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Aberrant deposition of stress granule-resident proteins linked to C9orf72-associated TDP-43 proteinopathy



A G4C2 hexanucleotide repeat expansion in the noncoding region of C9orf72 is the major genetic cause of frontotemporal dementia and amyotrophic lateral sclerosis (c9FTD/ALS). Putative disease mechanisms underlying c9FTD/ALS include toxicity from sense G4C2 and antisense G2C4 repeat-containing RNA, and from dipeptide repeat (DPR) proteins unconventionally translated from these RNA products.


Intracerebroventricular injections with adeno-associated virus (AAV) encoding 2 or 149 G4C2 repeats were performed on postnatal day 0, followed by assessment of behavioral and neuropathological phenotypes.


Relative to control mice, gliosis and neurodegeneration accompanied by cognitive and motor deficits were observed in (G4C2)149 mice by 6 months of age. Recapitulating key pathological hallmarks, we also demonstrate that sense and antisense RNA foci, inclusions of poly(GA), poly(GP), poly(GR), poly(PR), and poly(PA) DPR proteins, and inclusions of endogenous phosphorylated TDP-43 (pTDP-43) developed in (G4C2)149 mice but not control (G4C2)2 mice. Notably, proteins that play a role in the regulation of stress granules – RNA-protein assemblies that form in response to translational inhibition and that have been implicated in c9FTD/ALS pathogenesis – were mislocalized in (G4C2)149 mice as early as 3 months of age. Specifically, we observed the abnormal deposition of stress granule components within inclusions immunopositive for poly(GR) and pTDP-43, as well as evidence of nucleocytoplasmic transport defects.


Our in vivo model of c9FTD/ALS is the first to robustly recapitulate hallmark features derived from both sense and antisense C9orf72 repeat-associated transcripts complete with neurodegeneration and behavioral impairments. More importantly, the early appearance of persistent pathological stress granules prior to significant pTDP-43 deposition implicates an aberrant stress granule response as a key disease mechanism driving TDP-43 proteinopathy in c9FTD/ALS.


A hexanucleotide repeat expansion consisting of hundreds to thousands of G4C2 repeats located in a non-coding intronic region of chromosome 9 open reading frame 72 (C9orf72) is the most frequent genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS), collectively referred to as c9FTD/ALS. FTD is second only to Alzheimer’s disease (AD) as a cause of dementia in patients under 65 [46], and encompasses a group of disorders characterized clinically by changes in personality, behavior, and/or language. ALS, a common motor neuron disease, is characterized by selective degeneration of lower and upper motor neurons, leading to muscle weakness, spasticity, and atrophy, and ultimately resulting in paralysis. Given that FTD and ALS patients often share clinical, genetic, and neuropathological features, including the aggregation of phosphorylated TAR DNA-binding protein 43 (pTDP-43) [47], common disease mechanisms are believed to underlie both disorders.

Potential mechanisms implicated in the pathogenesis of c9FTD/ALS include the loss of C9ORF72 protein function, repeat RNA-mediated toxicity, and toxicity from the accumulation of dipeptide repeat (DPR) proteins produced by repeat-associated non-ATG (RAN) translation (reviewed [19, 55, 56]). For instance, foci containing sense G4C2 or antisense G2C4 repeat RNA bidirectionally-transcribed from the C9orf72 expansion are observed in c9FTD/ALS postmortem brain tissues, cultured cells, and neurons, and may disrupt RNA metabolism and nucleocytoplasmic transport through sequestration of various RNA-binding proteins [11, 14, 18, 22, 23, 31, 42, 43]. Moreover, RAN translation of repeat RNA produces poly-glycine-alanine (GA) and poly-glycine-arginine (GR) from sense G4C2 transcripts, poly-proline-alanine (PA) and poly-proline-arginine (PR) from antisense G2C4 transcripts, and poly-glycine-proline (GP) from both sense and antisense transcripts [2, 18, 43, 44, 65]. In postmortem c9FTD/ALS brains, poly(GA) and poly(GP) inclusions are more frequent than poly(GR), while poly(PA) and poly(PR) inclusions are comparatively rare [35, 36]. Although poly(GP) is believed to be relatively benign, poly(GA) deposition is linked to ubiquitin proteasome dysfunction, ER stress, and nucleocytoplasmic transport defects [21, 39, 62, 63]. In addition, despite being less abundant than poly(GA), several reports have demonstrated that poly(GR) and poly(PR) are particularly toxic in a variety of cell and animal models, leading to nucleolar stress and impairment of vital cellular functions including nucleocytoplasmic transport, stress granule (SG) dynamics, and protein translation [17, 25, 29, 41, 52, 54, 57, 61]. Nevertheless, how the many pathognomonic features of c9FTD/ALS cause disease remains to be determined, an effort that is hindered by the lack of a comprehensive model that recapitulates the hallmark features derived from both sense and antisense C9orf72 repeat expansion transcripts, including TDP-43 pathology.

We previously described the development and characterization of a mouse model of c9FTD/ALS whereby the expression of (G4C2)66 throughout the central nervous system (CNS) by means of somatic brain transgenesis using an adeno-associated virus (AAV) vectors resulted in the development of C9orf72-associated pathological and behavioral abnormalities by 6 months of age [9]. Specifically, sense RNA foci, inclusions of poly(GP), poly(GA), and poly(GR), pTDP-43 pathology, gliosis, and neuronal loss were detected in the brain of (G4C2)66 mice [9]. In the present study, we describe the characterization of an AAV mouse model in which a longer repeat is expressed. Similarly to (G4C2)66 mice, G4C2-derived RNA foci and DPR proteins accumulate in (G4C2)149 mice, and they develop TDP-43 pathology, neurodegeneration, gliosis, and behavioral abnormalities. Most remarkably, however, was our finding that antisense G2C4 RNA-derived foci and DPR proteins were also present in (G4C2)149 mice, thus providing an in vivo model that develops all pathological features of c9FTD/ALS with which to explore disease mechanisms. Furthermore, we demonstrate that several SG-associated proteins localize to inclusions in (G4C2)149 mice, offering additional support to the growing body of evidence that aberrant regulation of SG biology contributes to c9FTD/ALS [4, 5, 27, 32, 37, 38, 59]. SGs are dynamic, membraneless structures that transiently form in the cytoplasm in response to various stressors, and subsequently dissolve upon stress resolution. However, chronic cellular stress and a persistent SG response have been proposed to mediate the formation of irreversible, pathological inclusions by providing an environment in which TDP-43 and other aggregation-prone proteins and RNAs are focally concentrated. In support of this idea, knockdown of SG components or inhibition of SG formation was recently shown to decrease c9FTD/ALS pathophysiology and reverse nucleocytoplasmic transport defects [59]. By revealing colocalization of poly(GR) and pTDP-43 with SG-resident proteins within inclusions combined with evidence of nucleocytoplasmic trafficking abnormalities in (G4C2)149 mice, our present study now provides insight on the interplay among SG biology, nucleocytoplasmic transport, G4C2/G2C4-associated pathologies and TDP-43 deposition.


All animal procedures were performed in accordance with the National Institutes of Health Guide for Care and Use of Experimental Animals, and approved by the Mayo Clinic Institutional Animal Care and Use Committee (IACUC).

Generation of (G4C2)2 and (G4C2)149 AAV vectors

AAV vectors were generated as previously described [9]. Briefly, the (G4C2)2 or (G4C2)149 repeats, along with 119 and 100 base pairs of the 5′ and 3′ flanking regions of the C9orf72 gene, respectively, were inserted into an AAV expression vector (pAM/CBA-pl-WPRE-BGH) containing inverted terminal repeats of serotype 2. AAV-(G4C2)2 and AAV-(G4C2)149 particles were packaged into serotype 9 type capsid and purified using standard methods [64]. AAV was generated by co-transfection with helper plasmids into HEK293T cells. Cells were harvested 48 h after transfection, and lysed with 0.5% sodium deoxycholate and 50 Units/ml Benzonase (Sigma-Aldrich) by freeze thaw. The virus was then purified using a discontinuous iodixanol gradient, and the genomic titer of each virus determined by qPCR. AAV solutions were diluted with sterile phosphate-buffered saline (PBS).

Neonatal viral injections

Intracerebroventricular injections of AAV were performed as previously described with some minor modifications [7, 28]. Briefly, a 32-gauge needle (product #7803–04, 0.5 in. custom length, point style 4, 12 degrees, Hamilton Company) attached to a 10 μl syringe (Hamilton Company) was inserted into the lateral ventricle of cryoanesthetized C57BL/6J pups at postnatal day 0. The needle was inserted at a 30-degree angle from the surface of the head, and held at a depth of approximately two millimeters. Two microliters (1.5E10 genomes/μl) of AAV2/9-(G4C2)2 or AAV2/9-(G4C2)149 solution was manually injected into each lateral ventricle. Following injection, pups were placed on a heated pad until they recovered from anesthesia, at which time they were placed back into their home cage.

Behavioral tests

Cohorts of 3-month-old mice expressing (G4C2)2 (n = 17) or (G4C2)149 (n = 17), and 6-month-old mice expressing (G4C2)2 (n = 14) or (G4C2)149 (n = 11) underwent a battery of behavioral tests, including the open field assay, hanging wire test, and contextual fear conditioning test. All mice were acclimated to the testing room for 1–2 h prior to testing. All behavioral equipment was cleaned with 30% ethanol prior to use and between each animal. All mice were returned to their home cages and home room following completion of each test.

Open field assay

Mice were placed in the center of an open field apparatus, and allowed to explore the area for 15 min. Movement was monitored through the use of an overhead camera with AnyMaze software (Stoelting Co.), and total distance traveled was tracked.

Hanging wire test

A 2 mm thick wire tied to two vertical stands, approximately 55 cm apart, was maintained 35 cm above a layer of bedding material to prevent injury when an animal fell from the wire. Upon grasping the wire, the number of times the mouse fell from the wire within a 2 min time period were recorded.

Contextual fear conditioning test

This test was conducted in a test chamber with a grid floor capable of delivering an electric shock. Mice were initially placed in the chamber and left undisturbed for 2 min. An 80-dB white noise served as the conditioned stimulus (CS) and was presented for 30 s followed by a mild (2 s, 0.5 mA) foot shock serving as the unconditioned stimulus (US). A second CS-US pair was presented after 2 min, and the mouse was removed from the apparatus 30 s later and returned to its home cage. Twenty-four hours later, each mouse was returned to the test chamber and their freezing behavior was recorded for 5 min (in the absence of a CS-US pairing).

RNA fluorescence in situ hybridization (FISH)

Mice were euthanized by carbon dioxide, and their brain and spinal cord were rapidly removed. Hemi-brains and the cervical half of the spinal cord was fixed in 4% paraformaldehyde for at least 48 h, and subsequently embedded in paraffin and sectioned at 5 μm (sagittal sections for brain, coronal sections for spinal cord). Paraffin sections were mounted on positively-charged glass slides, dried overnight, and the RNA FISH protocol was performed as previously described [9] with some modifications. In brief, tissue sections were deparaffinized in xylene, rehydrated through a series of ethanol solutions, permeabilized with ice cold 2% acetone/1xDEPC-PBS for five minutes, washed twice with DEPC-water, and then dehydrated through a series of ethanol solutions. To detect sense RNA foci, sections were incubated with pre-hybridization buffer (50% formamide [Midsci], 10% dextran sulfate [Millipore], 2x saline-sodium citrate buffer [SSC], 50 mM sodium phosphate buffer pH 7.0) for 20–30 min at 66 °C, and then hybridized for 24 h at 66 °C in a dark, humidified chamber with a fluorescently-labeled locked nucleic acid (LNA) probe [30] (TYE563-[CCCCGGCCCCGGCCCC]; Exiqon product number 500150, design id: 283117) diluted to a final concentration of 40 nM. To detect antisense foci, sections were first incubated with pre-hybridization buffer (50% formamide [MidSci], 10% dextran sulfate [Millipore], 2xSSC, 50 mM lithium phosphate buffer pH 7.0), and then incubated for 24 h at 60 °C in a dark, humidified chamber with an LNA probe [30] (TYE563-[GGGGCCGGGGCCGGGG]; Exiqon product number: 500150, design id: 345686) diluted to final concentration of 40 nM. Next, sections were washed with 2x SSC/0.1% Tween-20 at room temperature for 5 min, and then washed twice with pre-warmed 0.2x SSC at 60 °C for 10 min in the dark. Following these washes, slides were coverslipped using Vectashield mounting media with DAPI (Vector Laboratories). Representative images of sense and antisense RNA foci in the motor cortex, hippocampus, cerebellum and spinal cord were taken with an AxioImager Z1 fluorescent microscope (Carl Zeiss MicroImaging) under 63x magnification. Quantitative analysis of cells containing sense and antisense RNA foci in (G4C2)149 mice (n = 6 from each age group) was completed for the following regions: motor cortex (n = 300–400 cells), hippocampus (n = 500 cells), and cerebellar Purkinje cells (n = 100 cells).

Immunohistochemistry and quantitative analysis of DPR protein inclusions

Tissue sections were deparaffinized in xylene and rehydrated through a series of ethanol solutions. Antigen retrieval was performed in distilled water or pH 9 Tris-EDTA (DAKO) for 30 min. Sections were then immunostained with rabbit polyclonal antibodies against poly(GA) (1:50,000), poly(GP) (1:10,000), poly(GR) (1:2500), poly(PA) (1:3500), or poly(PR) (1:500) using the DAKO Autostainer (Universal Staining System) and the DAKO+HRP system. Other antibodies used for immunohistochemical analysis were those for the detection of SG components (G3BP1 [1:100, Abclonal, A5342], eIF3Abclonal, A5342 [1:2000, Santa Cruz Biotechnology, sc-16,377], ataxin-2 [1:500, Proteintech, 21,776–1-AP]), RanGAP1 [1:100, Santa Cruz Biotechnology, sc-25,630], glial fibrillary acidic protein (GFAP, 1:2500, Biogenex) and neuronal nuclei (NeuN, 1:5000, Millipore). Sections were counterstained with hematoxylin, dehydrated through a series of ethanol and xylene washes, and coverslipped with Cytoseal mounting media (Thermo Fisher Scientific, Inc). Slides were scanned with a ScanScope® AT2 (Leica Biosystems) at 40x magnification, and representative images taken with ImageScope® software (v12.1; Leica Biosystems). Quantitative analysis of DPR protein burden in (G4C2)149 mice (n = 8 per age group) was performed by evaluating poly(GA), poly(GP), and poly(GR) protein inclusions in the motor cortex, and poly(PA) and poly(PR)-positive inclusions in the entire cortex. Quantitative analysis of the number of ataxin-2-positive inclusions in the motor cortex or hippocampus was performed on (G4C2)149-mice (n = 7 for 3 month; n = 9 for 12 month cohort). Quantification of the number of RanGAP1 nuclear invaginations in the cortex was performed on animals at 3 months [n = 6 for (G4C2)2-mice; n = 7 for (G4C2)149-mice] and 12 months of age [n = 6 for (G4C2)2-mice; n = 9 for (G4C2)149-mice].


Tissue sections were deparaffinized in xylene and rehydrated through a series of ethanol solutions. Antigen retrieval was performed by steaming in sodium citrate buffer (10 mM sodium citrate, 0.05% Tween-20, pH 6) for 30 min. Tissues were immunostained with antibodies against poly(GR) (1:1000, EMD Millipore, MABN778), TIA1 (1:50, Santa Cruz Biotechnology, sc-1751), ataxin-2 (1:500, Proteintech, 21,776–1-AP), and/or pTDP-43 (1:1000, Cosmo, CAC-TIP-PTD-P02) overnight at 4 °C. Sections were subsequently incubated with corresponding secondary antibodies (1:500, Molecular Probes) and coverslipped with Vectashield with DAPI. Images were taken with Zeiss LSM 800 confocal microscope.

Digital pathology

Percentage of GFAP immunoreactivity and NeuN-positive neuronal density were quantified using Aperio® ePathology technology (Leica Biosystems) as previously described [9]. Briefly, stained slides were scanned and digitized with ScanScope® AT2 (Leica Biosystems), and ImageScope® software (v12.1; Leica Biosystems) was used to annotate the cortex on serial sections stained for GFAP or NeuN. GFAP immunolabeling was quantified by a custom-designed positive pixel count algorithm [45], which provided the percent burden of positively-stained pixels per each annotated region as the output parameter (n = 8 per age group). NeuN-positive neurons were quantified using an algorithm designed to detect nuclei. The output parameter was the number of NeuN-positive neurons per mm2 of the annotated cortical region (n = 6 per age group).

pTDP-43 immunohistochemistry

Immunohistochemistry for pTDP-43 was performed using the VECTASTAIN® Elite® ABC (Vector Laboratories) kit, with minor modifications to the manufacturer’s protocol. Tissue sections were deparaffinized and rehydrated in a graded series of xylene and ethanol washes prior to antigen retrieval by steaming for 30 min in sodium citrate buffer (10 mM sodium citrate, 0.05% Tween-20, pH 6.0). Slides were allowed to slowly cool for 15–20 min, and then gently flushed with distilled water for 15 min. Tissue sections were incubated with Dako Dual Endogenous Enzyme Block (DAKO) and then rinsed three times with 1x PBS for five minutes at room temperature. Sections were blocked with 2% normal goat serum in 1xPBS for one hour at room temperature, and then incubated with pTDP-43 antibody (pS409/410, generated in-house [9, 10], 1:500) overnight at 4 °C. The following day, slides were washed with 1xPBS at room temperature (three 5 min washes), and then incubated with biotinylated goat anti-rabbit secondary (1:200) for 2 h at room temperature. Slides were subsequently washed with another round of 1xPBS (three 5 min washes), incubated with avidin-biotin complex solution for 30 min, and washed again in 1xPBS (three 10 min washes). 3,3′-diaminobenzidine (Acros Organics) was activated with hydrogen peroxide, and the reaction stopped by rinsing slides in distilled water. Slides were then counterstained with hematoxylin, dehydrated through a series of ethanol washes and xylene, and coverslipped with Cytoseal mounting media (Thermo Fisher Scientific, Inc). Slides were scanned with a ScanScope® AT2 (Leica Biosystems) at 40x magnification. Quantitative analysis of pTDP-43 inclusions in the cortex of (G4C2)149 (n = 6 per age group) was performed with ImageScope® software (v12.1; Leica Biosystems).

Statistical analysis for behavioral studies and quantification of pathology

To determine whether statistically significant differences in RNA foci, DPR protein burden or pTDP-43 inclusions were observed among (G4C2)149 mice of different ages, 1-way ANOVA followed by a Tukey’s posthoc test for multiple comparisons was used. To compare NeuN and GFAP immunoreactivity between (G4C2)2 and (G4C2)149 mice at 3 or 6 months of age, a 2-way ANOVA with a Tukey’s posthoc test was used. To compare the performance of (G4C2)2 and (G4C2)149 mice in behavioral tests (i.e., the open field assay, the hanging wire test and the contextual fear conditioning test), unpaired two-tailed t tests were performed. All statistical analyses were performed in GraphPad Prism. Data are presented as mean +/− SEM, with p < 0.05 considered statistically significant.


Behavioral abnormalities coincide with neurodegeneration in (G4C2)149 mice

Intracerebroventricular injections were performed to deliver AAV encoding (G4C2)2 or the expanded (G4C2)149 to the murine CNS on postnatal day 0, followed by behavioral and histopathological analysis of c9FTD/ALS features. To first characterize behavioral consequences of CNS (G4C2)149 expression, we subjected mice to an open field assay, a hanging wire test, and a contextual fear conditioning test. Consistent with our (G4C2)66 mouse model [9], 3- and 6-month-old (G4C2)149 mice displayed hyperactivity in the open field assay (Fig. 1a, Additional file 1: Figure S1a). However, motor deficits, as evidenced by an increased number of falls in the hanging wire test, were observed in 6- but not 3-month-old (G4C2)149 mice (Fig. 1b, Additional file 1: Figure S1b). (G4C2)149 mice also exhibited signs of cognitive dysfunction in the contextual fear conditioning test at 6 months of age. Specifically, the significant decrease in the amount of time (G4C2)149 mice spent freezing in this test is indicative of their impaired ability to associate the test environment with a mild electrical shock, and is suggestive of hippocampal dysfunction (Fig. 1c, Additional file 1: Figure S1c).

Fig. 1

(G4C2)149–mice exhibit hyperactivity, motor deficits, and memory loss at 6 months of age. a Significant increase in distance traveled in (G4C2)149 mice in open field analysis indicative of hyperactivity. b Hanging wire test revealed an increase in the number of falls in (G4C2)149 mice relative to age-matched (G4C2)2 mice. c Cognitive function was assessed by contextual fear conditioning, which demonstrated a significant reduction in freezing in (G4C2)149 mice, indicative of cognitive impairment. d Quantitative analysis of the number of NeuN-positive neurons per mm2 of cortex reveals neuronal loss in (G4C2)149 mice at 6 months of age, but no difference with (G4C2)2 mice at 3 months. e The percent of GFAP immunoreactivity in the cortex demonstrates a significant increase in gliosis in (G4C2)149 mice at both 3 and 6 months relative to control (G4C2)2 mice. Data represent the mean ± SEM. *p < 0.05, **p < 0.01,***p < 0.001, and ****p < 0.0001 as analyzed by unpaired two-tailed t tests (a-c) or 2-way ANOVA (d-e) followed by Tukey’s post-hoc analysis

To determine whether behavioral abnormalities are associated with markers of neurodegeneration in (G4C2)149 mice, we evaluated astrogliosis and neuronal loss. Compared to (G4C2)2 mice, (G4C2)149 mice showed significantly elevated immunoreactivity for the astrocytic marker GFAP in the cortex at both 3 and 6 months of age (Fig. 1e, Additional file 1: Figure S2a). However, a significant loss of NeuN-positive cortical neurons was only evident at 6 months of age, but not at 3 months of age (Fig. 1d, Additional file 1: Figure S2b), suggesting that astrogliosis precedes neurodegeneration in (G4C2)149 mice. Collectively, our findings indicate that the early development of astrogliosis and hyperactivity precede significant neurodegeneration in (G4C2)149 mice, and that the development of cognitive and motor deficits follow the time course of neuronal loss (Fig. 1, Additional file 1: Figure S1–2).

(G4C2)149 mice develop sense and antisense RNA foci

To determine whether behavioral abnormalities and neurodegeneration in (G4C2)149 mice are related to the accumulation of C9orf72 repeat-associated pathologies, we first performed RNA FISH using a probe to detect sense G4C2 repeat RNA. This analysis revealed intranuclear foci of G4C2 repeat RNA (sense foci) in various regions of the CNS in (G4C2)149 mice, including the motor cortex (Fig. 2a, bottom panel), the hippocampus, the Purkinje cell layer of the cerebellum, the thalamus, and, to a lesser extent, the ventral horn of the spinal cord (Additional file 1: Figure S3a). No sense RNA foci were detected in (G4C2)2 mice at any age (Fig. 2a, top panel).

Fig. 2

Sense and antisense RNA foci observed in the CNS of (G4C2)149–mice. a) Sense RNA foci (white arrowheads) were detected throughout the CNS with representative images from the motor cortex of 3, 6, and 12 month (G4C2)149–mice (bottom panel, a), but not in control (G4C2)2–mice (top panel, a). b-d Percentage of cells containing sense RNA foci in the motor cortex (b), CA1 through CA3 region of the hippocampus (c), and Purkinje layer of the cerebellum (d) in (G4C2)149 mice at 3, 6, and 12 months of age. e) Antisense RNA foci (white arrowheads) were detected throughout the CNS in (G4C2)149–mice (bottom panel, e) but not in control (G4C2)2–mice (top panel, e) at 3, 6, and 12 months of age, with representative images from the motor cortex. f-h) Percentage of cells containing antisense RNA foci in the motor cortex (f), CA1 through CA3 region of the hippocampus (g), and Purkinje layer of the cerebellum (h) in 3, 6, and 12-month (G4C2)149–mice. Data represent the mean ± SEM. *P < 0.05 and ***P < 0.001, as analyzed by one-way ANOVA followed by Tukey’s post-hoc analysis. Scale bar represents 5 μm

To assess whether aging exacerbates RNA foci accumulation, we quantified sense RNA foci in (G4C2)149 mice at 3, 6, and 12 months of age in brain regions with the highest foci burden (i.e., motor cortex, hippocampal CA1–CA3 regions, cerebellar Purkinje cell layer). The number of foci-positive cells was approximately 28, 39, and 56% in the motor cortex of (G4C2)149 mice at 3, 6, and 12 months of age, respectively, with a significant increase in foci burden detected in 12-month-old mice compared to younger mice (Fig. 2b). Of these foci-positive-cells, approximately 70% harbored one or two RNA foci per cell, while the remaining 30% of cells contained three or more foci (with no significant difference across age groups; Additional file 1: Figure S3d). In the hippocampus, approximately 26 to 40% of cells in the CA1–CA3 regions contained RNA foci in (G4C2)149 mice but no significant difference was seen among the three age groups (Fig. 2c). Consistent with results from c9FTD/ALS postmortem tissues [13], the cerebellar Purkinje cell layer had the highest burden of sense RNA foci among the three regions, with approximately 52 to 58% of cells containing nuclear RNA foci (Fig. 2d). However, as in the hippocampus, the percentage of sense foci in Purkinje cells did not significantly differ with age.

Given that foci of antisense G2C4 transcripts are also detected in postmortem brain tissues of c9FTD/ALS patients [12, 13, 18], and that inverted terminal repeats present within the AAV vector both 5′ and 3′ of the G4C2 repeat have been shown to exert promoter-like activity [16], we next evaluated whether antisense G2C4 repeat RNA was present in (G4C2)149 mice by RNA FISH. Antisense RNA foci were observed in the same brains regions in which sense RNA foci were detected, albeit at a much lower frequency (Fig. 2e bottom panel, Additional file 1: Figure S3b). Approximately 4 to 6% of cells in the motor cortex, and 5 to 10% of cells in the hippocampus contained antisense RNA foci with minimal differences in frequency seen across the three age groups (Fig. 2f-g, Additional file 1: Figure S3d). Again, the cerebellar Purkinje cell layer exhibited the highest burden of foci among the three assessed regions, with approximately 18 to 24% of cells bearing antisense foci among the three age groups (Fig. 2h). Overall, age appeared to have minimal effect on antisense RNA foci burden.

(G4C2)149 mice develop sense and antisense DPR protein pathology

Neuronal inclusions of DPR proteins generated from sense and antisense repeat RNA are a prominent hallmark of c9FTD/ALS. To characterize DPR protein pathology in the CNS of (G4C2)2 and (G4C2)149 mice, a panel of polyclonal antibodies specific to each of the DPR proteins was used for immunohistochemical analyses. We observed cytoplasmic aggregates immunopositive for poly(GA), poly(GP), or poly(GR) in various neuroanatomical regions of (G4C2)149 mice that were reminiscent of inclusions detected in c9FTD/ALS postmortem brains (Fig. 3). From 3 months of age, these inclusions were present in all layers of the cortex, CA1–CA3 regions of the hippocampus (less frequently observed in the dentate gyrus), the cerebellum, and the spinal cord (Additional file 1: Figure S4a-c). Additionally, diffuse nuclear poly(GP) was readily detected (Fig. 3b, Additional file 1: Figure S4a-c), as was diffuse cytosolic poly(GR) (Fig. 3c, Additional file 1: Figure S4a-c). Poly(GA), poly(GP) and poly(GR) inclusions increased in size, number, and stained more intensely across aging, suggestive of progressive aggregation over time. Indeed, quantitative analysis of poly(GA) (Fig. 3f), poly(GP) (Fig. 3g), and poly(GR) (Fig. 3h) inclusions in the motor cortex demonstrated an age-dependent increase from 3 to 12 months of age. Poly(GA) and poly(GP) inclusions were more frequent than poly(GR) inclusions (Fig. 3f-h), recapitulating the inclusion profile in c9FTD/ALS [35].

Fig. 3

Sense and antisense DPR protein inclusions in (G4C2)149–mice. a-e Representative images of immunohistochemical analysis of poly(GA), poly(GP), poly(GR), poly(PA), and poly(PR) proteins in the motor cortex of (G4C2)149 mice at 3, 6, and 12 months of age. f-h Quantitative analysis of the number of poly(GA) (f), poly(GP) (g), or poly(GR) (h) inclusions observed per mm2 of motor cortex in (G4C2)149–mice at 3, 6, and 12-months. i-j Quantitative analysis of poly(PA) (i) or poly(PR) (j) inclusions observed in the cortex of 3, 6, and 12-month (G4C2)149–mice. Data represent the mean ± SEM. *p < 0.05, **p < 0.01,***p < 0.001, and ****p < 0.0001 as analyzed by 1-way ANOVA followed by Tukey’s post-hoc analysis. Scale bar represents 20 μm

Of importance, we also detected inclusions throughout the cortex that were immunopositive for poly(PA) (Fig. 3d) and poly(PR) (Fig. 3e), the two DPR proteins uniquely produced from antisense G2C4 RNA. However, their frequency was much lower relative to poly(GA), poly(GP) and poly(GR) inclusions, again mimicking observations from c9FTD/ALS postmortem brain tissues [18, 35, 65]. The number of poly(PA) and poly(PR) inclusions increased with age, with the majority of inclusions detected in the cortex and exhibiting a cytoplasmic localization, although a small fraction did localize to the nucleus (Fig. 3d-e, i-j). Poly(PA) and poly(PR) inclusions were also occasionally observed in the hippocampus of (G4C2)149 mice at 12 months of age, but were rarely found in other regions of the CNS (not shown). To assess whether repeat length influences antisense DPR protein production, we examined mice injected with an AAV vector encoding a shorter 66-mer G4C2 repeat [9]. (G4C2)66 mice were positive for both poly(PA) and poly(PR) inclusions at 6 months of age; however, the frequency of these inclusions was significantly lower relative to those in mice expressing 149 G4C2 repeats (Additional file 1: Figure S5). Neither sense nor antisense DPR protein pathology was detected in the CNS of (G4C2)2 mice at any age (Additional file 1: Figure S6). These results indicate that the expression of (G4C2)149 in mice is associated with an age-dependent accumulation of DPR proteins derived from both sense and antisense repeat RNA, providing a valuable model to test the efficacy of therapeutic strategies targeting either sense (G4C2) or antisense (G2C4) RNA transcripts or DPR proteins.

(G4C2)149 mice develop progressive pTDP-43 pathology

Since pTDP-43 pathology tracks with neurodegeneration in c9FTD/ALS [34], we evaluated the temporal profile of pTDP-43 pathology in (G4C2)149-AAV mice. Inclusions containing pTDP-43 were absent in (G4C2)2 mice (Fig. 4a-c, Additional file 1: Figure S7a), but small cytoplasmic pTDP-43 inclusions reminiscent of those observed in c9FTD/ALS were detected in the cortex (Fig. 4d) and hippocampus (Additional file 1: Figure S7b top panel) of 3-month-old (G4C2)149 mice. By 6 and 12 months of age, the number of cytoplasmic pTDP-43 inclusions was significantly increased in the cortex (Fig. 4e-g) and the hippocampus (Additional file 1: Figure S7b middle, bottom panel). These findings indicate that aging exacerbates the accumulation and aggregation of pTDP-43 in (G4C2)149 mice.

Fig. 4

Cortical pTDP-43 (pS409/410) pathology detected in (G4C2)149–mice. a-f Representative images of immunohistochemical analysis of pTDP-43 in the cortex of (G4C2)2 (a-c) and (G4C2)149 mice (d-f) at 3, 6, and 12 months of age. g Quantitative analysis of pTDP-43 inclusions in the cortex. Data represent the mean ± SEM. ****p < 0.0001 as analyzed by 1-way ANOVA followed by Tukey’s post-hoc analysis. Scale bar represents 20 μm

(G4C2)149 mice exhibit aggregation of stress granule-associated proteins and nucleocytoplasmic transport defects

Given that TDP-43 localizes to SGs [32, 38], and that aberrant SG responses have been implicated in the pathogenesis of c9FTD/ALS [6, 8, 20], we investigated whether the expression of (G4C2)149 in the murine CNS was associated with the abnormal deposition of SG-resident proteins. To do so, we immunostained mouse brain sections for essential protein components and modulators of SG assembly, including: G3BP stress granule assembly factor 1 (G3BP1), ataxin-2, and eukaryotic initiation-factor 3η (eIF3η). Inclusions immunopositive for these three SG proteins were detected in the brains of (G4C2)149 mice but not control (G4C2)2 mice (Fig. 5a-c, Additional file 1: Figure S8a). Of note, the number of ataxin-2-positive inclusions increased in an age-dependent manner in the cortex and hippocampus (Fig. 5d-f), suggesting that the aberrant deposition of SG components, like that of pTDP-43, was both chronic and progressive. Since we recently reported that another SG component, T cell intracellular antigen 1 (TIA-1), colocalizes to poly(GR)-positive inclusions in the brains of (G4C2)66 and (G4C2)149 mice [61], we examined whether the same was true for ataxin-2. As shown in Fig. 6a-b, both ataxin-2 and TIA1 colocalized with aggregated, but not diffuse, poly(GR) in (G4C2)149 mice. What is more, TIA1/poly(GR)-positive inclusions were also immunopositive for pTDP-43 (Fig. 6b, Additional file 1: Figure S8b).

Fig. 5

Deposition of stress granule-associated proteins in (G4C2)149–mice. a-c Representative images of immunohistochemical analysis of G3BP1 (a), eIF3η (b), and ataxin-2 (c) in the cortex of (G4C2)2 and (G4C2)149 mice at 12 months of age, with inclusions indicated by black arrowheads. d Representative images of ataxin-2-positive inclusions in the cortex and hippocampus of (G4C2)149 mice at either 3 or 12 months of age. e-f Quantitative analysis of the number of ataxin-2 inclusions per mm2 of cortex (e) or hippocampus (f) in (G4C2)149 mice. Data represent the mean ± SEM. ****p < 0.0001 as analyzed by unpaired two-tailed t test. Scale bar represents 20 μm

Fig. 6

Stress granule markers colocalize with poly(GR) and pTDP-43 in (G4C2)149–mice. a-b Representative immunofluorescent images depicting colocalization between poly(GR) and either ataxin-2 (a) or TIA-1 and pTDP-43 (b) in (G4C2)149 mice, with no pathology detected in control (G4C2)2 mice. Nuclei are labeled with DAPI. Scale bar represents 5 μm

Considering the recent finding that aberrant SG assembly can disrupt nucleocytoplasmic transport [59], we examined the cellular distribution of RanGAP1, an essential regulator of nucleocytoplasmic transport that has been shown to be mislocalized in Drosophila expressing the G4C2 repeat, as well as in iPSCs and motor cortex from a C9orf72 ALS patient [60]. In (G4C2)149 mice, we observed a significant increase in the abnormal localization of RanGAP1 to nuclear invaginations relative to control (G4C2)2 mice as early as 3 months of age (Fig. 7). Collectively, these results provide new insight into the mechanism by which pTDP-43 accumulates in (G4C2)149 mice, and suggest that aberrant SG dynamics, poly(GR) deposition and nucleocytoplasmic transport defects are key drivers of TDP-43 pathology in c9FTD/ALS.

Fig. 7

Mislocalization of RanGAP1 in (G4C2)149–mice. a Representative images of immunohistochemical analysis of RanGAP1 in the cortex of (G4C2)2 and (G4C2)149 mice at 3 and 12 months of age, with nuclear invaginations indicated by black arrowheads. b Quantitative analysis of the number of RanGAP1-positive nuclear invaginations per mm2 of cortex. Data represent the mean ± SEM. **p < 0.01, ****p < 0.0001 as analyzed by 2-way ANOVA followed by Tukey’s post-hoc analysis. Scale bar represents 20 μm


We developed a novel mouse model that accurately recapitulates several pathologic features of c9FTD/ALS, including both sense and antisense RNA foci and DPR protein burden. These features are accompanied by gliosis, neuronal loss, pTDP-43 aggregation, as well as motor and cognitive dysfunction. (G4C2)149-mice also display nucleocytoplasmic transport defects and an abnormal accumulation of SG-resident proteins within inclusions immunopositive for poly(GR) and pTDP-43, findings that provide new insight into the relationship between C9orf72 repeat-associated pathologies and TDP-43 proteinopathy. Given that aberrant SG assembly has been shown to perturb nucleocytoplasmic trafficking [59], and SG-resident proteins have been detected within TDP-43 inclusions [5, 26, 32, 40], these results combined with the current data suggest SG dynamics, nucleocytoplasmic transport, and TDP-43 are key hubs in a pathogenic feedforward cycle.

To elucidate the role of poly(GR) in these events, in a prior study we used alternate codons to drive expression of poly(GR)100 in the murine CNS, in which virtually no pTDP-43 pathology or nucleocytoplasmic transport defects were detected [61]. Furthermore, the poly(GR) in these GFP-(GR)100-expressing mice, which was diffuse and cytoplasmic, did not colocalize with SG proteins. While colocalization with other DPRs has yet to be assessed, these data suggest that only aggregated poly(GR) (as occurs in (G4C2)149-mice) induces spontaneous SG formation or sequesters SG-resident proteins, enhances TDP-43 pathology, and perturbs nucleocytoplasmic transport. The data also suggest that merely expressing poly(GR) in vivo is not sufficient to cause its aggregation. Rather, in order to aggregate, poly(GR) may need to reach a certain threshold level and/or be accompanied by additional C9orf72 repeat-associated pathologies, such as poly(GA) [58]. Since G4C2-repeat RNA, like poly(GR), stimulates SG formation, sequesters ribosomal subunits, and inhibits global translation [15, 20, 53, 61], a synergistic effect of G4C2-repeat RNA and poly(GR) may promote TDP-43 phosphorylation and aggregation through translational inhibition and chronic SG formation.

Findings from bacterial artificial chromosome (BAC) transgenic mouse models, which express expanded C9orf72 repeats at lower levels than in our (G4C2)149-mice and (G4C2)66-mice (reviewed [3]), also suggest that repeat RNA and/or DPR protein concentrations influence the development of key c9FTD/ALS features. Sense and antisense RNA foci and certain DPR proteins were observed in the four BAC mouse models (reviewed [3]). However, two models showed no abnormalities in TDP-43 [48, 49]; one developed an increase in insoluble pTDP-43 in brain lysates but displayed no TDP-43 mislocalization or aggregation [24], and the model with the most aggressive phenotype exhibited TDP-43 aggregates at end-stage disease [33]. Of the two models that showed TDP-43 abnormalities (i.e., increased TDP-43 phosphorylation in the model created by Lagier-Tourenne and colleagues [24], and TDP-43 pathology in the mice from the Ranum group [33]), poly(GR) was examined only in the former and found to form inclusions. While this may support our finding that poly(GR) in the presence of G4C2 repeat RNA is linked to TDP-43 abnormalities, a more comprehensive characterization of all DPR proteins, especially poly(GR), in these models is required to probe this question more thoroughly. Nevertheless, data from human postmortem tissues offer support linking poly(GR) to TDP-43 pathology. Saberi and colleagues have reported that poly(GR) inclusions co-localize with TDP-43 in dendritic structures in the motor cortex of patients with c9ALS [50]. In addition, our recent findings demonstrate that the density and distribution of poly(GR) inclusions in C9orf72 repeat expansion carriers differs from that of poly(GA) and poly(GP), with poly(GR) inclusions associating with neurodegeneration [51] similarly to what has been reported for TDP-43 pathology [34]. Moreover, the relative abundance of poly(GR) inclusions is highest in patients with the most severe clinicopathologic phenotype (frontotemporal lobar degeneration with motor neuron disease) [51]. These data, along with those from the present study and from our poly(GR) mouse model [61], offer compelling evidence for a role of poly(GR) in eliciting TDP-43 pathology and neurodegeneration. This contrasts with early studies investigating associations between the neuroanatomical distribution of DPR proteins and neurodegeneration in C9orf72 expansion carriers [34], which largely focused on poly(GA) and poly(GP). Indeed, the contribution of DPR proteins versus repeat RNA to c9FTD/ALS pathogenesis has been, and remains, a topic of vigorous debate [1]. However, our production of a mouse model with both sense and antisense RNA and DPR protein pathology will help us answer this important question by dramatically facilitating both mechanistic and preclinical studies.


Our in vivo model of c9FTD/ALS, the first to robustly recapitulate hallmark features derived from both sense and antisense C9orf72 repeat-associated transcripts, and to display neurodegeneration and behavioral impairments, provides novel insight into the mechanism driving TDP-43 proteinopathy in c9FTD/ALS. In future studies, it will be of particular interest to evaluate the relationship(s) between the primary C9orf72 repeat-associated pathologies, the abnormal deposition of SG-resident proteins, nucleocytoplasmic trafficking defects, and TDP-43 pathology, and to determine the critical pathologic features that need to be targeted in order to rescue neuronal loss and behavioral deficits. Such studies could be accomplished through the use of antisense oligonucleotides (ASOs) that target sense versus antisense repeats, or antibodies that target specific DPR proteins. Moreover, given the abundance of SG protein pathology in our (G4C2)149-mice, the model provides the means to test potential therapeutics targeting the SG pathway in vivo, such as ataxin-2 ASOs [4] or small molecules (i.e., ISRIB) [59]. These approaches, used in parallel or simultaneously, will also provide new insight into the feasibility and/or requirements of reversing pTDP-43 aggregation, neurodegeneration and functional deficits.



Adeno-associated virus


Amyotrophic lateral sclerosis


Antisense oligonucleotide


Bacterial artificial chromosome


Chromosome 9 open reading frame 72


Central nervous system


Conditioned stimulus


Dipeptide repeat


Eukaryotic initiation factor 3η


fluorescence in situ hybridization


Frontotemporal dementia


G3BP stress granule assembly factor 1




Glial fibrillary acidic protein










Repeat-associated non-ATG


Stress granules


TAR DNA-binding protein 43


T cell intracellular antigen 1


Unconditioned stimulus


  1. 1.

    Arzberger T, Schludi MH, Lehmer C, Schmid B, Edbauer D. RNA versus protein toxicity in C9orf72 ALS/FTLD. Acta Neuropathol. 2018;135:475–9.

    Article  PubMed  Google Scholar 

  2. 2.

    Ash PE, Bieniek KF, Gendron TF, Caulfield T, Lin WL, Dejesus-Hernandez M, van Blitterswijk MM, Jansen-West K, Paul JW 3rd, Rademakers R, Boylan KB, Dickson DW, Petrucelli L. Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS. Neuron. 2013;77:639–46.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  3. 3.

    Batra R, Lee CW. Mouse models of C9orf72 Hexanucleotide repeat expansion in amyotrophic lateral sclerosis/ frontotemporal dementia. Front Cell Neurosci. 2017;11:196.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  4. 4.

    Becker LA, Huang B, Bieri G, Ma R, Knowles DA, Jafar-Nejad P, Messing J, Kim HJ, Soriano A, Auburger G, Pulst SM, Taylor JP, Rigo F, Gitler AD. Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice. Nature. 2017;544:367–71.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  5. 5.

    Bentmann E, Neumann M, Tahirovic S, Rodde R, Dormann D, Haass C. Requirements for stress granule recruitment of fused in sarcoma (FUS) and TAR DNA-binding protein of 43 kDa (TDP-43). J Biol Chem. 2012;287:23079–94.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  6. 6.

    Boeynaems S, Bogaert E, Kovacs D, Konijnenberg A, Timmerman E, Volkov A, Guharoy M, De Decker M, Jaspers T, Ryan VH, Janke AM, Baatsen P, Vercruysse T, Kolaitis RM, Daelemans D, Taylor JP, Kedersha N, Anderson P, Impens F, Sobott F, Schymkowitz J, Rousseau F, Fawzi NL, Robberecht W, Van Damme P, Tompa P, Van Den Bosch L. Phase separation of C9orf72 dipeptide repeats perturbs stress granule dynamics. Mol Cell. 2017;65:1044–55 e1045.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  7. 7.

    Chakrabarty P, Rosario A, Cruz P, Siemienski Z, Ceballos-Diaz C, Crosby K, Jansen K, Borchelt DR, Kim JY, Jankowsky JL, Golde TE, Levites Y. Capsid serotype and timing of injection determines AAV transduction in the neonatal mice brain. PLoS One. 2013;8:e67680.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  8. 8.

    Cheng W, Wang S, Mestre AA, Fu C, Makarem A, Xian F, Hayes LR, Lopez-Gonzalez R, Drenner K, Jiang J, Cleveland DW, Sun S. C9ORF72 GGGGCC repeat-associated non-AUG translation is upregulated by stress through eIF2alpha phosphorylation. Nat Commun. 2018;9:51.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  9. 9.

    Chew J, Gendron TF, Prudencio M, Sasaguri H, Zhang YJ, Castanedes-Casey M, Lee CW, Jansen-West K, Kurti A, Murray ME, Bieniek KF, Bauer PO, Whitelaw EC, Rousseau L, Stankowski JN, Stetler C, Daughrity LM, Perkerson EA, Desaro P, Johnston A, Overstreet K, Edbauer D, Rademakers R, Boylan KB, Dickson DW, Fryer JD, Petrucelli L. Neurodegeneration. C9ORF72 repeat expansions in mice cause TDP-43 pathology, neuronal loss, and behavioral deficits. Science. 2015;348:1151–4.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  10. 10.

    Clippinger AK, D'Alton S, Lin WL, Gendron TF, Howard J, Borchelt DR, Cannon A, Carlomagno Y, Chakrabarty P, Cook C, Golde TE, Levites Y, Ranum L, Schultheis PJ, Xu G, Petrucelli L, Sahara N, Dickson DW, Giasson B, Lewis J. Robust cytoplasmic accumulation of phosphorylated TDP-43 in transgenic models of tauopathy. Acta Neuropathol. 2013;126:39–50.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  11. 11.

    Conlon EG, Lu L, Sharma A, Yamazaki T, Tang T, Shneider NA, Manley JL. The C9ORF72 GGGGCC expansion forms RNA G-quadruplex inclusions and sequesters hnRNP H to disrupt splicing in ALS brains. Elife. 2016;5.

  12. 12.

    Cooper-Knock J, Higginbottom A, Stopford MJ, Highley JR, Ince PG, Wharton SB, Pickering-Brown S, Kirby J, Hautbergue GM, Shaw PJ. Antisense RNA foci in the motor neurons of C9ORF72-ALS patients are associated with TDP-43 proteinopathy. Acta Neuropathol. 2015;130:63–75.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  13. 13.

    DeJesus-Hernandez M, Finch NA, Wang X, Gendron TF, Bieniek KF, Heckman MG, Vasilevich A, Murray ME, Rousseau L, Weesner R, Lucido A, Parsons M, Chew J, Josephs KA, Parisi JE, Knopman DS, Petersen RC, Boeve BF, Graff-Radford NR, de Boer J, Asmann YW, Petrucelli L, Boylan KB, Dickson DW, van Blitterswijk M, Rademakers R. In-depth clinico-pathological examination of RNA foci in a large cohort of C9ORF72 expansion carriers. Acta Neuropathol. 2017;134:255–69.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  14. 14.

    DeJesus-Hernandez M, Mackenzie IR, Boeve BF, Boxer AL, Baker M, Rutherford NJ, Nicholson AM, Finch NA, Flynn H, Adamson J, Kouri N, Wojtas A, Sengdy P, Hsiung GY, Karydas A, Seeley WW, Josephs KA, Coppola G, Geschwind DH, Wszolek ZK, Feldman H, Knopman DS, Petersen RC, Miller BL, Dickson DW, Boylan KB, Graff-Radford NR, Rademakers R. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron. 2011;72:245–56.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  15. 15.

    Fay MM, Anderson PJ, Ivanov P. ALS/FTD-associated C9ORF72 repeat RNA promotes phase transitions in vitro and in cells. Cell Rep. 2017;21:3573–84.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  16. 16.

    Flotte TR, Afione SA, Solow R, Drumm ML, Markakis D, Guggino WB, Zeitlin PL, Carter BJ. Expression of the cystic fibrosis transmembrane conductance regulator from a novel adeno-associated virus promoter. J Biol Chem. 1993;268:3781–90.

    CAS  PubMed  Google Scholar 

  17. 17.

    Freibaum BD, Lu Y, Lopez-Gonzalez R, Kim NC, Almeida S, Lee KH, Badders N, Valentine M, Miller BL, Wong PC, Petrucelli L, Kim HJ, Gao FB, Taylor JP. GGGGCC repeat expansion in C9orf72 compromises nucleocytoplasmic transport. Nature. 2015;525:129–33.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  18. 18.

    Gendron TF, Bieniek KF, Zhang YJ, Jansen-West K, Ash PE, Caulfield T, Daughrity L, Dunmore JH, Castanedes-Casey M, Chew J, Cosio DM, van Blitterswijk M, Lee WC, Rademakers R, Boylan KB, Dickson DW, Petrucelli L. Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS. Acta Neuropathol. 2013;126:829–44.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  19. 19.

    Gendron TF, Petrucelli L. Disease mechanisms of C9ORF72 repeat expansions. Cold Spring Harb Perspect Med. 2018;8.

  20. 20.

    Green KM, Glineburg MR, Kearse MG, Flores BN, Linsalata AE, Fedak SJ, Goldstrohm AC, Barmada SJ, Todd PK. RAN translation at C9orf72-associated repeat expansions is selectively enhanced by the integrated stress response. Nat Commun. 2017;8:2005.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  21. 21.

    Guo Q, Lehmer C, Martinez-Sanchez A, Rudack T, Beck F, Hartmann H, Perez-Berlanga M, Frottin F, Hipp MS, Hartl FU, Edbauer D, Baumeister W, Fernandez-Busnadiego R. In situ structure of neuronal C9orf72 poly-GA aggregates reveals proteasome recruitment. Cell. 2018;172:696–705 e612.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  22. 22.

    Haeusler AR, Donnelly CJ, Periz G, Simko EA, Shaw PG, Kim MS, Maragakis NJ, Troncoso JC, Pandey A, Sattler R, Rothstein JD, Wang J. C9orf72 nucleotide repeat structures initiate molecular cascades of disease. Nature. 2014;507:195–200.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  23. 23.

    Jain A, Vale RD. RNA phase transitions in repeat expansion disorders. Nature. 2017;546:243–7.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  24. 24.

    Jiang J, Zhu Q, Gendron TF, Saberi S, McAlonis-Downes M, Seelman A, Stauffer JE, Jafar-Nejad P, Drenner K, Schulte D, Chun S, Sun S, Ling SC, Myers B, Engelhardt J, Katz M, Baughn M, Platoshyn O, Marsala M, Watt A, Heyser CJ, Ard MC, De Muynck L, Daughrity LM, Swing DA, Tessarollo L, Jung CJ, Delpoux A, Utzschneider DT, Hedrick SM, de Jong PJ, Edbauer D, Van Damme P, Petrucelli L, Shaw CE, Bennett CF, Da Cruz S, Ravits J, Rigo F, Cleveland DW, Lagier-Tourenne C. Gain of toxicity from ALS/FTD-linked repeat expansions in C9ORF72 is alleviated by antisense oligonucleotides targeting GGGGCC-containing RNAs. Neuron. 2016;90:535–50.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  25. 25.

    Jovicic A, Mertens J, Boeynaems S, Bogaert E, Chai N, Yamada SB, Paul JW 3rd, Sun S, Herdy JR, Bieri G, Kramer NJ, Gage FH, Van Den Bosch L, Robberecht W, Gitler AD. Modifiers of C9orf72 dipeptide repeat toxicity connect nucleocytoplasmic transport defects to FTD/ALS. Nat Neurosci. 2015;18:1226–9.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  26. 26.

    Kim HJ, Kim NC, Wang YD, Scarborough EA, Moore J, Diaz Z, MacLea KS, Freibaum B, Li S, Molliex A, Kanagaraj AP, Carter R, Boylan KB, Wojtas AM, Rademakers R, Pinkus JL, Greenberg SA, Trojanowski JQ, Traynor BJ, Smith BN, Topp S, Gkazi AS, Miller J, Shaw CE, Kottlors M, Kirschner J, Pestronk A, Li YR, Ford AF, Gitler AD, Benatar M, King OD, Kimonis VE, Ross ED, Weihl CC, Shorter J, Taylor JP. Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS. Nature. 2013;495:467–73.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  27. 27.

    Kim HJ, Raphael AR, LaDow ES, McGurk L, Weber RA, Trojanowski JQ, Lee VM, Finkbeiner S, Gitler AD, Bonini NM. Therapeutic modulation of eIF2alpha phosphorylation rescues TDP-43 toxicity in amyotrophic lateral sclerosis disease models. Nat Genet. 2014;46:152–60.

    CAS  Article  PubMed  Google Scholar 

  28. 28.

    Kim JY, Grunke SD, Levites Y, Golde TE, Jankowsky JL. Intracerebroventricular viral injection of the neonatal mouse brain for persistent and widespread neuronal transduction. J Vis Exp. 2014;51863.

  29. 29.

    Kwon I, Xiang S, Kato M, Wu L, Theodoropoulos P, Wang T, Kim J, Yun J, Xie Y, McKnight SL. Poly-dipeptides encoded by the C9orf72 repeats bind nucleoli, impede RNA biogenesis, and kill cells. Science. 2014;345:1139–45.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  30. 30.

    Lagier-Tourenne C, Baughn M, Rigo F, Sun S, Liu P, Li HR, Jiang J, Watt AT, Chun S, Katz M, Qiu J, Sun Y, Ling SC, Zhu Q, Polymenidou M, Drenner K, Artates JW, McAlonis-Downes M, Markmiller S, Hutt KR, Pizzo DP, Cady J, Harms MB, Baloh RH, Vandenberg SR, Yeo GW, Fu XD, Bennett CF, Cleveland DW, Ravits J. Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration. Proc Natl Acad Sci U S A. 2013;110:E4530–9.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  31. 31.

    Lee YB, Chen HJ, Peres JN, Gomez-Deza J, Attig J, Stalekar M, Troakes C, Nishimura AL, Scotter EL, Vance C, Adachi Y, Sardone V, Miller JW, Smith BN, Gallo JM, Ule J, Hirth F, Rogelj B, Houart C, Shaw CE. Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxic. Cell Rep. 2013;5:1178–86.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  32. 32.

    Liu-Yesucevitz L, Bilgutay A, Zhang YJ, Vanderweyde T, Citro A, Mehta T, Zaarur N, McKee A, Bowser R, Sherman M, Petrucelli L, Wolozin B. Tar DNA binding protein-43 (TDP-43) associates with stress granules: analysis of cultured cells and pathological brain tissue. PLoS One. 2010;5:e13250.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  33. 33.

    Liu Y, Pattamatta A, Zu T, Reid T, Bardhi O, Borchelt DR, Yachnis AT, Ranum LP. C9orf72 BAC mouse model with motor deficits and neurodegenerative features of ALS/FTD. Neuron. 2016;90:521–34.

    CAS  Article  PubMed  Google Scholar 

  34. 34.

    Mackenzie IR, Arzberger T, Kremmer E, Troost D, Lorenzl S, Mori K, Weng SM, Haass C, Kretzschmar HA, Edbauer D, Neumann M. Dipeptide repeat protein pathology in C9ORF72 mutation cases: clinico-pathological correlations. Acta Neuropathol. 2013;126:859–79.

    CAS  Article  PubMed  Google Scholar 

  35. 35.

    Mackenzie IR, Frick P, Grasser FA, Gendron TF, Petrucelli L, Cashman NR, Edbauer D, Kremmer E, Prudlo J, Troost D, Neumann M. Quantitative analysis and clinico-pathological correlations of different dipeptide repeat protein pathologies in C9ORF72 mutation carriers. Acta Neuropathol. 2015;130:845–61.

    CAS  Article  PubMed  Google Scholar 

  36. 36.

    Mackenzie IR, Frick P, Neumann M. The neuropathology associated with repeat expansions in the C9ORF72 gene. Acta Neuropathol. 2014;127:347–57.

    CAS  Article  PubMed  Google Scholar 

  37. 37.

    Mackenzie IR, Nicholson AM, Sarkar M, Messing J, Purice MD, Pottier C, Annu K, Baker M, Perkerson RB, Kurti A, Matchett BJ, Mittag T, Temirov J, Hsiung GR, Krieger C, Murray ME, Kato M, Fryer JD, Petrucelli L, Zinman L, Weintraub S, Mesulam M, Keith J, Zivkovic SA, Hirsch-Reinshagen V, Roos RP, Zuchner S, Graff-Radford NR, Petersen RC, Caselli RJ, Wszolek ZK, Finger E, Lippa C, Lacomis D, Stewart H, Dickson DW, Kim HJ, Rogaeva E, Bigio E, Boylan KB, Taylor JP, Rademakers R. TIA1 mutations in amyotrophic lateral sclerosis and frontotemporal dementia promote phase separation and Alter stress granule dynamics. Neuron. 2017;95:808–16 e809.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  38. 38.

    Markmiller S, Soltanieh S, Server KL, Mak R, Jin W, Fang MY, Luo EC, Krach F, Yang D, Sen A, Fulzele A, Wozniak JM, Gonzalez DJ, Kankel MW, Gao FB, Bennett EJ, Lecuyer E, Yeo GW. Context-dependent and disease-specific diversity in protein interactions within stress granules. Cell. 2018;172:590–604 e513.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  39. 39.

    May S, Hornburg D, Schludi MH, Arzberger T, Rentzsch K, Schwenk BM, Grasser FA, Mori K, Kremmer E, Banzhaf-Strathmann J, Mann M, Meissner F, Edbauer D. C9orf72 FTLD/ALS-associated Gly-ala dipeptide repeat proteins cause neuronal toxicity and Unc119 sequestration. Acta Neuropathol. 2014;128:485–503.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  40. 40.

    McGurk L, Lee VM, Trojanowksi JQ, Van Deerlin VM, Lee EB, Bonini NM. Poly-a binding protein-1 localization to a subset of TDP-43 inclusions in amyotrophic lateral sclerosis occurs more frequently in patients harboring an expansion in C9orf72. J Neuropathol Exp Neurol. 2014;73:837–45.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  41. 41.

    Mizielinska S, Gronke S, Niccoli T, Ridler CE, Clayton EL, Devoy A, Moens T, Norona FE, Woollacott IOC, Pietrzyk J, Cleverley K, Nicoll AJ, Pickering-Brown S, Dols J, Cabecinha M, Hendrich O, Fratta P, Fisher EMC, Partridge L, Isaacs AM. C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins. Science. 2014;345:1192–4.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  42. 42.

    Mizielinska S, Lashley T, Norona FE, Clayton EL, Ridler CE, Fratta P, Isaacs AM. C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci. Acta Neuropathol. 2013;126:845–57.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  43. 43.

    Mori K, Arzberger T, Grasser FA, Gijselinck I, May S, Rentzsch K, Weng SM, Schludi MH, van der Zee J, Cruts M, Van Broeckhoven C, Kremmer E, Kretzschmar HA, Haass C, Edbauer D. Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins. Acta Neuropathol. 2013;126:881–93.

    CAS  Article  PubMed  Google Scholar 

  44. 44.

    Mori K, Weng SM, Arzberger T, May S, Rentzsch K, Kremmer E, Schmid B, Kretzschmar HA, Cruts M, Van Broeckhoven C, Haass C, Edbauer D. The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS. Science. 2013;339:1335–8.

    CAS  Article  PubMed  Google Scholar 

  45. 45.

    Murray ME, Vemuri P, Preboske GM, Murphy MC, Schweitzer KJ, Parisi JE, Jack CR Jr, Dickson DW. A quantitative postmortem MRI design sensitive to white matter hyperintensity differences and their relationship with underlying pathology. J Neuropathol Exp Neurol. 2012;71:1113–22.

    Article  PubMed Central  PubMed  Google Scholar 

  46. 46.

    Neary D, Snowden JS, Gustafson L, Passant U, Stuss D, Black S, Freedman M, Kertesz A, Robert PH, Albert M, Boone K, Miller BL, Cummings J, Benson DF. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology. 1998;51:1546–54.

    CAS  Article  PubMed  Google Scholar 

  47. 47.

    Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, Chou TT, Bruce J, Schuck T, Grossman M, Clark CM, McCluskey LF, Miller BL, Masliah E, Mackenzie IR, Feldman H, Feiden W, Kretzschmar HA, Trojanowski JQ, Lee VM. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science. 2006;314:130–3.

    CAS  Article  PubMed  Google Scholar 

  48. 48.

    O'Rourke JG, Bogdanik L, Muhammad A, Gendron TF, Kim KJ, Austin A, Cady J, Liu EY, Zarrow J, Grant S, Ho R, Bell S, Carmona S, Simpkinson M, Lall D, Wu K, Daughrity L, Dickson DW, Harms MB, Petrucelli L, Lee EB, Lutz CM, Baloh RH. C9orf72 BAC transgenic mice display typical pathologic features of ALS/FTD. Neuron. 2015;88:892–901.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  49. 49.

    Peters OM, Cabrera GT, Tran H, Gendron TF, McKeon JE, Metterville J, Weiss A, Wightman N, Salameh J, Kim J, Sun H, Boylan KB, Dickson D, Kennedy Z, Lin Z, Zhang YJ, Daughrity L, Jung C, Gao FB, Sapp PC, Horvitz HR, Bosco DA, Brown SP, de Jong P, Petrucelli L, Mueller C, Brown RH Jr. Human C9ORF72 Hexanucleotide expansion reproduces RNA foci and dipeptide repeat proteins but not neurodegeneration in BAC transgenic mice. Neuron. 2015;88:902–9.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  50. 50.

    Saberi S, Stauffer JE, Jiang J, Garcia SD, Taylor AE, Schulte D, Ohkubo T, Schloffman CL, Maldonado M, Baughn M, Rodriguez MJ, Pizzo D, Cleveland D, Ravits J. Sense-encoded poly-GR dipeptide repeat proteins correlate to neurodegeneration and uniquely co-localize with TDP-43 in dendrites of repeat-expanded C9orf72 amyotrophic lateral sclerosis. Acta Neuropathol. 2018;135:459–74.

    CAS  Article  PubMed  Google Scholar 

  51. 51.

    Sakae N, Bieniek KF, Zhang YJ, Ross K, Gendron TF, Murray ME, Rademakers R, Petrucelli L, Dickson DW. Poly-GR dipeptide repeat polymers correlate with neurodegeneration and Clinicopathological subtypes in C9ORF72-related brain disease. Acta Neuropathol Commun. 2018;6:63.

    Article  PubMed Central  PubMed  Google Scholar 

  52. 52.

    Suzuki H, Shibagaki Y, Hattori S, Matsuoka M. The proline-arginine repeat protein linked to C9-ALS/FTD causes neuronal toxicity by inhibiting the DEAD-box RNA helicase-mediated ribosome biogenesis. Cell Death Dis. 2018;9:975.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  53. 53.

    Tabet R, Schaeffer L, Freyermuth F, Jambeau M, Workman M, Lee CZ, Lin CC, Jiang J, Jansen-West K, Abou-Hamdan H, Desaubry L, Gendron T, Petrucelli L, Martin F, Lagier-Tourenne C. CUG initiation and frameshifting enable production of dipeptide repeat proteins from ALS/FTD C9ORF72 transcripts. Nat Commun. 2018;9:152.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  54. 54.

    Tao Z, Wang H, Xia Q, Li K, Li K, Jiang X, Xu G, Wang G, Ying Z. Nucleolar stress and impaired stress granule formation contribute to C9orf72 RAN translation-induced cytotoxicity. Hum Mol Genet. 2015;24:2426–41.

    CAS  Article  PubMed  Google Scholar 

  55. 55.

    Taylor JP, Brown RH Jr, Cleveland DW. Decoding ALS: from genes to mechanism. Nature. 2016;539:197–206.

    Article  PubMed Central  PubMed  Google Scholar 

  56. 56.

    Todd TW, Petrucelli L. Insights into the pathogenic mechanisms of chromosome 9 open reading frame 72 (C9orf72) repeat expansions. J Neurochem. 2016;138(Suppl 1):145–62.

    CAS  Article  PubMed  Google Scholar 

  57. 57.

    Wen X, Tan W, Westergard T, Krishnamurthy K, Markandaiah SS, Shi Y, Lin S, Shneider NA, Monaghan J, Pandey UB, Pasinelli P, Ichida JK, Trotti D. Antisense proline-arginine RAN dipeptides linked to C9ORF72-ALS/FTD form toxic nuclear aggregates that initiate in vitro and in vivo neuronal death. Neuron. 2014;84:1213–25.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  58. 58.

    Yang D, Abdallah A, Li Z, Lu Y, Almeida S, Gao FB. FTD/ALS-associated poly(GR) protein impairs the notch pathway and is recruited by poly(GA) into cytoplasmic inclusions. Acta Neuropathol. 2015;130:525–35.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  59. 59.

    Zhang K, Daigle JG, Cunningham KM, Coyne AN, Ruan K, Grima JC, Bowen KE, Wadhwa H, Yang P, Rigo F, Taylor JP, Gitler AD, Rothstein JD, Lloyd TE. Stress granule assembly disrupts nucleocytoplasmic transport. Cell. 2018;173(958–971):e917.

    CAS  Article  Google Scholar 

  60. 60.

    Zhang K, Donnelly CJ, Haeusler AR, Grima JC, Machamer JB, Steinwald P, Daley EL, Miller SJ, Cunningham KM, Vidensky S, Gupta S, Thomas MA, Hong I, Chiu SL, Huganir RL, Ostrow LW, Matunis MJ, Wang J, Sattler R, Lloyd TE, Rothstein JD. The C9orf72 repeat expansion disrupts nucleocytoplasmic transport. Nature. 2015;525:56–61.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  61. 61.

    Zhang YJ, Gendron TF, Ebbert MTW, O'Raw AD, Yue M, Jansen-West K, Zhang X, Prudencio M, Chew J, Cook CN, Daughrity LM, Tong J, Song Y, Pickles SR, Castanedes-Casey M, Kurti A, Rademakers R, Oskarsson B, Dickson DW, Hu W, Gitler AD, Fryer JD, Petrucelli L. Poly(GR) impairs protein translation and stress granule dynamics in C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis. Nat Med. 2018;24:1136–42.

    CAS  Article  PubMed  Google Scholar 

  62. 62.

    Zhang YJ, Gendron TF, Grima JC, Sasaguri H, Jansen-West K, Xu YF, Katzman RB, Gass J, Murray ME, Shinohara M, Lin WL, Garrett A, Stankowski JN, Daughrity L, Tong J, Perkerson EA, Yue M, Chew J, Castanedes-Casey M, Kurti A, Wang ZS, Liesinger AM, Baker JD, Jiang J, Lagier-Tourenne C, Edbauer D, Cleveland DW, Rademakers R, Boylan KB, Bu G, Link CD, Dickey CA, Rothstein JD, Dickson DW, Fryer JD, Petrucelli L. C9ORF72 poly(GA) aggregates sequester and impair HR23 and nucleocytoplasmic transport proteins. Nat Neurosci. 2016;19:668–77.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  63. 63.

    Zhang YJ, Jansen-West K, Xu YF, Gendron TF, Bieniek KF, Lin WL, Sasaguri H, Caulfield T, Hubbard J, Daughrity L, Chew J, Belzil VV, Prudencio M, Stankowski JN, Castanedes-Casey M, Whitelaw E, Ash PE, DeTure M, Rademakers R, Boylan KB, Dickson DW, Petrucelli L. Aggregation-prone c9FTD/ALS poly(GA) RAN-translated proteins cause neurotoxicity by inducing ER stress. Acta Neuropathol. 2014;128:505–24.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

  64. 64.

    Zolotukhin S, Byrne BJ, Mason E, Zolotukhin I, Potter M, Chesnut K, Summerford C, Samulski RJ, Muzyczka N. Recombinant adeno-associated virus purification using novel methods improves infectious titer and yield. Gene Ther. 1999;6:973–85.

    CAS  Article  PubMed  Google Scholar 

  65. 65.

    Zu T, Liu Y, Banez-Coronel M, Reid T, Pletnikova O, Lewis J, Miller TM, Harms MB, Falchook AE, Subramony SH, Ostrow LW, Rothstein JD, Troncoso JC, Ranum LP. RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia. Proc Natl Acad Sci U S A. 2013;110:E4968–77.

    CAS  Article  PubMed Central  PubMed  Google Scholar 

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This work was supported by the National Institutes of Health/National Institute of Neurological Disorders and Stroke [R35NS097273 (LP), P01NS084974 (LP, DWD), P01NS099114 (TFG, MDD, JDR, LP)]; Mayo Clinic Foundation (LP); the Amyotrophic Lateral Sclerosis Association (YJZ, TFG, LP); the Robert Packard Center for ALS Research at Johns Hopkins (LP) and the Target ALS Foundation (YJZ, TFG, LP).

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JC carried out the animal studies; JC and CC performed the statistical analysis; JC, CC, YJZ and TFG wrote the manuscript; YJZ, KJW, GDR, LMD, MCC, AK, JDS, MDD, JDR, DWD and JDR made substantial contributions to acquisition and/or interpretation of data; LP conceived of the study, obtained study funding, participated in its design, and assisted with manuscript preparation. All authors critically read and approved the final manuscript.

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Correspondence to Yong-Jie Zhang or Leonard Petrucelli.

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Chew, J., Cook, C., Gendron, T.F. et al. Aberrant deposition of stress granule-resident proteins linked to C9orf72-associated TDP-43 proteinopathy. Mol Neurodegeneration 14, 9 (2019).

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  • C9orf72
  • Stress granules
  • Frontotemporal dementia
  • Amyotrophic lateral sclerosis
  • TDP-43
  • Neurodegeneration