlying sedc rather than a sequence polymorphism. The gene symbol for the sedc mutation has subsequently been assigned Col2a1sedc.
Skeletal abnormalities detected by X-rays and morphometrics
Visual examination of sedc/sedc mice showed shortening of the trunk and long bones. Body weight of sedc/sedc males and females compared with unaffected controls was reduced by approximately 20% at 4 weeks of age and by 30% at 8, 12, and 16 weeks of age. Tail length was reduced by approximately12% in both male and female sedc/sedc mice at 4, 8, 12, and 16 weeks compared with gender-matched unaffected mice, and back length in sedc/sedc males and females was reduced by an average of 14% from 4 to 16 weeks of age. Radiographic examination at ×3 and ×5 magnification showed that the thoracic and lumbar vertebral bodies of sedc/sedc mice were shorter and wider than those of unaffected (sedc/+) littermates (Fig. 2). Skeletal indices of vertebra and long bones (Fig. 3) showed that bones of sedc/sedc mice were significantly shorter but wider than controls (Table 2). In addition, sedc/sedc mice had shortened skulls, whereas height and width of the skull were unaffected. Measurements of nine sedc/sedc mice and six controls demonstrated that the skull length in affected mice was reduced by 5%; upper jaw length was reduced by 4%; and lower jaw length was reduced by 10%, compared with controls.
Abnormal growth plates by histology and dynamic histomorphometry
Longitudinal sections of the spine and spinal cord were prepared from sedc/sedc and control mice at 4, 8, and 16 weeks of age, and similar histological pathology was seen at all ages. The intervertebral disc cartilage in heterozygous control mice was well organized into annulus fibrosus and nucleus pulposus as shown at 16 weeks (Fig. 4A). A comparable section from a 16-week-old sedc/sedc mouse (Fig. 4B) showed shorter and wider vertebral bodies. The end plates of the vertebral bodies were splayed and irregular with no defined growth plate. In addition, the intervertebral disc cartilage was disorganized in mice at all ages examined, and the border between annulus fibrosus and nucleus pulposus of the disc was unclear. A dramatic example of the increased size of the central vertebral body is shown in Fig. 4D. This cross-section of L5 was taken from a 1-year-old sedc/sedc female with severe protrusion of the proliferative cartilage in the dorsal vertebral body, causing compression of the spinal cord. A cross-section of L5 from a normal mouse is shown in Fig. 4C for comparison.
Longitudinal sections of the distal femur from 16-week-old sedc/sedc and control mice are shown in Figs. 5A and 5B. Comparison of the sedc/sedc to the control showed an enlarged and disorganized growth plate with irregularly thickened articular cartilage. A similar section from a 1-year-old affected mouse is shown in Fig. 5C and exhibits the degeneration of articular cartilage often seen in older sedc/sedc mice, whereby the superficial layers of the articular cartilage separate from the deeper layers. Although we cannot explain why the overgrowth of the vertebral body is greater than enlargement of the growth plate in the femur, in our studies of mice, it is not uncommon to find that the skeletal response to environmental and genetic influences varies from one bone site to another.
Mid-frontal sections of the proximal growth plate of the femur from 2- and 6-week-old sedc/sedc and control mice are shown in Figs. 6A–6D. Mutant mice showed an absence of the typical columnar arrangement of cells with a reduction in the number of proliferating and hypertrophic chondrocytes (Figs. 6B and 6D). These observations were more evident in 6-week-old mice (Fig. 6D) than in younger mice (Fig. 6B). However, no reduction of the height of growth plate cartilage was seen at any age in affected mice. The distribution of primary spongiosa in sedc/sedc mice was slightly irregular and shorter than in control mice. However, TRACP+ osteoclasts in the zone of resorption were uniformly distributed both in the sedc/sedc and control mice (data not shown). Invasion of blood vessels into empty lacunae showed no distinct differences between the groups. There was no noticeable difference in intramembranous bone formation in calvaria examined by H&E- and toluidine blue-stained sections between affected mice and controls (data not shown).
Histomorphological parameters of longitudinal growth rate, bone formation rate, and bone resorption rate measured in this study all significantly decreased with age in both sedc/sedc and normal mice, while there was no significant effect of age on bone volume or trabecular thickness in either sedc/sedc or control mice (Table 3). Consistent with the reduced longitudinal bone growth in sedc/sedc mice, as determined by femur and back length, the longitudinal growth rate in mutant mice was significantly less than in control animals by an average of 38% at each age examined. Bone volume and trabecular thickness in sedc/sedc mice were significantly less (17% and 15%, respectively). Osteoid volume, mineral apposition rate, bone formation rate, and osteoclast number in the sedc/sedc mice were significantly less by an average of 33%, 15%, 30%, and 32%, respectively. Eroded and osteoclast surface were not significantly different between sedc/sedc and control groups.
Impaired hearing and retinoschisis
Mice homozygous for the sedc mutation exhibit head bobbing and circling behavior. Such balance defects indicate vestibular dysfunction of the inner ear, which often is associated with cochlear dysfunction. Therefore, we assessed hearing in these mice by auditory brainstem response (ABR) threshold analysis. At 10–15 weeks of age, 1 of the 12 sedc/sedc mice tested was completely deaf, failing to respond to the most intense auditory stimuli presented. All of the remaining 11 sedc/sedc mice exhibited significant hearing impairment, with ABR thresholds 35–50 dB above +/+ mice from the progenitor strains. No abnormalities were apparent at the light microscopic level in whole mounts and cross sections of inner ears from sedc/sedc mice; consequently, the head bobbing behavior remains unexplained.
Examination of eyes from mutant mice revealed that most had an unusual retinal lesion. Portions of the inner nuclear layer (INL) had split apart such that clefts formed between the inner and outer aspects of the INL. This finding was quite distinct from the common artifact of retinal detachment in which clefts appear between the photoreceptor layer and the pigment epithelial layer. The INL clefts varied in size and location from mouse to mouse in sedc/sedc mutants, and sections of eyes of some mutants had no retinal lesions. The lesion was never observed in control mice. Clefting within the INL occurs in humans and is called retinoschisis. A more comprehensive description of this lesion will be published elsewhere.
At least 20 mutations have been identified in the human gene encoding type II collagen,(1) each resulting in a somewhat different clinical phenotype. Linkage studies have identified patients with chondrodysplasias of one variety or other that are associated with each of these mutations, including both missense and nonsense types.(12,14,23–25) The correlation between each type of mutation or the site of the mutation and the clinical phenotype are not well understood.(1,13,14) Genetic analyses have shown that different mutations in the same gene may result in the same clinical phenotype, or a slightly different phenotype, and that locus heterogeneity exists, whereby clinically indistinguishable phenotypes are caused by mutations in different genes.(26,27) A possible explanation for locus heterogeneity is that many of the genes responsible for the formation of cartilage code for molecules with multiple domains involved in different interactions and participating in the formation of multimeric structural complexes or multistep signaling pathways.(28) Thus, genetic and phenotypic analyses of the large variety of chondrodysplasias identified in both humans and mice provide insight into the complex pathways of skeletal development.(29,30)
We have described here a new mutation in the mouse that is analogous to the mutation in the human COL2A1 gene responsible for spondyloepipyseal dysplasia (SED) congenita in two human patients reported to date.(14,15) In the sedc mouse, there is a missense mutation in exon 48 that changes codon 1417 CGC to TGC, causing an arginine to a cysteine change in the COL2A1 protein. In the two human patients with relatively severe SED congenita, the arginine to cysteine substitution occurs at position 789.(14,15) The substitution of a cysteine for an arginine in the Y-position of the Gly-X-Y triplet is of special interest because cysteine is not normally found in the triple-helical domain of type II collagen in any species.(13) A cysteine at this position provides the opportunity for disulfide bonds to form, thus disrupting the formation of collagen fibrils.(31,32) In humans, three arginine to cysteine mutations in the COL2A1 gene have been found at positions 75, 519, and 789, with SED varying in severity; all three mutations have been found in more than one unrelated individual.(13) The sedc mouse model shares not only unique molecular similarity with human SED but also the most common clinical phenotypes including abnormal epiphyses, flattened vertebral bodies, and involvement of the eyes and ears. As in the human, defects in the sedc mouse skeleton are specific to tissues with type II collagen, that is, endochondral bone, whereas intramembranous bone is normal. The eye phenotype, however, differs between human SED patients and the sedc mouse. Whereas SED patients often have myopia with vitreal degeneration and retinal detachment,(12,25)sedc mice have retinoschisis, characterized by clefts between the inner and outer aspects of the inner nuclear layer. Both human SED congenita patients(33) and sedc mice suffer hearing loss.
Recently, a transgenic mouse model was constructed using a type II collagen transgene with an arginine to cysteine switch at position 789 and a murine Col2a1 promoter directing the gene expression to cartilage.(34) Mice carrying the transgene were shorter overall, had shorter limbs with disorganized growth plates, a short nose, cleft palate, and died at birth. Using cell culture experiments and molecular modeling Gaiser et al.(34) suggested that this Y-position mutation acts in a dominant negative way resulting in destabilization of collagen molecules during assembly, reduction in the number of fibrils formed, and abnormal cartilage template function. Although our recessive naturally occurring sedc mutation is molecularly similar, the resulting phenotype is much less severe, whereby mice survive to adulthood and reproduce normally. It is possible that the endogenous COL2A1 protein in the transgenic mouse is overwhelmed by the quantity of abnormal COL2A1 induced by the transgene, resulting in a dominant-negative effect and a more severe phenotype. It is also possible that the insertion site of the transgene has disrupted an additional gene causing a change in the transgenic phenotype. The naturally occurring mutation in sedc mice is likely to be more similar to the mutation in human SED congenita patients because both involve only one gene; thus, sedc mice offer a better tool to further investigate the unique function of the arginine to cysteine substitution in this Y-position than does the transgenic model.
Other mouse models with mutations in the type II collagen gene have been studied, including numerous transgenics(35–38) and one other naturally occurring mutation, disproportionate micromelia (Dmm).(39) The resulting phenotypes in all of the highly expressing transgenic mice, each somewhat different depending on the transgene construct, include an assortment of features associated with human chondrodysplasias-short limbs, disproportionately short stature, small jaw, cleft palate, small thorax, and distended abdomen. All homozygotes were neonatal or perinatal lethal, some because of the inability to breathe.(35,37,40) One transgenic line expressing at low levels developed age-related joint abnormalities that were similar to human osteoarthrosis.(41,42) Transgenic lines were also constructed to overexpress the normal type II collagen gene.(43) In highly expressing lines, thick bundles of collagen fibrils were seen in the growth plate, suggesting that proper assembly of cartilage collagen is dependent on appropriate production of type II collagen. In humans, an example of underproduction of type II collagen is the Stickler syndrome wherein mutations of the human COL2A1 gene results in null alleles.(25)
The opportunity to study chondrodysplasias in humans is limited because of the high number of mutations found in the COL2A1 gene and the variability in the clinical phenotype. Variation in the phenotypic expression of the same mutation in different individuals suggests that other genetic and environmental effects play a part in the final clinical expression. These quantitative and epigenetic effects are difficult to understand in the heterozygous human population. Additionally, different mutations in the COL2A1 gene may result in slightly different clinical presentations, complicating molecular diagnosis. Animal models can help to interpret the clinical phenomena. The sedc mutant strain represents a unique opportunity to study the physiological consequence of a particular Col2a1 mutation in an infinite number of genetically identical individuals. In addition, this viable model of SED congenita allows testing of new treatment modalities for skeletal dysplasias and offers the potential for experimental gene therapy.
We thank Coleen Marden for her help in maintaining our colony of sedc mice; Joiel Buschatz for her characterization of the craniofacial abnormalities, and Jennifer Smith for her help in preparing the graphics for this paper. We also thank Drs Wesley Beamer and Patsy Nishina for their careful review of this manuscript. This study was supported by National Institutes of Health Grants RR01183, CA34186, EY07758, DE13078, and AG19698 (SM).
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