Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function
Nemaline myopathy is characterized by muscle weakness and the presence of rod-like (nemaline) bodies. The genetic etiology of nemaline myopathy is becoming increasingly understood with mutations in ten genes now known to cause the disease. Despite this, the mechanism by which skeletal muscle weakness occurs remains elusive, with previous studies showing no correlation between the frequency of nemaline bodies and disease severity. To investigate the formation of nemaline bodies and their role in pathogenesis, we generated overexpression and loss-of-function zebrafish models for skeletal muscle α-actin (ACTA1) and nebulin (NEB). We identify three distinct types of nemaline bodies and visualize their formation in vivo, demonstrating these nemaline bodies not only exhibit different subcellular origins, but also have distinct pathological consequences within the skeletal muscle. One subtype is highly dynamic and upon breakdown leads to the accumulation of cytoplasmic actin contributing to muscle weakness. Examination of a Neb-deficient model suggests this mechanism may be common in nemaline myopathy. Another subtype results from a reduction of actin and forms a more stable cytoplasmic body. In contrast, the final type originates at the Z-disk and is associated with myofibrillar disorganization. Analysis of zebrafish and muscle biopsies from ACTA1 nemaline myopathy patients demonstrates that nemaline bodies also possess a different protein signature. In addition, we show that the ACTA1D286G mutation causes impaired actin incorporation and localization in the sarcomere. Together these data provide a novel examination of nemaline body origins and dynamics in vivo and identifies pathological changes that correlate with muscle weakness.
KeywordsNemaline Myopathy Zebrafish Actin Protein aggregation
Nemaline myopathy is a congenital skeletal muscle disease characterized by muscle weakness and low muscle tone, except in a few rare patients with hypertonia . Severe nemaline myopathy results in death within the first few months of life; however, individuals displaying milder forms are able to walk despite reduced muscle function . Mutations in ten different genes cause nemaline myopathy: skeletal muscle α-actin (ACTA1) , nebulin (NEB) , α-tropomyosin , β-tropomyosin , troponin T1 , cofilin 2 (CFL2) , KBTBD13 , KLHL40 , KLHL41  and leiomodin 3 (LMOD3) . All of these genes either encode components of the thin filament or regulate thin filament organization and stability. NEB, which plays an important role in regulating thin filament length, is the most frequently affected gene in nemaline myopathy with patients exhibiting muscle weakness and reduced force generation [37, 40]. Deletion of exon 55, causing a common form of autosomal recessive nemaline myopathy , results in shortened thin filaments, alterations in cross-bridge cycling kinetics, and reduced calcium sensitivity [37, 38].
Nemaline myopathy patients present with a range of clinical phenotypes, but the presence of nemaline (rod-shaped) bodies in skeletal muscles is the defining feature [30, 52]. These structures are thought to derive from the Z-disk and contain Z-disk proteins such as α-actinin [21, 53], although nemaline bodies have also been described in the absence of Z-disk thickening . While nemaline bodies are a hallmark of the disease, their frequency does not correlate with disease severity [3, 17, 28, 41, 42]. In addition, they are sometimes found at the myotendinous junction in healthy skeletal muscle [18, 27] and in healthy ocular muscles .
Mutations in ACTA1 account for ~25 % of nemaline myopathy cases and ~50 % of severe presentations . The majority of ACTA1 patients carry a single, de novo, dominant mutation but approximately 10 % carry genetic or functional null mutations which are recessively inherited . The dominant ACTA1D286G mutation produces a very severe form of nemaline myopathy [3, 12, 31]. In cell culture experiments, ACTA1D286G expression resulted in the formation of rod-like bodies [7, 49] and the mutant protein demonstrated reduced incorporation into sarcomeric structures . Expression of ACTA1D286G in transgenic mice produced granulofilamentous accumulations in their skeletal muscle. These accumulations stained positive for both phalloidin (labeling F-actin) and α-actinin, and the mice displayed skeletal muscle weakness [41, 42]. Importantly, varying the proportion of mutant actin in this mouse model identified that disease severity correlated with the ratio of mutant to wild-type protein, suggesting a dominant negative action for ACTA1D286G .
To investigate the origin of nemaline bodies and to uncover the cause of skeletal muscle weakness, we developed overexpression and loss-of-function zebrafish models for ACTA1-related and a loss-of-function model for NEB-related nemaline myopathy. Remarkably, the in vivo examination of nemaline body formation and progression in Tg(ACTA1D286G-eGFP) fish demonstrates that nemaline bodies emanate from the myosepta and are dynamic and transitory in nature. We demonstrate that the breakdown of these early forming nemaline bodies coincides with the formation of globular aggregates that sequester actin-binding proteins and correlates with reduced muscle activity. Conversely, we show that a reduction in α-actin produces a distinct type of Z-disk-derived nemaline body, which extends across the sarcomere, and causes the formation of cytoplasmic α-actinin-rich aggregates. These types of nemaline bodies contribute to impaired muscle function and myofibrillar disarray. From the examination of Neb knockdown fish, we suggest that disruption of α-actin stoichiometry may be a common mechanism of disease for nemaline myopathy. Finally, we also show that the ACTA1D286G mutation has impaired incorporation in the sarcomere, reducing muscle activity, and compounding the effects of the nemaline bodies.
Materials and methods
Fish maintenance and handling were carried out as per standard operating procedures approved by the Monash Animal Services Ethics Committee and the creation of transgenic lines approved by the School of Biological Sciences Animal Ethics Committee (BSCI/2011/18). For patient samples, all experiments were approved by the Children’s Hospital at Westmead Ethics Committee (CHW 2005/042) and the Monash University Human Research Ethics Committee review panel (CF15/743-2015000336).
Production of transgenic constructs
Zebrafish were maintained as previously described . Transgenic constructs were assembled with the modular tol2 kit . C-terminal eGFP-tagged ACTA1 constructs were created using the following clones: p5E-Bact2, pME-loxP-mCherry-pA-loxP (Genbank accession: KF753698), pME-iCre (Genbank accession: KF753697), pME-ACTA1D286G-EGFP, p3E-ACTA1D286G-EGFP (Biomatik), p3E-ACTA1wildtype (Biomatik), p5E-actc1b , p3E-pA, pDEST-Tol2-pA2 and pDEST-Tol2pA-cryaa:GFP . Transgenic strains generated were Tg(βAct:loxP-mCherry-pA-loxP:Hs.ACTA1_D286G-eGFP), Tg(βAct:loxP-mCherry-pA-loxP:Hs.ACTA1-eGFP) and Tg(actc1b:iCre). Crossing of the Tg(actc1b:iCre) strain to either Tg(βAct:loxP-mCherry-pA-loxP:Hs.ACTA1_D286G-eGFP) or Tg(βAct:loxP-mCherry-pA-loxP:Hs.ACTA1-eGFP) results in the excision of the loxP-mCherry-pA-loxP cassette. The strains generated from this cross are Tg(βAct:Hs.ACTA1_D286G-eGFP and Tg(βAct:Hs.ACTA1-eGFP) referred to hereafter as Tg(ACTA1D286G-eGFP) and Tg(ACTA1wildtype-eGFP), respectively. For cardiac actin expression, the actc1a ORF was amplified by PCR from IMAGE clone 6893985 (Imagenes), fused to mCherry, and expressed using the actc1b promoter  cloned into the pDEST-Tol2-pA2 vector.
cDNA synthesis and quantitative RT-PCR
Total RNA was extracted using TRI Reagent (Sigma). cDNA was synthesized by Superscript III Reverse Transcriptase (Invitrogen Life Technologies). Quantitative RT-PCR (qRT-PCR) was performed using a Lightcycler (Roche) using SYBR Green Master mix (Roche). Primers used for RT-PCR analysis of morpholinos are listed in Supplementary Table 1.
Gomori trichrome and immunohistochemistry staining
For Gomori trichrome staining on zebrafish tissues, 50-h post-fertilization (hpf) embryos injected with actc1b;ACTA1D286G-eGFP were anesthetized and snap frozen. Transverse sections (12 μm) were cut using a Leica CM 1850 cryostat. These were imaged for eGFP using a Zeiss Axiophot compound fluorescent microscope. Sections were then stained with modified Gomori trichrome and imaged using a Zeiss Axioskop 2 microscope. Fluorescent and Gomori stained images for the same section were then overlaid for analysis. For immunostaining on zebrafish tissues, 4 % paraformaldehyde (PFA)-fixed 2 dpf whole-mount or 4 dpf vibratome-sectioned embryos were incubated for 10 min in 100 % acetone at −20 °C, washed 3 times in phosphate-buffered saline (PBS) with 0.02 % Tween 20 (PBT), and then incubated for 7 min in trypsin and 3 min in 4 % PFA. Tissues were then washed in PBT and incubated in blocking solution containing the appropriate primary antibody. Antibodies used were anti-α-actinin2 (Sigma clone A7811, 1:100), anti-GFP (Invitrogen A-11122), anti-GFP (DSHB clone 12A6), and AlexaFluor™-labeled-488 and AlexaFluor™-labeled-596 secondary antibodies (Molecular Probes, 1:200). The anti-α-actinin3 antibody was a kind gift of Prof Kathryn North (Murdoch Children’s Research Institute, Melbourne, Australia). The phalloidin used was rhodamine tagged (Molecular Probes, 1:200). Imaging was performed with a LSM 710 confocal microscope (Zeiss), and a 20× 1.0 numerical aperture water-dipping objective for time-lapse experiments or 63× 1.4 numerical aperture oil immersion objective for fixed specimens. All analyses used the ImageJ package Fiji .
For nemaline myopathy patient muscle biopsies , 8 µm cryosections were collected on glass slides and stained either with Gomori trichrome as described  or with anti-α-actinin2 and phalloidin. Immunohistochemistry staining was performed as described . In brief, following air drying, sections were blocked in 2 % BSA–PBS for 15 min before being incubated in blocking solution containing the appropriate primary antibody for 16 h. The anti-α-actinin2 antibody was a kind gift of Prof Alan Beggs (Boston Children’s Hospital, Boston, USA, clone 4B3, diluted 1:1000). The sections were then washed 3 times in PBS and re-blocked for 15 min before being incubated in AlexaFluor™-548 (Molecular Probes, 1:250) and AlexaFluor™-488-phalloidin (Molecular Probes, 1:40) for 1 h. Sections were mounted using Immu-Mount™ (cat #9990402, Thermo Scientific). All sections were imaged using a Zeiss Axioskop 2 microscope.
Electron microscopy (EM)
For EM 50 hpf, zebrafish embryos were anesthetized and immediately fixed in 2 % PFA/2 % glutaraldehyde in 0.1 M sodium cacodylate buffer (pH 7.5). Samples were post-fixed in 1 % osmium, gradually dehydrated in ethanol, and embedded in Epon epoxy resin using a Pelco Biowave Pro. Ultrathin (90 nm) sagittal sections were cut using an Ultracut UCT ultramicrotome (Leica). For correlative light electron microscopy (CLEM), samples were initially fixed in 4 % paraformaldehyde (PFA)/0.4 % glutaraldehyde in 0.1 M phosphate buffer (pH 7.4) to an equal volume of zebrafish embryo water for 10 min, followed by post-fixation in 2 %PFA/0.2 % glutaraldehyde in 0.1 M phosphate buffer (pH 7.4) overnight at 4 °C. Processing of tissue for ultrathin cryosectioning was carried out as described . For CLEM, the zebrafish were embedded in gelatin blocks and the blocks were infiltrated overnight with 2.3 M sucrose at 4 °C, mounted on aluminum pins, and frozen in liquid nitrogen. Sections were cut on an Ultracut UC7 (Leica) and placed on 50 mesh hexagonal copper grids. The combined immunofluorescence labeling was carried out as described  using a biotinylated anti-eGFP antibody (1:300, Rockland #600-106-215), rabbit anti-biotin (1:10.000, Rockland #100-4198), and a goat anti-rabbit AlexaFluor™-488-labeled secondary antibody (Molecular Probes, 1:300). Fluorescence imaging was performed using a Leica AF6000LX Live cell microscope. EM images were taken using an 80 kV Hitachi S-7500 TEM equipped with a Gatan Multiscan digital camera.
Fluorescence recovery after photobleaching (FRAP) experiments
Two-day-old embryos expressing either ACTA1D286G-eGFP or ACTA1wildtype-eGFP were anesthetized in 0.16 % tricaine methanesulfonate and laterally mounted in 1 % low melting agarose. Imaging was carried out on a LSM 710 confocal microscope (Zeiss) equipped with a 20× 1.0 numerical aperture water-dipping objective and a 488-nm laser. A precise region of the muscle fiber was bleached with four iterations of 100 % laser and imaged every 20 s for 10 min after bleaching. Four images were taken prior to bleaching and averaged to obtain the pre-bleach value. Fiji  was used to determine fluorescence intensity of bleached and unbleached areas at each time point. FRAP data analysis was carried out as previously described .
Morpholino antisense oligonucleotides (MOs) targeted against nebulin (exon 5 MO: 5′ TACAGTTCATACCTCACTTAGCTGC, exon 35 MO: 5′ GTCAGTATAGGAATCATACCTGGCT), actc1b exon 2 (ex 2) MO (5′ TGCAGTGTTTTTTTCACCTGGTGAC) and actc1b 5′ UTR MO (5′ GGTCAAGTTGTTATCACAAGACTGA) (Gene Tools) were diluted in distilled water and co-injected with Cascade Blue-labeled dextran (Molecular Probes) into one- to four-cell embryos at a final concentration of 0.5 μM. The embryos were sorted for Cascade Blue labeling prior to analysis.
Western blot analysis
100 μg of total protein was extracted from 2 dpf embryos and electrophoresed through a 12.5 % polyacrylamide SDS gel. Protein was transferred to a nitrocellulose membrane and probed with either; anti-α-actin (Sigma clone A2066, 1:400) or β-tubulin (1:5000, Millipore). Secondary HRP antibodies were all used at 1:5000 (Chemicon).
Touch-evoked response assays were performed at 2 dpf. Zebrafish larvae were imaged using a high-speed infrared camera (1000 frames per second) following a gentle tap of the head using a blunt needle. The maximum acceleration of the fish was extracted using the ZebraLab software (ViewPoint Life Sciences) with a low detection threshold of 6 mm/s. The Tg(actc1b-eGFP) zebrafish line was used as a control.
Locomotor activity was examined at 6 dpf by recording the larval activity and swimming distance during a 10-min period using a Zebrabox (ViewPoint Life Sciences). Larvae were gently pipetted into 48-well plates and allowed to habituate in the light for 5 min before the experiment started. Using a high-speed infrared camera (25 frames per second), the embryos were tracked in the dark for 10 min with the following parameters: inactivity threshold of 6 mm/s, detection threshold of 25 mm/s, and activity burst threshold of 30 mm/s. Both the number of small movements (above inactivity threshold and below activity burst threshold) and total distance swum in a 10-min period were extracted using the ZebraLab software (ViewPoint Life Sciences). The Tg(actc1b-eGFP) zebrafish line was used as a control.
For statistical analysis, a Student’s t test assuming equal variance was used to determine significance and performed using Excel (Microsoft) and graphs were prepared in Prism.
Overexpression of ACTA1D286G-eGFP in zebrafish recapitulates the nemaline myopathy phenotype
Nemaline bodies are highly dynamic and transitory in Tg(ACTA1D286G-eGFP) fish
Cytoplasmic actin aggregates correlate with reduced skeletal muscle function
Using time-lapse analysis, we observed the formation of globular aggregates in the skeletal muscle and hypothesize that these may contribute to muscle weakness. To test this, we overexpressed a human wild-type ACTA1 eGFP-tagged transgene in the zebrafish skeletal muscle (Supplementary Figure S1). We constructed transgenic strains with high and low levels of ACTA1wildtype-eGFP expression (Tg(ACTA1wildtype-eGFP)high and Tg(ACTA1wildtype-eGFP)low, respectively) (Fig. 4b). In contrast to the rod-shaped nemaline bodies observed in Tg(ACTA1D286G-eGFP)high fish, expression of ACTA1wildtype-eGFP never induced the formation of rod-like structures (Supplementary Movie S3). Rather, Tg(ACTA1wildtype-eGFP)high fish only produced globular aggregates that formed at the myosepta and showed an identical immunological signature to those observed in Tg(ACTA1D286G-eGFP)high fish (Fig. 5, Supplementary Figure S2). This demonstrates that globular aggregates are a result of increased ACTA1 and not specifically caused by the ACTA1D286G mutation. These globular aggregates were formed at earlier developmental stages in Tg(ACTA1wildtype-eGFP)high fish (Supplementary Movies S3 and S4) compared to Tg(ACTA1D286G-eGFP)high fish (Supplementary Movie S2).
To assess the pathogenicity of globular aggregates in the skeletal muscle, we examined muscle function in both Tg(ACTA1wildtype-eGFP) and Tg(ACTA1D286G-eGFP) transgenic strains at 2 and 6 dpf. Using a touch-evoked escape response assay, we were able to determine the maximum acceleration of 2 dpf larvae as a direct measure of muscle force. We found a significant decrease in the maximum acceleration of both Tg(ACTA1wildtype-eGFP)high and Tg(ACTA1D286G-eGFP)high compared to control zebrafish, demonstrating that cytoplasmic actin is pathogenic (Fig. 4a). We also recorded the swimming performance at 6 dpf and observed a significant decrease in the number of movements and in the distance traveled by both Tg(ACTA1wildtype-eGFP)high and Tg(ACTA1D286G-eGFP)high strains compared to controls (Fig. 4d).
In addition, we assayed the activity of the low-expressing zebrafish strains. While the swimming abilities of Tg(ACTA1wildtype-eGFP)low fish were comparable to control fish, Tg(ACTA1D286G-eGFP)low fish displayed significantly reduced swimming at 6 dpf (Fig. 4c, d). This reduction in swimming activity correlated with the level of transgene expression (Fig. 4b). These findings demonstrate that cytoplasmic actin aggregates correlate with reduced skeletal muscle performance.
When neb morpholinos were injected singularly and in combination into both the high- and low-expressing Tg(ACTA1wildtype-eGFP) strains we observed an increase in eGFP-positive accumulations at the myosepta (Fig. 8a). These accumulations were also phalloidin positive (Fig. 8b), akin to those observed in Tg(ACTA1D286G-eGFP)high and Tg(ACTA1wildtype-eGFP)high zebrafish, and were not observed in control embryos.
Loss of α-actin results in Actinin2 accumulation and reduced skeletal muscle function
Our analysis has shown that overexpression of ACTA1D286G produces nemaline bodies and causes detrimental effects on muscle function. However, nemaline bodies have been reported in patients carrying recessive ACTA1 mutations leading to an absence of skeletal muscle α-actin protein. Skeletal muscle biopsies from these patients contain disorganized myofibrils and nemaline bodies, presumably caused by an imbalanced stoichiometry between sarcomeric components .
We injected the actc1b morpholino into the Tg(ACTA1wildtype-eGFP)low strain and analyzed the results using in vivo time-lapse imaging. We showed that unlike early forming nemaline bodies in Tg(ACTA1D286G-eGFP) muscle, these nemaline bodies were stable in the skeletal muscle, forming from 32 hpf. They were located both at the myosepta and scattered throughout the muscle fibers (Supplementary Movie S5) and were not observed in control embryos (Supplementary Movie S6).
ACTA1D286G is mislocalized and more rapidly exchanged in the sarcomere
During the FRAP analysis, we observed that the localization of the two proteins within the sarcomere differed. While the ACTA1wildtype-GFP protein demonstrated a clear striated pattern, with well-defined Z-disk structures, ACTA1D286G-eGFP showed more generalized distribution throughout the length of the thin filament (Fig. 13a). We quantified this difference by comparing the fluorescence intensity of the Z-disk to the rest of the filament in both Tg(ACTA1D286G-eGFP)high and Tg(ACTA1wildtype-eGFP)high fish. We found a significant decrease in the ratio of Z-disk/filament eGFP intensity in Tg(ACTA1D286G-eGFP)high (1.3 ± 0.07) compared to Tg(ACTA1wildtype-eGFP)high (1.6 ± 0.1) fish. This finding suggested that ACTA1D286G is preferentially localized along the thin filament (Fig. 13b).
We describe the generation of zebrafish ACTA1 nemaline myopathy models allowing us to investigate disease pathogenesis in vivo. Utilizing the advantages of the zebrafish system we analyze, for the first time, nemaline body formation and dynamics in vivo. Through the overexpression of an eGFP-tagged ACTA1 variant or knockdown of α-actin in the skeletal muscle, we observed the formation of three distinct types of nemaline bodies. ACTA1D286G expression resulted in the formation of actinin-negative nemaline bodies at the myosepta, whereas reduction of actin resulted in Z-disk thickening and nemaline bodies within the myofibril and the formation of Actinin2-positive nemaline bodies at the myosepta.
We found that the early forming nemaline bodies in Tg(ACTA1D286G-eGFP)high fish are highly dynamic within the cell This is both spatially, with nemaline bodies forming close to the myosepta before moving rapidly throughout the cytoplasm, and temporally, as they form around 48 hpf and degrade by 96 hpf. The transitory nature of the nemaline bodies may explain why there is no correlation between their frequency and disease severity [17, 44]. Following the breakdown of the nemaline bodies, we observe the formation of actin-positive globular aggregates. Swimming behavior at 6 dpf, following the transition from nemaline bodies to globular actin aggregates was impaired, suggesting that cytoplasmic actin accumulation may be detrimental to muscle function.
To test this, we created a line overexpressing the wild-type form of ACTA1. Tg(ACTA1wildtype-eGFP)high fish formed globular aggregates, in the absence of nemaline bodies and had reduced muscle performance, indicating that these aggregates likely contribute to reduced skeletal muscle function. Intriguingly, the earlier detection of the aggregates in the Tg(ACTA1wildtype-eGFP)high fish rather than in the Tg(ACTA1D286G-eGFP)high suggests that the nemaline bodies might delay the formation of these aggregates, most likely through the sequestration of actin. The nemaline bodies may therefore be part of a protective mechanism as suggested for intranuclear rod myopathy , and by the observation of rod formation in wild-type muscle under conditions of extreme stress .
As our experimental system overexpressed ACTA1, we examined a model of recessive nemaline myopathy to see if similar cytoplasmic actin aggregates were present. Examining Neb morphant embryos, we identified a shortening of the sarcomere length as observed in NEB-deficient animal models [4, 36, 48] and NEB-related nemaline myopathy patients carrying deletions in exon 55 . Neb morphants also displayed accumulations of globular cytoplasmic actin aggregates comparable to those identified in the ACTA1 models, suggesting this may be a common phenotype in the disease, despite a different genetic cause. Recent data have demonstrated an increase in F-actin accumulation, coupled with increased expression of α-actin isoforms in Cfl2 knockout mice [2, 14] and in patients carrying CFL2 mutations . Furthermore, it has recently been shown that loss of KLHL40 causes a reduction in NEB, leading to destabilization of the thin filament  and increased actin was observed in patients with mutations in KLHL40 . Together with our data, this suggests that the accumulation of actin in the cytoplasm is one of the contributing factors to reduced muscle performance in nemaline myopathy.
However, the formation of nemaline bodies can not only be caused by the presence of mutant actin, and neither can the accumulation of actin in the cytoplasm be the sole cause of muscle weakness, since loss of ACTA1 also results in the disease . We therefore examined the consequence of reducing actin in the skeletal muscle. We used two different morpholinos to reduce actin levels in the skeletal muscle, both of which resulted in the formation of two further forms of Actinin2-rich nemaline bodies. One originated in the cytoplasm, in the vicinity of the myosepta, and the other appeared to form from Z-disk thickenings that expanded to engulf an entire sarcomere. The cytoplasmic Actinin2-rich aggregates were also positive for actin, suggesting they further deplete the sarcomeric pool of actin, and may impair muscle function in this way. The electron-dense material engulfing the sarcomere would be expected to form a non-contractile region in the fiber reducing function. EM analyses showed that these sarcomeric nemaline bodies were concentrated around regions of fiber disorganization and dissolution, suggesting that their presence interferes with normal sarcomere function causing an inherent structural weakness. This is consistent with a recent analysis of muscle biopsies from NEB-related nemaline myopathy patients that showed myofibrillar dissociation appeared to be an important cause of muscle weakness rather than the frequency or position of nemaline bodies within muscle fibers, which inversely correlated with severity . Functional analysis of Actc1b morphants demonstrated significantly reduced skeletal muscle function at both 2 dpf and 6 dpf, proportional to the loss of α-actin in the skeletal muscle. In Actc1b morphants, we observed electron-dense projections extending from the myosepta, a structure analogous to the myotendinous junction. While disruptions to the myotendinous junction are not thought to be common in patients with ACTA1 mutations, the recessive ACTA1V154L mutation results in a dystrophic phenotype, alongside Z-disk streaming and infrequent nemaline bodies , consistent with dystrophic disruption to this structure.
The frequent presence of Z-disk thickening in nemaline myopathy has led to the prevalent theory that nemaline bodies originate from, and are tethered to, the Z-disk [9, 40, 41, 57]. Our observations show that only one of the three types of nemaline bodies originates within the Z-disk. This is supported by reports of nemaline patients with nemaline bodies but without Z-disk thickening  and the observation of nemaline bodies in proximity to the myotendinous junction. The subtypes of nemaline bodies we identified in the zebrafish can be distinguished immunologically. To determine if the same was true in patients, we examined muscle biopsy samples from ACTA1 nemaline myopathy patients and also found variations in phalloidin and actinin2 labeling of nemaline bodies. In ACTA1T66I muscle biopsy samples, nemaline bodies contained both phalloidin and actinin2. However, in ACTA1I136M, both actinin2-positive and -negative nemaline bodies were identified, confirming previous reports in cell culture [12, 18, 50], and likely corresponding to those identified in the fish. The different composition of the nemaline bodies may allow the subtypes to be used as indicators of the mechanism triggering nemaline body formation and potentially aid in the identification of the causative mutation. Further support for the formation of different types of nemaline bodies comes from examining other nemaline myopathies, such as those caused by a CFL2 mutation, which have identified a mixture of aggregates, some that stained for F-actin and actinin2, and others that did not . It should be noted that despite the lack of phalloidin labeling, these nemaline bodies in our ACTA1D286G model fish contain actin. The lack of labeling therefore reflects differences in the conformation of actin in the bodies, compared to sarcomeres, preventing binding of phalloidin.
Both our overexpression and loss-of-function ACTA1 nemaline myopathy models show that actin imbalance in the skeletal muscle has pathogenic consequences. In addition to the formation of nemaline bodies and actin aggregates, ACTA1 mutation can also directly affect its sarcomeric function. The ACTA1D286G mutation lies near the hydrophobic pocket, which is important for actin–actin interactions . Due to this location, and the reduced incorporation of ACTA1D286G into actin filaments reported in myoblasts, it has been suggested that the polymerization of ACTA1D286G could be impaired . We directly examined actin dynamics identifying a more rapid exchange of ACTA1D286G compared to ACTA1wildtype protein. Although the mutant actin was incorporated into the sarcomere, we identified a reduced affinity for the Z-disk and increased affinity for the thin filament. These changes in dynamics and sub-sarcomeric localization, coupled with a reduction in binding strength at the actomyosin interface , will impact thin filament function in the sarcomere, leading to muscle weakness. Similarly, mutation-specific contributions to muscle weakness are observed in NEB-related nemaline myopathy, where altered thin filament lengths reduce muscle contractile performance [37, 38].
Our study identifies multiple subtypes of nemaline bodies and characterizes, in vivo, their origin within the skeletal muscle. We demonstrate that these subtypes can be differentiated immunologically in skeletal muscle biopsies from ACTA1 nemaline myopathy patients, potentially providing markers for disease severity and aiding in the identification of the causative mutation. We further identify accumulation of cytoplasmic actin, myofibrillar disarray, sarcomeric disruption, and actin depletion as contributors to muscle weakness. Our analysis of a NEB-related nemaline myopathy model and data from other forms of nemaline myopathy suggest that these mechanisms may be common across nemaline myopathy. Furthermore, the generation of these zebrafish models has additionally established an ideal platform for the development and evaluation of therapies.
We would like to thank Professor Kathryn North for her assistance in obtaining biopsy material. The research was funded by an Australian National Health and Medical Research Council (NHMRC) Project Grant (APP1010110). STC is supported by a NHMRC Career Development Fellowship (APP1048816). MY is supported by a NHMRC Project Grant (APP1080587). NGL and PDC are supported by NHMRC Principal Research Fellowships (APP1002147, APP1041885), and KJN by an Australian Research Council Future Fellowship (FT100100734).
- 2.Agrawal PB, Joshi M, Savic T et al (2012) Normal myofibrillar development followed by progressive sarcomeric disruption with actin accumulations in a mouse Cfl2 knockout demonstrates requirement of cofilin-2 for muscle maintenance. Hum Mol Genet 21:2341–2356. doi:10.1093/hmg/dds053 PubMedCentralCrossRefPubMedGoogle Scholar
- 13.Gupta VA, Ravenscroft G, Shaheen R, Todd EJ et al (2013) Identification of KLHL41 mutations implicates BTB-Kelch-mediated ubiquitination as an alternate pathway to myofibrillar disruption in nemaline myopathy. Am J Hum Genet 93:1108–1117. doi:10.1016/j.ajhg.2013.10.020 PubMedCentralCrossRefPubMedGoogle Scholar
- 17.Hutchinson DO, Charlton A, Laing NG et al (2006) Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindred. N Neuromuscul Disord 16:113–121. doi:10.1016/j.nmd.2005.11.004 CrossRefGoogle Scholar
- 39.North KN, Ryan MM (1993) Nemaline myopathy. In Pagon RA, Adam MP, Ardinger HH, et al (editors) GeneReviews. University of Washington, Seattle (WA)Google Scholar
- 56.Westerfield M (2007) The zebrafish book. A guide for the laboratory use of zebrafish (Danio rerio). Univ of Oregon Press, EugeneGoogle Scholar
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.