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Growth Differentiation Factor 6 As a Putative Risk Factor in Neuromuscular Degeneration

  • Michèle G. DuVal,

    Affiliation Department of Biological Sciences, University of Alberta, Edmonton AB, Canada

  • Matthew J. H. Gilbert,

    Affiliation Department of Biological Sciences, University of Alberta, Edmonton AB, Canada

  • D. Ezekiel Watson,

    Affiliations Department of Biological Sciences, University of Alberta, Edmonton AB, Canada, Centre for Prions and Protein Folding Disease, University of Alberta, Edmonton AB, Canada

  • Tanja C. Zerulla,

    Affiliation Department of Biological Sciences, University of Alberta, Edmonton AB, Canada

  • Keith B. Tierney,

    Affiliation Department of Biological Sciences, University of Alberta, Edmonton AB, Canada

  • W. Ted Allison

    Affiliations Department of Biological Sciences, University of Alberta, Edmonton AB, Canada, Centre for Prions and Protein Folding Disease, University of Alberta, Edmonton AB, Canada, Department of Medical Genetics, University of Alberta, Edmonton AB, Canada


Mutation of Glass bottom boat, the Drosophila homologue of the bone morphogenetic protein or growth/differentiation factor (BMP/GDF) family of genes in vertebrates, has been shown to disrupt development of neuromuscular junctions (NMJ). Here we tested whether this same conclusion can be broadened to vertebrate BMP/GDF genes. This analysis was also extended to consider whether such genes are required for NMJ maintenance in post-larval stages, as this would argue that BMP genes are viable candidates for analysis in progressive neuromuscular disease. Zebrafish mutants harboring homozygous null mutations in the BMP-family gene gdf6a were raised to adulthood and assessed for neuromuscular deficits. Fish lacking gdf6a exhibited decreased endurance (∼50%, p = 0.005) compared to wild type, and this deficit progressively worsened with age. These fish also presented with significantly disrupted NMJ morphology (p = 0.009), and a lower abundance of spinal motor neurons (∼50%, p<0.001) compared to wild type. Noting the similarity of these symptoms to those of Amyotrophic Lateral Sclerosis (ALS) model mice and fish, we asked if mutations in gdf6a would enhance the phenotypes observed in the latter, i.e. in zebrafish over-expressing mutant Superoxide Dismutase 1 (SOD1). Amongst younger adult fish only bigenic fish harboring both the SOD1 transgene and gdf6a mutations, but not siblings with other combinations of these gene modifications, displayed significantly reduced endurance (75%, p<0.05) and strength/power (75%, p<0.05), as well as disrupted NMJ morphology (p<0.001) compared to wild type siblings. Bigenic fish also had lower survival rates compared to other genotypes. Thus conclusions regarding a role for BMP ligands in effecting NMJ can be extended to vertebrates, supporting conservation of mechanisms relevant to neuromuscular degenerative diseases. These conclusions synergize with past findings to argue for further analysis of GDF6 and other BMP genes as modifier loci, potentially affecting susceptibility to ALS and perhaps a broader suite of neurodegenerative diseases.


Development, growth and stabilization of neuromuscular junctions (NMJ) in larval Drosophila require the bone morphogenetic protein (BMP) gene glass bottom boat (gbb) [1]. Here we tested whether this same conclusion can be broadened to vertebrates, and extended this analysis to consider whether such genes are required for vertebrate NMJ maintenance in post-larval stages. Gbb is the Drosophila homolog of a family of vertebrate genes including the BMP and growth/differentiation factor ligands (BMP/GDF Family), which is itself a sub-family of the transforming growth factor β (TGFβ) genes [1][3]. Extending their role to encompass vertebrate NMJs would embolden speculation that mutations in BMP/GDF genes can sensitize patients to progressive late-onset neuromuscular disease. This affirmation would support the contended relevance of several intriguing cellular and molecular mechanisms of neuromuscular degeneration, derived from Drosophila studies (see Discussion), that are hypothesized to impinge upon the development of treatments or diagnostics of neuromuscular disease.

Indeed the synthesis of disparate literature by several authors has recently suggested that mutations in BMP/GDFs are good candidates for sensitizing patients to amyotrophic lateral sclerosis (ALS), if not representing causal instigators of disease etiology [4], [5]. This suggestion was based not only on the aforementioned role of Gbb [1], [2], but also upon the requirement for the proteins constituting Gbb receptors in NMJ development [6][8]. BMP/GDFs have also been implicated in ALS progression via a separate line of inquiry, in that a Drosophila model of familial ALS8 demonstrates disrupted BMP signaling at their NMJs; Thus mutations in VAPB (vesicle-associated membrane protein B) cause ALS8 [9], [10] and altering VapB disrupts BMP signaling at the Drosophila NMJ [11]. A role for BMP/GDFs in other neuromuscular diseases has also been proposed, including Spinal Muscular Atrophy, Hereditary Spastic Paraplegias, Multiple Sclerosis and Huntington's Disease [4].

BMPs are most widely recognized for their fundamental roles in development across vertebrates, including patterning the dorsoventral axis of the body, CNS and retina [12][17]. BMP/GDF proteins heterodimerize or homodimerize to signal through BMP receptors, and canonically through phosphorylating SMAD proteins, though several other signaling cascades can be important in many instances [18].

ALS is a progressive neuromuscular disease caused by motoneuron loss, though the etiology of motoneuron death is unknown. Candidate causes include glutamate excitotoxicity, oxidative stress, and RNA processing defects. Symptoms in patients, recapitulated in animal models overexpressing mutant SOD1, include progressive muscle weakness and decreased endurance, altered gait, motor neuron death and progressive paralysis. Genetics of familial ALS (fALS) include lesions in TARDBP, FUS/TLS, C9orf72 and SOD1. Identification of misfolded SOD1 in sporadic ALS argues for a central role for SOD1 in ALS regardless of genetic or environmental initiators [19]. SOD1G93A mice are an indispensable staple in the ALS field because they exhibit many etiological similarities to, and present with disease progression that has fidelity to, clinical ALS presentation. Zebrafish, with conserved CNS and motoneuron physiology/genetics, have proven very useful to study the genetic relationships between fALS genes via loss-of-function analyses [20][27]. Furthermore, toxic gain-of-function zebrafish have been generated overexpressing mutant SOD1 and that recapitulate all hallmark attributes of fALS [28], [29]. A substantial percentage of fALS remains to be explained, and genes that modify such susceptibility have potential to be influential in late-onset disorders with complex interactions of genetics and/or environmental factors.

The proposed requirement for BMP/GDF6 family genes in vertebrate NMJs is supported by at least three previous lines of inquiry. First, disruption of intracellular trafficking led to NMJ deficits in zebrafish mutants of atlastin, and it was argued that this deficit was due to disrupted trafficking of BMP Receptors [30]. Second, BMPs and BMP Receptors are increased in expression at NMJs during recovery from experimentally induced traumatic injury in mice [5]. Third, a role for TGFβ/BMP/GDF signaling in ALS progression is suggested by the increase in pSMADs in ALS inclusions observed in both patient pathology and mouse models [31][33]. Although these lines of evidence are encouraging and suggestive, a role for BMP ligands in vertebrate neuromuscular degeneration remains unaddressed.

Our recent success in raising topical mutant zebrafish to adulthood [34] enabled us to address the questions above regarding a role for BMPs in the maintenance of vertebrate NMJs. Zebrafish harboring a null mutation in a homolog of GDF6 were outcrossed, establishing a viable and fecund line of homozygous gdf6a mutants. Increased cell death in at least some CNS neurons was reported during early development of these mutants [34]. This encouraged us to explore a potential role for gdf6a in neuromuscular degeneration, which would potentially implicate BMP/GDF6 genes as candidate loci in neuromuscular disease. We document progressive neuromuscular deficits in these mutants, including reduced muscle endurance, neuromuscular junction anomalies and loss of spinal motor neurons. Further, this mutation in gdf6a increased disease severity in a zebrafish model of ALS that over-expresses mutant SOD1. These data integrate to compel GDF6 as a candidate locus that increases susceptibility to or progression of ALS.


Gdf6−/− zebrafish do not display motoneuron axonopathy in early development

Because Gdf6−/− mice are not viable beyond embryonic stages [34], we considered alternate animal models and asked if zebrafish deficient in a GDF6 homologue might present with neuromuscular deficits akin to ALS. Our recent work employed several generations of out-crosses to successfully isolate a viable line of homozygous null gdf6as327/s327 fish (ZFin ID: ZDB-ALT-050617-10) that can be raised to adulthood [34]. This nonsense mutation occurs in the pro-domain, at residue 55, abrogating production of mature Gdf6a ligand and herein we refer to these mutants as gdf6a−/−. These fish display microphthalmia [34], but are otherwise normal in development (Figure 1A), adult morphology, and fecundity. A decreased longevity in gdf6a−/− fish compared to their siblings was noted, not reaching statistical significance in a small cohort (Figure 1B).

Figure 1. Zebrafish harboring homozygous mutations in gdf6 can be raised to adulthood and do not display overt skeletal defects.

A. gdf6−/− fish are viable into adulthood, exhibit variably penetrant microphthalmia and normal body morphology. B. gdf6−/− fish exhibit somewhat decreased survival compared to gdf6+/+ siblings (n = 11 gdf6−/− fish; n = 4 gdf6+/+ siblings). C, D. gdf6−/− fish lack overt skeletal phenotypes, as revealed by (C) clearing and staining or by (D) microCT analysis. The latter is further represented as Supplemental Movie S1. Scale bars are 5 mm. A variety of fin morphologies were present in the fish examined, but these were neither different between experimental groups (genotypes) nor a significant covariant with swim performance (see Results).

To assess if gdf6a−/− embryos display motoneuron disease, we utilized sensitive assays of motoneuron disease/ALS that are deployed frequently in embryonic zebrafish, consisting of examining branching and pathfinding defects in GFP-positive primary motoneurons of transgenic fish [20][22], [24][27]. gdf6a−/− embryos did not display a significant increase in motoneuron pathfinding or axonopathies as determined in a transgenic background that enables sensitive detection of motoneuron morphology based on GFP fluorescence; both gdf6a−/− and siblings had a low rate of abnormalities in this scoring system (Supplemental Figure S1; p≥0.315, n≥9 larvae per genotype). We confirmed that this assay was sensitive to ALS-related genetic lesions in our hands by delivering mRNA encoding human SOD1 with or without mutations associated with familial ALS (5.7 and 0.18 primary motoneurons affected per fish injected with SOD1A4V or SOD1WT, respectively p<0.05), consistent with past results [26], [27].

Considering ALS is a late-onset disease, it was of interest to characterize adult gdf6a−/− zebrafish with respect to ALS-like phenotypes. We examined fish at 9 to 18 months old (zebrafish are considered to be ‘adult’ at sexual maturity, ∼3 months old and can thrive for 3–5 years of age) regarding muscle endurance, gait, motoneuron abundance and character of their neuromuscular junctions.

gdf6a loss in adult zebrafish leads to neuromuscular disease, including deficits in endurance

Deficits in muscle endurance is a hallmark of ALS progression consistently observed in murine and fish models [28]. We quantified muscle endurance in gdf6a−/− and sibling fish by assessing their ability to swim against a strong, accelerating water current [35], from which we determined the critical swimming speed (Ucrit, the water flow velocity at which a fish can no longer maintain its position [35]; See Methods). At 9 months of age, gdf6a−/− fish were found to have substantially reduced swimming endurance, with mean Ucrit values approximately half those of gdf6+/+ siblings (Figure 2A,B; p = 0.005, n = 12 and 9 fish, respectively). At 18 months of age, the same significant difference was observed between genotypes (Figure 2B, p<0.0005, n = 4 and n = 3). Endurance was lower in the older fish within each genotype, though this difference between ages was not significantly different when comparing within genotypes.

Figure 2. Zebrafish harboring homozygous mutations in gdf6 exhibit decreased endurance.

A. gdf6−/− fish have a lower endurance compared to gdf6+/+ siblings as measured by increasing water velocity in a swim channel to determine the Ucrit i.e. ‘critical swimming speed’ which is taken to be the highest speed that a fish can swim at for a period of several minutes before exhaustion. Each fish tested at 9 months is plotted. B. The same data in panel A (9 month) plotted along with 18 month old siblings. gdf6−/− fish have approximately 50% lower endurance compared to gdf6+/+ siblings at each age (*p = 0.005, **p<0.01). Endurance trends towards being decreased in older fish of each genotype, but this difference is not significant. C. Open field tests of average swim velocity during 10 minutes of each hour through a circadian cycle, in tanks replicating lifetime husbandry conditions, show a lower mean movement at night (in either genotype, **p<0.01) but no difference between genotypes in any measure during day (p = 0.247) or night (p = 0.814).

The swim endurance (Ucrit) values in the wild type fish above are within the range of values obtained in past studies, being higher than [28], lower than [36], [37] or comparable to [38] previous results. Differences between studies are likely due to methodology, including duration of water velocity steps and flow chamber construction that can affect absolute values; thus comparisons between experimental configurations can be challenging, but the results are robust when compared within an experiment or laboratory.

An alternative interpretation of our endurance data is that fish were less able to perform the swimming test because of decreased availability of visual cues, due to microphthalmia. To rule out any confounding role for the visual deficits, swimming performance was assessed in a dark room under infrared light, which zebrafish are unable to detect (lighting conditions of the swimming endurance assay and zebrafish light sensitivity are characterized in Supplemental Figure S2). A further alternative is that the fish have decreased endurance due to decreased activity patterns in their typical husbandry conditions, perhaps predicting decreased muscle fitness. Open field tests on groups of fish were performed in conditions closely mimicking the husbandry conditions in which these fish were raised, and conducted in multiple replicates during each hour through a full circadian cycle. No significant difference in activity was found, arguing against mean activity as a confounding factor in these fish (Figure 2C, Supplemental Figure S2). The methods deployed were sensitive enough to detect lower average swim velocity in night vs. day (regardless of genotype, p<0.001), however no difference was detected between genotypes for average swim velocity during day (p = 0.247) or night (p = 0.814) (Figure 2C).

A small difference was noted between genotypes in the open field test, only during mating activity at light onset (Supplemental Figure S2), which accounted for the small non-significant decrease in overall activity of the gdf6a−/− fish. The difference observed during breeding is not relevant to the fish under consideration here, because they were raised and maintained in tanks that included sibling fish with normal eyes. When housed with normophthalmic siblings (our standard practice), gdf6a−/− fish had ample activity during breeding times and coordinately robust fecundity; this contrasts groups comprised solely of gdf6a−/− fish that had no breeding success. Thus the open field test we deployed under-represented the gdf6a−/− fish's activity during mating behaviour at light onset. In sum, the data argue against visual system deficits playing either an acute or long-term role in the muscle deficits of microphthalmic gdf6a−/− fish.

A further alternative explanation for deficits in swimming performance could be morphological changes resulting from long-term loss of gdf6a. Skeletal changes might be anticipated from BMP namesake functions in bone morphogenesis, from skeletal defects observed in patients with GDF6 mutations [39][42] or past analysis of zebrafish gdf6a morphants [43]. In adult zebrafish, skeletal deficits in the axial skeleton were not observed (Figure 1, Supplemental Movie S1). Body morphology was also assessed, and no significant morphometric covariates of Ucrit were observed, including condition factor (Figure S2). Caudal fin length was not different between experimental groups (One-way ANOVA F5,31 = 1.320 p = 0.28) and was not a significant covariant in the relationship between experimental group and swimming performance (MLR: F1,31 = 0.36 p = 0.55). Thus there was no evidence for a role of skeletal system malformation in the swimming deficits of gdf6a−/− zebrafish.

gdf6a loss in adult zebrafish leads to neuromuscular disease, including disruption of neuromuscular junctions

Histological hallmarks of ALS include neuromuscular deficits, comprising loss of motoneurons at the level of the spinal cord and abnormal structure of neuromuscular junctions (NMJ). Nine month old gdf6a−/− zebrafish were noted to have disrupted NMJ, including increased mean volume and greater variation of the presynaptic motoneuron compartment compared to wild type siblings (Figure 3). This presynaptic motoneuron volume, when normalized to the post-synaptic volume, was nearly 3-fold greater in gdf6a−/− mutants (p = 0.009, n = 5 fish per genotype). Co-localization of pre- and post-synaptic compartments was not significantly different based on genotype (Figure 3). Increased volume of pre-synaptic compared to post-synaptic NMJ compartments has also been observed in ALS model zebrafish overexpressing mutant SOD1 [28].

Figure 3. Zebrafish harboring homozygous mutations in gdf6 exhibit altered neuromuscular junctions and fewer spinal motor neurons.

A–B. Assessment of neuromuscular junction (NMJ) morphology including presynaptic (synaptophysin) and postsynaptic (αBTX) compartments in 9 month old gdf6−/− and gdf6+/+ siblings by immunohistochemistry. C. ALS-like increases in motoneuron pre-synaptic volumes are observed in gdf6−/− fish when normalized to post-synaptic volumes (**p = 0.009, n = 5 fish per genotype). Coefficients of colocalization for pre- and post-synaptic compartments are not altered, as is expected in later-stage zebrafish ALS models. D–E. Motor neuron cell bodies were identified in cross-sections of spinal cord using immunohistochemistry against choline acetyl transferase (ChAT, e.g. arrowheads) in nine month old gdf6+/+ and gdf6−/− fish (panels A and B, respectively). Bottom panels affirm motoneuron cell body identification using actin and nuclear counter-stains. F. gdf6−/− fish have approximately 50% the abundance of spinal motor neurons compared to sibling gdf6+/+ fish. (Mann-Whitney U Test, *** p<0.001, n>50 sections from 4 fish per genotype, researcher blinded to genotype during quantification). Scale bar = 60 µm in A,B and 50 µm in D,E.

Further, gdf6a−/− fish at nine months of age were noted to have approximately 50% fewer spinal motoneurons compared to wildtype fish (p<0.001, Figure 3, n>50 sections from 4 fish per genotype), akin to changes observed in ALS model fish overexpressing mutant SOD1 [28].

Disruption of gdf6 hastens disease progression in a zebrafish model of ALS

We reasoned that if gdf6a mutation hastens disease progression, or increases susceptibility to ALS, then this should be recognizable in ALS animal models lacking gdf6a function. We bred gdf6a mutants to an established zebrafish model of ALS: transgenic os10 zebrafish that over-express zebrafish Sod1G93R and develop symptoms of ALS very reminiscent of transgenic mice over-expressing human SOD1G93A [28]. Breeding gdf6a+/−;Tg(sod1:sod1G93R,hsp70l:DsRed)os10 fish generated six genotypes, consisting of three gdf6a genotypes (+/+, +/− or −/−), each with the os10 transgene being present or absent. Herein we define ‘bigenic’ fish as those both homozygous null for gdf6a and possessing the os10 transgene, i.e. gdf6a−/−;Tg(sod1:sod1G93R,hsp70l:DsRed)os10.

Similar to the observations on fish larvae with gdf6a lesions alone, no significant increase in axonopathy was noted in primary motoneurons when os10 was also present in the larval genome (Supplemental Figure S1). In older fish, amongst the six genotypes examined, it was apparent that a subset of bigenic gdf6a−/−;os10 fish failed to thrive. The time to reach 75% survival was approximately 6 months in bigenic ALS model zebrafish lacking normal gdf6a function, but more than 13 months in all other genetic combinations, including the same ALS model fish with at least partial gdf6a function (Figure 4A).

Figure 4. Mutations in gdf6 sensitize SOD1∧G93R zebrafish to develop ALS-like symptoms.

Six genotypes combining gdf6−/− alleles and SOD1∧G93R alleles were examined in endurance and sprint tests, which primarily measure red and white muscle respectively. The SOD1∧G93R fish mimic many aspects of ALS progression [28]. Swimming performance was measured in all six genotypes (determined by outcrosses and examining progeny) at 4.5 months of age. A. bigenic fish, i.e. gdf6−/− mutants expressing SOD1∧G93R, had decreased survival compared to all other genotypes, i.e. their siblings ( = gdf6+/+ or gdf6+/−) with or without SOD1∧G93R. B. bigenic gdf6−/− mutants expressing SOD1∧G93R had significantly lower endurance compared to heterozygous siblings also expressing SOD1∧G93R, and to WT and heterozygous siblings without SOD1∧G93R. C. Sprint test demonstrates a significant deficit in white muscle function only when SOD1∧G93R and gdf6−/− genotypes are combined ( = 25% deficit). (ANOVA and multiple linear regression, p<0.05; sample size indicated below graph).

Muscle endurance was assessed in bigenic gdf6a−/−;os10 fish and their siblings, using younger fish (4 months old) in an effort to capture any potential acceleration of disease progression. Deficits in swimming endurance attributable to gdf6a genotype alone were less dramatic at this young age: gdf6a−/− fish (lacking the os10 transgene) had Ucrit values approximately 75% those of their siblings but these differences were not statistically different (Figure 4B). This smaller endurance deficit in young fish contrasts the significant reductions observed at 9 and 18 months of age (where Ucrit was ∼50% that of siblings, Figure 2B), providing additional support for the contention that gdf6a loss of function leads to neuromuscular degeneration in a progressive manner.

Similarly, young os10 fish consistently displayed decreased endurance within each gdf6a genotype, similar to what was observed previously for older os10 animals [28], though in no case did this rise to the level of statistical significance (Figure 4B). Only when the genetic lesions were combined were statistical differences attained, such that bigenic gdf6a−/−;os10 fish had Ucrit values approximately 65% those of wild type fish (Figure 4B, p<0.05 by MANOVA, sample size = 37, with 5–7 individuals per genotype as indicated on Figure abscissa). Thus, in young adult fish, gdf6a and os10 genotypes both imposed effects on muscle endurance that were consistent with neuromuscular disease, but these deficits only reached statistical significance when both genetic lesions were combined.

Muscle strength/power was also assessed in these six genotypes, by documenting the ability of the fish to sprint against increasing velocities of water flow. This constant acceleration test was similar to the Ucrit endurance test, but with water velocity increased at an accelerated rate such that fast-twitch white muscle became dominant, allowing the velocity at fatigue (Umax) to be calculated [44], [45]. Neither the presence of the os10 transgene nor loss of gdf6a function were individually potent in reducing swimming strength in these young fish (Figure 4C). Only when the two genetic lesions were combined was any statistically significant deficit in swimming power observed, compared to wild type fish. Thus bigenic gdf6a−/−;os10 fish had Umax values approximately 75% those of wildtype fish (Figure 4C, p<0.05 by MANOVA, sample size = 37, with 5–7 individuals per genotype as indicated on the Figure).

These same bigenic gdf6a−/−;os10 fish and their siblings were subsequently examined for neuromuscular junction abnormalities. Both os10 and bigenic gdf6a−/−;os10 fish at 7 months of age had increased presynaptic/postsynaptic volume ratios compared to wildtype siblings, though the differences did not reach statistical significance (Figure 5A, B. Kruskall-Wallis ANOVA p = 0.134, n = 6 WT, 4 os10, 6 gdf6a−/−;os10). Further, NMJs in bigenic gdf6a−/−;os10 had significantly decreased overlap of synaptic compartments compared to either os10 or wildtype siblings (Figure 5B) (Kruskall-Wallis ANOVA, p<0.001). Mander's colocalization coefficients for the postsynaptic compartment were significantly lower for bigenic gdf6a−/−;os10 fish, implying loss of synaptic connectivity because postsynaptic compartments were less colocalized with presynaptic compartments despite the increase in presynaptic size (Figure 5B) (Kruskall-Wallis ANOVA, p<0.05). Thus the gdf6a−/− mutation does not alter co-localization of NMJ pre- and post-synaptic compartments on its own (Figure 3C), but it further exacerbates the ALS-like NMJ abnormalities observed in bigenic fish expressing overexpressing mutant SOD1.

Figure 5. Disruption of gdf6 function exacerbates neuromuscular junction abnormalities in ALS model zebrafish.

ALS model zebrafish possess disruptions to neuromuscular junctions (NMJ), and loss of gdf6 function exacerbates this by 7 months of age. A. The presynaptic junctions (labeled with synaptophysin antibody) and postsynaptic junctions (labeled with fluorescently tagged αBTX) in ALS model zebrafish expressing the mutant SOD1G93R show punctate morphology, deviations in presynaptic volume and less overall colocalization compared to WT sibling junctions. Some abnormalities are exacerbated in bigenic siblings expressing the mutant SOD1G93R that are also gdf6−/− (scale bar is 40 µm). B. Quantification of these NMJs suggests the presynaptic/postsynaptic volume ratios of SOD1G93R and bigenic gdf6−/−;SOD1G93R zebrafish are larger than those of WT siblings at this age, though these differences do not rise to statistical significance (Kruskall-Wallis ANOVA, p = 0.134; n = 6,4,6 for WT, SOD1G93R, and bigenic fish respectively). Colocalization coefficients, that measure overall colocalization of presynaptic and postsynaptic junctions, are altered in these fish. The values for SOD1G93R zebrafish are significantly lower than wild type sibling values, indicating that presynapses and postsynapses overlap less, as characterized previously for this transgenic ALS model [28]. Bigenic SOD1G93R zebrafish that are also gdf6−/− have a dramatically lower coefficient than either sets of siblings, including being 30% lower than ALS model SOD1G93R fish with normal gdf6a (*p<0.05; ***p<0.001. Kruskall-Wallis ANOVA with pairwise comparisons).

Overall, loss of Gdf6 function led to an acceleration of disease progression in this ALS animal model, as measured by longevity, integrity of neuromuscuslar junctions, muscle endurance and muscle strength. These data are in good accordance with the hypothesis that deficits at the GDF6 locus can sensitize animals to onset and/or progression of neuromuscular degeneration akin to ALS.


Zebrafish harboring homozygous null mutations in a GDF6 homologue were found to be viable, fecund and robust into adulthood, though exhibiting somewhat reduced longevity. Homozygous gdf6a−/− fish had progressively severe deficits in endurance, loss of spinal motoneurons and disrupted neuromuscular junctions compared to the wild type siblings, very much akin to ALS model zebrafish. Furthermore, progression of neuromuscular disease in ALS model zebrafish was accelerated when this homologue of GDF6 was mutated: older zebrafish expressing mutant SOD1 exhibit ALS-like symptoms, but young fish only exhibited significant ALS-like neuromuscular deficits when on a gdf6a−/− background.

Regarding ALS and other neuromuscular diseases, support for a BMPs' relevance is continuing to be revealed by genetic studies in Drosophila, including that a homologue of BMPs and homologues of BMP receptors are each required for normal NMJ development in flies [1], [4], [46], [47], but suggestions of such functions for BMP pathway components rarely extend to vertebrates. Within vertebrates, BMP receptor type II has recently been localized to mouse NMJs, and one of its ligands BMP4 was found in close proximity [48]. BMP4, BMP5 and their receptors have also been shown to have a role at some synapses in the CNS [49]. A role for BMPs in the vertebrate neuromuscular system has more frequently been suggested following motoneuron or spinal cord injury [50]. Recent work has also demonstrated a role for proper trafficking, including that of BMP receptors, in primary motor axon outgrowth during zebrafish development [30], instigating a search for which component of the BMP gene family might underpin this effect. A potential example may be GDF15, a member of the BMP subfamily with divergent properties and typically associated with macrophage recruitment and inflammation, in that GDF15 disruption causes loss of motoneurons in mice [51]. A link between BMP signaling and neuromuscular disease is suggested by the observation of phosphoSMAD proteins (downstream signaling components of TGFβ/BMP/GDF signaling) being enriched in pathological ALS inclusions [31][33], [52]. Human genetics suggests that loci associated with hereditary spastic paraplegia, including ATLASTIN, can regulate BMP receptor trafficking and effect neuromuscular disease [30], [50]. Despite this substantial level of interest, we are not aware of previously published data from vertebrate experiments or human genetics directly linking BMP/GDF gene family members (ligands or receptors) with ALS or any neuromuscular disease.

A substantial proportion of ALS susceptibility remains unexplained with respect to human genetics. Analyses herein support GDF6, a member of the BMP family, as worthy of further consideration. A role for GDF6 homologues in progressive, late-onset neuromuscular disease was supported herein by muscle physiology, histopathology and behavioural assessment of zebrafish carrying mutations in gdf6a. Further, gdf6a loss of function accelerated disease progression in a zebrafish model of ALS. The synthesis of this data combines with recent reports of a role for GDF6 in congenital and late-onset photoreceptor degenerations [34], [53] to compel a role for GDF6 as a modifier gene in the etiology of disparate neuropathies.

BMPs in neurodegenerative disease

Inappropriate growth factor expression and signaling have been linked to inflammation and apoptosis in other neural diseases such as Alzheimer's, Parkinson's and, in one instance, Creutzfeldt-Jakob Disease, which are characterized by inappropriate accumulation of misfolded proteins, leading to neuron death via a multitude of proposed pathological pathways [54][56]. TGFβ1 and TGFβ2 expression are high in brains afflicted with Alzheimer's, causing inflammation, astrogliosis and neuron death through such pathways as NADPH oxidase-induced oxidative stress and caspases [57], [58]. Xenopus TGFβ1, a member of the same gene superfamily as GDF6, is released from Schwann cells and can promote synaptogenesis at NMJ [59]. TGFβ1 is an effector of motoneuron survival (refs in [60]) and has been proposed as a mediator of increased ALS susceptibility in athletes abusing anabolic steroids [60]. Based on these similarities, it is plausible that GDF6 dysfunction could contribute to any of these pathways as they play out in ALS. Based on our data, we believe the expansion of ALS studies to the investigation of TGFβ signaling is warranted, beginning with GDF6.

Therapeutic implications

Application of BMPs as treatment has been investigated previously [50], especially following injury, suggesting that further knowledge of GDF6 function could lead to strategies that replace BMP function. A number of TGFβ superfamily members are neuroprotective, such as BMP7 in cerebral ischemia and GDF5 in Parkinson's disease [61], [62]. GDF15 plays a role in the pathology of motoneuron loss, but is also required to effect the therapeutic effects of GDNF [51], [63], illustrating how these signaling factors are able to participate in either neuroprotection or degeneration.

Therapeutic potential also exists in small molecules such as aminopropyl carbazoles and their derivatives. For example it has recently been demonstrated that P7C3 can ameliorate phenotypes in zebrafish gdf6a mutants [34], and P7C3 has also recently been shown to be efficacious in mouse models of ALS and Parkinsons Disease [64], [65]. Efficacy of P7C3 seems to be driven by a combination of pro-neural and neuroprotective signals, and identifying the mechanisms that underpin this could be aided by zebrafish models and/or by investigation of its etiological effects in diverse neurodegenerations.

Finally, GDF6 may represent an entry-point into unexplored pathogenic mechanisms of vertebrate neuromuscular degeneration. In cases where such mechanisms have been identified, the etiology of ALS can be associated with a variety of cellular mechanisms. Ferraiuolo and colleagues [66] review these to include oxidative stress, RNA processing, endosomal trafficking, protein degradation, cytoskeletal integrity and glutamate excitotoxicity. It is conspicuous that, despite being a member of the BMP family with diverse functions, GDF6 is not currently associated with any of these etiological categories.

Three mechanisms whereby BMP ligands and receptors affect NMJs can be suggested as potential routes to explore in the zebrafish system. First, retrograde signaling of BMP ligand from the muscle to the NMJ, and retrograde transport of receptors to activate transcription in the nucleus of motoneurons is important for motoneuron survival in Drosophila [4], [50]. Second, BMP in Drosophila is required for stabilizing the NMJ through non-canonical signaling via LIM Kinase domain 1 [4], [50]. Third, vertebrate BMP ligands have recently been revealed to bind Agrin [67], and thus directly affect the clustering of acetylcholine receptors during formation and stabilization of the NMJ. In support of the latter we found that the NMJ morphology, as measured by α-bungarotoxin labelling of acetylcholine receptors, was disrupted in gdf6a−/− mutants (Figures 3, 5), suggesting one priority for future analysis.


In summary, past conclusions regarding a role for Drosophila BMP ligands in effecting NMJ can be extended to vertebrates, supporting conservation of mechanisms that may be of substantial import to degenerative neuromuscular diseases. Zebrafish present a tractable system for assessing the role of BMP/GDF ligands (data herein) and their receptors [30] with respect to neuromuscular disease. The data also synergize to argue for further analysis of GDF6 and other BMP genes as modifier loci, affecting susceptibility to ALS and perhaps a broader suite of neurodegenerative diseases. Further efforts to assess the role of vertebrate BMPs in motoneuron disease are warranted.


Ethics statement

All fish husbandry and procedures were completed with approval of the University of Alberta Animal Care and Use Committee: Biosciences, in accordance with the Canadian Council on Animal Care.

Zebrafish husbandry and establishment of mutants and transgenic crosses

Zebrafish bearing gdf6as327/s327 (also known as radar s327/s327 [13], Zfin ID ZDB-ALT-050617-10), referred to here as gdf6−/−, previously identified as larval lethal, were recently acquired as viable adults through breeding of heterozygous mutants, preceded by backcrosses onto an AB background [34]. Homozygous gdf6as327/s327 larvae were identified by the presence of microphthalmia at 3dpf and were raised separately from their siblings. Mutants and siblings were confirmed in several cases by genotyping from finclip derived DNA at adulthood (using primers 5′-TGTGAGACACGGCTCCACTT-3′ and 5′-GCAGGACGAGAGCTTACCAA-3′) and/or by examining the Mendelian frequency with which their progeny exhibited microphthalmia. At 9 and 18 months, Gdf6as327/s327 adults and WT siblings underwent a swim channel assay and were subsequently sacrificed for NMJ and spinal cord immunocytochemistry.

ALS model zebrafish, expressing mutant SOD1G93R under control of the zebrafish sod1 promoter [28], were generously provided by Christine E. Beattie. The fish, Tg(sod1:sod1G93R,hsp70l:DsRed)os10 (ZFin ID: ZDB-GENO-101006-6), herein referred to as os10, can be readily identified from their expression of DsRed under a promoter that is independent of the sod1 expression cassette, but linked immediately contiguous to it in the construct. The os10 line was crossed to gdf6as327/s327 fish, and screened for the presence of os10 transgene following heat shock at 2dpf [28]; the resultant compound heterozygous fish were inbred to acquire the combinations of gdf6as327 and os10 in the various combinations reported.

Zebrafish husbandry and breeding used standard methods [68], with 14∶10 L∶D light cycle, 1300±100 µS conductivity at 28±1°C water temperature. Fish were fed a diet dominated by brine shrimp and trout chow.

Assessing primary motoneuron axonopathy in embryonic zebrafish

Zebrafish embryos were scored for abnormal primary motoneuron axonopathy, as previously described [27], in transgenic animals where primary motoneurons abundantly express GFP under control of the promoter mnx1 (also known as hb9, Zfin ID: ZDB-GENO-080606-250). Breeding created gdf6a+/−;Tg(mnx1:GFP)ml2 fish. These were bred to gdf6a+/−;Tg(sod1:sod1G93R,hsp70l:DsRed)os10 fish described above to generate genotypes including gdf6a−/− fish and siblings with labelled motoneurons and/or expressing mutant Sod1G93R.

At 30hpf, larvae were visualized under a Leica MZ16F fluorescent stereomicroscope and axon branching was scored while the researcher was blind to genotype. As per established methods [27], branching of the GFP positive motoneurons was considered abnormal if it initiated at or above the ventral aspect of the notochord. Branching that was observed below this point was considered normal. The yolk sac extension was used as a landmark, and only the ten motoneurons immediately above it were scored for defects (Figure S1). Subsequent to quantifying its axonopathy, each of the larvae was reared individually in 24 well plates until they were old enough to assess genotypes based on microphthalmia, and heat-shocked for one hour prior to screening for DsRed expression associated with os10. To assess the sensitivity of the axonopathy assay in our hands, Tg(mnx1:GFP)ml2 fish were injected with 900 pg of mRNA encoding wildtype or A4V human SOD1. mRNAs were synthesized and delivered as per previous methods [69]. Axonopathy scores per fish were analyzed using a Kruskall-Wallis ANOVA followed by a pairwise Mann-Whitney U-test, calculated in SYSTAT 12. All p-values reported are two-tailed and significance was set at p<0.05.

Adult fish - assessing endurance in swim channel assay and activity in open field test

Individual fish were tested for their critical sustained swimming (Ucrit), which was the maximum velocity at which they could swim for a set period in a 10 L modified Brett-style swim tunnel (Loligo Systems, DK). Fish were placed in the swim tunnel under blackout hoods with infrared lighting (see below for characterization of lighting) and allowed to acclimate for 30 minutes to a low velocity current (5 cm/s). The flow rate was then increased every 10 minutes by 4 cm/s. Fish were monitored via infrared camera (SAV-CD120; Matco, QE) and Elgato video capture software (Elgato Systems, CA), and were considered to have reached maximum velocity when they were no longer able to maintain position in the current and fell into a screen at the back of the swim chamber. After fish fatigued the test was halted and the fish removed following a cool-down swimming period of 10 minutes at low velocity. The four month old fish were allowed to recover in the chamber at 5 cm/s for 45-minutes before completing a second test with shortened, one-minute steps to determine their maximum sprint swimming speed (Umax). The Ucrit and Umax values were calculated using the Brett formula [70]. All fish were measured for morphological traits that are potential covariates of swimming endurance [36], [38]. Morphology measurements included: head length, muscle length, standard length, fork length, total length, body height, body width, caudal peduncle, and mass. Condition factor was determined using the standard formula from mass (g) and body length (BL; mm), calculated as 105·mass/BL3.

Open field tests on zebrafish were carried out on groups of three fish per tank under conditions nearly identical to their normal husbandry conditions regarding temperature, water chemistry, water flow rates and lighting (except that IR lights were used to enable video recording in the dark). Fish were transferred from their housing tanks to test tanks of the same dimensions and were acclimated for one hour prior to the start of testing (N = 6 tanks with 3 fish each). Zebrafish motion was then recorded from above for 10-minutes every hour for 24-hours, using IR-lit cameras (as above) and video surveillance software (Visio-soft; Matco, QE). Average swimming speeds were determined from video (15 measures per second) for each fish using behavioural analysis software (Ethovision XT8.5; Noldus, NL). Infrared lighting was characterized using a calibrated spectrophotometer (USB4000-UV-VIS Ocean Optics, Dunedin FL) connected to a 455 micron optical fiber (QP450-2-XSR, Ocean Optics) held at the approximate position that fish maintained during trials. Spectra were recorded to Spectra Suite software (Ocean Optics).

Differences in the day- and night-time swimming speed between gdf6−/− and wild-type fish were assessed using a two-way repeated measures analyses of variance with a Holm-Sidak post-hoc test. Differences in Umax (BL/s) and Ucrit (cm/s) between genotypes were analyzed using one-way ANOVA's with Holm-Sidak post-hoc tests. Holm-Sidak adjusted p-values were reported. All swimming performance and open field test data were log transformed to achieve normality. All data were tested for normality (Shapiro-Wilk) and equal variance (Levene's test) prior to the use of parametric statistics. Multiple linear regression analyses were also performed using standard body length and genotype as explanatory variables of swimming performance to ensure that the detected differences were independent of fish size. The statistical analysis of swimming performance and activity was conducted using SPSS 20.0 (SPSS IBM, Chicago, IL) and Sigmaplot 11 (Systat Software, CA).

Adult zebrafish tissue preparation and immunocytochemistry

To assess neuromuscular junctions (NMJ), muscles from adult zebrafish were removed, cut transversely into quarters (anterior to posterior) and fixed in 4% paraformaldehyde/0.1 M PO4 for 24 hours at 4°C. Samples were prepared for cryosectioning as per previous methods [71] by washing thrice in 5% sucrose/0.1 M PO4 (20 minutes), once in 12.5% sucrose/0.1 M PO4 (30 minutes), and overnight in 20% sucrose/0.1 M PO4. Samples were embedded and frozen in OCT media (Tissue-Tek 62550-12). 16 µm sections were serially placed on Superfrost Plus microscope slides (Fisherbrand 12550-15). All sections used in immunocytochemistry were of the second-most anterior quarter of muscle.

NMJs were visualized by labeling pre-synaptic terminals and post-synaptic terminals as reported previously [28]. Briefly, slides were blocked for 60 minutes in 10% NGS/PBSTw and incubated in 1∶50 rabbit anti-synaptophysin (Invitrogen 180130) in 2% NGS/PBSTw overnight at 4°C. Slides were washed with PBSTw and incubated in 1∶500 AlexaFluor 488 chicken anti-rabbit (Invitrogen A21441)/1∶100 AlexaFluor 555-tagged α-bungarotoxin (Invitrogen B35451)/2% NGS/PBSTw overnight at 4°C. Sections were viewed with a Zeiss LSM 700 confocal mounted on a Zeiss Axio Observer.Z1 microscope and imaged with ZEN 2010 (version 6.0) software (Carl Zeiss MicroImaging).

To quantify motoneuron abundance, spinal cords were dissected whole and fixed in 4% paraformaldehyde/0.1 M PO4 for 24 hours at 4°C. The spinal cords were then prepared for cryosectioning as previously described. Transverse sections (20 µm) of each sample were serially placed on 6 Superfrost Plus microscope slides. Motor neurons were labeled as previously described [28]. Briefly, slides were incubated in 0.003% H2O2/PBS for 20 minutes, blocked for 1 hour in 5% normal donkey serum (NDS)/1% DMSO/PBSTw, washed, and incubated in 1∶100 goat anti-ChAT (Chemicon AB 144P)/2% NDS/1% DMSO/PBSTw for 3 days at 4°C. Slides were rinsed and washed in PBSTw, and incubated in 1∶500 Alexafluor 555 or Alexafluor 488 donkey anti-goat (Invitrogen A-21432 and A-11055)/2% NDS/1% DMSO/PBSTw overnight at 4°C. Actin was labelled using phalloidin conjugated to AlexaFluor-488 (Invitrogen #A12379). Nuclei were stained with TO-PRO-3 (Invitrogen, #T3605). After three 30-minute washes with PBSTw, slides were coverslipped and imaged. Sections were viewed with a Zeiss LSM 700 confocal mounted on a Zeiss Axio Observer.Z1 microscope and imaged with ZEN 2010 (version 6.0) software (Carl Zeiss MicroImaging). Powerpoint 2008 for Mac (Microsoft) was used to assemble figures following being merged and/or linearly manipulated for brightness and contrast in Photoshop CS3, Zen confocal software (Zeiss), and/or Imaris ×64 7.4.0 (Bitplane).

Histological analysis

NMJ volumes were measured using the voxel counter plugin for ImageJ 1.45 (Wayne Rasband, National Institutes of Health; and colocalization was analyzed in Imaris ×64 (version 7.4.0, Bitplane). Researcher was blinded to genotype prior to image analysis. Values were normalized to WT values and statistical analysis was performed with Kruskall-Wallis ANOVA (volume and colocalization measurements) and Mann-Whitney U test (colocalization measurements) on SYSTAT 12.

Motoneurons in spinal cord cross-sections were quantified as per established methods [28] by averaging the number of motoneuron cell bodies, identified as ChAT-positive objects greater than 10 µm, per section. Researcher was blinded to genotype during quantification and analysis. Statistical analysis was performed with Kruskall-Wallis ANOVA in SYSTAT 12.

Clearing and staining of skeletal elements

Clearing and staining of cartilage and bone was performed using established protocols [72]. Briefly, adult fish were fixed whole in 4% paraformaldehyde overnight, rinsed in distilled water and preserved step-wise in 30%, 70% and 95% ethanol. The fish were then placed in alcian blue stain (cartilage) (Sigma-Aldrich A5268) in 30% acetic acid/70% EtOH for 6 hours and placed in saturated sodium borate overnight. Depigmentation was performed using 15% peroxide/85% KOH for 25–50 minutes or until pigment was removed. Fish were partially cleared in 30% saturated sodium borate with 1∶250 tissue culture grade trypsin (VWR, CA97061-708)(1/16 teaspoon/30 mL). Bones were stained using a 1∶1000 dilution of stock alizarin red dye (Sigma-Aldrich A5533) in 1% KOH for 1 hour, or until sufficiently pink. Afterward, fish were fully cleared in trypsin solution and preserved step-wise in 30% and 70% glycerin/1% KOH. Fishes were finally stored and imaged in 100% glycerin.

Imaging skeletal elements in zebrafish by microCT

Intact fish were fixed in 4% paraformaldehyde/5% sucrose in 0.1 M PO4 buffer for 24 hours and washed in 0.1 M PO4 pH 7.4. buffer 3-times for 20 minutes to remove fixative. Fish were incubated overnight in Lugol solution (Sigma-Aldrich; No. L-6146) with gentle agitation followed by three 20-minute baths in 0.1 M PO4 buffer. Tissue was dehydrated in a graded ethanol series and kept at −20°C. To orient the specimen appropriately for scanning, it was partially embedded vertically in 2% agarose, caudal fin down, with the top half of a 15 mL Falcon tube serving as a mold. Imaging was performed on a SkyScan1174 (Bruker; Kontich, BE) compact Micro CT (50 kV x-ray source and inbuilt 1.3 MP cooled x-ray camera). Raw data obtained from the scanner was initially reconstructed using NRecon v. 1.6.6 (Bruker; Kontich, BE) and further processed to optimize viewing of structures of interest using Osirix v. 5.0.2 (Open-source DICOM Viewer). 360° rotating specimen videos were produced using Osirix v. 5.0.2 for viewing.

Supporting Information

Figure S1.

In larval zebrafish, mutations in gdf6a do not appreciably sensitize SOD1∧G93R zebrafish to develop ALS-like symptoms. Four genotypes combining Gdf6−/− alleles and SOD1∧G93R alleles were examined in Tg(HB9:eGFP) zebrafish expressing GFP in the axons of primary motor neurons (PMN), or via immunohistochemistry. A. Bracket indicates position of axons quantified, magnified in B,C. B. Normal primary motor axons. C. An example of an abnormal PMN axon (arrow). D. Quantification of primary motor axons in 30 hour post-fertilization embryosshow no difference based on gdf6a genotype; Thus effects are not developmental, and accord with a late-onset phenotype. Results indicated no significant effect of Gdf6 on the presence of axonopathies (p≥0.315, n≥5 larvae per genotype), although the highest rate of PMN axon abnormalities were observed in gdf6a−/−;SOD1+/G93R larvae.


Figure S2.

Eliminating alternate hypotheses that might account for differences in swimming behaviour between gdf6a−/− zebrafish and their siblings. Our overall conclusion is that gdf6a mutants have deficits in endurance due to a progressive loss of spinal motor neurons and disrupted neuromuscular junctions. Alternative explanations for these fish having reduced endurance are eliminated here. A. Body morphology was not significantly different based on genotype. Condition factor was determined using the standard formula from mass (g) and body length (BL, in mm), calculated as 100000Xmass/BL3. Condition factor did not vary based on genotype. Sample sizes (number of fish) indicated at the bottom of graph. B. Acute deficits in vision cannot account for differences between microphthalmic gdf6a−/− fish and their wildtype siblings. Infrared lighting conditions during behavioural tracking of zebrafish excludes a role for visual dysfunction in the assays of fish activity, power or endurance. Grey trace indicates photons available to fish during recording sessions. Arrows annotate the maximal wavelength of sensitivity of photoreceptors in zebrafish [73]: rod photoreceptors (grey) and cone photoreceptors (coloured to indicate spectral sensitivity, magenta for ultraviolet-sensitive cone, and blue-, green- and red-sensitive cones are indicated by the cognate colour) are documented. In sum, the infrared conditions used prevented vision from impacting behaviour of wild type or mutant fish the during tracking of fish movement in the open field test, endurance tests or sprint tests. C. gdf6a−/− zebrafish in open field test shows no significant difference in average movement compared to wild type siblings. Fish movement tracked over 24 hours, bar below abscissa indicates lights on and off. Mutant fish had near-normal activity levels throughout the circadian cycle. A lower average movement in mutants is noted immediately after the lights turn on (0800–0900 h, compared to siblings), though this difference is not expected to occur in normal husbandry conditions: The data herein tracked groups of mutant fish, or groups of sibling fish, maintained in separate tanks (because automated video tracking of individuals in mixed populations was unreliable), whereas in normal husbandry conditions the microphthalmic gdf6a−/− mutants were housed in the same tanks as their siblings. This is impactful, because breeding is cued by lights turning on, and microphthalmic fish had increased movement during breeding (and bred successfully) only if housed with normal fish. If all fish in a tank are microphthalmic gdf6a−/−, they fail to exhibit breeding behaviour and thus have less vigorous movement. Because our gdf6a−/− fish were raised in mixed populations with normophthalmic siblings, they likely had near-normal movement activity when the lights were automatically turned on each morning. This data is summarized in Figure 4C, concluding no significant difference in total movement between genotypes.


Movie S1.

gdf6−/− fish have normal skeletal morphology compared to wildtype siblings. See Figure 1 regarding scale bars.



We thank Bradley Scott and Allison Murray for use of their MicroCT scanner and training. We received technical support from Neel Doshi and Aleah McCorry. Christine Beattie was generous in sharing her os10 line of transgenic zebrafish. We appreciate the generous constructive comments made by Simonetta Sipione and Kelvin Jones on an earlier draft of this manuscript. The Zebrafish International Resource Center (ZIRC) provided the transgenic line mnx1:gfp.

Author Contributions

Conceived and designed the experiments: MGD MJHG KBT WTA. Performed the experiments: MGD MJHG DEW TCZ KBT WTA. Analyzed the data: MGD MJHG DEW TCZ KBT WTA. Wrote the paper: MGD WTA. Critically edited the manuscript: MGD MJHG DEW TCZ KBT WTA.


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