Introduction

Amyotrophic lateral sclerosis (ALS) is a fatal neurological disorder characterized primarily by the rapid degeneration of motor neurons (MNs). Mutations in over 20 genes account for about 10% of cases1, but how mutations in each of these functionally diverse genes cause selective MN degeneration is unknown. The identification of the DNA/RNA-binding protein TDP-43 as a component of abnormal, cytoplasmic inclusions in sporadic ALS patients2 and the later discovery of ALS-causing mutations in the TDP-43 gene (TARDBP)3 led to the identification of causal mutations in the gene encoding the related protein FUsed in Sarcoma (FUS)4,5. Together, these findings suggested that aberrant RNA processing may underlie common mechanisms of neurodegeneration in ALS6 and focused attention on the normal activities of TDP-43, FUS and other ALS-associated RNA-binding proteins7.

Over 50 mutations in FUS have been found in ALS families8, the majority of which are dominant, missense changes clustered in and around the C-terminal nuclear localization signal9. FUS mutations are associated with a broad range of clinical phenotypes including some of the most aggressive, juvenile-onset forms of the disease10. How mutant FUS causes ALS is unknown, but both gain- and loss-of-function mechanisms have been proposed8. The toxic gain of function may relate to the formation of abnormal aggregates of FUS in the nucleus and cytoplasm of affected neurons and glia in ALS patients with FUS mutations11,12. Alternatively, an excess of FUS activity may lead to MN degeneration, as suggested by the identification of non-coding mutations that increase the levels of non-mutant FUS13 in ALS patients and by the finding that overexpression of wild-type (WT) FUS in mice causes MN degeneration14.

FUS is a predominantly nuclear protein that plays multiple roles in DNA damage repair and in RNA transcription, splicing, transport and translation15,16. In neurons, FUS is also localized to dendrites and accumulates at excitatory synapses as an RNA–protein complex17 associated with N-methyl-D-aspartate receptor (NMDA) receptors18 and in RNA transporting granules in the soma and dendrites19. These data suggest that FUS, like TDP-43 (ref. 20), could play a role in the modulation of synaptic activity in the central nervous system by regulating mRNA transport and local translation in neurons. Whether any of these diverse activities of FUS is required for MN survival is not known. Thus, the role of FUS function in ALS remains to be determined.

To study the mechanisms of mutant FUS-mediated MN degeneration, we generated an allelic series of targeted, conditional transgenic mice in which a single-copy, WT or ALS-associated mutant human FUS (hFUS) is conditionally expressed from the MAPT (tau) locus. Analysis of these mutants reveals progressive, age- and mutation-dependent MN degeneration that faithfully models several key aspects of the ALS phenotype, including selectivity for MN subtypes most vulnerable in the human disease. MN loss in this model is associated with early synaptic failure and withdrawal of the motor axon from the neuromuscular junction. We demonstrate that expression of mutant hFUS is sufficient to cause MN degeneration, and that alleles associated with aggressive, juvenile-onset forms of ALS are more pathogenic in our disease models.

To determine whether the toxicity of mutant hFUS is a consequence of FUS loss of function, we generated a conditional FUS knockout mouse to demonstrate that long-term survival of MNs in vivo is not dependent on postnatal FUS. These data provide genetic evidence that MN degeneration in ALS-FUS is not a consequence of FUS loss of function, but a toxic gain of function conferred by ALS-associated FUS mutations. To test whether this novel toxic function depends on the presence of WT FUS, we combined the FUS transgenic and knockout mutants to express exogenous mutant FUS in the context of reduced postnatal FUS. These studies demonstrate in vivo that the ALS mutant hFUS is not dependent on endogenous FUS to initiate MN degeneration, arguing against a ‘seeding’ mechanism21 in which mutant hFUS interacts with WT FUS to induce the formation of toxic aggregates. Moreover, the finding that FUS elimination has no effect on the onset of MN degeneration in our model argues that an excess of FUS activity alone does not cause MN degeneration. Together, these data support a disease model in which ALS mutant FUS causes MN degeneration through a toxic gain of function mechanism that does not involve the normal activity of FUS.

Results

Generation and characterization of ALS-FUS mutant mice

To investigate the mechanisms by which ALS-associated mutations in FUS cause MN degeneration, we generated a series of targeted transgenic mouse lines expressing WT or ALS-associated, mutant human FUS from the mouse MAPT (tau (τ)) locus22. cDNAs encoding WT human FUS (hFUSWT) or one of two mutant isoforms—hFUSR521C associated with typical, adult-onset ALS, and hFUSP525L found in patients with an aggressive, juvenile-onset form of the disease10—were introduced (Fig. 1a,b) into the first coding exon of tau, preceded by an N-terminal myc tag to label the exogenous hFUS protein. The τ-hFUS alleles were made conditional by placing a transcriptional stop flanked by loxP sites 5′ of the hFUS cDNA (Fig. 1a) so that the recombinant tau allele is silent until activated by Cre-mediated recombination (Supplementary Fig. 1A). The three conditional τ-myc-hFUS mouse lines are referred to as τOFFhFUSWT, τOFFhFUSR521C and τOFFhFUSP525L.

Figure 1: Conditional expression of myc-tagged hFUS from the MAPT locus reveals increased stability of ALS mutant protein.
figure 1

(a) Organization of the endogenous (τ) and targeted (τOFF) MAPT locus on mouse Chromosome 11. An hFUS expression cassette (light blue) was introduced into exon 2 of MAPT, replacing the endogenous start codon. Excision of the LOX-STOP-LOX transcriptional stop sequence by Cre-mediated recombination allows expression of the myc-tagged hFUSWT, hFUSR521C and hFUSP525L cDNAs from the τON allele of the MAPT locus. (b) Southern blot analysis of targeted ES cell clones following BamHI digestion and hybridization with a 5′ external probe (green, a). Wild-type ES cells (left, +/+) display a 9.0-kb band. Targeted ES cells (right, +/τOFF) yielded a 3.3-kb band corresponding to the τOFF allele in addition to the 9.0-kb band corresponding to the untargeted allele at the MAPT locus. (c) RT–qPCR analysis of hFUS transcripts in total brain and total spinal cord (p90, N=4). Data are represented as mean and s.e.m. (d) Western blot analysis of total spinal cord, brain and sciatic nerve extracts. 7x myc-tagged hFUS migrated at a higher molecular weight (90 kDa) relative to endogenous mouse FUS (73 kDa). Immunoblotting with anti-FUS antibody did not detect myc-hFUS. All mutants analysed were heterozygous for the τONhFUS alleles (with the exception of Supplementary Fig. 4A–C) and tau expression was maintained in these animals. (e) Immunoprecipitation of P90 mouse spinal cord extracts with anti-myc or anti-FUS antibodies. myc-hFUS bands were detected with an anti-FUS antibody following immunoprecipitation with an anti-myc antibody. (f) Western blot analysis of cyclohexamide (CHX)-treated embryonic stem cell-derived motor neurons (ESMNs). At 16 h post CHX treatment, myc-hFUS was no longer detected with anti-myc antibody in cells derived from τONhFUSWT animals but persisted in τONhFUSR521C and τONhFUSP525L samples. Levels of endogenous mouse FUS detected with anti-FUS antibody were similarly decreased in all samples. CyclinB1 was used as an internal positive control for CHX treatment efficacy. (g) Quantification of myc-hFUS levels, normalized to myc-hFUS levels at 0 h, in CHX-treated ESMNs. Data are represented as mean and s.e.m. of N=3 differentiations.

Full size image

To express hFUS constitutively in all τ-expressing cells, we crossed the three τOFF conditional mouse lines to the Prm1-Cre23 germline CRE deleter to generate the τONhFUSWT, τONhFUSR521C and τONhFUSP525L lines. In each of the three, heterozygous τONhFUS mouse lines, no significant change in the level of endogenous mouse FUS (mFUS) or tau was observed (Fig. 1d). Compared with endogenous mouse FUS (mFUS), the slowly migrating (90 kDa) myc-hFUS protein was expressed at low levels and could not be detected by western blot analysis of spinal cord extracts by any one of a series of FUS antibodies (Fig. 1d; antibodies listed in Supplementary Table 1). However, after enrichment by myc or FUS immunoprecipitation followed by western blot analysis with a FUS or myc antibody, respectively, exogenous hFUS was detected in the τONhFUSR521C and τONhFUSP525L samples (Fig. 1e).

Western blot analysis also showed that the levels of hFUSR521C and hFUSP525L were ∼4 times higher than hFUSWT in the spinal cord and brain (Fig. 1d). All hFUS transcript levels were equivalent in brain and spinal cord of the three lines (Fig. 1c; primers listed in Supplementary Table 2), so this increase could not be explained at the level of transcription. However, cyclohexamide blockade of translation in embryonic stem cell-derived MNs from each of the three τhFUS mutants revealed decreased turnover of the mutant protein (Fig. 1f,g). Together these data demonstrate that the accumulation of mutant versus WT hFUS is due to increased stability of the ALS-associated mutant proteins.

Mislocalization of ALS mutant human FUS in MNs

In ALS patients with mutations in FUS, the predominantly nuclear FUS protein is mislocalized to the cytoplasm of neurons and glia24. Immunohistochemical analysis of the τONhFUS mutants demonstrated expression of myc-hFUS in neurons and non-neuronal cells (Fig. 2a) in a pattern consistent with the known pattern of MAPT expression in the spinal cord25,26,27,28. In the myc-hFUSWT control mice, both hFUS and mFUS remained predominantly nuclear (Fig. 2a,c), however, in the τONhFUSR521C and τONhFUSP525L mutants, myc-hFUS was found mislocalized to the cytoplasm and dendrites of τ-expressing MNs (Fig. 2a,b), and mutant hFUS protein was also detected peripherally in the sciatic nerve (Figs 1d and 2c). Notably, the more pathogenic hFUSP525L protein mislocalized to a greater degree compared with hFUSR521C, as shown by a higher cytoplasmic/nuclear ratio (Supplementary Fig. 2B). In contrast, endogenous mFUS remained localized to the nucleus and below levels of detection in the cytoplasm of the τONhFUSR521C and τONhFUSP525L mutants. Despite the marked cytoplasmic mislocalization of mutant hFUS, we observed no large, discrete cytoplasmic aggregates in lumbar spinal MNs in the τONhFUSR521C or hFUSP525L mice. These data demonstrate that ALS-associated mutations in hFUS result in the marked mislocalization of FUS in the cytoplasm, axon and dendrites of neurons, modelling a pathological hallmark of ALS-FUS. Moreover, the degree of mislocalization of hFUSP525L versus hFUSR521C in this mouse model correlates with the relative toxicity of the respective mutant FUS alleles in ALS patients.

Figure 2: Diffuse cytoplasmic mislocalization of mutant FUS extends to sensory and motor axons in the peripheral nerve.
figure 2

(a) Confocal images of L5 spinal cord cross-sections of hFUSWT (left), ALS mutant R521C (centre) and P525L (right) animals immunostained with anti-myc and anti-FUS antibodies. hFUS was detected by anti-myc antibodies in both the grey and the white matter (boundary marked by the dotted white line), consistent with the normal pattern of Tau (MAPT) expression in all neurons and in subpopulations of glia, including oligodendroglia and astrocytes25,26,27. Scale bar, 100 μm. (b) Higher magnification confocal images of L5 MNs, as in a. hFUS-WT protein was detected with anti-myc antibody (top, left) exclusively in the nucleus, whereas hFUS-R521C (top, centre) and hFUS-P525L (top, right) were detected both in the nucleus and in the cytoplasm of the MNs. Immunohistochemical staining with anti-FUS antibody (bottom) detected nuclear but not cytoplasmic FUS in all samples. Scale bar, 25 μm. (c) Cross-sections of sciatic nerves stained with anti-myc (red), anti-ChAT (green) and anti-MBP (myelin basic protein, blue) antibodies. hFUS-R521C and hFUS-P525L proteins, but not hFUS-WT, were detected in motor and sensory axons in the peripheral sciatic nerve. Scale bar, 40 μm.

Full size image

Selective MN loss and weakness in ALS-FUS mutants

To determine if ALS mutant FUS expression in the τONhFUSR521C and hFUSP525L mice was associated with MN degeneration, we used an antibody against choline acetyl transferase (ChAT) to visualize and count spinal MNs at lumbar level 5 (L5; Fig. 3a). At postnatal day 10 (p10), there was no significant difference in the number of ChAT+ L5 MNs in the mutants compared with age-matched τONhFUSWT and WT littermate controls (Fig. 3b), demonstrating that expression of hFUSR521C or hFUSP525L had no developmental effect on the number of MNs generated. We observed the first significant loss of MNs at p30 in the τONhFUSP525L mutant, but no significant MN loss in the τONhFUSR521C at that age (Fig. 3b). However, the number of ChAT+ MNs was significantly reduced in both the τONhFUSR521C and τONhFUSP525L mice at p60 (Fig. 3b). MN loss progressed steadily in both mutants to p360, but was more pronounced in the τONhFUSP525L mutant (∼30%), compared with the τONhFUSR521C mice (∼20%; Fig. 3b), demonstrating that the mutant allele associated with juvenile-onset ALS is also more pathogenic in this mouse model of the disease. Moreover, only mutant hFUS was toxic to MNs in this system as, in contrast, no significant loss of L5 MNs was observed in the τONhFUSWT control (Fig. 3b).

Figure 3: Progressive and selective loss of motor neurons in the lumbar spinal cord of mice expressing ALS mutant FUS.
figure 3

(a) Representative images of L5 spinal cord cross-sections of control τONhFUSWT and τONhFUSP525L p360 animals immunostained with anti-ChAT antibody. Scale bar, 100 μm. (b) MN survival in τONhFUSWT (grey), τONhFUSR521C (blue) and τONhFUSP525L (red) animals calculated from the number of MNs in the L5 spinal cord normalized to that of non-transgenic wild-type controls (expressed as a percentage). (c) Representative images of parvalbumin-positive sensory neurons (PV, green, left) in the L5 DRG and MNs (ChAT, green, right) in the oculomotor nucleus in τONhFUSP525L animals. Scale bar, 50 μm (left), 100 μm (right). (d) The number of parvalbumin-positive sensory neurons in the L5 DRG (left) and the number of MNs in the oculomotor nucleus (right) in p360 τON animals normalized to non-transgenic wild-type controls (expressed as a percentage). (e) Evaluation of hind-limb motor function at p360 using the wire hang test. The latency for animals to fall was recorded over five trials with a 2-min rest period between each trial. (For b, d and e: N=4, *P<0.05, **P<0.01 and ***P<0.001 using one-way analysis of variance with Bonferroni’s post hoc test. Error bars represent s.e.m.).

Full size image

To determine if neuronal loss was selective to MNs in these mutants, we counted parvalbumin (PV)-positive, proprioceptive sensory neurons in the L5 dorsal root ganglia and found no significant difference at p360 in the τONhFUSP525L or FUSR521C mutants relative to controls (Fig. 3c,d). Also we found no significant MN loss at p360 in oculomotor nucleus (Fig. 3c,d), a MN subpopulation spared in ALS patients and in the mutant SOD1 model of disease29. However, as in ALS patients and the SOD1G93A mouse30,31,32,33,34, MN degeneration in the τONhFUS mutants was associated with marked astrocytosis and microgliosis, evidenced by an increase in both glial fibrillary acidic protein (GFAP) and Iba1 immunoreactivity in the ventral horn of the τONhFUSR521C and hFUSP525L mutants relative to the τONhFUSWT controls (Supplementary Fig. 1B).

Expression of mutant hFUS had no effect on the survival of the τONhFUS mice; however, MN loss in the lumbar spinal cord was also associated with significant hind-limb weakness. Wire hang analysis at p360 demonstrated that the average latency to fall for the τONhFUSR525L mutant was approximately half that of the τONhFUSWT and WT controls (Fig. 3e).

These data demonstrate that ALS mutant hFUS, but not the WT protein, is toxic to MNs in this model system, and that hFUSP525L, the more pathogenic allele in patients, also causes earlier and more pronounced MN loss in the mouse compared with hFUSR521C. Moreover, neurodegeneration in the τONhFUS mutants is selective to MNs and associated with significant motor dysfunction, reproducing key aspects of the ALS phenotype.

Early preferential denervation of fast twitch limb muscles

In ALS patients, fast-fatigable (FF) motor units are the earliest affected,35 and neurogenic changes in muscle can be observed before MN loss36. Similarly, MN loss in the SOD1 mouse is also preceded by denervation of skeletal muscles, with early and preferential involvement of FF motor units37,38. To determine whether expression of mutant hFUS results in the early withdrawal of motor axons from muscles innervated by FF motor units, we looked for evidence of denervation in three hind-limb muscles innervated by L5 MNs, the tibialis anterior (TA) innervated predominantly by FF MNs, the soleus (Sol) innervated mostly by slow (S) MNs and the gastrocnemius (GS) innervated by a mixture of S, fast fatigue resistant (FR) and FF motor units39.

Using an antibody against vesicular acetyl choline transporter (VAChT) to visualize motor axon terminals and a fluorescent conjugate of α-bungarotoxin (α-BTX) to label the post-synaptic surface of the neuromuscular junction (NMJ), we found no significant denervation of NMJs at p10 in any of the three τONhFUS mice (Fig. 4a,b). By p20, however, before MN loss was detected at L5, a significant number of NMJs (11.4%) in the TA of the τONhFUSP525L mutants had no associated input (Fig. 4a), demonstrating early retraction of motor axons. Similarly, in the τONhFUSR521C mice, we observed significant denervation of the TA at p40 before L5 MN loss at p60 (Fig. 3b). Denervation of the GS followed at p90 when ∼10% of NMJs were vacant in both the τONhFUSR521C and τONhFUSP525L mice (Fig. 4a). Denervation in both the TA and GS progressed steadily in these mutants so that at p360 in the τONhFUSR521C mouse, 30.2% and 13.9% of endplates were vacant in the TA and GS, respectively (Fig. 4a). Similarly, in the τONhFUSP525L mice 36.7% and 19.3% of NMJs were denervated in the TA and GS, respectively (Fig. 4a). In the predominantly slow Sol muscle, no significant denervation was noted at 1 year (p360) in the τONhFUSR521C, however, over 10% of Sol motor terminals were vacant in the τONhFUSP525L mutant at that time point (Fig. 4a). As further evidence of denervation, internal nuclei (Fig. 4b) and decreased fibre diameter (Supplementary Fig. 3B) were also observed in the TA of the τONhFUSP525L mutant. The same results were found using other pre-synaptic markers including synaptophysin, neurofilament and synaptic vesicle protein 2, demonstrating that the apparent denervation was not a consequence of VAChT downregulation in the mutants (Supplementary Fig. 3A). As τONhFUS is not expressed in the muscle, these data show that mutant FUS causes the early retraction of motor axons from the neuromuscular junction by a pre-synaptic mechanism, and that this pathology preferentially involves the motor units known to be most vulnerable in ALS.

Figure 4: Mutant FUS causes early synaptic changes at the neuromuscular junction, leading to progressive and selective denervation.
figure 4

(a) Denervated NMJs in the TA, GS and SOL of τONhFUSWT (grey), τONhFUSR521C (blue) and τONhFUSP525L (red) animals normalized to controls. N=4. *P<0.05, **P<0.01 and ***P<0.001 using one-way analysis of variance with Bonferroni’s post hoc test. Error bars represent s.e.m. (b) Co-localization of VAChT-positive motor terminals (green) with acetylcholine receptors (α-BTX, red) as a marker of innervated endplates. In τONhFUSP525L animals, denervated endplates (arrows, top right), partially innervated endplates (asterisk, top right) and internal nuclei (arrows bottom left) were observed. Scale bar, 40 μm (top), 20 μm (bottom). (c,d) Electron micrographs from TA NMJs in p30 τONhFUSWT (c) and τONhFUSP525L (d) animals, show that motor terminals (ax., green) were correctly opposed to postsynaptic folds (f) in the muscle (brown, m.f). Higher magnification of boxes 1 and 2 are shown in c1, d1 and c2, d2. In τONhFUSP525L animals, the distributions of mitochondria (purple) and synaptic vesicles (yellow) were altered. Pre- (white arrows, d1, d2) and post-synaptic structurally damaged mitochondria (yellow arrows, d2) with clear- and dark-vacuoles (d.v. and c.v., d2) were observed in τONhFUSP525Lanimals. Scale bar, 1 μm (c,d), 0.4 μm (for c1, c2 and d1,d2). (e) Quantification of synaptic vesicles, healthy mitochondria, postsynaptic folds and sarcomere length in NMJs from τONhFUSWT (grey) and τONhFUSP525L animals (red). N=6 junctions, 2 animals. (f) EMG responses in the TA following a 50-Hz, 1 s stimulation of the sciatic nerve in τONhFUSWT (left) and τONhFUSP525L (right) animals. The first and last four responses are shown in an expanded time scale below. Blue triangles mark the stimulus artefact. (g) M-responses at subsequent stimuli, normalized to the first response in τONhFUSWT (grey) and τONhFUSP525L (red) animals. (N=5. *P<0.05 using two-way analysis of variance with Fisher’s LSD post-hoc test. Error bars represent s.e.m.). (h) Spontaneous activity in the TA of τONhFUSWT (left) and τONhFUSP525L (right) animals. Examples of spontaneous activity are shown in insets 1–3. (i) Frequency of spontaneous events in τONhFUSP525L (red) and τONhFUSWT (grey) animals. (N=5. *P<0.01 using t-test. Error bars represent s.e.m.).

Full size image

As was the case with MN soma counts, no denervation of the TA, GS or Sol muscles was observed in the τONhFUSWT control, demonstrating that the phenotype was specific to mutant hFUS. Here we also used TA denervation as a sensitive measure of MN loss to test whether the selective toxicity of hFUSP525L and hFUSR521C is a result of higher steady-state levels of mutant versus WT hFUS. We analysed mutant mice that were homozygous for the τONhFUSWT or τONhFUSP525L allele. In each case, the level of hFUS RNA determined by reverse transcription–quantitative PCR (RT–qPCR) was double in the homozygous mutant compared with the respective heterozygous control (Supplementary Fig. 4A). Western blot analysis of the homozygous animals confirmed that the level of hFUS protein was twofold higher than in the corresponding heterozygote mutant, which was still too low to negatively regulate endogenous mFUS expression (Supplementary Fig. 4B). In the homozygous animals, the relative levels of hFUSP525L and FUSWT remained approximately 4 to 1 (Supplementary Fig. 4B). No denervation of the TA NMJs was detected in the homozygous τONhFUSWT animals at p90 (Supplementary Fig. 4C), demonstrating that hFUSWT even at twice the level expressed in the τONhFUSWT heterozygotes is not toxic to MNs. Further, analysis of the τONhFUSP525L homozygous mutants showed a comparable degree of TA denervation as in the heterozygous mutant control (Supplementary Fig. 4C).

Abnormal NMJ structure and function early in FUS mutants

Ultrastructural changes of NMJs in the TA muscle were also observed in the τONhFUSP525L mice at p30 when morphological changes were first seen by light microscopy (Fig. 4c,d). At this early time point, mutant NMJs showed pre-synaptic abnormalities, including a significant (∼40%) reduction in the density of synaptic vesicles (depicted in yellow in Fig. 4c1, c2, d1 and d2) in the pre-synaptic terminals of the mutant (39.7±1.4 per μm2) compared with aged-matched WT controls (64.3±6.6 per μm2; Fig. 4c–e). However, the number of active zones—the main apparatus for synaptic vesicle release—was unchanged in the τONhFUSP525L mice compared with the τONhFUSWT control (2.4±0.2 per μm−1 and 2.6±0.2 per μm−1, respectively). In the axon terminals of the τONhFUSP525L mutant, the number of morphologically normal mitochondria (6.3±2.0 per μm2) was significantly decreased compared with control terminals (34.1±10.1 per μm2; Fig. 4c,d, purple) and the remaining mitochondria appeared dilated and vacuolated with disorganized cristae and membranes (Fig. 4d and d1–2), comparable to that described in mutant SOD1 and TDP-43 transgenic models of ALS40. At the postsynaptic site, we also found evidence of muscle degeneration in the τONhFUSP525L mice including abnormal mitochondria (Fig. 4d). Further, the sarcomere length in TA muscle of the τONhFUSP525L mutant (1.83±0.2 μm) was significantly reduced compared with control fibres (3.04±0.05 μm; Fig. 4e). These data suggest that early synaptic changes in the τhFUS mutant mice lead to severe NMJ abnormalities and the consequent axonal detachment observed in our immunofluorescent studies.

To determine whether these ultrastructural changes are associated with physiological dysfunction at the NMJ, we used electromyography (EMG) to record spontaneous and evoked activity of TA MNs at the NMJ in the τONhFUSP525L and WT control mice. Using a novel, in vitro sciatic nerve-hind-limb preparation, we stimulated the sciatic nerve for 1 s at 10, 50 and 100 Hz and recorded the evoked motor response from the TA muscle. We detected no difference in the motor response in the τONhFUSP525L mice compared with controls at 2 weeks of age (Supplementary Fig. 5E,F), demonstrating no developmental abnormality in NMJ transmission. At 3 weeks of age, there was no significant difference in the average motor response between control and mutant mice with low frequency stimulation (10 Hz; Supplementary Fig. 5A,B). However, at 50 Hz there was a significant (∼45%) reduction of the motor response amplitude in the TA of mutant mice compared with controls (Fig. 4f,g), suggesting that mutant MNs cannot sustain reliable neurotransmission at the NMJs and exhibit abnormal signs of synaptic depression. At 100 Hz, both control and mutant mice exhibited synaptic depression as measured by the average amplitude of the motor response (Supplementary Fig. 5C,D), however, in contrast to the controls, the motor response in mutant TA MNs was often completely absent, indicating a failure of neurotransmission. As further evidence of dysfunction at the NMJ in the FUS mutant mice, we observed a significant increase in spontaneous activity in the τONhFUSP525L mutants, a sign of active denervation of neurogenic origin (Fig. 4h,i). Although the frequency and amplitude of these events were variable between mutants, control animals did not exhibit any spontaneous events. Together, these results provide strong evidence that in τONhFUSP525L mutant mice, functional abnormalities in neurotransmission at the NMJ precede gross morphological changes and motor axon withdrawal.

Cell autonomous MN degeneration in FUS mutant mice

To test whether expression of mutant FUS in MNs alone is sufficient to cause MN degeneration, we used a ChAT-Cre deleter strain crossed to the conditional τOFFhFUSWT, hFUSR521C and hFUSP525L lines to express each hFUS isoform selectively in MNs (Fig. 5a). We refer to this series of mice as the τMN lines. Immunohistochemical analysis of the τMNhFUSR521C and τMNhFUSP525L spinal cords revealed marked mislocalization of mutant hFUS to the cytoplasm, dendrites and axons of MNs (Fig. 5a,b). In contrast, WT hFUS remained localized to MN nuclei in the τMNhFUSWT mice, similar to what we observed in the τONhFUSWT controls (Figs 5a and 2b). Immunohistochemical (Fig. 5b) and western blot analysis (Fig. 1d) of sciatic nerve also detected myc-hFUSR521C and -hFUSP525L, but not -hFUSWT in the periphery, confirming that ALS mutant FUS is selectively mislocalized to motor axons in the τMN mutants.

Figure 5: Motor neuron-selective expression of mutant FUS results in degeneration of MNs and denervation of fast muscles.
figure 5

(a) Conditional expression of myc-tagged hFUS proteins (grey, top) in cholinergic cells of τMNhFUSWT, τMNhFUSR521C and τMNhFUSP525L animals. hFUS expression was restricted to cholinergic cells, as determined by the co-localization of myc (red, bottom) with ChAT (green, bottom). Scale bar, 100 μm. (b) Cross-sections of the sciatic nerves from τMNhFUSWT (left) and τMNhFUSP525L (right) animals stained with anti-myc (red), anti-ChAT (green) and anti-MBP (blue) antibodies. Co-localization of hFUS and ChAT in motor axons (yellow) was observed in τMNhFUSP525L but not in τMNhFUSWT animals. Scale bar, 20 μm. (c) MN survival in τMNhFUSWT (light grey), τMNhFUSR521C (light blue) and τMNhFUSP525L (orange) animals calculated from the number of MNs in the L5 spinal cord normalized to that of non-transgenic wild-type controls (expressed as a percentage). (d) Percentages of denervated NMJs in the tibialis anterior, gastrocnemius and soleus muscles of τMNhFUSWT (light grey), τMNhFUSR521C (light blue) and τMNhFUSP525L (orange) animals normalized to non-transgenic wild-type controls. (For c and d: *P<0.05, **P<0.01 and ***P<0.001 using one-way analysis of variance at each time point with Bonferroni’s post hoc test. Error bars represent s.e.m. N=4 for all genotypes.)

Full size image

To determine whether the selective expression of ALS mutant FUS in MNs caused cell autonomous degeneration in vivo, we counted all ChAT+ MNs at L5 (Fig. 5c). At p10, there was no significant difference in the number of L5 MNs in the τMN mutants compared with the τMNhFUSWT and WT controls. At p30, we observed significant MN loss in the τMNhFUSP525L (11.8%, Fig. 5c) mutant mice compared with both τMNhFUSWT and control animals. Significant degeneration was first noted in the τMNhFUSR521C at p60 when 10% of all L5 MNs were lost (Fig. 5c). This degeneration progressed in both ALS mutants until approximately p240, and measured at p360 there were 18.6% and 22.6% fewer MNs overall in the L5 segment of τMNhFUSR521C and τMNhFUSP525L mutants, respectively, compared with age-matched controls (Fig. 5c).

MN loss in the τMNhFUS mutants was also associated with significant (∼10%) denervation of the TA NMJs, first observed at p20 of in the τMNhFUSP525L mutants (Fig. 5d) before any detectable MN loss at L5 (Fig. 5c), and at p60 in the τMNhFUSR521C mice (Fig. 5d). Denervation of the TA muscle progressed with age, and at p360 ∼30% and ∼25% of NMJs were denervated in the τMNhFUSP525L and τMNhFUSR521C mutants, respectively (Fig. 5d). Significant denervation was first noted much later (p120) in the GS in both the τMNhFUSP525L (∼13%) and τMNhFUSR521C (∼10%) mice (Fig. 5d), but even at p360, no significant denervation was noted in the Sol in any of the genotypes we analysed. Together, these data demonstrate that selective expression of mutant hFUS in MNs is sufficient to cause muscle denervation and MN degeneration by cell autonomous mechanisms, preferentially affecting MN subtypes most vulnerable in ALS.

FUS loss of function alone does not cause MN degeneration

In ALS-FUS, mutant hFUS may cause MN degeneration either by acting as a dominant-negative to inhibit normal FUS activity or through a novel, toxic gain of function. A loss-of-function mechanism would be consistent with our observation that mutant hFUS as well as endogenous mFUS was excluded from the nucleus in a significant subset of MNs in the τONhFUS mutants (Fig. 6a), as reported in ALS-FUS patients24. At p120, FUS exclusion was observed in ∼5–10% of L5 MNs in the τONhFUSR521C and τONhFUSP525L mutants, and rarely in the τONhFUSWT and WT controls. Nuclear exclusion of hFUS and endogenous mFUS was also observed in a proportion of MNs in the τMNhFUS mutant mice (Supplementary Fig. 2C).

Figure 6: Motor neuron-selective deletion of FUS does not cause MN degeneration.
figure 6

(a) MNs of τONhFUSWT (left), τONhFUSR521C (centre) and τONhFUSP525L (right) animals immunostained with anti-myc (red, top) and anti-FUS (green, bottom) antibodies. White arrows indicate cells with no nuclear staining for myc-hFUS (red) and endogenous mFUS (green). Scale bar, 25 μm. (b) Illustration of the conditional FUS allele (FUSFLOX) and the null FUS allele (FUSKO*). In the FUSFLOX allele, exons 4–6 of murine FUS are flanked by LoxP (red triangles) recombination sites. Cre-dependent excision of exons 4–6 produces the FUSKO* allele. (c) Western blot analysis of total brain extracts with anti-FUS antibody in p10 wild-type controls (WT/WT) and animals homozygous for the conditional FUS allele (FLOX/FLOX). (d) Using primers specific to exons 12–14, in p0 total brain extracts, FUS transcript abundance in FUS null (FUSKO*/KO*, light grey) was 4.1±0.3% relative to wild-type controls (dark grey) animals. Similar results (6.7±0.8%) were obtained using primers specific to exons 1–3 (N=3). (e) Western blot analysis of total brain extracts from p0 wild-type (WT/WT), heterozygous FUS null (WT/KO*) and homozygous FUS null (KO*/KO*). No protein products were observed in FUSKO*/KO* animals using N-terminal anti-FUS antibody (ab84078). Similar results were obtained using antibodies raised to the middle and the C-terminus of the FUS protein (Supplementary Fig. 4D). (f) Quantification of the fraction of MNs (ChAT+) that were also FUS+ in control (black) and FUS-KOMN (grey) animals. The majority of MNs (67.1±5.6%) were already immunonegative for FUS by p4 and by p30 the elimination of FUS from MNs was complete (99.5±0.3%). N=3. (g) Immunostaining of L5 spinal cords from p360 control (left) and FUS-KOMN (right) animals for FUS (red) and ChAT (white). Boxed area is reproduced at higher magnification in the bottom panels. Scale bar, 100 μm (top), 25 μm (bottom). (h) Percentage of MNs in the L5 spinal cord normalized to control (top) and the percentages of innervated NMJs in the TA muscle (bottom) in p360 control (dark grey) and FUS-KOMN (light grey) animals. N=4. (For f–h: Control=FUSFLOX/WT;ChAT-Cre+/− and FUS-KOMN=FUSFLOX/KO;ChAT-Cre+/−).

Full size image

To explore the role of FUS loss of function on MN degeneration in the τONhFUS mutants, we generated a novel, conditional FUS knockout (FUSFLOX) allele (Fig. 6b) to overcome the perinatal lethality of the constitutive FUS knockout mutation41. FUS transcript (by RT–qPCR (N=3)) and protein (Fig. 6c) levels in the postnatal brain were equivalent in the FUSFLOX/FLOX and WT control, and homozygous FUSFLOX/FLOX and FUSFLOX/KO mutants showed normal postnatal survival. Together, these findings demonstrate that before recombination, the conditional FUSFLOX allele is fully functional and able to rescue the perinatal lethality of FUS deficiency. We then crossed the FUSFLOX mice to a germline Cre deleter strain to generate a constitutive FUS knockout allele (FUSKO*; Fig. 6b) and found that homozygous FUSKO*/KO* mutants die at birth and express no detectable level of FUS transcript or protein at p0 (Fig. 6d,e). These data demonstrate that upon recombination, FUSFLOX generates a null (FUSKO*) allele.

To determine whether FUS deficiency in MNs causes neurodegeneration, we used ChAT-Cre to selectively eliminate FUS from MNs by generating mice heterozygous for the FUSFLOX, FUSKO and ChAT-Cre alleles (referred to as FUS-KOMN mutants). We reasoned that if ALS mutant FUS acts as a dominant negative to cause MN degeneration in the τhFUS mutants and ALS-FUS patients, then the complete deletion of FUS from MNs would result in at least comparable if not more severe loss of MNs in the FUS-KOMN mice. Analysis of the FUS-KOMN mutants revealed selective and nearly complete elimination of FUS from MNs in the ventral horn of the L5 spinal cord by the end of the second postnatal week (Fig. 6f,g). Remarkably, despite this cell autonomous loss of FUS, no appreciable MN degeneration was observed in the FUS-KOMN mutant compared with controls even at 1 year of age (p360), as measured by the number of L5 MN somata and the extent of denervation of NMJs in the TA muscle (Fig. 6h).

As a further test of whether FUS loss of function could cause MN degeneration, we used a ubiquitously expressed, tamoxifen-inducible Cre deleter (UBC-CreERT2 (ref. 42)) to induce widespread, postnatal elimination of FUS in the central nervous system (see Methods for details). Early postnatal FUSFLOX recombination (Fig. 7a) led to the loss of FUS immunoreactivity in a large majority of all neuronal and non-neuronal cells in the L5 spinal cord (shown at p240, Fig. 7b). Again, despite this early and efficient elimination of FUS expression, no significant loss of L5 MNs or denervation of the TA muscle was detected at p240 (Fig. 7c), well after MN degeneration was observed in the τONhFUSR521C and τONhFUSP525L mice. Together, these data demonstrate that postnatal FUS expression is not required for the long-term survival of MNs in vivo and that FUS elimination does not reproduce the MN degenerative phenotype observed in the τhFUS mutants.

Figure 7: Widespread postnatal deletion of FUS does not cause MN degeneration.
figure 7

(a) Experimental paradigm for early postnatal induction of CreERT2 activity. Mice were treated with tamoxifen at postnatal days 1–5 and were analysed at p240. (b) L5 spinal cords of p240 control (FUSFLOX/WT; UBC-CreERT2+/−, left) and FUS-KOUBC (FUSFLOX/KO; UBC-CreERT2+/−, right) animals immunostained for FUS (red) and ChAT (white). Outlined areas of top panels are reproduced at higher magnification in the bottom panels. Loss of FUS immunoreactivity was observed in 96.0±3.8% of NeuN-IR neurons and 83.0±4.8% of NeuN-negative cells. N=3. Scale bar, 200 μm (top), 50 μm (bottom). (c) The numbers of MNs in the L5 spinal cord normalized to control (top) and the percentage of innervated NMJs in the tibialis anterior (TA) muscle (bottom) in p240 control (dark grey) and FUS-KOUBC (white) animals. N=3. (d) Representative images of L5 MNs in τONhFUSP525L/control (left) and τONhFUSP525L/FUS-KOUBC animals (right). (e) Percentage of denervated NMJ’s in the TA muscle of τONhFUSP525L/control (red) and τONhFUSP525L/FUS-KOUBC (green) animals (N=4 for all groups. For d and e, the genotypes of the τONhFUSP525L/control and the τONhFUSP525L/FUS-KOUBC animals were τONhFUSP525L;FUSFLOX/WT;UBC-CreERT2+/− and τONhFUSP525L;FUSFLOX/KO;UBC-CreERT2+/−, respectively.)

Full size image

FUS toxicity is unrelated to endogenous mouse FUS expression

The absence of a MN phenotype in the postnatal FUS knockout mutant leads to the conclusion that MN degeneration in the τhFUS mutant mice is caused by a toxic gain of function. Although mutant hFUS protein in the τON mice is expressed far below the levels of endogenous mFUS (Fig. 1d), MN toxicity may be a consequence of excess of FUS activity. Our finding that the ALS-related mutations increase the stability and steady-state level of hFUS (Fig. 1d,f) is consistent with the idea that MN toxicity is a function of increased FUS expression. Alternatively, mutant hFUS may interact with mFUS to seed the formation of toxic aggregates21,43,44. To test these possible gain-of-function mechanisms, we generated inducible FUS knockout (FUSFLOX/KO; UBC-CreERT2) mice that were also heterozygous for the τONhFUSP525L allele to determine whether the elimination of endogenous mFUS would delay the onset of MN degeneration in the τONhFUS mutant. Postnatal treatment of these mutants with tamoxifen (Fig. 7a) again resulted in elimination of endogenous mFUS from a large majority (∼90.0%) of NeuN+ L5 spinal neurons (Fig. 7d). We used denervation of the TA muscle at p60 as a measure of disease initiation to determine whether this loss of endogenous FUS had any effect on the onset of the τONhFUSP525L MN phenotype. Despite the widespread elimination of mFUS, we found no difference in the degree of TA denervation in this tamoxifen-treated mutant (∼12%) compared with littermate controls (∼13%) in which mFUS was expressed in all cells (Fig. 7e). These data provide functional evidence that the toxicity of mutant hFUS is not a consequence of an excess of total FUS. Consistent with our finding that mutant hFUS and endogenous mFUS do not interact physically (Fig. 1e), these data also demonstrates that mutant hFUS toxicity does not depend on an interaction between mutant and WT protein.

Together, our data demonstrate that the selective toxicity of mutant hFUS in the τON mice is not due to an excess of total FUS or the mutation-related increase in hFUS stability, but rather to a toxic gain-of-function specific to the ALS-associated mutant protein.

Discussion

Advances in ALS genetics have led to the identification of a multitude of genes in which mutations cause selective MN degeneration. The discovery of each new ALS gene presents an opportunity to generate novel models with which to explore mechanisms of disease and to identify therapeutic targets shared between distinct, familial and sporadic forms of ALS. ALS-FUS is unusual in that a wide variety of clinical phenotypes are associated with FUS mutations, ranging from common presentations of the disease to the most aggressive, juvenile-onset forms of ALS reported. Here using a series of novel mouse models of ALS-FUS, we demonstrate that FUS loss of function is not sufficient to cause the selective and progressive loss of MNs associated with ALS mutant FUS and that the toxicity conferred by ALS mutations on FUS does not involve an excess of FUS activity or require the interaction of mutant and WT FUS.

FUS expression is highly regulated and existing animal and cellular models have shown that an excess of WT FUS activity is toxic14, although not necessarily in a way that is relevant to ALS. We modelled FUS-ALS by generating a series of targeted transgenic animals in which equivalent levels of exogenous hFUS transcript are stably expressed from a defined locus in a consistent pattern, at or below endogenous FUS levels so as to avoid any variance in the lines that may influence the MN phenotype. Analysis of animals expressing mutant hFUS selectively from spinal MNs (τMN) or more broadly from all τ-expressing neurons and non-neuronal cells (τON) revealed progressive MN degeneration that selectively involves spinal MNs and spares neuronal populations normally unaffected in ALS, including oculo-MNs and other long projection neurons like muscle spindle (IA) afferents in the dorsal root ganglia. We also observed the preferential involvement of fast versus slow twitch motor units in our models, demonstrating the selective loss of specific, functional subtypes of spinal MNs most vulnerable in patients and SOD1 mutant mice37. In contrast, no MN loss or muscle denervation was observed in the heterozygous or homozygous hFUSWT animals, demonstrating that the MN phenotype we describe is dependent on the ALS-causing mutation in hFUS. The molecular and cellular selectivity of mutant FUS toxicity in this system demonstrates the relevance of the τON-hFUS mouse model to FUS-ALS. However, the selective involvement of a specific subset of MNs—while sufficient to cause significant hind-limb weakness—does not influence the lifespan of these mutants. Although this is in some respects a limitation of the model, the early onset and steady progression of MN degeneration, together with the specific, qualitative aspects of the MN phenotype make the τON-hFUS mutants a highly ALS-relevant system in which to explore disease mechanisms and to test potential therapeutics.

The conditional nature of the τ-hFUS alleles allowed us to explore whether cell autonomous and non-autonomous mechanisms contribute to mutant FUS-dependent MN degeneration, as in SOD1 mice45,46,47,48. We found that selective expression of mutant hFUS in MNs caused MN degeneration with the same selectivity as in the τON mutants. These data do not argue that ALS-FUS is a cell autonomous disease, only that expression of mutant FUS in MNs alone is sufficient to cause MN loss. Even in the τMN mutants, evidence of astrocytosis and microgliosis suggests that secondary, non-autonomous mechanisms may also contribute to the MN phenotype in this model. Comparison of the τMN- and the corresponding τON-hFUS mutant (Supplementary Fig. 3D) did not reveal a significant non-autonomous effect in the hFUSR521C model, but in the hFUSP525L mice the extent of MN loss and the degree of denervation was significantly greater in the τON versus τMN mutant, but only after p240. These studies show that cell non-autonomous expression of mutant hFUSP525L had no effect on the onset of MN degeneration, but did accelerate disease progression in this mouse model of ALS-FUS. The specific cell type(s) involved in the cell non-autonomous mechanisms of disease progression in the τON mice remains to be determined, but the predominant expression of MAPT in neurons and oligodendroglia (Supplementary Fig. 3C) implicates these MN partners in FUS-mediated MN degeneration.

MN degeneration in the τ-hFUS mutants progresses slowly, but the first evidence of pathology is detected remarkably early in the most vulnerable motor units of the τONhFUSP525L mice. By the third postnatal week, structural and functional evidence of synaptic failure at the NMJ is first observed. Pre- and postsynaptic changes in the ultrastructure of the NMJ—including abnormal mitochondria and reduced synaptic vesicle density—are associated with electrophysiological evidence of active denervation of the TA muscle, including increased spontaneous activity and sensitivity to high-frequency stimulation. These early changes at the NMJ anticipate the retraction of the motor axon ∼10 days later in the τONhFUSP525L mouse and precede loss of MN somata. These data are consistent with a model of axonal ‘die-back’ described in the SOD1 mutant by which degenerative changes at the NMJ occur in advance of neuronal loss in distinct subpopulations of MNs49. The mechanism that underlies these early physiological and morphological changes at the NMJ is not known, but overexpression of mutant FUS has been reported to impair axonal transport50,51,52. The reported roles of FUS in mRNA transport and local translation17 are perturbed by ALS-associated mutations53,54, suggesting that—as with mutant TDP-43 (ref. 20)—mutant FUS may impair the transport of mRNA to the periphery and decrease axonal translation required for axonal maintenance55.

The discovery of novel ALS genes leads first to the question of whether causal mutations result in a loss of function of the encoded protein or a gain of toxic properties, related or not to its normal activity. Structural and functional similarities between TDP-43, FUS and other ALS-associated RNA-binding proteins encouraged the view that the role of these proteins in MN disease relates to the normal RNA processing functions of these regulatory factors. Physical interaction between FUS and TDP-43 as well as evidence of their shared role in genetic pathways required for survival and motor function56,57 further implicated the normal activities of these proteins in MN survival in ALS. These early observations led to the suggestion that mutant FUS acts as a dominant negative to interfere with the normal activity of the WT FUS protein to cause a partial or complete loss of function, leading to MN degeneration in ALS-FUS. Our data demonstrating that postnatal FUS elimination has no effect on MN survival even in the most vulnerable MN pools provide unequivocal evidence that FUS loss-of-function alone does not underlie MN degeneration in ALS.

In ALS patients, FUSP525L is associated with juvenile-onset and rapidly progressive MN disease. In the τONhFUS mice, this allele is also more pathogenic than hFUSR521C both in terms of onset and progression of the MN degeneration. This provides further evidence that the τ-hFUS mice reliably model key aspects of ALS-FUS. However, the basis of this enhanced toxicity is not clear. In the τ-hFUSP525L mice, mutant FUS is localized to the cytoplasm to a much greater extent than hFUSR521C, and the more pronounced MN phenotype is consistent with previous studies that correlate toxicity with the degree of cytoplasmic mislocalization of FUS58. However, although the accumulation of cytoplasmic FUS correlates with the severity of the MN phenotype in our model, we find no evidence that this is associated with the formation of large cytoplasmic inclusions characteristic of ALS-FUS.

Toxicity in the τ-hFUS mice was also associated with an increase in the steady-state level of mutant hFUS protein relative to the hFUSWT control, which does not reflect a difference in the levels of hFUS mRNA in the three τON-hFUS mice, but an increase in the stability of hFUS conferred by ALS-causing mutations—in agreement with a recent in vitro study59. However, the selective toxicity of mutant hFUS does not appear to be a quantitative/dose-dependent effect in this system as doubling of hFUSWT levels in the homozygous τON mutant does not result in MN degeneration, and twice the level of mutant hFUSP525L does not exacerbate the MN phenotype. Rather, these data support a mechanism by which ALS-related mutations confer qualitative changes on hFUS that underlie the toxic gain of function.

Insight into the mechanism by which mutant FUS causes MN degeneration in the τON mice comes from our finding that the postnatal elimination of the endogenous FUS in our most severe hFUSP525L mutant had no effect on the initiation and early progression of MN loss. These data argue that mutant FUS toxicity does not involve an excess of FUS activity, as suggested by the finding that mutations in the 3′UTR of FUS13 cause ALS by perturbing the autoregulation of FUS expression60 and increasing FUSWT levels13, and by previous studies showing that overexpression of FUSWT is toxic to neurons. Our data also demonstrate that the toxicity of mutant FUS does not depend on a physical or functional interaction with the much more14,61 abundant endogenous FUS protein, arguing against the ‘seeding’ hypothesis of FUS toxicity by which mutant hFUS accelerates the aggregation of mFUSWT, resulting in selective toxicity to MNs.

In light of our conclusion that the activity of FUS is not required for the long-term survival of MNs, the question remains then as to how the structural and functional similarities between FUS-, TDP-43- and other ALS-associated hnRNP’s relate to their role in the disease. One intriguing idea is that these ALS proteins all contain low-complexity ‘prion-like’ sequences (and possibly other domains62) that are not only a key determinant of their normal function, but also of their role in the pathogenesis of ALS. These domains appear to mediate the movement of these regulatory proteins in and out of subcellular, RNA-containing structures like stress granules43,44 and permit reversible and regulated44,63,64 interactions with a large variety of partner proteins. Under pathological conditions, these same regions may mediate the irreversible formation of abnormal aggregates that are selectively toxic to subpopulations of neurons. The natural propensity of these proteins to anneal leads to a model of disease in which the low probability of WT protein to form these toxic aggregates is increased by disease-causing mutations, leading to the onset of neurodegeneration7. Although our data does not support the seeding of endogenous FUS by the mutant, aberrant interactions of mutant hFUS with other factors could underlie its toxicity, and the ALS-FUS models we present offer a highly disease-relevant, in vivo system in which to explore these interactions and to elucidate mutant FUS-dependent mechanisms of disease.

Methods

Generation of mice and mouse genetics

All procedures were performed in accordance with the National Institutes of Health Guidelines on the Care and Use of Animals and approved by the Institutional Animal Care and Use Committee at Columbia University.

The τOFFhFUS mouse lines were generated using a vector modified from that designed to target the mouse MAPT (tau) genomic locus by homologous recombination65. This targeting vector was modified to include a LoxP-flanked transcriptional ‘stop’ sequence (poly-A3) followed by a myc-tagged human FUS cDNA (hFUSWT, hFUSR521C or hFUSP525L generously provided by Brian McCabe).

The FUSFLOX mouse line in which FUS exons 4–6 are flanked by LoxP sites was created from ES cells obtained from the International Knockout Mouse Consortium Project: 84575.

Muscle innervation analysis

Cryosections of muscle (30 μm) were stained with antibodies against VAChT to identify the pre-synaptic terminal, and tetramethylrhodamine-conjugated α-BTX (Invitrogen) to detect post-synaptic acetylcholine receptors. Images were acquired using Zeiss Pascal LSM 510 confocal microscope using a × 10 objective. Percentage (%)NMJ innervation was determined by dividing the total number of areas of overlap between VAChT and α-BTX signals (total number innervated endplates) by the number of areas α-BTX signal (total number of endplates).

MN counts

The lateral motor column of lumbar spinal segment L5 was imaged as a z-series of confocal optical sections at a × 20 magnification (z-step of 1.5 μm). MNs labelled with an anti-ChAT antibody were counted by outlining the cell body in the confocal plane of the nucleolus using ImageJ.

Electron microscopy

Animals were deeply anaesthetized using ketamine (100 mg kg−1) and xylazine (10 mg kg−1) and transcardially perfused with 0.1 M PBS followed by 2.5% glutaraldehyde and 4% paraformaldehyde (EMS) in PBS. TA muscles were post-fixed at 4 °C overnight and sectioned using a vibrating blade microtome (200 μm; Leica VT 1000S) and processed for reduced osmium tetroxide-thiocarbohydrazide—osmium (ROTO) method66. After dehydration and resin infiltration (EPON 812; EMS), samples were cured at 70 °C for 3 days. Blocks were sectioned in a UC7 Ultramicrotome (Leica) with a 35° Diamond knife (Diatome). Ultra-thin serial sections (40 nm) were collected on Kapton66, post-stained (1% uranyl acetate, 5 min; 2% lead citrate, 1 min), mounted in silicon wafers (Universal Wafers) and carbon coated (custom built coater). Backscattered images were collected using ATLAS (FIBICS) at 3 nm pixel resolution (3 ms dwell) in a SIGMA FESEM electron microscope (Zeiss).

NMJ functional assays

Mice were terminally anaesthetized with isoflurane followed by decapitation. The M-response in TA muscles was assessed in an isolated sciatic nerve-hind-limb preparation in vitro. Muscles were perfused with oxygenated (95%O2+5%CO2) artificial cerebrospinal fluid (CSF) (12.83 mM NaCl, 0.4 mM KCl, 0.05 mM NaH2PO4, 2.1 mM NaHCO3, 1.5 mM CaCl2, 1 mM MgSO4, 30 mM glucose). A suction stimulating electrode was placed on the sciatic nerve and EMG recordings were obtained using a concentric needle electrode (P12CEA3, Microprobes) placed in the belly of the muscle. The maximum M-response was obtained following stimulation of the sciatic nerve for 0.2 ms at supramaximal stimulus intensity. The signal was amplified ( × 1,000; acquired by MultiClamp 700B, Molecular Devices), filtered (0.1–3 kHz) and digitized for offline analysis.

Spontaneous muscle activity was recorded for 60 s immediately after placement of the EMG electrode. A two Standard Deviations (2s.d.) window discriminator of the peak-to-peak baseline signal (calculated from 5 different and random time points during EMG acquisition) was used to calculate spontaneous events above the baseline recording.

Subsequently, a train of stimuli was delivered at 10, 50 and 100 Hz to the sciatic nerve for 1 s duration. The change of the M-response (measured peak-to-peak) at different frequencies was calculated and expressed as a percentage change from the first response for each frequency.

Statistical analysis

For all statistical tests, Graph Pad Prism 6 software was used. Statistical analysis of mean differences between groups was performed using either one- or two-way analysis of variance, followed by a Bonferroni post hoc analysis or Fisher’s least significant difference (LSD) test depending on the number of variables and time points in each experiment. The statistical tests, P values and n values are indicated in figure legends.

See Supplementary Methods for details.

Additional information

How to cite this article: Sharma, A. et al. ALS-associated mutant FUS induces selective motor neuron degeneration through toxic gain of function. Nat. Commun. 7:10465 doi: 10.1038/ncomms10465 (2016).