Carbonic Anhydrase-Related Protein VIII Deficiency Is Associated With a Distinctive Lifelong Gait Disorder in Waddles Mice
Yan Jiao, Jian Yan, Yu Zhao, Leah Rae Donahue, Wesley G. Beamer, Xinmin Li, Bruce A. Roe, Mark S. LeDoux, Weikuan Gu


The waddles (wdl) mouse is a unique animal model that exhibits ataxia and appendicular dystonia without pathological abnormalities of either the central or the peripheral nervous systems. A 19-bp deletion in exon 8 of the carbonic anhydrase-related protein VIII gene (Car8) was detected by high-throughput temperature-gradient capillary electrophoresis heteroduplex analysis of PCR amplicons of genes and ESTs within the wdl locus on mouse chromosome 4. Although regarded as a member of the carbonic anhydrase gene family, the encoded protein (CAR8) has no reported enzymatic activity. In normal mice, CAR8 is abundantly expressed in cerebellar Purkinje cells as well as in several other cell groups. Compatible with nonsense-mediated decay of mutant transcripts, CAR8 is virtually absent in mice homozygous for the wdl mutation. These data indicate that the wdl mouse is a Car8 null mutant and that CAR8 plays a central role in motor control.

RODENTS, mainly spontaneously mutant mice with movement disorders, have revealed molecules and cellular pathways involved in motor control. Examples of deficient or defective proteins in mice with motor dysfunction include Scn8a (type VIII α-subunit of voltage-gated sodium channel) in MedJ mice (Burgess et al. 1995), Grid2 (delta2 glutamate receptor) in lurcher mice (Zuo et al. 1997), Kcnj6 (potassium inwardly rectifying channel subfamily J member 6) in weaver mice (Patil et al. 1995), Agtpbp1 (ATP/GTP-binding protein 1) in Purkinje cell degeneration mice (Fernandez-Gonzalez et al. 2002), and Cacna1a (P/Q type calcium channel α-1A subunit) in tottering mice (Fletcher et al. 1996). Although these models have shed considerable light on signaling and second messenger pathways, the relationship between cellular dysfunction due to these mutations and motor control at the systems level remains unclear. This disconnect is largely due to the ubiquitous expression of the encoded proteins within neural tissues. Furthermore, many mutant rodents with movement disorders exhibit overt structural and histological abnormalities of the central nervous system, extraneural disease, or early death. Thus, in many cases, the mutant gene may have deleterious effects on several local-area neural networks in addition to systemic effects that severely compromise attempts to correlate genotype with particular motor phenotypes (e.g., ataxia, Parkinsonism, dystonia, spasticity, or myoclonus). Identification of additional mutant genes with restricted expression in neural tissue and causally associated with distinct motor syndromes may help to bridge the gaps between the molecular and systems neurobiology of movement disorders. As part of this effort, we chose to study waddles (wdl) mice.

The wdl mutation was discovered at The Jackson Laboratory (TJL) in 1995 in C57BL/KS mice ( The wdl phenotype is very similar to that of another model, waddler (wd), which was discovered in 1959 and is now thought to be extinct (Yoon 1959). The gait of wdl mice is characterized by wobbly side-to-side ataxic movements that are readily seen when mice reach 2 weeks of age. The gait disorder of wdl mice persists throughout their life span.

In addition to ataxia, wdl mice exhibit frequent tail elevation and intermittent Straub tail. During ambulation, the trunks of wdl mice are abnormally elevated, particularly their caudal portions. Resting forelimb and hindlimb tone is normal. However, action dystonia with apparent cocontraction of knee and elbow flexors and extensors is exacerbated by ambulation (Jinnah and Hess 2004). This appendicular dystonia produces nearly straight limbs with minimal flexion at the knee and elbow joints, elevation of the pelvis, and a “bouncy” or “waddling” motion during ambulation, particularly at higher velocities. Occasionally, wdl mice fall to their sides.

Pathological examination of wdl mice at TJL was unremarkable except for one isolated case of hydrocephalus. In addition, vision and hearing were normal in the mutants. An early genetic study indicated that wdl mice were autosomal recessive mutants. Linkage mapping at TJL placed the wdl mutation in close approximation to the wd locus on mouse chromosome 4, although tests for allelism were not conducted since wd is extinct.



One homozygous waddles (wdl/wdl) mouse and its heterozygous littermate (+/wdl) from (L.R.D.) mouse mutant stock resource colonies at TJL were sent to (W.G.) University of Tennessee Health Science Center (UTHSC). Then a breeding colony was established by mating them at UTHSC. Experimental animal procedures and mouse husbandry were performed in accordance with the National Institute of Health's Guide for the Care and Use of Laboratory Animals and approved by the UTHSC Institutional Animal Care and Use Committee.

Motor function examination:

Adult (2–4 months) wdl/wdl mice and wild-type (+/+) littermates were used for quantitative analyses of motor function. The open field behavior of additional wdl mice along with heterozygote (+/wdl) and +/+ littermates was observed in both home cages and bedless arenas. Digital videos were analyzed for the presence of distinguishing behaviors. Analysis of variance was conducted for the significance between the homozygous wdl (wdl/wdl) and their normal littermates (+/wdl or +/+) whenever necessary.


Mice were acclimated to a rotarod (San Diego Instruments) rotating at 5 rpm for 5 min prior to data acquisition. Three 2-min trials were performed at each target speed (5, 10, 20, 30, 40, and 50 rpm) with an intertrial interval of 5 min. The rotarod was accelerated to target speeds >1 min. Median values were used for statistical comparisons.

Footprint analysis:

Mouse forepaws and hindpaws were dipped in nontoxic water-based paints. Mice were then allowed to run down a runway lined with white paper. Three trials were performed with intertrial intervals of at least 5 min. Two to four steps from the middle portion of each run were measured for (1) stride length, (2) hind-base width (the distance between the right and left hindlimb strides), (3) front-base width (the distance between the right and left forelimb strides), and (4) overlap between forepaw and hindpaw placement. At least seven steps were measured for each mouse. Mean values were used for statistical analyses.

Tail suspension:

This test involved the response of each mouse to 1 min of suspension from the tail. Some mice with neurological dysfunction exhibited hindlimb and/or forelimb clasping during this maneuver.

Righting reflex:

To obtain righting reflex times, mice were placed in the supine position and then released. The time required for all four limbs to contact the tabletop was measured for three trials. Median values were used for statistical comparisons.

Vertical rope climbing:

Mice were acclimated to a vertical 40-cm-long, 10-mm-thick rope prior to testing. The bottom of the rope was suspended 15 cm above a padded base and the top entered an escape box. Three trials with a 5-min intertrial interval were completed for each mouse and median times were used for statistical analyses.

Raised-beam task:

Mice were acclimated to an 80-cm-long, 26-mm-wide beam elevated 50 cm above a padded foundation. A 60-W lamp at the start served as an aversive stimulus whereas the opposite end of the beam entered an escape box. Slips were counted as mice traversed the beam. Falls were counted as five slips.

Genome information:

Information on microsatellite markers and their locations were obtained from the Mouse Genome Database search forms ( The locations of microsatellite markers on genome sequences and physical chromosomal distances were obtained by searching the Ensembl mouse genome database (; data used in this article are from its updated information as of March 20, 2005.

High-throughput screening of the wdl locus:

Liver genomic DNA (gDNA) from +/+, +/wdl, and homozygous (wdl/wdl) mice was extracted for temperature-gradient capillary electrophoresis (TGCE) and sequence analysis. On the basis of the Ensembl and National Center for Biotechnology Information (NCBI) databases, primer pairs flanking the exons of known and predicted genes (including ESTs) within the wdl locus were designed with Primer3 software ( Primers were located ∼100 bp 5′ or 3′ to each exon and, in general, produced 300- to 400-bp DNA fragments. Several primer pairs were required for complete coverage of some exons. PCR amplification of gDNA was performed in a 96-well plate format and consisted of 30–35 cycles at three temperatures: strand denaturation at 96° for 30 sec, primer annealing at 54°–60° for 60 sec, and primer extension at 72° for 120 sec. TGCE (SpectruMedix, State College, PA) was used to analyze amplicons from +/+, +/wdl, and wdl/wdl mice mixtures. The SpectruMedix system includes a high-throughput capillary electrophoresis instrument capable of analyzing 96 samples every 140 min. Heteroduplex analysis was subsequently performed offline using SpectruMedix software. Amplicons from wdl mice were sequenced if they differed from normal.


Total RNA was extracted from cerebellum and liver with Trizol reagent (Invitrogen, San Diego). Total RNA integrity was confirmed with the Agilent Bioanalyzer 2100. Reverse transcription and PCR were conducted using a one-step RT-PCR kit from Invitrogen. Reactions were performed in a total volume of 50 μl with 8 ng/μl of total RNA and 0.2 μm forward (CCAAAACAATTCCATGCTTTAAT) and reverse (GTATGAATTCCAGAAGCTGTGGT) primers used to amplify exons 6–9 of Car8. First, cDNA synthesis and predenaturation were performed in single cycles at 50° for 40 min and 94° for 2 min. Next, PCR amplification was performed for 35 cycles: 94° for 30 sec, 54°–58° for 36 sec, and 72° for 2 min.

DNA sequencing:

DNA sequencing was conducted to verify the deletion in the gDNA and cDNA of Car8. PCR products from both genomic and cDNA were purified using an AMPure PCR Purification Kit (Agencourt Beverly, MA) and the purified products were sequenced using a BigDye Terminator v3.1 Cycle Sequencing (Applied Biosystems, Foster City, CA). A total of 5-μl sequencing reactions, including 2-μl of Big Dye (plus Half-BD), 10–23 ng of purified DNA template, and 1–3 pmol of either forward or reverse universal sequencing primers, were incubated for 37 cycles at 96° for 180 sec, 50° for 30 sec, and 60° for 180 sec. Unreacted primers were removed by ethanol-acetate precipitation (3.75% 3 m NaOAc, 87.5% nondenatured 100% EtOH, and 8.75% dH2O, pH 4.6). The labeled products were dissolved in 0.02 mm EDTA in HiDi formamide prior to electrophoretically loading onto the SpectruMedix 96 capillary sequencing system. The same primers in the amplification of DNA fragments from either genomic DNA or mRNA were also used in the sequencing. Sequencing was conducted two times to verify the result for either gDNA or cDNA.

Expression of recombinant CAR8:

Normal (accession no. NM_007592) and mutant Car8 cDNA was amplified (forward primer, CACCATGGCTGACCTGAGCTTCATTG; reverse primer, CTGAAAGGCCGCTCGGATGACTCTAT) and cloned into Invitrogen's pET102/D-TOPO vector in-frame for transcription. A single colony of Escherichia coli BL21 (DE3) transformed with the Car8 expression vector was inoculated into 10 ml of Luria-Bertani medium containing 100 μg/ml ampicillin; this was incubated at 37° for 10 hr. Then 0.5 ml of the culture was inoculated into 50 ml of Luria-Bertani medium containing 100 μg/ml ampicillin. This culture was incubated at 37° until it reached an OD600 of 0.7. At that point, isopropyl-d-thiogalactoside was added to a final concentration of 0.5 mm and incubation was continued at 37° for 3 hr; cells were harvested by centrifugation. Protein products were analyzed on 8% SDS-PAGE gels. Calculated molecular weights for normal and mutant CAR8 fusion proteins are 46.09 and 45.49 kD, respectively.

Northern blot hybridization:

After isolation of total RNA from mouse cerebella, mRNA (from 20 mice: +/+, 7; wdl/wdl, 7; +/wdl, 6) was extracted and purified with the MicroPoly(A)Purist kit from Ambion (Austin, TX). The mRNA was electrophoretically resolved on denaturing gels and transferred to positively charged nylon membranes. Radiolabeled ([32P]UTP) complementary RNA (cRNA) probes were generated by in vitro transcription using T7 RNA polymerase. The location of Car8 probe in the cDNA of Car 8 gene is from 205 to 650 bp. After ultraviolet crosslinking, blots were prehybridized and then hybridized overnight with both Car8 and β-actin cRNA probes. After washing, blots were exposed to Kodak Biomax MR radiographic film prior to development.

Antibody production:

A rabbit polyclonal antibody to CAR8 was generated by immunizing rabbits with a peptide sequence unique to CAR8 (DANGEYQSPINLNSREC) and encoded by nucleotides 27–71 from the second exon of Car8 (AnaSpec, San Jose, CA). This peptide shows no sequence similarity with other carbonic anhydrases. Serum was immunoaffinity purified.

Western blot analysis:

Cerebellar cortex was harvested from mice, rinsed in PBS, and homogenized in chilled NP-40 lysis buffer containing a protease inhibitor cocktail (Sigma, St. Louis). Lysates were clarified by centrifugation. Protein concentrations were determined with the Bio-Rad (Hercules, CA) DC protein assay kit using BSA standards. Equal amounts of proteins were electrophoretically resolved on 4–20% Tris-HCl Criterion precast gels (Bio-Rad) and then transferred onto Immunoblot PVDF membranes (Bio-Rad). Membranes were washed in Tris-buffered saline with 0.1% Tween, blocked in 5% nonfat dry milk, and then incubated in affinity-purified rabbit anti-CAR8 (1:2000) or rabbit anti-inositol 1,4,5-triphosphate receptor (IP3R1) (1:2000, A. G. Scientific, San Diego) antibodies. After washing, blots were incubated in horseradish-peroxidase-conjugated secondary antibodies (1:5000, Amersham, Buckinghamshire, UK). Targeted proteins were visualized with the ECL Plus chemiluminescent kit from Amersham. For loading controls, membranes were stripped and reprobed with a mouse anti-β-tubulin antibody (1:5000; Chemicon, Temecula, CA).


Mice and rhesus monkeys were perfusion fixed with saline/4% paraformaldehyde. Brains were postfixed and then cryoprotected in 30% sucrose/phosphate buffer. Mouse brains and monkey cerebella were sectioned parasagitally on a cryostat and collected onto Superfrost-Plus glass slides (Fisher). Mouse spinal cords were sectioned horizontally. Brain sections were processed for immunocytochemical detection of CAR8 (affinity-purified rabbit antibody, 1:20,000), calbindin (rabbit polyclonal antibody, 1:5000; Chemicon), and IP3R1 (rabbit polyclonal antibody, 1:2000). For light microscopic visualization, tissues were sequentially exposed to a biotinylated goat anti-rabbit polyclonal antibody (1:500; Vector, Burlingame, CA), streptavidin, and diaminobenzidine. Cy2- and rhodamine red-X-conjugated (Jackson ImmunoResearch, West Grove, PA) secondary antibodies were applied for confocal microscopy.


Motor dysfunction in wdl mice:

To characterize the motor function of wdl mice, several experiments were performed to compare the mutants with +/+ littermates. There were no differences between wdl and +/+ mice in their responses to tail suspension. Furthermore, righting times and vertical rope climbing, respectively, did not differ between the mutants and their normal littermates, suggesting that the wdl mice have normal axial and appendicular motor power. In contrast, the results of footprint analysis (Figure 1, A and B), rotarod (Figure 1C), and the raised-beam task were compatible with significant motor disability in wdl mice. Although traversal times on the raised-beam task did not differ significantly between wdl mice and +/+ littermates, the mutants had many more slips (19.0 ± 1.7) than normal (0.8 ± 0.3) littermates (P < 0.0001). In wdl mice, paws were abnormally everted and hindpaw (red) placement was rostral to the location of forepaw (green) prints (Figure 1A). However, there were no differences in either stride length or the distance of paw overlap between wdl and +/+ mice (Figure 1B). At all speeds, wdl mice showed shorter latencies to fall off the rotarod than +/+ littermates (P < 0.05, for all).

Figure 1.—

Behavioral analysis of wdl mice and +/+ littermates. (A) Representative footprint patterns from +/+ and wdl/wdl mice. (B) Quantitative footprint analysis. (C) Latency to fall off the rotarod plotted vs. speed in revolutions per minute (rpm). (*P < 0.05). The error bar denotes standard deviation.

High-throughput screening of the wdl locus on chromosome 4:

According to data from the Jackson Laboratory web page (, the recombination estimates with standard errors and the best gene order were: centromere—D4Mit149 1.79 ± 1.02 cM—wdl—0.81 ± 0.80 cM (D4Mit181, D4Mit99)—7.65 ± 4.16 cM—D4Mit97—2.52 ± 2.47cM—D4Mit39—1.62 ± 1.60 cM—D4Mit5. To begin with, we searched the Ensembl database ( to locate genetic markers flanking the wdl locus. Initially, D4mit149 (at 0 cM), the nearest marker on the centromeric side of the wdl locus, was mapped between 3,584,271 and 3,584,381 bp. D4mit181 (at 2.5 cM), the nearest marker on the telomeric side, was mapped between 9,500,798 and 9,500,930 bp (Figure 2A). Another marker on the telomeric side, D4mit99, was mapped between 12,496,147 and 12,496,289 bp. However, the initial mapping data from TJL were based on 86 F2 mice. By examining the genomic information, we found that the region from centromere to 12,500,000 bp is a gene-poor region with 68 genes and 41 ESTs, mainly from the region between 6,500,000 and 12,500,000 bp (Figure 2A). Those genetic elements were then analyzed with TGCE. Every exon and at least 50 bp of intron sequences on both sides from wdl and normal mice were amplified and carefully compared on the SpectruMedix system. During this screening process, we found that only the Car8 exon 8 amplicon was smaller in wdl mice than in +/+ littermates (forward primer, AATTGTCTCCCAAAATCCCATC; reverse primer, CAGCATGCTTTCTTAACCACTG) (Figure 2B). Every DNA fragment from other genes was the same between wdl and its +/+ littermates. After verification of this difference by PCR amplification of Car8 exon 8 (Figure 2C), we conducted a comparison of PCR products from eight mouse strains and wdl/wdl mice (Figure 2D), and the data indicated that the deletion found in wdl mice did not exist in any of these normal mouse strains (Figure 2E). At that point, we felt confident that a deletion within exon 8 of Car8 caused the wdl disease. We then sequenced exon 8 and discovered that 19 nucleotides were deleted in the mutant mice (Figure 2F).

Figure 2.—

A genomic map of the wdl locus (A) shows the relative locations of microsatellite markers. TGCE detected an abnormality in exon 8 of the Car8 gene (B). PCR amplification of Car8 exon 8 generated a smaller band in wdl/wdl mice, a larger band in +/+ mice, and two bands in +/wdl mice (C). Comparison of PCR products from eight mouse strains and wdl/wdl mice (D) revealed that the deletion does not exist in any normal mouse strains (E). DNA sequence analysis revealed a 19-bp deletion in Car8 exon 8 from wdl/wdl mice (F).

Car8 mutation:

Car8 has nine exons (ENSMUSG00000041261). Total RNA from normal and wdl mice was extracted for RT-PCR amplification of 3′ Car8 transcript (exons 6–9) (Figure 3A). Smaller amplicons were found in cerebella (Figure 3A) and extraneural tissue (liver, lung, and kidney) from wdl mice (data not shown). Direct sequencing of Car8 cDNA from normal and wdl mice confirmed the 19-nucleotide deletion (Figure 3B). In the region of deletion, 15 nucleotides are flanked by two AAGG motifs. The deleted 19 nucleotides include the 15 nucleotides and one AAGG motif, leaving the other AAGG motif in the genome. Thus, the deletion either starts at the first AAGG motif and stops at the second AAGG motif or starts immediately after the first AAGG motif and stops after the second motif. Due to frameshifting, wdl Car8 cDNA is predicted to encode a protein that is 29 amino acids shorter than +/+ CAR8 secondary to elimination of 50 +/+ amino acids and addition of 21 novel residues before terminating in a stop codon (Figure 3B).

Figure 3.—

Analysis of Car8 transcript with RT-PCR. (A) Amplification of Car8 transcript from total RNA extracted from cerebella of +/+ and wdl/wdl mice. (B) Derived amino acid sequences of normal (black) and mutant CAR8 (brown).

Car8 transcript and protein (CAR8):

To determine the molecular impact of the Car8 deletion mutation, we compared mutant and +/+ Car8 at the transcriptional and translational levels. Six bands were identified on Northern blotting of mRNA from both +/+ and wdl mice (Figure 4A). However, a striking global reduction of Car8 transcript was detected in wdl mice (Figure 4A). The larger bands on the Northern blot were barely detectable in the mutants. Quantities of Car8 mRNA were intermediate in +/wdl animals. With Western blotting, our affinity-purified rabbit polyclonal antibody to CAR8 identified both full-length recombinant +/+ and wdl CAR8 in different sizes (Figure 4B). In contrast, we were unable to detect CAR8 in cerebellar tissue lysates from wdl mice although a Purkinje cell marker, the type 1 IP3R1, was expressed at normal levels in the mutants (Figure 4C).

Figure 4.—

The wdl Car8 mutation has dramatic effects at the transcriptional and translational levels. (A) Northern blot analysis of cerebellar mRNA. (B) Western blot analysis of recombinant wild-type (rCAR8-WT) and mutant (rCAR8-wdl) proteins. (C) Western blot analysis of cerebellar lysates from +/+, +/wdl, and wdl/wdl mice; β-tubulin was the loading control.

Immunolocalization of CAR8:

Immunohistochemistry was then used to examine the patterns of CAR8 expression in +/+ and wdl mice (Figure 5). In +/+ mice, CAR8 was expressed in cerebellar Purkinje cells as well as in cerebellar nuclei and brainstem (Figure 5A). Immunohistochemically, CAR8 expression was greatest in cerebellar Purkinje cells and minimal to absent in the spinal cord and cerebral cortex. In line with the Western blotting results, CAR8 expression was virtually undetectable in wdl mice (Figure 5B). The potential importance of CAR8 to humans is suggested by its prominent expression in Purkinje cells from a nonhuman primate (Figure 5C). CAR8 is abundantly present in the somas, axons, and entire dendritic arbors of cerebellar Purkinje cells (Figure 5, D and E). The common Purkinje cell marker, calbindin, showed immunoreactivity in cerebellar cortex that did not differ between normal and mutant mice (Figure 5, F and G). Furthermore, at the level of confocal microscopy, the density and intracellular localization of IP3R1 was normal in wdl mice (Figure 5, H and I).

Figure 5.—

Immunocytochemistry for CAR8 and Purkinje cell markers in +/+ and wdl/wdl mice and a rhesus monkey (R.Monkey). CAR8 in the cerebellum from +/+ (A, D, and E) and wdl/wdl (B) mice and a rhesus monkey (C). Also shown is calbindin (F and G) and IP3R1 (H, I) expression in +/+ (F and H) and wdl/wdl (G and I) mice. Bars: A and B, 1 mm; C, 500 μm; D, 100 μm; E–I, 50 μm.


Our data strongly suggest that the 19-bp deletion in Car8 described here is causally associated with the wdl phenotype. We provide several lines of evidence to support this claim. First, Car8 is located within the genetic region of the wdl locus. Second, the Car8 deletion was the only defect detected among genes and ESTs within the wdl locus from wdl mice. Because the wdl mutation was derived from the C57BLKS inbred strain and there are no other differences between wdl mice and their littermates, it is unlikely that another mutation causes the movement disorder exhibited by wdl mice. Third, work on the cDNA sequence agreed with the genomic data. Finally, we showed a virtual absence of CAR8 expression in wdl mice but not in wild-type littermates.

Our molecular analysis of the wdl mouse model has shown that CAR8 is essential for motor control. Moreover, the relative preponderance of CAR8 in cerebellar Purkinje cells suggests that the wdl mouse can be used as a tool to precisely investigate the effects of Purkinje cell dysfunction on local and wide-area motor networks. In contrast to several other mouse mutants with ataxia, there is no loss or overt morphological abnormalities of Purkinje cells in wdl mice. Although CAR8 is a member of the carbonic anhydrase family of zinc metalloenzymes that catalyze the reversible hydration of CO2, CAR8 lacks catalytic activity by virtue of missing critical amino acid residues required for zinc binding (Sjoblom et al. 1996; Taniuchi et al. 2002). Recombinant CAR8 generated by introducing R117H and E115Q mutations into the wild-type protein is able to bind zinc and catalyze the hydration of CO2. CAR8 may contribute to the pathophysiology of ataxia in other mouse models. For instance, Kelly et al. (1994) reported the absence of Car8 transcript in the cerebella of lurching mice years before the actual causal mutation was identified.

The reduced Car8 transcript and barely detectable CAR8 protein in wdl mice is indicative of nonsense-mediated decay (NMD). NMD, first documented by Losson and Lacroute (1979) >20 years ago, is a proofreading mechanism that enables eukaryotic cells to detect and degrade mRNAs that contain premature termination codons (PTCs). About one-third of inherited genetic disorders and many forms of cancer are caused by frameshift or nonsense mutations, which result in the generation of PTCs (Frischmeyer and Dietz 1999; Holbrook et al. 2004). Although mRNA containing a PTC may initially be translated into a truncated protein, cells can initiate the NMD mechanism to recognize and degrade the mutant transcripts if the truncated protein is deleterious (Wagner and Lykke-Andersen 2002).

With respect to the cellular effects of CAR8 deficiency, it has been shown that CAR8 binds to the modulatory domain of IP3R1, which is an intracellular IP3-gated Ca2+ channel (Hirota et al. 2003). CAR8 inhibits IP3 binding to IP3R1 by reducing the affinity of the receptor for IP3 (Hirota et al. 2003). IP3 is an intracellular second messenger for calcium release. Increased cytosolic-free calcium concentration is a stimulatory signal for diverse calcium-dependent mechanisms such as secretion, contraction, or alterations in membrane excitability. Therefore, CAR8 deficiency may cause ataxia by altering calcium homeostasis and disturbing the normal physiology of cerebellar Purkinje cells.

Our study also demonstrates a useful strategy for simplifying positional cloning. Most procedures employed in traditional positional cloning have been labor intensive and time consuming. As described in materials and methods, our strategy includes identifying a target genomic region on the basis of linkage mapping, identifying every gene and biologically functional element within the candidate region, TGCE heteroduplex analysis (Chou et al. 2005; Girald-Rosa et al. 2005), confirmation of suspected mutations by cDNA sequencing, and, finally, investigatation of the encoded protein. Using a similar approach, we recently identified the causal mutation in a mouse disease model of spontaneous fractures (Jiao et al. 2005). In that study, mapping of the mutation locus was followed by positional cloning. In this study, mapping information on the TJL webpage allowed us to define a target genomic region. The mutant gene was discovered in less than half a year from the start of the project, thereby offering the possibility of rapid identification of mutations with only crude mapping data. We believe that our strategy will be particularly useful for familial human diseases with small kindreds. Furthermore, in the setting of rodent models with spontaneous mutations, mutations can be rapidly identified without the excessive cost and time associated with the extensive breeding programs required for high-resolution mapping.

In summary, we have identified a 19-bp deletion in exon 8 of Car8 in wdl mice using a positional candidate cloning approach. This loss-of-function mutation of Car8 may underlie the ataxic phenotype of wdl mice. Since we did not find an obvious change in the morphology of Purkinje cells or the distribution of the CAR8-binding target, IP3R1, the cellular pathways by which CAR8 deficiency causes ataxia and dystonia remain uncertain. Thus, the role of CAR8 cerebellar neurophysiology warrants additional study.


Special recognition and gratitude are offered to Belinda Harris of The Mouse Mutant Resource at The Jackson Laboratory for providing mice and to Feng Jiao of the University of Tennessee Health Science Center for mouse breeding, tissue collection, and management of this work. Major support for this work was provided by the Center of Genomics and Bioinformatics (W.G.) and the Center in Connective Tissue Research (W.G.), at University of Tennessee Health Science Center. Additional support was from the Dystonia Medical Research Foundation (M.S.L.), the Veterans Administration at Memphis Medical Center (W.G.), National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health (NIH; R01 AR51190 to W.G.; RR01183 to L.R.D.); National Eye Institute, NIH (R01 EY12232 to M.S.L.; R01 EYO15073 to L.R.D.); National Institute of Neurological Diseases and Stroke, NIH (R01 NS048458 to M.S.L.).


  • Communicating editor: M. Justice

  • Received April 14, 2005.
  • Accepted July 29, 2005.


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