- Open Access
Dipeptide repeat proteins activate a heat shock response found in C9ORF72-ALS/FTLD patients
Acta Neuropathologica Communications volume 6, Article number: 55 (2018)
A hexanucleotide (GGGGCC) repeat expansion in C9ORF72 is the most common genetic contributor to amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD). Reduced expression of the C9ORF72 gene product has been proposed as a potential contributor to disease pathogenesis. Additionally, repetitive RNAs and dipeptide repeat proteins (DPRs), such as poly-GR, can be produced by this hexanucleotide expansion that disrupt a number of cellular processes, potentially contributing to neural degeneration. To better discern which of these mechanisms leads to disease-associated changes in patient brains, we analyzed gene expression data generated from the cortex and cerebellum. We found that transcripts encoding heat shock proteins (HSPs) regulated by the HSF1 transcription factor were significantly induced in C9ORF72-ALS/FTLD patients relative to both sporadic ALS/FTLD cases and controls. Treatment of human neurons with chemically synthesized DPRs was sufficient to activate a similar transcriptional response. Expression of GGGGCC repeats and also poly-GR in the brains of Drosophila lead to the upregulation of HSF1 and the same highly-conserved HSPs. Additionally, HSF1 was a modifier of poly-GR toxicity in Drosophila. Our results suggest that the expression of DPRs are associated with upregulation of HSF1 and activation of a heat shock response in C9ORF72-ALS/FTLD.
Amyotrophic lateral sclerosis (ALS) is an adult onset neurodegenerative disease characterized by the loss of upper and lower motor neurons and muscle atrophy. Patients become progressively paralyzed and develop difficulty speaking, swallowing, and eventually breathing. Survival is typically limited to 2–5 years from the time of onset, and current treatment options remain limited. About 90% of cases are seemingly “sporadic” without a family history of disease and about 10% are familial. Hundreds of distinct variants in more than a dozen genes, many of which act with high penetrance, can increase a person’s risk of developing ALS [46, 51].
The most common genetic contributor to ALS is a hexanucleotide (GGGGCC) repeat expansion within the first intron of C9ORF72 [14, 45]. Carriers of the C9ORF72 expansion can also present with frontotemporal dementia (FTD), which is characterized by frontotemporal lobar degeneration (FTLD) of the brain. In many cases, these initially diverse diagnoses can progress towards the inclusion of neurological features from each condition leading many to believe they are spectrums of the same disorder . In addition, both diseases can be characterized by the presence of TDP-43 positive inclusions .
Three distinct mechanisms have been proposed for how the C9ORF72 expansion contributes to the development of ALS and FTLD. First, C9ORF72-ALS brains display reduced abundance of C9ORF72 transcripts, suggesting that a loss-of-function mechanism may contribute to disease . Although complete loss of C9ORF72 in mice leads to fatal autoimmunity and changes in microglia, no obvious signs of neurodegeneration or neural dysfunction have yet been reported in these animals [8, 23, 39]. Second, mutant transcripts containing the GGGGCC repeats form intranuclear RNA foci that may sequester RNA binding proteins and lead to nucleolar stress [14, 20]. Finally, dipeptide repeat proteins (DPRs) were unexpectedly found to be translated from both sense and antisense transcripts containing these repeats . Several DPRs are toxic when overexpressed in model systems [11, 26, 33, 55], and have been shown to affect diverse cellular pathways, including RNA processing and nucleocytoplasmic transport [51, 52, 56].
The transcriptional response that occurs in various brain regions in ALS and FTLD patients has the potential to provide useful insights into whether genetic subgroups of patients display common or divergent mechanisms, and for validating proposed mechanisms through which mutations act. Here, we explored RNA-sequencing data from C9ORF72 and sporadic patients, and identified distinct transcriptional responses in these two patient classes. We validate a C9ORF72-specific transcriptional signature in a large patient cohort. Additionally, we find that similar transcriptional changes occur in human neurons treated with DPRs and in gain-of-function Drosophila models.
The processed gene expression count matrix of the brain-derived RNA-seq datasets from Prudencio et al. were obtained via GEO (GSE67196). The data was analyzed using the R library “edgeR” as described by Prudencio et al., with modifications as follows [41, 47]. Statistical inference was performed with two methods which we refer to as “double cut-off” and “FDR”. For the “double cut-off” method, as described by Prudencio et al., differentially expressed genes called by this approach had to pass two filters: one cut-off of absolute log2fold change > 2 and a second cut-off of unadjusted p-value < 0.05. For the “FDR” method, the false discovery rate was controlled using the Benjamini-Hochberg method  and all genes below a threshold FDR of 0.05 were considered to be significantly differentially expressed. Additionally, a generalized linear model (glmFit() in edgeR) was used to model the effect of gender rather than the exactTest() function, which resulted in slight differences in the number of differentially expressed genes found using the double cut-off method when compared to the original published analysis. Hypergeometric tests were used to compare sets of genes. Note that a pseudocount of 0.01 was used for plotting log2(CPM).
Protein-protein interaction networks were generated using GeNets hosted at the Broad Institute (apps.broadinstitute.org/genets) based on the InWeb network . Associated gene ontology (GO) terms for biological process based on the GO Consortium were obtained with multiple testing correction for p-values using g:Profiler . GO term clustering was performed with Revigo (reduce and visualize gene ontology, http://revigo.irb.hr/)  to support the identification of representative biological processes terms.
Protocols were approved by the Mayo Clinic IRB and Ethics Committee on Human Experimentation. Informed consent for post-mortem tissue was obtained from all individuals or the appropriate next-of-kin. The diagnosis of ALS and/or FTLD was based on neurological and pathological examination and C9ORF72 repeat expansion status was determined using repeat-primed PCR and the cohort was described in Prudencio et al., including TDP-43 pathology . See Additional file 1: Table S1 for patient characteristics. For transcript measurements by quantitative RT-PCR on human brains, total RNA was extracted and 500 ng of RNA with RNA integrity values (RIN) higher than 7, measured by an Agilent Bioanalyzer, and was used for reverse transcription to synthesize cDNA as previously described . Using a SYBR green assay (Life Technologies) samples were run in triplicate on an ABI Prism 7900HT Real-Time PCR System (Applied Biosystems). Relative mRNA expression of examined genes was normalized to GAPDH and RPLP0 values, the endogenous transcript controls. Primer sequences are provided in Additional file 2: Table S2. Statistical differences were calculated by one-way ANOVA followed by Dunn’s multiple comparison tests using GraphPad Prism. Associations between HSF1 and heat shock related transcripts were evaluated using a Spearman’s test of correlation.
Neuron production and cell culture experiments
Neurons were generated from HuES-3-Hb9:GFP based on the following neuron differentiation protocol . Human embryonic stem cells were cultured in mTeSR (Stemcell technologies) on matrigel (Corning)-coated plates. For motor neuron differentiation, the media was changed to 1:1 Neurobasal:DMEM/F12 (Life Technologies) supplemented with N2 (StemCell Technologies), B27 (Life technologies), Glutamax (Life Technologies), non-essential amino acids (Life technologies). For the first week, this neural media was supplemented with retinoic acid (Sigma Aldrich, 1 μM), smoothened agonist (SAG, DNSK, 1 μM), BMP inhibitor (LDN-193189, DNSK, 100 nM) and TGF-beta inhibitor (SB431542, DNSK, 10 μM). Then, for the second week, this neural media was supplemented with retinoic acid, smoothened agonist, GSK3-beta inhibitor (SU-5402, DNSK, 4 μM), and gamma-secretase inhibitor (DAPT, DNSK, 5uM). Upon completion of the differentiation protocol, cells were dissociated with accutase (Innovative Cell Technologies) to single cells and sorted via flow-cytometry for GFP-positive cells to yield GFP-positive neurons, which were plated on poly-D-lysine(Sigma Aldrich)/laminin(Life Technologies)-coated plates. Neurons were maintained in Neurobasal medium supplemented with N2, B27, Glutamax, non-essential amino acids, and neurotrophic factors (BDNF, GDNF, CNTF), and allowed to mature for two weeks before experiments with dipeptide repeat proteins (DPRs). Recombinant biotin-tagged DPRs, (each 20 amino acids in length (poly-GA, poly-GP, or poly-GR with 10 repeats or scrambled control poly-GAPR with 5 repeats) were synthesize by Anaspec with > 95% purity and dissolved in DMSO (Sigma). Following DPR treatment, RNA was extracted after 24 h via an RNeasy Minikit (Qiagen), and cDNA prepared with iScript (Bio-Rad). qRT-PCR reactions were performed with iTaq SYBR green (Bio-Rad) on a C1000 touch thermal cycler with CFX real-time system (Bio-rad). Relative expression was normalized to GAPDH. Primers were designed from the MGH PrimerBank and synthesized by IDT. Primer sequences are provided in Additional file 2: Table S2. Viability was measured with CellTiter-Glo (Promega) on a Cytation3 reader (Biotek). All cell lines tested negative for mycoplasma using the MycoAlert detection kit (Lonza LT07–518).
Animals were raised and maintained at 18 °C on standard cornmeal-molasses food. The UAS-(G4C2)n transgenic models [9, 25], UAS-(GR)36 model , and the HSF overexpression (OE) mutant, HSF[+t8] , are previously defined. UAS-(GR)36, control, and mutant HSF[+t8] were obtained from Bloomington Drosophila Stock Center.
qPCR in the adult fly nervous system
UAS-(G4C2)n or UAS-(GR)36 transgenes were driven by elavGS, a drug-inducible Gal4 driver that expresses only in neurons. Crosses were setup and maintained at 24 °C. Female progeny with the desired genotype were collected and matured to 1-3d before being transferred to vials containing 40μg/ml of RU486. Animals were aged on RU486-infused food 16d while being flipped onto fresh drug-infused food every 2-days. Total RNA was collected from heads of frozen animals using Trizol, converted to cDNA using random primers, and analyzed by qPCR using SYBR Green. All primers were previously developed with the exception of dHSF1, dHSP70, dBAG3, dStip1, dFkbp4 (Fkbp59), and dChordc1 [5, 12]. Data was normalized to the housekeeping gene, RP49 . Primer sequences are provided in Additional file 2: Table S2. Full genotypes for (G4C2)n are as follows: w1118/yw;; UAS-(G4C2)n, elavGS/+. (GR)36 animals, w1118/yw; UAS-(GR)36/+; elavGS/+, were compared to controls, w1118/yw;;. For analysis of HSF mutant expression, briefly, male HSF OE mutant flies were crossed to w1118 virgin females and maintained at 24 °C. Male progeny were collected and aged to 5d before analysis. Full genotype: w1118;; HSF[+t8]/+. Control w1118 males were maintained and aged in parallel.
External eye analysis
Scoring of the external eye phenotype for (G4C2)49 was done using a 0–8 scale previously defined where 0 = WT eye and 8 = lethality (extreme toxicity) . (G4C2)49 expression causes an average degenerative score of 4–5 across multiple studies. Scoring of the external eye phenotype for (GR)36 was done using a 0–11 scale where 0 = WT eye and 11 = lethality (extreme toxicity) (Additional file 3: Figure S5). (GR)36 expression causes an average degenerative score of 5–6 across multiple studies.
For optimal eye phenotypes, crosses for (G4C2)n were setup and maintained at 24 °C and (GR)36 at 21 °C. Male progeny with the desired genotype were collected daily and matured to 1-2d before imaging on a Leica Apo16 microscope. Severity of the external eye phenotype was determined post-imaging while looking for changes in red pigmentation, ommatidial organization, and eye size. Full genotypes for (G4C2)n are as follows: “Control” = w1118;; UAS-(G4C2)n, Gmr-Gal4/+ and “HSF OE” = w1118;; UAS-(G4C2)n, Gmr-Gal4/HSF[+t8]. Full genotypes for (GR)36 are as follows: “Control” = w1118; UAS-(GR)36/+; Gmr-Gal4/+ and “HSF OE” = w1118; UAS-(GR)36/+; Gmr-Gal4/HSF[+t8].
Drosophila beta-galactosidase western blots
Western blots are as previously described .
Identification of a C9ORF72-associated transcriptional signature in patient brain samples
There remains much to be learned concerning the mechanisms by which the repeat expansion in C9ORF72 contributes to ALS and FTLD. Recently, RNA-sequencing datasets were generated from the frontal cortex as well as the cerebellum of sporadic ALS cases, C9ORF72-ALS cases and controls . In Prudencio et al., a “double-cutoff method” was used for identifying genes whose expression was significantly changed in each class of ALS patient relative to controls (methods). Although such methods are useful for identifying changes in gene expression, they tend to be more sensitive to large fold-changes in less abundant transcripts, while modest fold-changes in abundant transcripts may go undetected (Additional file 4: Figure S1) [3, 29]. We reasoned that further analyses of these data might provide new insights into the disease mechanisms acting in C9ORF72 and sporadic patients, respectively. Utilizing a false discovery rate (FDR) threshold of 5%, we sought to identify changes in abundantly-expressed transcripts and found 56 transcripts that were differentially expressed between C9ORF72-ALS cortex and controls at this confidence interval (Additional file 4: Figure S1, methods). Comparison of sporadic ALS patient and control cortex with these same metrics identified 65 differentially expressed transcripts, most (61) of which were downregulated. Consistent with the previous report that sporadic and C9ORF72 ALS patients display distinct transcriptional signatures relative to controls, we found no overlap in the identity of transcripts that we identified as differentially expressed in the cortex of sporadic ALS and C9ORF72 ALS patient classes (Fig. 1b) . However, the majority of the genes we had found as likely to be differentially expressed in sporadic and C9ORF72-ALS patients had not been previously identified , validating the importance of reanalyzing these sequencing data using the methods we employed (Additional file 5: Table S3, Additional file 4: Figure S1, see Methods).
In C9ORF72-ALS, the cortex is characterized by distinct p62-positive DPR neuronal inclusions and the cerebellum contains abundant DPR inclusions [1, 30, 34, 41]. Hence, we reasoned that identifying transcripts with expression changes shared in both the frontal cortex and the cerebellum might lead us to genes and pathways that were reproducibly induced by the C9ORF72 repeat expansion. Strikingly, 27 of the 56 transcripts differentially expressed in the C9ORF72-ALS cortex were also significantly changed in the C9ORF72-ALS cerebellum (p = 2.93*10− 40; Fig. 1c). Comparison of the fold expression changes in these 27 transcripts between these two regions in C9ORF72-ALS brains revealed a strong positive correlation (R2 = 0.88). Notably, we identified increased abundance for 26 of these 27 transcripts in both brain regions relative to controls (Fig. 1d). The one exception was the C9ORF72 transcript itself which showed reduced abundance (57% cortex, FDR = 0.0169; 42% cerebellum, FDR = 2.75*10− 5), in agreement with previous studies of patient brains [14, 52, 53]. In contrast to a prior analysis, we detected no significant transcriptional changes between the cerebellum of sporadic ALS cases and controls (Fig. 1b), consistent with this region being histologically unremarkable in sporadic cases .
To determine if the transcripts significantly changed in C9ORF72 and sporadic ALS cortex pointed to particular pathways that might be responding to disease processes, we carried out gene ontology (GO) analysis. Transcripts identified in C9ORF72-ALS were significantly associated with response to topologically incorrect proteins (p = 2.13*10− 6) and protein folding (p = 4.57*10− 7) (Fig. 1e). In contrast, differentially expressed transcripts detected in sporadic ALS were associated with functions in the mitochondrial respiratory chain complex assembly (p = 8.53*10− 21) and related terms (Fig. 1f), and included 9 members of the NADH dehydrogenase (complex I) enzyme and 6 components of cytochrome oxidase C (complex IV) (Additional file 6: Figure S2A). These findings suggest that the transcriptional responses in the C9ORF72 and sporadic ALS cortex might be reflective of changes in protein and mitochondrial homeostasis, respectively. We also asked whether any of the C9ORF72-associated transcripts encoded proteins that interact in particular complexes. Using the InWeb protein-protein interaction network , analysis of the 56 differentially expressed transcripts from C9ORF72 cortex identified an interaction network involving heat shock proteins (HSPs) and protein chaperones, with HSPA1B (HSP70) and HSPB1 (HSP27) at its hubs (Fig. 1g). Examination of protein interactions from the 221 transcripts differentially expressed in the C9ORF72 cerebellum revealed a similar and expanded network of more than 80 interactors that was centered on the same core HSPs (Additional file 6: Figure S2B).
Activation of the HSF1 pathway in C9ORF72-ALS/FTLD
A well-established regulator of HSP and protein chaperone expression is the transcription factor heat shock factor 1 (HSF1) . Hence, we wondered if the transcriptional response we observed in the C9ORF72 brain might be at least in part mediated by activation of HSF1. To explore this possibility, we turned our attention to established HSF1 target genes previously identified by ChIP-seq and genome-wide methods [31, 32, 49]. Consistent with the notion that a portion of the response in C9ORF72 patient brain was mediated by HSF1, 13 of the 27 transcripts identified as significantly changed in both the cerebellum and frontal cortex were among 812 genes bound by HSF1 after heat shock treatment across three human cell lines (p = 1.22*10− 12) , including several HSPs shown to be upregulated in the initial small C9ORF72-ALS cohort .
As a next step towards investigating whether activation of the HSF1 might be responsible for the induction of these genes in C9ORF72 patients, we used quantitative RT-PCR to measure the transcript abundance of HSF1 and 11 of these conserved HSP-associated transcripts in a much larger patient cohort that also included patients diagnosed with FTLD and both ALS and FTLD (n = 56 C9ORF72-ALS/FTLD, n = 46 sporadic ALS/FTLD, n = 8 controls). In the frontal cortex, expression of each of these 11 HSF1 target genes was significantly increased in the C9ORF72-ALS/FTLD cohort relative to controls (p < 0.05 or lower for each gene) and to sporadic cases (p < 0.01 or lower) (Fig. 2a, Additional file 7: Table S4). Next, we extended our expression analyses of these 11 HSF1 targets to the cerebellum, and again found that the abundance of each transcript gene was significantly elevated in C9ORF72-ALS/FTLD relative to both controls and sporadic ALS cases (Additional file 8: Figure S3A, Additional file 7: Table S4). For example, we found a significant, two orders of magnitude induction of the HSP70 transcript HSPA1B in C9ORF72-ALS/FTLD cases relative to controls. To investigate if the larger number of genes initially detected only in the C9ORF72 cerebellum might also be reflective of a heat shock response, we examined another HSF1 target gene CRYAB and found it was significantly upregulated in both C9ORF72 brain regions in this larger patient cohort (Fig. 2a, Additional file 8: Figure S3A).
Evaluation of HSF1 expression in these same samples demonstrated that it was significantly more abundant in both the cortex and cerebellum relative to sporadic ALS cases (P < 0.05) (Fig. 2b). We found a strong and consistent correlation between the levels of HSF1 and each of these C9ORF72-chaperome transcripts in both brain regions (p < 0.0001 for each gene, Additional file 8: Figure S3B). For instance, the relationship between the transcript levels of HSF1 and HSPB1 yielded an R2 value of 0.73 (95% CI 0.63–0.81) in the cortex and 0.65 (95% CI 0.52–0.75) in the cerebellum. Taken together, these findings indicate that HSF1 is activated in C9ORF72-ALS and FTLD patient brains and suggests that it is regulating the expression of the HSPs we found to be induced there.
DPRs are sufficient to induce a C9ORF72-associated transcriptional changes
The C9ORF72 GGGGCC repeat expansion is translated from both sense and anti-sense transcripts through non-ATG translation to generate 5 distinct dipeptide repeat proteins (DPRs), e.g. poly-glycine-arginine (poly-GR) [18, 34, 52]. We wondered if DPRs alone were sufficient to induce the upregulation of C9ORF72 signature transcripts. Therefore, we tested the effects of synthetic DPRs in human stem cell-derived neurons . GP10, GA10 and a scrambled GAPR5 control were not acutely toxic to the parental human stem cell line or stem-cell derived neurons. In contrast poly-GR10 resulted in a dose-dependent decrease in the viability of stem cell-derived neurons, but not the stem cell from which they were produced (Fig. 3b). In human neurons, we found that both poly-GA and poly-GR led to the significant upregulation of HSPA1B (p < 0.01), as well as additional C9ORF72 signature transcripts (Fig. 3c). Given that poly-GA is not associated with decreased viability in these conditions, this suggests that the observed transcriptional changes are not simply a consequence of general neuronal toxicity. There was a strong correlation (R2 = 0.58) between the degree of induction of these transcripts in human neurons by poly-GR and the changes present specifically in C9ORF72 brains. Upon measuring HSF1, there was a trend for increased levels with poly-GA and poly-GP, and the greatest increase was again observed with poly-GR (Fig. 3d). These findings support the notion that gain-of-function effects from DPRs are sufficient to induce HSF1 target genes that are upregulated in C9ORF72-associated disease.
Detection of C9ORF72-associated transcriptional changes in gain-of-function Drosophila models
To test for correlations in DPR production and altered HSF1 target gene expression in vivo, we evaluated a Drosophila gain-of-function transgenic model engineered to express 49 pure GGGGCC repeats driven by a drug-inducible neuronal-specific ElavGS-GAL4 driver [25, 33]. Fly models expressing toxic GGGGCC repeats produce DPRs and RNA foci [16, 33, 54]. We found significant increased expression of the Drosophila orthologs of conserved C9ORF72-associated HSPs and protein chaperones in flies expressing 49 repeats in neurons compared to controls (Fig. 4a). Upregulation of HSF1-associated genes was observed in the absence of significant animal death, arguing that the effect is specific to expression of (GGGGCC)49. Note that these expression changes are likely to be an underestimation of the actual changes caused by the repeats in vivo since (GGGGCC)49 was only expressed in neurons while gene expression changes were assayed using whole heads, including non-neuronal tissue. Additionally, we detected an increase in HSF1 expression similar to that observed in C9ORF72 patient brains (Fig. 4a). This demonstrates that at least part of the transcriptional response to the C9ORF72 repeat expansion is conserved in Drosophila, and is consistent with gain-of-function effects of the C9ORF72 repeat expansion driving the expression of HSF1 target genes.
Activation of the HSF1 pathway has been proposed to be protective in several neurodegenerative diseases associated with protein aggregation as a means to combat the cellular effects of toxic proteins . Given that we observed an HSF1 heat shock response in C9ORF72 patients and model systems, we wondered whether HSF1 may be a potential modifier of C9ORF72 gain-of-function toxicity. To investigate this idea, we selected a fly line harboring an additional allele of the Drosophila HSF1 ortholog (dHSF1) . We confirmed increased dHSF1 expression in this line and noted that it was comparable to the relative increase in dHSF1 expression observed in response to the GGGGCC repeat expansion (Fig. 4b). The presence of additional dHSF1 did not affect the expression of a control LacZ transgene (Fig. 4c). We next asked if this increase in dHSF1 would have an effect on GGGGCC-mediated toxicity and used the Gmr-Gal4 driver to specifically express the repeats in the fly optic system to assess the effect on the eye. Consistent with prior observations, GGGGCC49 expression in the eye during development led to generation of animals with eye degeneration and disruption of the highly regular ommatidial structure, reduced eye size, and loss of pigment (Fig. 4d) [25, 33]. dHSF1 upregulation by itself did not affect eye structure in the presence of a control GGGGCC8 (Fig. 4d). Surprisingly, we found that GGGGCC49-induced toxicity in the external eye was enhanced in the presence of dHSF1 overexpression (Fig. 4d, e).
Among the repeat expansion encoded DPRs, arginine-rich DPRs are particularly toxic in model systems, including Drosophila . Given that the expression of GGGGCC49 is associated with the production of both DPRs and potentially toxic RNA, we assayed the transcriptional effects of poly-GR in vivo. There was significant upregulation of dHSF1 and many HSF1-regulated transcripts in Drosophila expressing a poly-GR100 transgene in neurons compared to non-transgenic controls (Additional file 9: Figure S4). We additionally tested the effects of modulating dHSF1 levels in the optic system of poly-GR Drosophila again using Gmr-GAL4 to drive transgene expression. We observed exacerbation of poly-GR36 external eye toxicity in the presence of dHSF1 upregulation (Fig. 4h, j). These results argue that the changes in toxicity caused by added dHSF1 in the GGGGCC49 model is in part due to the effects of GR-dipeptide. Taken together, these findings suggest that augmentation of HSF1 activity may enhance DPR-mediated toxicity in Drosophila.
In this study, we have identified novel differentially expressed transcripts in C9ORF72-ALS based on analysis of two brain regions compared to controls. Every C9ORF72-associated transcript was not significantly altered in sporadic ALS, suggesting that the observed changes in this set of transcripts are not just an indicator of neuronal loss but rather reflective of C9ORF72-specific pathogenesis. Furthermore, we validated our C9ORF72 transcriptional signature in a large ALS/FTLD patient cohort and gain-of-function models.
Our findings specifically link activation of the HSF1 pathway to C9ORF72-ALS/FTLD. The HSF1 pathway is highly conserved from budding yeast to mammals and is an important mediator of the compensatory response to disruptions in proteostasis, such as heat shock . Impairment of HSF1 activity and loss of protein chaperone function have been reported to occur with ageing and in the setting of age-related neurodegeneration [7, 21, 35]. For instance, in models of poly-glutamine repeat-associated Huntington disease decreased expression of HSF1 target genes is observed and may contribute to protein aggregation . Likewise, decreased expression of a particular set of protein chaperones, including HSP90, occurs in Alzheimer disease and Parkinson disease . In C9ORF72-ALS/FTLD, we found robust increased expression of a family of protein chaperones and co-chaperones, consistent with activation of a heat shock response in this particular disease. Our study may provide the first evidence of increased, rather than impaired, activity of HSF1 based on human brain samples for a specific neurodegenerative disease. In addition, HSF1 is generally not thought to be regulated at the transcriptional level in the context of neurodegeneration. We found upregulation of HSF1 itself in C9ORF72-ALS/FTLD and a strong correlation between levels of HSF1 and its target genes. It will be important to examine transcriptional changes in HSF1 in post-mortem brain samples of additional neurodegenerative diseases.
Prior studies in model systems have suggested that HSF1 is a protective factor that helps neurons cope with cellular stress associated with misfolded proteins and protein aggregates . Unexpectedly, we observed that having additional HSF1 in the developing eye in two Drosophila models of C9ORF72-ALS/FTLD was not beneficial. Additional studies in these Drosophila models that characterize the functional consequences of the loss of individual HSF1-associated protein chaperones and HSPs may be useful to further dissect the relationship between this pathway and C9ORF72-related pathology. Pharmacological activation of HSF1 has been proposed as a therapeutic strategy to enhance protein chaperone function and neuronal survival in neurodegenerative disease . For instance, arimoclomol, which may act to enhance HSF1-pathway activation, has been shown to delay disease progression in an SOD1 overexpression mouse model . A phase II clinical trial for arimoclomol was recently conducted for a subtype of familial ALS associated with mutations in SOD1 and was found to be well-tolerated . Our findings suggest that additional pre-clinical studies may be warranted if this strategy is applied to other forms of ALS, especially the most common type of ALS, C9ORF72-ALS, and associated dementias. Additionally, the transcriptional differences present among distinct cohorts of ALS/FTLD patients re-emphasizes the potential importance of patient stratification by genotype for future clinical trials.
Several studies have aimed to identify the specific transcriptional changes and pathways affected by the C9ORF72 repeat expansion in patient-based cellular models, including iPSC-derived neurons, with little concordance among them [13, 15, 27, 48]. Gene expression changes have also been explored in a few animal models for this disease. In a loss-of-function mouse model lacking both copies of C9ORF72, transcriptional analysis of the spinal cord from C9ORF72−/− animals revealed significant changes in several pathways related to inflammation . On the other hand, gain-of-function bacterial artificial chromosome (BAC) transgenic mouse models harboring the human C9ORF72 repeat expansion have been generated with varying phenotypes and transcriptional changes. In one model containing exons 1–6 of human C9ORF72 with approximately 500 hexanucleotide repeats, no significant changes in the transcriptome of the frontal cortex at 6 months of age were reported . In another BAC mouse model with 100–1000 repeats, immunomodulatory and extracellular matrix pathways were identified as being altered in the frontal cortex also at 6 months of age . Although both of these BAC mouse models exhibit DPR inclusions in the nervous system that increase with age, evidence of neurodegeneration was not observed. One possibility is that DPRs did not reach sufficient levels in these models at the examined time points to induce neurodegeneration or the transcriptional changes described herein. Indeed, robust expression of DPRs using an adeno-associated viral vector with 66 repeats was sufficient to induce DPR aggregates, TDP-43-positive inclusions, neuronal loss, and behavioral deficits in mice . However, gene expression studies have not yet been performed in this viral mouse model.
Using two gain-of-function Drosophila models, we found upregulation of many Drosophila orthologs of the same genes that were upregulated in C9ORF72 patient brains. This is consistent with the notion that more potent expression of DPRs in models is essential to recapitulate C9ORF72 transcriptional changes and disease phenotypes. Our approach and findings starting with unbiased transcriptional analysis of patient samples may be useful for the characterization and assessment of existing and new models employed to study C9ORF72 disease.
Based on our findings, we propose the following model. The presence of the C9ORF72 repeat expansions results in the production of various toxic DPRs. In early life, neurons can degrade DPRs or perhaps sequester them into protective p62-positive inclusions. With aging, there is a decreased capacity of neurons to maintain proteostasis, and environmental insults may be associated with additional proteotoxic stress. This leads to the gradual accumulation of DPRs and the activation of a heat shock response to increase protein chaperones, perhaps in an attempt to refold inherently unstructured DPRs. However, increased HSF1 activity may actually contribute to DPR-dependent toxicity. One possibility is that the resulting increased levels of protein chaperones may promote the solubility or the stability of toxic DPRs. This model could partially explain the variable disease penetrance and expressivity by which the C9ORF72 repeat expansion acts to cause ALS and/or FTLD. It could be that natural human variation in the HSF1 response influences when and where the repeat expansion results in neurodegeneration.
In summary, we have identified specific gene expression changes in C9ORF72 disease that are consistent with the activation of a HSF1-associated transcriptional response. We found that the expression levels of HSF1 and protein chaperones are increased in C9ORF72-ALS/FTLD patients and in gain-of-function model systems. Our results suggest that DPRs encoded by the C9ORF72 hexanucleotide repeat expansion are sufficient to lead to the upregulation of HSF1 and its target genes. The effects of the HSF1 pathway on C9ORF72 pathogenesis in models of disease that express DPRs warrants further investigation.
Agosta F, Ferraro PM, Riva N, Spinelli EG, Domi T, Carrera P, Copetti M, Falzone Y, Ferrari M, Lunetta C, Comi G, Falini A, Quattrini A, Filippi M (2017) Structural and functional brain signatures of C9orf72 in motor neuron disease. Neurobiol Aging. https://doi.org/10.1016/j.neurobiolaging.2017.05.024
Al-Sarraj S, King A, Troakes C, Smith B, Maekawa S, Bodi I, Rogelj B, Al-Chalabi A, Hortobagyi T, Shaw CE (2011) p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS. Acta Neuropathol 122:691–702. https://doi.org/10.1007/s00401-011-0911-2
Anders S, Huber W (2010) Differential expression analysis for sequence count data. Genome Biol 11:R106. https://doi.org/10.1186/gb-2010-11-10-r106
Benatar M, Wuu J, Andersen PM, Atassi N, David W, Cudkowicz M, Schoenfeld D (2018) Randomized, double-blind, placebo-controlled trial of arimoclomol in rapidly progressive SOD1 ALS. Neurology 90:e565–e574. https://doi.org/10.1212/WNL.0000000000004960
Berson A, Sartoris A, Nativio R, Van Deerlin V, Toledo JB, Porta S, Liu S, Chung CY, Garcia BA, Lee VM, Trojanowski JQ, Johnson FB, Berger SL, Bonini NM (2017) TDP-43 promotes neurodegeneration by impairing chromatin remodeling. Curr Biol 27:3579–3590 e3576. doi:https://doi.org/10.1016/j.cub.2017.10.024
Boulting GL, Kiskinis E, Croft GF, Amoroso MW, Oakley DH, Wainger BJ, Williams DJ, Kahler DJ, Yamaki M, Davidow L, Rodolfa CT, Dimos JT, Mikkilineni S, MacDermott AB, Woolf CJ, Henderson CE, Wichterle H, Eggan K (2011) A functionally characterized test set of human induced pluripotent stem cells. Nat Biotechnol 29:279–286. https://doi.org/10.1038/nbt.1783
Brehme M, Voisine C, Rolland T, Wachi S, Soper JH, Zhu Y, Orton K, Villella A, Garza D, Vidal M, Ge H, Morimoto RI (2014) A chaperome subnetwork safeguards proteostasis in aging and neurodegenerative disease. Cell Rep 9:1135–1150. https://doi.org/10.1016/j.celrep.2014.09.042
Burberry A, Suzuki N, Wang JY, Moccia R, Mordes DA, Stewart MH, Suzuki-Uematsu S, Ghosh S, Singh A, Merkle FT, Koszka K, Li QZ, Zon L, Rossi DJ, Trowbridge JJ, Notarangelo LD, Eggan K (2016) Loss-of-function mutations in the C9ORF72 mouse ortholog cause fatal autoimmune disease. Sci Transl Med 8:347ra393. https://doi.org/10.1126/scitranslmed.aaf6038
Burguete AS, Almeida S, Gao FB, Kalb R, Akins MR, Bonini NM (2015) GGGGCC microsatellite RNA is neuritically localized, induces branching defects, and perturbs transport granule function. Elife 4:e08881. https://doi.org/10.7554/eLife.08881
Chafekar SM, Duennwald ML (2012) Impaired heat shock response in cells expressing full-length polyglutamine-expanded huntingtin. PLoS One 7:e37929. https://doi.org/10.1371/journal.pone.0037929
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 (2015) Neurodegeneration. C9ORF72 repeat expansions in mice cause TDP-43 pathology, neuronal loss, and behavioral deficits. Science 348:1151–1154. https://doi.org/10.1126/science.aaa9344
Colinet H, Lee SF, Hoffmann A (2010) Temporal expression of heat shock genes during cold stress and recovery from chill coma in adult Drosophila melanogaster. FEBS J 277:174–185. https://doi.org/10.1111/j.1742-4658.2009.07470.x
Cooper-Knock J, Bury JJ, Heath PR, Wyles M, Higginbottom A, Gelsthorpe C, Highley JR, Hautbergue G, Rattray M, Kirby J, Shaw PJ (2015) C9ORF72 GGGGCC expanded repeats produce splicing dysregulation which correlates with disease severity in amyotrophic lateral sclerosis. PLoS One 10:e0127376. https://doi.org/10.1371/journal.pone.0127376
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 (2011) Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 72:245–256. https://doi.org/10.1016/j.neuron.2011.09.011
Donnelly CJ, Zhang PW, Pham JT, Haeusler AR, Mistry NA, Vidensky S, Daley EL, Poth EM, Hoover B, Fines DM, Maragakis N, Tienari PJ, Petrucelli L, Traynor BJ, Wang J, Rigo F, Bennett CF, Blackshaw S, Sattler R, Rothstein JD (2013) RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention. Neuron 80:415–428. https://doi.org/10.1016/j.neuron.2013.10.015
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 (2015) GGGGCC repeat expansion in C9orf72 compromises nucleocytoplasmic transport. Nature 525:129–133. https://doi.org/10.1038/nature14974
Gabler M, Volkmar M, Weinlich S, Herbst A, Dobberthien P, Sklarss S, Fanti L, Pimpinelli S, Kress H, Reuter G, Dorn R (2005) Trans-splicing of the mod(mdg4) complex locus is conserved between the distantly related species Drosophila melanogaster and D. Virilis. Genetics 169:723–736. https://doi.org/10.1534/genetics.103.020842
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 (2013) Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS. Acta Neuropathol 126:829–844. https://doi.org/10.1007/s00401-013-1192-8
Gomez-Pastor R, Burchfiel ET, Thiele DJ (2018) Regulation of heat shock transcription factors and their roles in physiology and disease. Nat Rev Mol Cell Biol 19:4–19. https://doi.org/10.1038/nrm.2017.73
Haeusler AR, Donnelly CJ, Rothstein JD (2016) The expanding biology of the C9orf72 nucleotide repeat expansion in neurodegenerative disease. Nat Rev Neurosci 17:383–395. https://doi.org/10.1038/nrn.2016.38
Hartl FU, Bracher A, Hayer-Hartl M (2011) Molecular chaperones in protein folding and proteostasis. Nature 475:324–332. https://doi.org/10.1038/nature10317
Jedlicka P, Mortin MA, Wu C (1997) Multiple functions of Drosophila heat shock transcription factor in vivo. EMBO J 16:2452–2462. https://doi.org/10.1093/emboj/16.9.2452
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 (2016) Gain of toxicity from ALS/FTD-linked repeat expansions in C9ORF72 is alleviated by antisense oligonucleotides targeting GGGGCC-containing RNAs. Neuron 90:535–550. https://doi.org/10.1016/j.neuron.2016.04.006
Kieran D, Kalmar B, Dick JR, Riddoch-Contreras J, Burnstock G, Greensmith L (2004) Treatment with arimoclomol, a coinducer of heat shock proteins, delays disease progression in ALS mice. Nat Med 10:402–405. https://doi.org/10.1038/nm1021
Kramer NJ, Carlomagno Y, Zhang YJ, Almeida S, Cook CN, Gendron TF, Prudencio M, Van Blitterswijk M, Belzil V, Couthouis J, Paul JW 3rd, Goodman LD, Daughrity L, Chew J, Garrett A, Pregent L, Jansen-West K, Tabassian LJ, Rademakers R, Boylan K, Graff-Radford NR, Josephs KA, Parisi JE, Knopman DS, Petersen RC, Boeve BF, Deng N, Feng Y, Cheng TH, Dickson DW, Cohen SN, Bonini NM, Link CD, Gao FB, Petrucelli L, Gitler AD (2016) Spt4 selectively regulates the expression of C9orf72 sense and antisense mutant transcripts. Science 353:708–712. https://doi.org/10.1126/science.aaf7791
Kwon I, Xiang S, Kato M, Wu L, Theodoropoulos P, Wang T, Kim J, Yun J, Xie Y, McKnight SL (2014) Poly-dipeptides encoded by the C9orf72 repeats bind nucleoli, impede RNA biogenesis, and kill cells. Science 345:1139–1145. https://doi.org/10.1126/science.1254917
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 (2013) Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration. Proc Natl Acad Sci U S A 110:E4530–E4539. https://doi.org/10.1073/pnas.1318835110
Li T, Wernersson R, Hansen RB, Horn H, Mercer J, Slodkowicz G, Workman CT, Rigina O, Rapacki K, Staerfeldt HH, Brunak S, Jensen TS, Lage K (2017) A scored human protein-protein interaction network to catalyze genomic interpretation. Nat Methods 14:61–64. https://doi.org/10.1038/nmeth.4083
Love MI, Huber W, Anders S (2014) Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol 15:550. https://doi.org/10.1186/s13059-014-0550-8
Mackenzie IR, Frick P, Grasser FA, Gendron TF, Petrucelli L, Cashman NR, Edbauer D, Kremmer E, Prudlo J, Troost D, Neumann M (2015) Quantitative analysis and clinico-pathological correlations of different dipeptide repeat protein pathologies in C9ORF72 mutation carriers. Acta Neuropathol 130:845–861. https://doi.org/10.1007/s00401-015-1476-2
Mahat DB, Salamanca HH, Duarte FM, Danko CG, Lis JT (2016) Mammalian heat shock response and mechanisms underlying its genome-wide transcriptional regulation. Mol Cell 62:63–78. https://doi.org/10.1016/j.molcel.2016.02.025
Mendillo ML, Santagata S, Koeva M, Bell GW, Hu R, Tamimi RM, Fraenkel E, Ince TA, Whitesell L, Lindquist S (2012) HSF1 drives a transcriptional program distinct from heat shock to support highly malignant human cancers. Cell 150:549–562. https://doi.org/10.1016/j.cell.2012.06.031
Mizielinska S, Gronke S, Niccoli T, Ridler CE, Clayton EL, Devoy A, Moens T, Norona FE, Woollacott IO, Pietrzyk J, Cleverley K, Nicoll AJ, Pickering-Brown S, Dols J, Cabecinha M, Hendrich O, Fratta P, Fisher EM, Partridge L, Isaacs AM (2014) C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins. Science 345:1192–1194. https://doi.org/10.1126/science.1256800
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 (2013) The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS. Science 339:1335–1338. https://doi.org/10.1126/science.1232927
Morimoto RI (2011) The heat shock response: systems biology of proteotoxic stress in aging and disease. Cold Spring Harb Symp Quant Biol 76:91–99. https://doi.org/10.1101/sqb.2012.76.010637
Neef DW, Jaeger AM, Thiele DJ (2011) Heat shock transcription factor 1 as a therapeutic target in neurodegenerative diseases. Nat Rev Drug Discov 10:930–944. https://doi.org/10.1038/nrd3453
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 (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314:130–133. https://doi.org/10.1126/science.1134108
O'Rourke JG, Bogdanik L, Muhammad AK, 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 (2015) C9orf72 BAC transgenic mice display typical pathologic features of ALS/FTD. Neuron 88:892–901. https://doi.org/10.1016/j.neuron.2015.10.027
O'Rourke JG, Bogdanik L, Yanez A, Lall D, Wolf AJ, Muhammad AK, Ho R, Carmona S, Vit JP, Zarrow J, Kim KJ, Bell S, Harms MB, Miller TM, Dangler CA, Underhill DM, Goodridge HS, Lutz CM, Baloh RH (2016) C9orf72 is required for proper macrophage and microglial function in mice. Science 351:1324–1329. https://doi.org/10.1126/science.aaf1064
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 (2015) Human C9ORF72 Hexanucleotide expansion reproduces RNA foci and dipeptide repeat proteins but not neurodegeneration in BAC transgenic mice. Neuron 88:902–909. https://doi.org/10.1016/j.neuron.2015.11.018
Prudencio M, Belzil VV, Batra R, Ross CA, Gendron TF, Pregent LJ, Murray ME, Overstreet KK, Piazza-Johnston AE, Desaro P, Bieniek KF, DeTure M, Lee WC, Biendarra SM, Davis MD, Baker MC, Perkerson RB, van Blitterswijk M, Stetler CT, Rademakers R, Link CD, Dickson DW, Boylan KB, Li H, Petrucelli L (2015) Distinct brain transcriptome profiles in C9orf72-associated and sporadic ALS. Nat Neurosci 18:1175–1182. https://doi.org/10.1038/nn.4065
Prudencio M, Gonzales PK, Cook CN, Gendron TF, Daughrity LM, Song Y, Ebbert MTW, van Blitterswijk M, Zhang YJ, Jansen-West K, Baker MC, DeTure M, Rademakers R, Boylan KB, Dickson DW, Petrucelli L, Link CD (2017) Repetitive element transcripts are elevated in the brain of C9orf72 ALS/FTLD patients. Hum Mol Genet 26:3421–3431. https://doi.org/10.1093/hmg/ddx233
Reimand J, Arak T, Adler P, Kolberg L, Reisberg S, Peterson H, Vilo J (2016) G:profiler-a web server for functional interpretation of gene lists (2016 update). Nucleic Acids Res 44:W83–W89. https://doi.org/10.1093/nar/gkw199
Reiner A, Yekutieli D, Benjamini Y (2003) Identifying differentially expressed genes using false discovery rate controlling procedures. Bioinformatics 19:368–375
Renton AE, Majounie E, Waite A, Simon-Sanchez J, Rollinson S, Gibbs JR, Schymick JC, Laaksovirta H, van Swieten JC, Myllykangas L, Kalimo H, Paetau A, Abramzon Y, Remes AM, Kaganovich A, Scholz SW, Duckworth J, Ding J, Harmer DW, Hernandez DG, Johnson JO, Mok K, Ryten M, Trabzuni D, Guerreiro RJ, Orrell RW, Neal J, Murray A, Pearson J, Jansen IE, Sondervan D, Seelaar H, Blake D, Young K, Halliwell N, Callister JB, Toulson G, Richardson A, Gerhard A, Snowden J, Mann D, Neary D, Nalls MA, Peuralinna T, Jansson L, Isoviita VM, Kaivorinne AL, Holtta-Vuori M, Ikonen E, Sulkava R, Benatar M, Wuu J, Chio A, Restagno G, Borghero G, Sabatelli M, Consortium I, Heckerman D, Rogaeva E, Zinman L, Rothstein JD, Sendtner M, Drepper C, Eichler EE, Alkan C, Abdullaev Z, Pack SD, Dutra A, Pak E, Hardy J, Singleton A, Williams NM, Heutink P, Pickering-Brown S, Morris HR, Tienari PJ, Traynor BJ (2011) A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 72:257–268. https://doi.org/10.1016/j.neuron.2011.09.010
Robberecht W, Philips T (2013) The changing scene of amyotrophic lateral sclerosis. Nat Rev Neurosci 14:248–264. https://doi.org/10.1038/nrn3430
Robinson MD, McCarthy DJ, Smyth GK (2010) edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics 26:139–140. https://doi.org/10.1093/bioinformatics/btp616
Sareen D, O'Rourke JG, Meera P, Muhammad AK, Grant S, Simpkinson M, Bell S, Carmona S, Ornelas L, Sahabian A, Gendron T, Petrucelli L, Baughn M, Ravits J, Harms MB, Rigo F, Bennett CF, Otis TS, Svendsen CN, Baloh RH (2013) Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansion. Sci Transl Med 5:208ra149. https://doi.org/10.1126/scitranslmed.3007529
Solis EJ, Pandey JP, Zheng X, Jin DX, Gupta PB, Airoldi EM, Pincus D, Denic V (2016) Defining the essential function of yeast Hsf1 reveals a compact transcriptional program for maintaining eukaryotic Proteostasis. Mol Cell 63:60–71. https://doi.org/10.1016/j.molcel.2016.05.014
Supek F, Bosnjak M, Skunca N, Smuc T (2011) REVIGO summarizes and visualizes long lists of gene ontology terms. PLoS One 6:e21800. https://doi.org/10.1371/journal.pone.0021800
Taylor JP, Brown RH Jr, Cleveland DW (2016) Decoding ALS: from genes to mechanism. Nature 539:197–206. https://doi.org/10.1038/nature20413
Todd TW, Petrucelli L (2016) Insights into the pathogenic mechanisms of chromosome 9 open reading frame 72 (C9orf72) repeat expansions. J Neurochem 138(Suppl 1):145–162. https://doi.org/10.1111/jnc.13623
Waite AJ, Baumer D, East S, Neal J, Morris HR, Ansorge O, Blake DJ (2014) Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion. Neurobiol Aging 35:1779 e1775–1779 e1713. https://doi.org/10.1016/j.neurobiolaging.2014.01.016
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 (2015) The C9orf72 repeat expansion disrupts nucleocytoplasmic transport. Nature 525:56–61. https://doi.org/10.1038/nature14973
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 (2016) C9ORF72 poly(GA) aggregates sequester and impair HR23 and nucleocytoplasmic transport proteins. Nat Neurosci 19:668–677. https://doi.org/10.1038/nn.4272
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 (2014) Aggregation-prone c9FTD/ALS poly(GA) RAN-translated proteins cause neurotoxicity by inducing ER stress. Acta Neuropathol 128:505–524. https://doi.org/10.1007/s00401-014-1336-5
Zou J, Guo Y, Guettouche T, Smith DF, Voellmy R (1998) Repression of heat shock transcription factor HSF1 activation by HSP90 (HSP90 complex) that forms a stress-sensitive complex with HSF1. Cell 94:471–480
We are grateful to all patients who donated tissues. We thank members of the Eggan laboratory and Camille Sindu for helpful discussion and Kasper Lage’s group for supporting GeNets. We thank Kiki Lilliehook for comments on the manuscript.
This work was supported by the NINDS R01NS089742 (K.E.), R35-NS097275 (N.B.), R21NS084528 (L.P.), R01NS088689 (L.P.), R01NS063964 (L.P.); R01NS077402 (L.P.); P01NS084974 (L.P.); R35NS097273 (L.P.), NCI 5T32CA009216-34 (D.A.M), NIA P50AG016574 (L.P.), NIEHS R01ES20395 (L.P.), Project ALS (K.E.), Mayo Clinic Foundation (L.P.) and Robert Packard Center for ALS Research at Johns Hopkins (L.P.), Target ALS (L.P. and K.E.), a pilot project from 5P50AG005134 (D.A.M.), and grants from the ALS Association to D.A.M., M.P., L.P., and K.E.
Availability of data and materials
The RNA-seq data used for analysis is available via NCBI GEO (Prudencio et al., GSE67196).
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Written informed consent was given by all participants or authorized family members in accordance with institutional review board guidelines of Mayo Clinic.
The authors declare that they have no competing interests.
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Additional file 1:
Table S1. Characteristics of patient cohort for brain samples used in qPCR analysis. (PDF 154 kb)
Additional file 2:
Table S2. Primer sequences for PCR. (PDF 167 kb)
Additional file 3:
Figure S5. External eye quantification scale for (GR)36 animals. For quantification of the enhancement effects of increased expression of HSF in the eye, (GR)36 animals received a score between 0 (normal eye) and 11 (extreme toxicity causing lethality). Across multiple studies control Gmr-GAL4 > (GR)36 animals receive a score between 5 and 6. (PDF 1969 kb)
Additional file 4:
Figure S1. Bioinformatic method comparison for gene expression analysis of C9ORF72-associated ALS and sporadic ALS (sALS) in the frontal cortex and cerebellum. (a-d) Gene density plots comparing the expression levels of differentially expressed transcripts as determined by the prior double cut-off method (|log2 fold change| ≥ 2 and p-value < 0.05) and the FDR method (FDR < 0.05), which was used in Fig. 1 and subsequent analysis. Note, no significant changes were detected in the sALS cerebellum using with FDR method. (e) Venn diagrams demonstrating considerable differences in the designated disease-associated transcripts between these bioinformatics methods in both brain regions. (f) Table of the number of differentially expressed transcripts as determined by Prudencio et al., the double cut-off method and the FDR method used here. (PDF 216 kb)
Additional file 5:
Table S3. Genes significantly changes in RNA-seq analysis from ALS patients. (XLSX 52 kb)
Additional file 6:
Figure S2. Gene networks in C9ORF72-ALS and sporadic ALS. (a) Protein-protein interaction network derived from differentially expressed transcripts in C9ORF72-ALS cerebellum. Those transcripts that are differentially expressed in both the frontal cortex and the cerebellum in C9ORF72-ALS are highlighted by dashed yellow circles, and predominantly consist of heat shock proteins and protein chaperones. (b) Protein-protein interaction network derived from differentially expressed transcripts in the sporadic ALS cortex. (PDF 164 kb)
Additional file 7:
Table S4. Values from qPCR analysis in brain samples. (PDF 178 kb)
Additional file 8:
Figure S3. Activation of HSF1 in C9ORF72-ALS, FTLD, and combined ALS/FTLD patients. (a) Quantitative real-time PCR (qRT-PCR) for HSF1 target genes in the cerebellum of sporadic and C9ORF72-associated disease (n = 56 C9ORF72-ALS/FTLD, n = 42 sporadic ALS/FTLD, n = 7 controls) (one-way ANOVA with Bonferonni post-hoc test for multiple comparisons * p < 0.05, ** p < 0.01, *** p < 0.001. Note, no significant changes were detected between the sporadic cases and controls. (b) Correlation of HSF1 levels and HSF1 target gene levels in the frontal cortex and cerebellum in C9ORF72-ALS/FTLD. Spearman’s R2 values are plotted for each target gene, error bars denote 95% confidence interval, p-value < 0.0001 in all cases. (PDF 209 kb)
Additional file 9:
Figure S4. poly-GR expression results in the upregulation of heat shock response genes and dHSF1 in the adult fly nervous system. UAS-(GR)36 was expressed in the adult fly nervous system using the drug-inducible Gal4 driver, elavGS, for 16d. qPCR analysis of endogenous HSF1-regulated genes and dHSF1 revealed significant upregulation of the Drosophila orthologs of many of the genes identified in patient studies, suggesting that poly-GR is contributing to the altered transcriptome in C9ORF72-ALS/FTLD patients. Control animals did not express a transgene. Differences in expression are likely underestimated as the analyses include neuronal and non-neuronal tissue while (GR)36 was expressed only in neurons. (n = 6, mean +/− SD, unpaired, student’s t-tests, p-value * < 0.05, ** < 0.01). (PDF 389 kb)
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Mordes, D.A., Prudencio, M., Goodman, L.D. et al. Dipeptide repeat proteins activate a heat shock response found in C9ORF72-ALS/FTLD patients. acta neuropathol commun 6, 55 (2018). https://doi.org/10.1186/s40478-018-0555-8
- Amyotrophic lateral sclerosis
- C9ORF72 repeat expansion
- Dipeptide repeat proteins
- Frontotemporal dementia
- Frontotemporal lobar degeneration
- Heat shock response