Abstract
Spinocerebellar ataxia (SCA) type 7 is an inherited neurodegenerative disorder caused by expansion of a polyglutamine tract within the ataxin-7 protein. To determine the molecular basis of polyglutamine neurotoxicity in this and other related disorders, we produced SCA7 transgenic mice that express ataxin-7 with 24 or 92 glutamines in all neurons of the CNS, except for Purkinje cells. Transgenic mice expressing ataxin-7 with 92 glutamines (92Q) developed a dramatic neurological phenotype presenting as a gait ataxia and culminating in premature death. Despite the absence of expression of polyglutamine-expanded ataxin-7 in Purkinje cells, we documented severe Purkinje cell degeneration in 92Q SCA7 transgenic mice. We also detected an N-terminal truncation fragment of ataxin-7 in transgenic mice and in SCA7 patient material with both anti-ataxin-7 and anti-polyglutamine specific antibodies. The appearance of truncated ataxin-7 in nuclear aggregates correlates with the onset of a disease phenotype in the SCA7 mice, suggesting that nuclear localization and proteolytic cleavage may be important features of SCA7 pathogenesis. The non-cell-autonomous nature of the Purkinje cell degeneration in our SCA7 mouse model indicates that polyglutamine-induced dysfunction in adjacent or connecting cell types contributes to the neurodegeneration.
- polyglutamine
- ataxin-7
- neurodegeneration
- Purkinje cell
- non-cell autonomous
- truncation
- proteolytic cleavage
The spinocerebellar ataxias (SCAs) are a group of inherited neurological disorders that share the common feature of cerebellar degeneration. Spinocerebellar ataxia type 7 (SCA7) is classified as an autosomal dominant cerebellar ataxia type II (ADCA II), because affected patients display retinal and brainstem degeneration (Enevoldson et al., 1994). Neuropathological examination corroborates the clinical picture, revealing marked atrophy of the cerebellar vermis, the inferior olivary nucleus, and the dentate nucleus (Weiner et al., 1967). Neuronal loss and degenerative changes are consequently greatest in the Purkinje cell layer of the cerebellum and in the inferior olivary complex.
A compelling feature of SCA7 is genetic anticipation (Enevoldson et al., 1994). On the basis of this observation, a repeat expansion was sought as the cause of SCA7, and an expanded CAG tract, ranging from 38 to >250 triplets, was identified (David et al., 1997). The CAG repeat encodes a run of glutamines in the ataxin-7 protein, placing SCA7 in a category of diseases caused by polyglutamine tract expansions. The CAG/polyglutamine repeat disease group consists of at least nine inherited neurodegenerative disorders, including spinal and bulbar muscular atrophy (SBMA), dentatorubral-pallidoluysian atrophy (DRPLA), Huntington's disease (HD), and six types of spinocerebellar ataxia (SCA1, -2, -3, -6, -7, and -17) (Zoghbi and Orr, 2000; Nakamura et al., 2001).
With the exception of SCA6, all of the polyglutamine repeat diseases involve expansion beyond a threshold of ∼35 glutamines, resulting in a change in the conformation of the protein. The transition to a novel conformation may be detected by antibodies directed against extended glutamine runs (Trottier et al., 1995), and the adoption of an altered conformation is hypothesized to underlie a toxic gain-of-function effect. Studies done on animals and in cell culture suggest that the mutant polyglutamine-containing protein (or a peptide fragment thereof) must localize to the nucleus to initiate pathogenesis (Klement et al., 1998; Saudou et al., 1998). Indeed, our recent work on the molecular basis of SCA7 retinal degeneration supports such a model (La Spada et al., 2001). Once in the nucleus, the polyglutamine-expanded protein or peptide fragment can interfere with the function of transcription factors or coactivators (McCampbell et al., 2000; Orr, 2001). Expanded polyglutamine tracts are also relatively resistant to proteasomal degradation via the ubiquitin pathway (Paulson, 1999), and this leads to the accumulation of polyglutamine-containing peptide fragments within the cell. In SBMA, HD, DRPLA, SCA1, SCA3, and SCA7, aggregates of polyglutamine-containing fragments form nuclear inclusions (NIs) within neurons (Paulson et al., 2000).
To advance our understanding of polyglutamine neurodegeneration, we have generated a mouse model for SCA7. Lines of transgenic mice expressing ataxin-7 with 92 glutamines developed a neurological phenotype presenting as a gait ataxia. Despite the absence of expression of polyglutamine-expanded ataxin-7 in Purkinje cells, we documented severe degeneration of cerebellar Purkinje cells in these mice. We observed NIs consisting of N-terminal truncations of polyglutamine-expanded ataxin-7 and were able to detect an N-terminal truncation fragment of ∼55 kDa in protein lysates from affected tissues. The appearance of NIs in cerebellar neurons coincides with the onset of a coordination defect in the SCA7 transgenic mice, suggesting that nuclear localization of the truncated mutant ataxin-7 correlates with the ability to initiate pathogenesis. The non-cell-autonomous nature of the Purkinje cell degeneration in this model implies that dysfunction in adjacent cell types may play a prominent role in SCA7.
MATERIALS AND METHODS
Transgenic mice. The generation of the SCA7 transgenic constructs and the production of the PrP-SCA7-c92Q and PrP-SCA7-c24Q transgenic mice have been described previously (La Spada et al., 2001).
Immunohistochemistry. Deeply anesthetized mice were perfused transcardially with 4% paraformaldehyde in 0.1 mphosphate buffer (PB), pH 7.4. The brain was removed, placed in paraformaldehyde for 4 hr, and cryoprotected in 10% sucrose and then 30% sucrose in PB. Parasagittal frozen sections were cut at 30 μm thickness on a sliding microtome. Immunohistochemistry (IHC) was performed on free-floating sections after blocking in 10% goat serum, 1% BSA, and 0.3% Triton X-100 in PBS, and the primary antibody was diluted in 0.3% Triton X-100 in PBS. The antibodies used and their respective dilutions are as follows: anti-ataxin-7 antibody A, 1:300 (La Spada et al., 2001); anti-ataxin-7 antibody K, 1:2000 (La Spada et al., 2001); expanded polyglutamine tract antibody 1C2, 1:1000 (Chemicon); HDJ-2, 1:500 (NeoMarkers); and Hsc-70, 1:200 (StressGen). Primary antibody staining was visualized with the ABC Vector elite kit (Vector Laboratories) using diaminobenzidine as a chromagen.
Western blot analysis. Protein lysates were obtained by homogenizing tissues in sample buffer (62.5 mmTris-HCl, pH 6.8, 4% SDS, 200 mm dithiothreitol, 10% glycerol, 0.001% Bromophenol blue) at a ratio of 1:10 (w/v) and then boiling. Nuclear extracts were prepared using the NE-PER Nuclear and Cytoplasmic Extraction Reagents Kit (Pierce). Protein samples were resolved by SDS-PAGE (8% acrylamide), transferred to nitrocellulose, and probed with antibody K (La Spada et al., 2001) or 1C2 antibody (Dako) or p44/42 MAP kinase antibody (Cell Signaling Technologies) at 1:1000 dilution in TBS containing 0.1% Tween 20 and 5% BSA, after membrane blocking in TBS with 0.1% Tween 20 and 5% non-fat dry milk. Antibody 1598, produced by Yvert et al. (2000), was kindly provided by J.-L. Mandel (Institut de Génétique et de Biologie Moléculaire et Cellulaire, Institute National de la Santéet de la Recherche Médicale, Strasbourg, France) and was also used at a dilution of 1:1000. The primary antibody was visualized with horseradish peroxidase-coupled anti-rabbit antibodies (Amersham) at 1:2000 dilution and Enhanced Chemiluminescence (Amersham).
Behavioral analysis. Mice of varying ages and genotype were assessed with four different behavioral tests in a blinded manner by investigators over the course of four successive days. The “clasping test” assessed whether mice would clasp their forelimbs and hindlimbs into their bodies or would splay their limbs when suspended by their tails (Lin et al., 2001). The “activity test” measured the activity of mice after removal of their cage lid. Normal “active” mice typically explore their cages when the lid is removed, whereas neurologically affected mice remain inactive or show enhanced exploration of their surroundings (Lin et al., 2001). The “ledge test” (which we developed) involved placing a mouse on the ledge of a cage and observing the response of the mouse to this predicament. Although normal mice either scurry along the bar of the cage and jump down without a problem, mice with neurological dysfunction typically freeze in place or fall into their cages. Finally, we determined the coordination and motor functions of the mice by performing rotarod testing with an Economex Accelerating Rotarod apparatus (Columbus Instruments). The speed of the rod was set to 4 rpm and increased to a final speed of 40 rpm at a rate of 0.1 rpm/sec, and latency to fall was measured in the best four of five daily trails over the course of 4 d. Performance on the rotarod was statistically compared by two-factor ANOVA (Microsoft EXCEL, Office 98).
Light microscopy. Mice were killed, and the brain was removed and immersed in a fixative consisting of 1.6% paraformaldehyde, 2.5% glutaraldehyde, 0.05% MgCl2 · 6H20, and 0.04m sucrose in 0.08 m PIPES buffer at pH 7. After washing, brains were secondarily fixed with 1% osmium tetroxide for 1 hr. A graded alcohol series (methanol or ethanol) was then used to dehydrate the brains: 35, 70, 95, and 100%, each 15 min per change. After three propylene oxide transition washings, brains were embedded in epoxy, and the propylene oxide was allowed to evaporate from the mixture overnight on a rotating shaker. The embedded brains were transferred to molds, and after hardening, the resulting blocks were sectioned on an ultramicrotome. One-micrometer-thick sections were cut and mounted on glass slides after immersion in 50% (v/v) Richardson's stain (sodium borate, Methylene blue, and Azure II, each at 1% w/v) in 0.1m dibasic sodium phosphate solution, pH 8.8.
Confocal microscopy. Free-floating 40 μm brain sections were blocked with 10% goat serum, 1% BSA, and 0.3% Triton X-100 in PBS for 1 hr and then incubated with antibody K (1:2000) and anti-calbindin (1:1000) in PBS containing 0.3% Triton X-100 for 48 hr at 4°C. After three washes with PBS, Alexa Fluor 488 anti-mouse IgG (Molecular Probes) at 1:100 dilution, Cy3 anti-rabbit IgG (Jackson ImmunoResearch) at 1:200 dilution, and 4′,6′-diamidino-2-phenylindole dihydrochloride (DAPI; Molecular Probes) at 1:10,000 dilution were applied to the sections and incubated together overnight at 4°C. After washing, the sections were mounted on glass slides and coverslipped in a medium of 90% glycerol and 10% phosphate buffer with n-propyl gallate added at a final concentration of 0.5% to reduce fluorescent label bleaching. The sections were viewed, and digital scans were recorded using a Zeiss 510 multiphoton nonlinear optics confocal microscope system. Digital imagez-stacks were created, and projections were made from them using the Zeiss AIM LSM software and the NIH Image J program (http://rsb.info.nih.gov/ij/).
RESULTS
Characterization of the SCA7 transgenic mice: expression pattern and aggregates
To produce a mouse model of SCA7, we inserted the ataxin-7 coding region with either 24 or 92 CAGs into the MoPrP expression vector to yield two transgenic constructs: PrP-SCA7-c24Q and PrP-SCA7-c92Q. PCR screening identified five founders (one PrP-SCA7-c24Q mouse and four PrP-SCA7-c92Q mice). As described previously, we determined the expression level of the ataxin-7 transgene in brain RNA samples from representative individuals for each available line and confirmed expression of full-length ataxin-7 protein (La Spada et al., 2001).
To study the expression pattern of ataxin-7 in the CNS, we immunostained frozen sections from our transgenic mice. We found that ataxin-7 is widely expressed in neurons throughout the CNS in the 92Q transgenic mice, but we observed no appreciable increase in ataxin-7 immunostaining in 92Q cerebellar Purkinje cells in comparison with 24Q and non-transgenic control mice (Fig. 1) (data not shown). Lack of transgene expression in Purkinje cells is a feature of the MoPrP construct and has been observed repeatedly (Borchelt et al., 1996; Schilling et al., 1999a,b). In the 92Q transgenic mice, there was intense nuclear staining of neurons, with especially dense staining noted in the granule cell layer of the cerebellum (Fig. 1A,B), pyramidal neurons, and dentate gyrus granule neurons of the hippocampus (Fig.1C,D), the pontine nucleus (Fig.1E), and the inferior olivary nucleus (Fig.1F). At higher magnification, this nuclear staining is clearly punctate with usually one or two dense regions of immunoreactivity (Fig. 1G,H). These densely stained structures resemble the NIs reported in other polyglutamine repeat diseases and mouse models (Ross, 1997) and could be detected with antibodies directed against polyglutamine expansion tracts or heat shock chaperones (1C2, HDJ2, Hsc-70; data not shown). We observed variation in the intensity of ataxin-7 immunoreactivity in NIs between transgenic individuals of the same line and of different lines (data not shown). The intensity of anti-ataxin-7 antibody staining increases with transgene expression level and with age, suggesting that ataxin-7 protein is accumulating in NIs over time.
PrP-SCA7-c92Q mice develop ataxia
The first sign of a neurological dysfunction in the PrP-SCA7-c92Q mice is an unsteady gait beginning at 8–15 weeks of age (Table1). The gait ataxia gradually progresses until the mice display a wide-based stride with occasional falling. The movement disorder then becomes more complicated, and the mice start to shudder and startle easily. The mice become less explorative and a chronic whole-body tremor eventually ensues. By this time, the PrP-SCA7-c92Q mice are significantly smaller in size than their non-transgenic littermates. Such phenotypically affected transgenic mice show decreased survival, with the most severely ill individuals of the highest expressing line (i.e., 6080) dying or requiring euthanasia at 13 weeks of age (Table 1). Despite high level expression of the ataxin-7 transgene in heart and kidney, necropsies performed on these affected mice found no non-neural pathology or obvious cause of death (data not shown). In contrast, the eldest PrP-SCA7-c24Q transgenic mice (1 year of age) show no visible signs of neurological disease and display no increased mortality.
To determine the nature of the behavioral abnormality and the timing of its onset in the SCA7 transgenic mice, we performed a series of four tests to gauge neurological function: clasping test, activity test, ledge test, and rotarod test (see Materials and Methods). Because of the difficulty in maintaining lines 6080 and 6561, we focused our behavioral testing on one high-expressing PrP-SCA7-c92Q line (i.e., 6076), one low-expressing PrP-SCA7-c92Q line (i.e., 6529), and the high-expressing PrP-SCA7-c24Q line (i.e., 6129). Although all tested mice performed all four paradigms at 4 weeks of age without significant differences, 92Q transgene-positive mice from line 6076 exhibited a significant impairment in rotarod function by 8 weeks of age (Fig.2). At 12 weeks of age, performance on the rotarod considerably worsened for line 6076 mice, and the performance difference became even more apparent. This was accompanied by abnormalities in the other testing paradigms, with 50% of the 12-week-old line 6076 92Q mice being classified as “claspers,” “inactive,” or failing the ledge test (data not shown). No functional deficits were noted in these three testing paradigms for comparably aged non-transgenic littermates or for younger (i.e., 4 and 8 week old) line 6076 92Q mice. Once line 6076 mice become visibly ataxic at 13–15 weeks of age, virtually all such mice display abnormal behaviors in all three of these paradigms. Line 6529 mice that express the ataxin-7 92Q transgene at levels less than endogenous, however, continued to perform comparably on the rotarod to aged-matched littermate controls when tested at ages beyond 1 year, as did the line 6129 PrP-SCA7-c24Q mice (data not shown).
Neurodegenerative changes in the cerebellum occur in the absence of apoptosis or significant neuronal loss
Because the neurological dysfunction in the SCA7 mice resembles the presentation of patients with cerebellar ataxia, we evaluated the CNS of our transgenic mice for neurodegenerative changes with particular emphasis on neuroanatomical analysis of the cerebellum. Using a basic dye stain (Richardson's), we examined the cerebella of PrP-SCA7-c92Q mice from line 6076 at 20 weeks of age and found marked histopathology and degenerative changes (Fig.3). Although the cerebella of non-transgenic littermate controls displayed Purkinje cells of typical morphology, the PrP-SCA7-c92Q cerebella consisted of Purkinje cells that were much smaller and shrunken by comparison. Instead of a normal cuboid appearance, the Purkinje cells of the line 6076 PrP-SCA7-c92Q mice were flattened and exhibited less dendritic arborization. The nuclei of the 92Q Purkinje cells revealed occasional invaginations and appeared granular. Despite the observation of degenerative changes in cerebella of PrP-SCA7-c92Q animals killed at end-stage disease, granule cells and Purkinje cells were not labeled by the terminal deoxynucleotidyl transferase-mediated biotinylated UTP nick end labeling method of apoptosis detection (data not shown). Furthermore, there was no obvious difference in the number of neurons within PrP-SCA7-c92Q cerebella immunoreactive for NeuN or microtubule-associated protein 2 (data not shown). These findings suggest that functional deficits develop in PrP-SCA7-c92Q mice without significant neuronal loss.
To determine the timing of aggregate formation relative to the onset of neurological dysfunction, cerebellar sections from SCA7 transgenic mice at 4, 8, and 13 weeks of age were double labeled with antibodies recognizing ataxin-7 and the Purkinje cell-specific calcium binding protein calbindin. Although 4-week-old PrP-SCA7-c92Q mice from line 6076 do not display ataxin-7-positive aggregates in cerebellar neurons, NIs are clearly visible in cerebellar granule cell neurons at 13 weeks of age in c92Q mice from line 6076 (Fig.4). Although NIs can be detected in non-Purkinje cell neurons of the molecular layer (such as stellate, basket, and Golgi cells), NIs are not visible in the Purkinje cells themselves, confirming that the MoPrP promoter does not drive expression in this cell type. Interestingly, detection of NIs in the granule cell layer and the molecular cell layer of the cerebella of the line 6076 mice first becomes apparent at 8 weeks of age (Fig. 4). The NIs are few in number at this age and accompanied by diffuse nuclear staining in a subset of cerebellar granule neurons, suggesting that accumulation of the polyglutamine-expanded ataxin-7 first becomes appreciable around this time. Despite the absence of expression of polyglutamine-expanded ataxin-7 in Purkinje cells, calbindin immunoreactivity in Purkinje cell dendrites was markedly decreased in both 8- and 13-week-old line 6076 transgenic mice (Fig. 4). These findings demonstrate that ataxin-7-containing NIs and non-cell-autonomous Purkinje cell abnormalities develop coincident with the onset of neurological dysfunction in the line 6076 SCA7 mice (Fig.1). IHC analysis of line 6129 ataxin-7 24Q mice and of low-expressing line 6529 ataxin-7 92Q mice revealed no loss of calbindin immunoreactivity or NI formation in individuals at 1 year of age (data not shown).
Ataxin-7 undergoes proteolytic cleavage
As we reported previously, affected PrP-SCA7-c92Q mice produce full-length ataxin-7 protein with 92 glutamines, but the soluble, monomeric form of polyglutamine-expanded ataxin-7 is only readily detectable before the onset of a phenotype (La Spada et al., 2001). With advancing age and neurological dysfunction, little of the full-length monomeric form of ataxin-7 is seen on Western blot analysis, but instead, insoluble immunostaining material tends to be seen in the stacking portion of polyacrylamide gels (La Spada et al., 2001). Inspection of Western blots, which we probed with antibody K raised against the N-terminal portion of ataxin-7, also reveals intense bands migrating at 50–60 kDa (Fig.5A). These bands appear specific to SCA7 transgenic mice that express the ataxin-7 transgene with either 24 or 92 glutamines, because they are not observed in non-transgenic littermate controls.
To confirm the existence of this truncation fragment in the PrP-SCA7-c92Q mice, protein lysates were generated from various tissues from a line 6076 individual and a non-transgenic control and probed with the 1C2 antibody after immunoblotting. The 1C2 antibody, which is directed against expanded polyglutamine tracts and has already been shown to successfully detect polyglutamine-expanded ataxin-7 (Trottier et al., 1995; Lindenberg et al., 2000), also identifies an ∼55 kDa fragment in the PrP-SCA7-c92Q mice (Fig. 5B). Using the 1C2 antibody, no such fragments are detected in non-transgenic littermate controls (as shown) or in PrP-SCA7-c24Q mice (data not shown). Furthermore, protein lysates from the fibroblasts of an affected SCA7 patient reveal a fragment of similar size when probed with the 1C2 antibody, whereas fibroblast lysates from two human controls yield no such fragment. An N-terminal ataxin-7 truncation fragment of comparable mobility is also apparent in protein lysates obtained from the occipital lobe of an unrelated SCA7 patient (data not shown). Interestingly, the amount of detectable fragment in the line 6076 SCA7 transgenic mice varies according to tissue, with heart showing the largest quantity. To verify that ataxin-7 does undergo proteolytic cleavage, we performed IHC analysis on brain sections from PrP-SCA7-c92Q mice with antibody 1598 (Yvert et al., 2000) directed against a C-terminal epitope of the ataxin-7 protein. Although brain sections immunostained with antibody K reveal obvious NIs (Figs. 1, 4), antibody 1598 did not detect NIs or show appreciable staining in transgene-positive mice beyond 4 weeks of age (data not shown). When used to probe Western blots, antibody 1598 could detect full-length ataxin-7 protein but did not identify a fragment specific to SCA7 transgenic mice (data not shown). Because a Northern blot survey of ataxin-7 expression revealed only a single 7.5 kb mRNA species in humans (David et al., 1997), independent detection of a 50–60 kDa protein with polyglutamine-directed and ataxin-7 N-terminal-directed antibodies suggests that this protein product is the result of proteolytic degradation. However, until the proteolytic enzyme is identified or the truncation fragment is peptide sequenced, other possible explanations, including alternative splicing, cannot be excluded.
DISCUSSION
We have generated a representative mouse model of SCA7 by expressing a human ataxin-7 transgene with 92 glutamines in the CNS. The behavioral phenotype observed in the PrP-SCA7-c92Q mice includes features common to SCA7 patients, including prominent gait ataxia. The neurological phenotype progresses to include tremors and hypokinesis. Despite the complexity of the phenotype, the SCA7 transgenic mice display expression of mutant ataxin-7 in the cerebellum, basis pontis, and inferior olivary nucleus, tissues of primary pathological importance in SCA7. The PrP-SCA7-c92Q mice show intense nuclear staining in neurons expressing the ataxin-7 transgene. In humans, ataxin-7 is normally expressed in both the nucleus and cytoplasm of neurons in the pons, inferior olive, cerebellum, thalamus, and striatum (Lindenberg et al., 2000). Studies of SCA7 patient material, however, suggest that this cytoplasmic staining gives way to intense nuclear staining and nuclear aggregate formation, perhaps reflecting relocalization of the polyglutamine-expanded ataxin-7 to the nucleus (Holmberg et al., 1998; Einum et al., 2001). The anti-ataxin-7 antibody used primarily in this study, antibody K, appears specific for human ataxin-7 because it fails to recognize murine ataxin-7. Antibody K immunostaining of transgenic brain sections primarily yields a nuclear pattern, suggesting that the PrP-SCA7-c92Q mice recapitulate the nuclear relocalization of polyglutamine-expanded ataxin-7 observed in SCA7 patients.
In SCA1 transgenic mice and in a striatal neuron model of HD, localization of polyglutamine-expanded protein to the nucleus is required for pathogenesis (Klement et al., 1998; Saudou et al., 1998). In SCA7 patients, however, NIs occur at high frequency in both affected and unaffected brain regions (Holmberg et al., 1998), suggesting that although nuclear localization is necessary to initiate pathogenesis, it is by no means sufficient. Lack of correlation between NI distribution and neurodegeneration has been established similarly for other polyglutamine repeat diseases (Ross et al., 1997; Becher et al., 1998). Additional studies report onset of neuronal dysfunction in the absence of NIs (Klement et al., 1998; Saudou et al., 1998; Hodgson et al., 1999), leading some workers to suggest that nuclear aggregate formation is a protective response by the cell (Sisodia, 1998). Indeed, impaired ubiquitin-proteasome function yielded fewer NIs but accelerated disease pathology in a mouse model of SCA1 (Cummings et al., 1999). Other investigators nonetheless argue that the process of aggregate formation is pathogenic, because development of NIs typically precedes onset of neuronal dysfunction (Perutz and Windle, 2001). In the PrP-SCA7-c92Q transgenic mice, nuclear aggregate formation in granule cell neurons and in neurons in the molecular layer is prominent, with virtually all of these neurons showing NIs when a visibly ataxic phenotype is detectable (Fig. 4). Furthermore, although presymptomatic line 6076 mice lack detectable aggregates, the development of NIs in these mice occurs at 8 weeks of age and coincides with the onset of impaired performance on the rotarod. Thus, it is the accumulation of polyglutamine-expanded ataxin-7 within neuronal nuclei that best correlates with the onset of neurological dysfunction in our model, indicating that once a sufficient quantity of the altered ataxin-7 conformer is present in the nucleus, the disease process is under way. Formation of nuclear aggregates corresponds to the achievement of this threshold and may serve as a useful marker for disease progression. Whether NIs themselves cause or contribute to the disease process or are solely a protective cellular response in our SCA7 transgenic mice and in polyglutamine disease pathogenesis, however, remains to be determined.
A feature of the PrP-SCA7-c92Q mouse model that appears relevant to the human disease is the production of an N-terminal ataxin-7 truncation fragment. Previous studies of HD, DRPLA, and SBMA have yielded evidence that N-terminal truncation fragments accumulate in the nuclei of neurons from brain and spinal cord tissues in affected patients (Li et al., 1998; Schilling et al., 1999a,b). For HD, DRPLA, and SCA7, analysis of transgenic mouse models by immunoblotting and immunostaining suggests that N-terminal truncation fragments are produced from the full-length proteins (Schilling et al., 1999a,b;Yvert et al., 2000). In the present study, we detected N-terminal truncation fragments of ataxin-7 in PrP-SCA7-c92Q and PrP-SCA7-c24Q mice with an ataxin-7-specific antibody. We and others (Yvert et al., 2000) have found that ataxin-7-positive NIs in transgenic mice lack C-terminal epitopes, indicating that N-terminal truncated forms are accumulating in the nucleus. We, however, additionally used the polyglutamine-specific 1C2 antibody to probe protein lysates and were able to detect an N-terminal truncation product in the ataxin-7 92Q mice. Interestingly, with this antibody, we also detected an N-terminal truncation fragment of ataxin-7 in SCA7 patient material, migrating at the same molecular weight position as the truncation fragment present in the SCA7 transgenic mice. The presence of an N-terminal truncation fragment of ataxin-7 in transgenic mice and in SCA7 patients is consistent with the detection of an N-terminal truncation fragment in DRPLA transgenic mice and patients by Schilling et al. (1999b).
Of the polyglutamine-expanded proteins responsible for human disease, huntingtin, the androgen receptor, atrophin-1, ataxin-1, and ataxin-3 can each be cleaved by caspases to generate proteolytic truncation fragments (Wellington et al., 1998). Caspases are cysteine-dependent aspartyl-directed proteases involved in both signal transduction and the execution of the apoptotic cascade (Stennicke and Salvesen, 1998). In some cases, the cytotoxicity of the polyglutamine-expanded protein appears to be dependent on caspase cleavage (Wellington et al., 1998; Ellerby et al., 1999). Interestingly, tissue culture cells expressing polyglutamine-expanded ataxin-7 recruit the active form of caspase-3 into NIs, and CNS tissue from SCA7 patients appears immunoreactive for the activated form of caspase-3 (Zander et al., 2001). This observation suggests that proteolytic processing of ataxin-7 may also be mediated by caspases. However, although the ataxin-7 protein contains several caspase consensus cleavage sites (DXXD), none of these optimal sites is located in a region of the protein that corresponds to the molecular weight of the N-terminal truncation fragment observed in SCA7 transgenic mice and patient material. Indeed, whether proteolysis of ataxin-7 is required for toxicity is not yet known. The goal of future studies will be to determine how the ataxin-7 truncation product is generated and what its role in cerebellar injury and dysfunction is.
In a recent study, Dyer and McMurray (2001) sought to determine whether the huntingtin N-terminal truncation product is generated from polyglutamine-expanded huntingtin or from the normal huntingtin protein product in human HD brains. Using the 1C2 antibody, these workers reported that polyglutamine-expanded huntingtin remains full length, whereas the normal huntingtin protein product is subject to proteolytic cleavage. Although the N-terminal truncation fragment of huntingtin appears to be generated from the normal huntingtin protein, our data and that of others respectively suggest that N-terminal truncation fragments of ataxin-7 and atrophin-1 do derive from the polyglutamine-expanded versions of these proteins (Schilling et al., 1999b; Yvert et al., 2000). Thus, although loss of normal huntingtin function caused by enhanced proteolytic degradation may contribute to the pathogenesis of HD, differences in protein metabolism in the non-HD polyglutamine repeat diseases may indicate that a corollary process of loss of normal function does not occur in all polyglutamine repeat diseases.
A significant feature of the PrP-SCA7-c92Q mouse model is the degeneration of cerebellar Purkinje cells despite the absence of expression of polyglutamine-expanded ataxin-7 in this cell type. To assist in the interpretation of this result, it is useful to consider previous studies of SCA7. Although Purkinje cell degeneration and loss are hallmarks of SCA7, immunostaining of human SCA7 cerebella from both juvenile and late onset patients reveals that few, if any, surviving Purkinje cells contain ubiquitinated NIs (Holmberg et al., 1998; Einum et al., 2001). Furthermore, when Yvert et al. (2000) generated SCA7 transgenic mice expressing ataxin-7 90Q protein at high levels exclusively in Purkinje cells, these mice remained normal beyond 1 year of age, ultimately showing a phenotype and neurodegeneration at 16 months of age. When this group directed high-level expression of polyglutamine-expanded ataxin-7 throughout the cerebellum and brainstem with the platelet-derived growth factor B promoter, however, a motor incoordination phenotype appeared at 3 months of age (Yvert et al., 2000). Our results, taken together with these studies, indicate that expression of polyglutamine-expanded ataxin-7 in neurons that synapse with or receive input from Purkinje cells may underlie the Purkinje cell degeneration in SCA7. Ubiquitinated NIs are most frequent in brainstem neurons in the basis pontis and inferior olive of SCA7 patients (Holmberg et al., 1998). As shown in Figure 1, these brainstem regions contain numerous NIs in our PrP-SCA7-c92Q mice.
What then is the mechanism of Purkinje cell degeneration in the PrP-SCA7-c92Q mice? A well recognized function of synaptic connections between communicating neurons is to provide neurotrophic support (Sofroniew et al., 2001). Members of the neurotrophin family, including brain-derived neurotrophic factor (BDNF), are believed to perform this function in both a retrograde and an anterograde manner (Nawa and Takei, 2001). In HD, a reduction in BDNF levels in corticostriatal projection neurons was found in transgenic mice and patients, suggesting that loss of striatal neurons in HD may involve withdrawal of trophic support (Zuccato et al., 2001). The non-cell-autonomous nature of Purkinje cell degeneration in our SCA7 mouse model could similarly stem from a loss of trophic support involving cerebellar synaptic interconnections. Inferior olivary neurons as well as deep cerebellar and brainstem nuclei are among the principal populations of neurons with which Purkinje cells synapse. Granule cell neurons and Bergmann glia (in the Purkinje cell layer) also show expression of polyglutamine-expanded ataxin-7 in the PrP-SCA7-c92Q mice and could similarly be involved in Purkinje cell degeneration. Whatever the molecular basis of this phenomenon, our SCA7 mouse model clearly demonstrates that Purkinje cell abnormalities develop without intrinsic expression of a polyglutamine-expanded protein, supporting the hypothesis that “murder” by adjacent, dysfunctional neurons or glia does occur in the polyglutamine repeat expansion diseases.
Footnotes
This work was supported by research funds from the University of Washington, by a generous gift from a Utah SCA7 family (Y.-H.F.), and in part by National Institutes of Health Grant NS31775 to R.S.M. We thank G. Nicholson, J. Christodoulou, and T. Bird for patient samples and D. Borchelt for the MoPrP vector.
Correspondence should be addressed to Dr. Albert R. La Spada, Department of Laboratory Medicine, University of Washington Medical Center, Box 357110, Room NW 120, Seattle, WA 98195-7110. E-mail:laspada{at}u.washington.edu.