Tuberous Sclerosis Complex (TSC) is a rare genetic disorder that results from a mutation in the TSC1 or TSC2 genes leading to constitutive activation of the mechanistic target of rapamycin complex 1 (mTORC1). TSC is associated with autism, intellectual disability and severe epilepsy. Cortical tubers are believed to represent the neuropathological substrates of these disabling manifestations in TSC. In the presented study we used high-throughput RNA sequencing in combination with systems-based computational approaches to investigate the complexity of the TSC molecular network. Overall we detected 438 differentially expressed genes and 991 differentially expressed small non-coding RNAs in cortical tubers compared to autopsy control brain tissue. We observed increased expression of genes associated with inflammatory, innate and adaptive immune responses. In contrast, we observed a down-regulation of genes associated with neurogenesis and glutamate receptor signaling. MicroRNAs represented the largest class of over-expressed small non-coding RNA species in tubers. In particular, our analysis revealed that the miR-34 family (including miR-34a, miR-34b and miR-34c) was significantly over-expressed. Functional studies demonstrated the ability of miR-34b to modulate neurite outgrowth in mouse primary hippocampal neuronal cultures. This study provides new insights into the TSC transcriptomic network along with the identification of potential new treatment targets.
Tuberous Sclerosis Complex (TSC) is a genetic disorder caused by mutations in either TSC1 or TSC2 genes, leading to the development of benign lesions/hamartomas in multiple organs1, 2. TSC often compromises the central nervous system resulting in complex neurological manifestations consisting of varying combinations of neurodevelopmental delay (including autism), various psychiatric disorders and severe epilepsy3,4,5. Cortical tubers, a form of focal cortical dysplasia, are thought to be major contributors to these disabling neurological manifestations in TSC and are targeted for surgical resection in TSC patients with pharmacologically intractable epilepsy6,7,8. Although the current surgical and pharmacological management of seizures in TSC often provide significant benefits5, 7, 9, 10, there is further need for a better understanding of the molecular and physiological basis of the neurological manifestations seen in TSC11.
Previous gene expression studies on TSC tuber specimens focused either on selected cDNA sequences12, 13 or used mRNA14 or microRNA (miRNA) microarray hybridization platforms15. Advances in high-throughput RNA sequencing (RNA-seq) technology coupled with sophisticated bioinformatics methods have provided a revolutionary means to systematically map transcriptional units of the human genome16, 17. Indeed, RNA-seq has led to a more profound appreciation of the intricate nature of both the coding and non-coding transcriptome of the human brain18, 19. Moreover, the non-coding units of the human transcriptome, particularly small RNA species that include miRNA, have emerged as important modifiers of the protein coding transcriptome and, in turn, disease phenotype19,20,21,22. A comprehensive, parallel scan of both the protein coding and small non-coding brain transcriptome of TSC patients by RNA-seq has never been performed. Thus, we here aimed to first map the protein coding and small non-coding RNA species in the brain transcriptome of TSC patients and second, to identify significantly altered cellular signaling pathways in TSC patients that may be modified by miRNA for a better delineation of the complex pathological signaling pathways and networks seen in TSC.
The protein coding transcriptome of tuberous sclerosis complex brain tissue
To characterize the brain transcriptome of TSC subjects, RNA-Seq was performed on mRNA extracted from tubers and normal control brain samples. The analysis included tubers from 12 TSC subjects (10 surgical specimens and 2 autopsy specimens) and 10 age-matched controls without a history of seizures or other neurological disease (See methods and Table 1). On average 23 million paired-end reads were produced per sample. After quality assessment and filtering ~20 million paired-end reads remained per sample, of which ~77% mapped concordantly to the GRCh38 reference genome. Differential gene expression analysis revealed 438 differentially expressed genes (absolute fold-change of >1.5 or <−1.5 and adjusted p-value < 0.05) in the TSC cortical tubers compared to control cortex, 269 of these genes were over-expressed and 169 under-expressed (Fig. 1a). The top 10 over-expressed and under-expressed protein-coding genes (ranked by fold-change) are listed in Table 2. Ingenuity pathway analysis revealed that genes with enhanced expression in tubers were associated with innate and adaptive immune response canonical signaling pathways, including the complement system, triggering receptor expressed on myeloid cells 1 (TREM1) signaling, and CD28 signaling in T helper cells (Fig. 1b). The complement system represented the most significant association, with increased expression of complement C1q A chain (C1QA) (3.5-fold), complement C1q B chain (C1QB) (3.9-fold), complement C1q C chain (C1QC) (3.5-fold), complement component 3 (C3) (9.2-fold) and complement C1r subcomponent (C1R) (2.2-fold) (Fig. 1c). No canonical signaling pathways were associated with genes that had decreased expression in TSC patients. RT-qPCR targeting a selection of complement system and TREM1 signaling genes validated the RNA-Seq data (Supplementary Fig. 1).
To gain a better understanding of potential cell-type specific gene expression related to TSC pathology an independent dataset of single-cell RNA-Seq from neurons, microglia, oligodendrocytes and astrocytes taken from healthy human cortex was analyzed (GSE67835)23. Genes from the single-cell RNA-Seq analysis were classified as microglia, oligodendrocyte, astrocyte or neuron specific based on expression values (greater than 10 read-counts in cell type of interest, less than 1 read count in all other cell-types). Of the 269 genes over-expressed in the TSC cortical tubers, 23 were specific to microglia, 3 to oligodendrocytes, 5 to neurons, and 8 to astrocytes (Supplementary Table 1). Amongst the 169 genes under-expressed in the TSC cortical tubers, 6 were specific to neurons, 2 to astrocytes, 1 to microglia and 1 to oligodendrocytes (Supplementary Table 1). A Fisher’s exact test revealed that amongst the significantly over-expressed genes there was significant enrichment for microglia specific (p-value < 2.2e-16) and astrocyte specific (p-value < 0.002) genes, amongst the significantly under-expressed genes there was a suggestive enrichment of neuron specific genes (p-value < 0.05). The 32 genes specific to microglia and astrocytes that were over-expressed in the TSC subjects included the complement system related genes, C1QA, C1QB, C1QC and C4B (Fig. 1c). We did not observe gene expression differences between important subgroups, that is individuals with TSC2 versus TSC1 mutations, or mild versus severe intellectual disability.
The small non-coding RNA landscape of tuberous sclerosis complex brain tissue
In order to further explore the brain transcriptome of TSC subjects relative to control subjects we performed small RNA-seq analysis on the same set of RNA samples (Table 1). Each sequencing run produced ~9 million paired-end reads for each sample. After quality assessment and filtering, ~5 million paired-end reads remained for each sample, of which ~82% were mapped to the reference genome (GRCh38). Differential expression analysis of the aligned small RNA transcripts revealed a total of 991 significantly altered transcripts, 59 were elevated and 932 were decreased in TSC cortical tubers compared to controls (Fig. 2a). The differentially expressed small RNAs were not only miRNAs but also other classes (Fig. 2b). The largest class of altered small non-coding RNA was the small nuclear RNA (snRNA). Other classes of altered small RNAs in TSC relative to control patients (in decreasing order) were the C/D box small nucleolar RNAs (snoRNAs), miRNAs, H/ACA box snoRNAs, orphan snoRNA and the small Cajal body RNAs (scaRNAs). Interestingly, the majority of snRNAs, snoRNAs and scaRNAs were under-expressed in TSC cortical tubers compared to control cortex (Fig. 2b; Supplementary Fig. 2). Highly expressed miRNAs in TSC subjects included, miR-34a (3.1-fold), miR-34b (2.6-fold), miR-34c (2.5-fold), miR-302a (2.2-fold), miR-577 (4-fold) and miR-21 (2.9-fold) (Fig. 2c), all members of the miR-34 family were validated using RT-qPCR (Supplementary Fig. 3).
Previously reports of age dependent miRNA expression patterns in the brain and cardiac tissue24, 25, notably of miR-34a26, coupled with the variability of age in our study cohort motivated us to evaluate the association of age to expression patterns of miR34a and the other members of the miR-34 family members. We found no significant correlation (Pearson’s correlation) between expression patterns of miR-34 family members and age (r < 0.41, p-value > 0.05) (Supplementary Fig. 4).
Gene co-expression network modules and miRNA targets
To better understand the organization of the protein coding and small non-coding RNA transcriptome in TSC and control subject brain tissue we applied an unsupervised weighted gene co-expression network approach (WGCNA)27, 28. On the basis of a Spearman’s correlation matrix, a weighted network of RNA transcripts was constructed that ensured scale-free topology (see Methods). Unsupervised hierarchical clustering uncovered 21 modules of highly inter-correlating transcripts, each harbouring more than 100 genes (Supplementary Table 2). Modules were analysed for over-representation of gene ontologies and illustrated by an unsupervised Cytoscape yFiles organic layout with each module colour coded (Fig. 3a and Supplementary Table 2). We found 11 modules (out of 21) to be over-represented for various cellular biological pathways, particularly innate immune response (green module), type-I interferon signalling pathway (light yellow module), synaptic signalling (red module), neurogenesis (black module) and extracellular matrix organization (magenta module) modules (Fig. 3a). Overlaying the fold expression (log2 transformed) of significantly differential genes between TSC and control subjects revealed the innate immune response and extracellular matrix organization modules harboured the majority of significantly elevated genes in TSC patients (Fig. 3b and c). Genes with significantly decreased expression in TSC patients were predominantly located in modules attuned to neuronal functions, for example the neurogenesis and glutamate receptor signaling module (Fig. 3b and c). Next, we sought to infer miRNA that potentially target genes within the gene co-expression network. To this aim we firstly leveraged the module eigengene concept (module first principal component) to test for correlations between miRNA expression indices and module expression patterns. Here, we focused our attention on miRNA with elevated patterns of expression in TSC patients relative to controls. In particular, we identified significant indirect negative correlations between the glutamate receptor signalling and neurogenesis modules with expression indices of miR-193, miR-200, and the miR-34 families (Pearson’s correlation) (Supplementary Fig. 5 and Supplementary Table 3). Using the miR-Walk 2.0 database29 we identified multiple genes in the neurogenesis and glutamate receptor signalling modules that are predicted targets of miR-34a, miR-34b and/or miR-34c (Fig. 3d, Supplementary Table 4). No overlap was found between the putative miR-34 family targets in the modules neurogenesis and glutamate receptor signalling and any cell-specific genes. Altogether, these results suggest that neurogenesis and glutamate receptor signalling modules may be targeted and, in turn, regulated by specific miRNA families altered in TSC brain tissue.
Cellular distribution of selected over-expressed miRNAs in TSC cortical tubers and control cortex
Thus far our findings suggest that typical neuronal cellular pathways were predicted targets of specific miRNA family members. Considering our analysis was centered upon complex brain tissue, which encompasses multiple cell-types, we here sought to gain insight into the cell-specific patterns of selected miRNA expression in TSC and control brain tissue, that is, the miR-34 family members, miR-34a and miR-34b. In line with our RNA-seq data, in situ hybridization targeting miR-34a-5p and miR-34b-5p showed low expression in control cortex for both miRNAs (Fig. 4a,e) and high expression in TSC tubers, specifically dysmorphic neurons, giant cells and in cells with astroglial morphology (Fig. 4b,d,f,h). Double labeling confirmed the expression of these miRNAs in NeuN (neurons) – and GFAP (astrocytes)- positive cells in TSC cortical tuber specimens (Fig. 4).
Overexpression of miR-34b increases expression of IL1B in human foetal astrocytes
To study the impact of miR-34a-5p and miR-34b-5p overexpression in foetal astrocytes two different assays were performed. First, in an attempt to induce miR-34a-5p and miR-34b-5p expression foetal astrocytes were stimulated with IL1β. No increase in the expression levels of miR-34a-5p and miR-34b-5p due to IL1 β were observed. Subsequently, the foetal astrocytes were transfected with a miR-34a-5p and a miR-34b-5p mimic. Foetal astrocytes transfected with the miR-34b-5p mimic had an associated up-regulation of IL1β (~4-Fold, p-value < 0.03) and the inflammatory marker IL6 (~2.3-fold, p-value < 0.03), (Supplementary Figure 6). Conversely, no increase in IL1β and IL6 levels was seen after transfection with the miR-34a-5p mimic, and a down regulation of COX2 (~1.5-fold, p-value < 0.03) was observed. This suggests that an overexpression of miR-34b-5p in astrocytes could activate an inflammatory response in astrocytes.
miR-34b modulates neurite outgrowth in mouse hippocampal neuronal cultures
To further explore the capacity of miR-34 family members to modulate neuronal characteristics, as predicted by our miRNA-to-module interaction framework, we selected miR-34b for further functional studies in vitro. In particular we investigated the impact of miR-34b overexpression on neurite outgrowth in a mouse hippocampal neuron model. Primary mouse neuronal cultures prepared from the hippocampi of postnatal day 0 (P0) C57Bl/6 mice were transfected at 1 day in vitro with either the miR-34b-5p mimic or the miRNA mimic negative control (Scr) and analyzed for neurite outgrowth at 4 days in vitro. Neurons transfected with miR-34b-5p mimic showed an increased number of longer neurites as compared to Scr transfected cultures (Fig. 5a,b). Quantification using the NeuroMath software showed a significant increase in the total length (Fig. 5c), number of neuritis (Fig. 5d) and an increase in soma size (Fig. 5e) of the miR-34b-5p mimic transfected neurons compared to Scr transfected cultures.
In this study we report a comprehensive analysis of the brain transcriptome in TSC patients relative to control subjects. Evaluation of both the protein coding and small non-coding RNA by RNA-seq revealed substantial alterations in TSC brain tissue. In particular, TSC cortical tubers had elevated expression of genes involved in innate immune pathways, such as complement system, concomitant with decreased expression of genes predominantly associated with neuronal cellular pathways, including neurogenesis and glutamate receptor signaling. A variety of small non-coding RNA transcripts, including miRNAs, were also significantly altered in TSC cortical tubers relative to controls. Application of a gene co-expression network approach and miRNA-to-target predictions allowed for the identification of functional modules of the brain transcriptome potentially modulated by miRNAs. Based on these predictions miR-34 family members, notably miR-34b, were assessed by functional in vitro studies and shown to possess a capacity to modulate neurite outgrowth and to activate an inflammatory response in astrocytes.
Heightened expression of genes involved in innate and adaptive immune pathways, such as complement system, TREM1 signaling and CD28 signaling was an overarching feature of the TSC cortical tuber protein coding transcriptome. These data extend on our previous study, a genome wide microarray analysis of a small cohort of TSC cortical tubers and four controls demonstrating up-regulation of genes related to the inflammatory response, including complement factors, chemokines and several cytokines14. Others have also shown differential inflammatory gene expression in TSC cortical tubers; albeit by targeted RT-qPCR and immunocytochemistry14, 30, 31, indicating that our data on mRNA expression changes in TSC cortical tubers were consistent across different sample cohorts and studies. The presence of biologically active fragments of C3 (C3c and C3d); and C4 (C4b) in TSC cortical tubers indicates that the activation of the complement cascade may be a key driver of the inflammatory response consistently observed in the TSC brain14, 30, 31. The complement cascade has been implicated in seizure generation and progression in numerous experimental epilepsy models32,33,34,35,36, human temporal lobe epilepsy37, and in epileptogenic glioneuronal tumors38. Also, our data suggest a role for TREM-1 signaling in TSC. TREM-1 can amplify Toll like receptor signaling, thereby increasing the production of a wide range of cytokines and chemokines39, 40. Interestingly, experimental studies support the role of these pathways in seizures35, 41, 42, suggesting that drugs targeting the TREM-1 signaling may have potential therapeutic benefit for seizures in TSC. Evaluation of fetal TSC brain revealed an activation of the innate and adaptive immune response early during brain development43 suggesting that the induction of this pathway could be intrinsic to the TSC developmental pathology and linked to the deregulation of the mTOR pathway44,45,46. Accordingly, a recent study shows over-activation of pro-inflammatory signaling pathways in astrocytes before epilepsy onset in a mouse model of TSC, pointing to the role of mTOR-mediated inflammatory mechanisms in TSC47. Amongst the significantly over-expressed genes in TSC subjects there was enrichment for microglial and astrocyte specific genes. Both microglia and astrocytes are involved in inflammation driven processes throughout the brain48, 49, suggesting that the TSC inflammatory processes may be driven by activation of microglia and astrocytes. Understanding whether changes in innate and/or adaptive immune gene expression represent the cause or the consequence of chronic pharmacoresistant seizure activity is extremely difficult since epilepsy surgery targeting cortical tubers or autopsy is performed several months or years after the start of seizures. Moreover, a comparison with non-epileptogenic tubers could not be performed, since this tissue is not resected during epilepsy surgery and infrequently available at autopsy. Nevertheless these findings provide further evidence for the activation of both the innate and adaptive immune response cascades in the pathophysiology of TSC.
Besides the protein coding transcriptome we also mapped the small non-coding RNA in TSC brain tissue relative to controls. We found that not only miRNA, extensively investigated as epigenetic effector molecules, were significantly altered in the TSC brain transcriptome but also other species of small RNA, notably snoRNAs, snRNAs and scaRNAs. These small RNA species represent an ancient group of non-coding RNA molecules, which in particular to snoRNA (including the H/ACA box and C/D box categories) may spread throughout the genome by retrotransposition, representing a new family of mobile genetic elements50, 51. These recently discovered small RNA have been shown to modify the chemical properties of ribosomal RNAs and transfer RNAs, impacting on mRNA translation, RNA silencing, alternative splicing52,53,54, as well as methylation and pseudouridylation of spliceosomal RNAs in the Cajal bodies of the nucleus55, 56. Notably, the disruption of snoRNA expression and/or function has been implicated in neurodevelopmental disorders such as Prader-Willi syndrome and autism spectrum disorders57, 58. These as yet under-explored classes of small non-coding RNA certainly warrant further investigation in TSC pathogenesis.
Through the use of an unsupervised systems-based computational technique, that is gene co-expression network construction, we identified multiple modules of tightly inter-correlating protein coding genes. This approach allowed for the construction of a holistic transcriptome model, thus not only those functions biased towards the response in TSC relative to control subjects (supervised analysis). This aspect is supported by the finding of modules enriched for genes involved in neuronal attuned biological functions, such as neurogenesis and glutamate receptor signalling, which would otherwise have been missed. Moreover, WGCNA has emerged as an important tool in integrative bioinformatics/genomics59. We reasoned that since miRNA are known to target and influence the expression of multiple genes involved in shared and distinct cellular processes, a modular approach may uncover functional units of distinct biological functions in the brain transcriptome potentially modulated by miRNA, rather than considering single transcripts. In so doing, we uncovered the miR-34 family (miR-34a, miR-34b and miR-34c) as predicted modifiers of neurogenesis and glutamate receptor signalling transcriptional output. These predictions were further tested experimentally using a miR-34b-5p overexpression system in mouse hippocampal neurons, demonstrating that miR-34b-5p can modulate neurite outgrowth. Reduced neurogenesis during chronic epilepsy could result in loss-of-function deficits and contribute to common TSC comorbidities such cognitive impairment or depression60, 61. Also, previous findings have demonstrated abnormal accumulation of extracellular glutamate occurring in human epileptogenic tissue, which is hypothesized as a key factor in recurrent seizures and neuronal death62. Mouse models have also shown that controlling seizures by antiepileptic drugs (AEDs) may act via alterations in brain glutamate dehydrogenase activity as well as the brain transcriptome including miRNAs63, 64. Both miR-34a and miR-34b have been previously identified as overexpressed miRNAs in tubers15, as well as key tumour suppressors downstream of the p53 pathway and have been suggested as potential targets of therapy in several cancers65, 66. Members of the miR-34 family have also been shown to regulate key pathways in neurodevelopment and cortical neurogenesis, such as the Notch67,68,69 and the Wnt signaling pathway70, 71. More specifically, it appears that miR-34a plays a role in neuronal differentiation72,73,74,75,76,77, where overexpression of miR-34a in mouse neural stem cells impairs both neuronal differentiation and synapse function74,75,76,77,78. Moreover, a recent study has demonstrated targeting of the TSC1 3′ UTR by miR-34a, supporting the role of this miRNA in tuber pathology15. In this particular study epileptogenic tubers were compared to adjacent non-tuber tissue indicating that elevated expression of miR-34 members may indeed represent an important feature of tuber physiology rather than an effect of AED treatment.
Our study has limitations. TSC patients received individually tailored AED regimens contrary to autopsy control subjects. Moreover, AEDs were given in multiple combinations, which precludes proper evaluation of the effects of AEDs on gene expression alterations in TSC tubers.
In conclusion, our study provides a comprehensive analysis of the coding and small non-coding transcriptional landscape of TSC cortical tubers. The TSC transcriptomic network reflects the prominent activation of both innate and adaptive immune response characteristic of cortical tubers, with identification of key pathways such as complement system, TREM1 and CD28 signaling. Notably, the under-expressed genes were linked to neurogenesis and glutamate receptor signaling. We identified a variety of small RNA molecules, including miRNA, snoRNA, snRNA and scaRNA, differentially expressed in TSC. Moreover, our study predicts an important role for the miR-34 family (miR-34a, miR-34b and miR-34c) as modifiers of neurogenesis and glutamate receptor signaling in TSC, which may potentially provide an epigenetic-driven therapeutic tool for epilepsy and cognitive disabilities in TSC.
The cortical specimens from TSC and control patients included in this study were selected from the archives of the departments of neuropathology of the Academic Medical Center (AMC, University of Amsterdam, The Netherlands), the University Medical Center Utrecht (UMCU, The Netherlands), Motol University Hospital (Prague, Czech Republic) and Medical University Vienna (MUV, Austria). Informed consent was obtained for the use of brain tissue and for access to medical records for research purposes. We evaluated 12 TSC specimens (10 surgical specimens and 2 autopsy specimens) from whom we obtained anatomically well-preserved neocortical tubers tissue and sufficient clinical data. All patients fulfilled the diagnostic criteria for definite TSC79, 80. The surgical cases had pharmacologically intractable epilepsy (daily seizures) and underwent extensive pre-surgical evaluation6. Patient characteristics are summarized in Table 1. The following clinical data were extracted from medical records: TSC1/TSC2 mutation status, gender, localization of the resected area, age at seizure onset, duration of active epilepsy, antiepileptic drug (AED) management at time of surgery and presence/absence of intellectual disability (ID; Mild = IQ 55–70; Moderate = IQ 40–55; Severe IQ 25–40) and autism. The majority of TSC patients harbored TSC2 gene mutations (66.6%; Table 1). The tissue specimens were age-matched with the controls (p-value > 0.86, two-sided t-test). Using a principal variance component analysis (PVCA) brain region and gender were shown to contribute minimally to the overall variation of the RNA-Seq results.
Perituberal frozen material was available for only 3 out of 10 TSC cases examined and two samples did not pass the minimal quality requirements; thus analysis of perituberal tissue was not performed. Histologically normal cortex was obtained at autopsy from 10 controls without a history of seizures or other neurological diseases (cause of death was acute cardiorespiratory failure; Table 1). We acknowledge that the choice of the control material is extremely difficult in human studies, particularly in case of pathologies affecting young patients, which limits the number of cases suitable for gene expression studies. We were fortunate to obtain the human postmortem from young controls, as well as autopsy TSC samples.
Tissue was obtained and used in accordance with the Declaration of Helsinki and the AMC Research Code provided by the Medical Ethics Committee and approved by the science committee of the UMC Utrecht Biobank. The local ethical committees of all participating centers gave permission to undertake the study.
Cortical specimens from control and TSC patients were snap frozen in liquid nitrogen and stored at −80 °C until use for RNA isolation. Additional tissue was fixed in 10% neutral buffered formalin and embedded in paraffin. Paraffin-embedded tissue was sectioned at 5 μm, mounted on pre-coated glass slides (Star Frost, Waldemar Knittel GmbH, Brunschweig, Germany) and used for in situ hybridizations and immunocytochemistry. One representative paraffin block per case was sectioned and processed for hematoxylin and eosin (HE) as well as for immunocytochemical staining for a number of neuronal and glial markers to confirm the diagnosis.
Frozen tissue material was homogenized in Qiazol Lysis Reagent (Qiagen Benelux, Venlo, The Netherlands). The total RNA including the miRNA fraction was isolated using the miR-Neasy Mini kit (Qiagen Benelux, Venlo, the Netherlands) according to manufacturer’s instructions. The concentration and purity of RNA were determined at 260/280 nm using a Nanodrop 2000 spectrophotometer (Thermo Scientific, Wilmington, DE, USA) and RNA integrity was assessed using a Bioanalyser 2100 (Agilent). Samples required an RNA integrity number (RIN) greater than 6.0 for use in down-stream sequencing.
RNA-seq library preparation and sequencing
Library preparation and sequencing were completed at ServiceXS, Plesmanlaan 1D, 2333 BZ, Leiden, Netherlands. The Illumina (San Diego, California, USA) mRNA-Seq and TruSeq Small RNA-Seq sample preparation kits were used to prepare sequencing libraries of mRNA and small RNA, respectively. Briefly, mRNA was selected by oligo-dT magnetic beads, fragmented and subjected to cDNA synthesis. Sequencing adapters were ligated to the cDNA fragments, followed by PCR amplification. Small RNA samples were processed by size exclusion gel electrophoresis subsequent to sequencing adaptor ligation. After gel excision and digestion, sequences were amplified by PCR. Clustering and DNA sequencing was performed using the Illumina cBot and HiSeq 2500. Each library was subjected to paired-end sequencing, producing reads 125 nucleotides in length.
Bioinformatics analysis of RNA-seq data
Read quality was assessed using FastQC v0.11.2 (Babraham Institute, Babraham, Cambridgeshire, UK), and Trimmomatic v0.33 was used to trim and filter reads of low quality81. Low quality leading and trailing bases were removed from each read, a sliding window trimming using a window of 4 and a phred33 score threshold of 20 was used to assess the quality of the body of the read. Reads that dropped below 36 and 18 nucleotides, respectively in our mRNA and small RNA datasets, as well as sequence reads lacking both forward and reverse orientations were excluded from further analysis.
Next, paired-end reads were aligned to the human reference genome (GRCh38) with TopHat2 v2.0.13 using the default settings82. No mismatches between the small RNA trimmed reads and reference genome were allowed. The aligned mRNA reads were assembled into individual transcripts and the abundance of each transcript was estimated using Cufflinks v2.2.183. For mRNA sequence data, expression level was calculated as fragments per kilobase of exon per million fragments mapped (FPKM). The Cufflinks transcript assembly was guided using the reference annotation file Gencode v2184. The transcript assemblies from each sample were then assembled into a single unified transcript catalog using Cuffmerge83. Finally, the merged transcript file along with the original alignment files produced from Tophat were analyzed using Cuffdiff. Libraries were quantile-normalized and differential expression analysis was performed considering genes with FPKM >1 in at least one of the sample groups. Small RNA count data were normalized (per 1 × 106 reads) and differential expression analysis between TSC and control patients was done by means of the limma method (version 3.14.4)85. Throughout Benjamini-Hochberg (BH)86 multiple comparison adjusted probabilities (P < 0.05) defined significance. Ingenuity Pathway Analysis (Ingenuity Systems IPA, www.ingenuity.com) was used to identify the associating canonical signaling pathways stratifying genes by over- and under-expressed patterns. The Ingenuity gene knowledgebase was selected as reference and human species specified. All other parameters were default. Fisher’s exact test BH-adjusted probabilities (P < 0.05) defined significance.
The mRNA sequence transcriptome was analyzed by means of a weighted gene coexpression network approach87, 88. A pair-wise Spearman’s correlation matrix of the top 10000 most variable unique genes (ranked by median absolute deviation) was transformed into an adjacency matrix by using a soft power function to ensure scale-free topology89. The adjacency matrix was further transformed into a topological overlap matrix to enable the identification of modules (clusters) of highly correlating genes by implementing a dynamic tree cut algorithm90, 91. Thus, each module representing a cluster of co-regulated genes with a distinct expression pattern from other identified modules. In order to define module “driver” genes we made use of the module eigengene concept, defined as the first principal component of the module expression matrix, and, the module membership measure, k90, 91. Significantly different miRNA expression indices between TSC and control patients were interrogated for their predicted interations with module-specific genes by means of the miR-Walk atlas, specifying the miR-Walk algorithm, of gene-miRNA-target interactions92. We selected for human species annotations and considered 3’UTR interactions as well as a minimum seed length equating to 7. All other parameters were default. Correlation analysis between miRNA profiles and module eigengenes was performed by Pearson’s method. Significant correlations were demarcated by p < 0.05.
Single cell RNA-seq analysis
Single cell RNA-Seq data sets produced by the Quake laboratory (Stanford University, CA), were retrieved from NCBI’s Gene Expression Omnibus (GEO) (accession no. GSE67835)93. Data was retrieved for four different cell types; neurons, oligodendrocytes, microglia and astrocytes, all from healthy human cortex. Three biological replicates for each cell type were used, giving 12 samples in total. Sequence reads were trimmed and filtered using FastQC v0.11.2 and Trimmomatic v0.33 as aforementioned. Paired-end reads were aligned to the human reference genome (GRCh38) with TopHat2 v2.0.13 using the default settings82. Next, the number of reads that mapped to each gene in the genome was calculated using featureCounts from the SubRead package94. The GRCh38 reference annotation file Gencode v21 was used as an input for featureCounts84. Data analysis and manipulation was performed in R (version 3.2.4). The count matrix was normalized using the R package DESeq295.
TSC1 and TSC2 mutation analysis was performed by sequence analysis of all coding exons and exon/intron boundaries. Mutations are described according to HGVS nomenclature (Accession number NM_000548.3)96.
In situ hybridization
In situ hybridization (ISH) for miR-34a-5p and miR-34b-5p were performed on 5 μm thick FFPE tissue using 5′ - 3′ double digoxygenin (DIG)-labeled probes as described previously97, 98. The probe sequences used were: miR-34b-5p: 5′ DIG-AugGcaGugGagTuaGugAuuG-DIG;from Ribotask ApS (Odense, Denmark) and miR-34a-5p: 5′ DIG- AcaAccAgcTaaGacAcuGccA-DIG (Exiqon A/s, Vedbaek, Denmark) (capital letter = LNA modification, small letter = 2-o-methyl modification). Briefly, after the sections were deparaffinized and heat-treated to undo protein crosslinks (10 min at 120 °C in a pressure cooker), the probes were hybridized at 56 °C for 1 h. The hybridization was detected with an alkaline phosphatase (AP)-labeled anti-DIG antibody (Roche Applied Science, Basel, Switzerland). NBT (nitro-blue tetrazolium chloride)/BCIP (5-bromo-4-chloro-3′-indolyphosphate p-toluidine salt) was used as chromogenic substrate for AP. Negative controls sections were without probes and without primary antibody. For the double-staining, combining immunohistochemistry with ISH, the sections were first processed for ISH and then processed for immunohistochemistry with glial fibrillary acidic protein (GFAP, astrocyte marker; monoclonal mouse, Sigma, St. Louis, Mo, USA; 1:4000), NeuN (neuronal nuclear protein; mouse clone MAB377; Chemicon, Temecula, CA, USA; 1:2000), and HLA-DP/DQ/DR (microglial marker, mouse clone CR3/43; Dako; 1:100). Signal was detected using the chromogen 3-amino-9-ethylcarbazole (Sigma-Aldrich, St. Louis, MO, USA).
Quantitative reverse-transcription PCR analysis (RT-qPCR)
miRNAs (miR-34a-5p, miR-34b-5p, miR-34c-5p, miR-302a-3p, miR-21-5p and the reference small nuclear RNAs, Rnu6B and Rnu44) expression was analyzed using Taqman micro RNA assays (Applied Biosystems, Foster City, CA). cDNA was generated using Taqman MicroRNA reverse transcription kit (Applied Biosystems, Foster City, CA) according to manufacturer’s instructions and the PCRs were run on a Roche Lightcycler 480 thermocycler (Roche Applied Science, Basel, Switzerland). Quantification of data was performed using the computer program LinRegPCR in which linear regression on the Log (fluorescence) per cycle number data is applied to determine the amplification efficiency per sample99, 100. The starting concentration of each specific product was divided by the starting concentration of reference genes (geometric mean of Rnu6B and Rnu44 values) and this ratio was compared between groups.
To evaluate expression of miRNA targets and inflammation-related genes, 2.5 µg of total RNA was reverse-transcribed into cDNA using oligodT primers. PCR primers (Eurogentec, Belgium) were designed using the Universal ProbeLibrary of Roche (https://www.roche-applied-science.com) on the basis of the reported cDNA sequences (Supplementary Table 5). For each PCR, a mastermix was prepared on ice, containing per sample: 1 µl cDNA, 2.5 µl of 2x SensiFASTTM SYBR Green Reaction Mix (Bioline Inc, Taunton, MA, USA), 0.4 µM of both reverse and forward primers and the PCRs were run on a Roche Lightcycler 480 thermocycler (Roche Applied Science, Basel, Switzerland). Quantification of data was performed as described for the Taqman PCR and the starting concentration of each specific product was divided by the geometric mean of the starting concentration of reference genes (EF1A, C1orf43 and SNRPD3) and this ratio was compared between patient/control groups.
Human astrocyte-enriched cell cultures
Primary foetal astrocyte-enriched cell cultures were prepared from tissue collected from donors from whom a written informed consent for the use of the material for research purposes has been obtained by the Bloemenhove Clinic (Heemstede, The Netherlands). Cell isolation was performed as described elsewhere98. Cell cultures were stimulated with human recombinant (r) IL1β (Peprotech, NJ, USA; 10 ng/ml) for 24 hours. For transfection Foetal astrocyte cultures were transfected with either mirVanaTM miR-34b-5p miRNA mimic or mirVana™ miRNA Mimic, Negative Control #1 (both from ThermoFisher Scientific, Landsmeer, Netherlands) at a final concentration of 50 nM using Lipofectamine® 2000 transfection reagent (ThermoFisher Scientific, Landsmeer, Netherlands). Cells were harvested after 24 hours of stimulation/transfection for RNA isolation and RT-qPCR (miR-34a-5p, miR-34b-5p, IL1β, IL6, COX2).
Primary mouse hippocampal neuron cultures, immunofluorescent staining and neurite growth analysis
Primary mouse hippocampal neuron cultures were prepared from postnatal day 0 (P0) C57BL/6 mouse brains. Cells were plated on 15 mm coverslips coated with poly-D-lysine (20 µg/ml) and laminin (40 µg/ml) in 24-well plates at a density of 100,000 cells/well. The cultures were grown in Neurobasal medium (NB) supplemented with B27, 0.35 mM HEPES, 200 mM L-glutamine, 14.3 mM β-mercaptoethanol and penicillin/streptomycin. Cultures were co-transfected at 1 day in vitro with miR-34b-5p miR-Vana mimic (Applied Biosystems, Life Technologies Europe BV, Bleiswijk, Netherlands) or the miR-IDIAN miRNA mimic negative control #1 (Dharmacon, GE Healthcare Europe, Eindhoven, the Netherlands) and a green fluorescent protein (GFP) vector at 50 pmol/well using Lipofectamine®-2000 (Thermo Fisher Scientific) as transfection reagent for 1 hour at 37 °C and 5% CO2. Cultures were fixed with 4% paraformaldehyde/4% sucrose in phosphate-buffered saline (PBS) at 4 days in vitro for 20 minutes and washed three times with PBS for 30 min at room temperature. The cultures were blocked with 0.1% PBS-Triton X-100 buffer with 3% Normal Goat serum and then incubated with primary antibodies in the blocking solution overnight at 4 °C. Subsequently, neurons were washed three times in PBS and incubated with AlexaFluor-conjugated secondary antibodies in the blocking buffer for 2 hr at RT. They were then washed 2 times with PBS and incubated with DAPI (nuclear) staining. After final washes with PBS for 20 min, the neurons were mounted on slides with Fluorsave (Merck Millipore) mounting medium. Images were obtained at 20x magnification with epifluoroscent Axioscope A1 (Zeiss) microscope. Neurite outgrowth was analyzed using NeuroMath developed at Weizmann Institute, Israel.
The datasets generated during and/or analyzed during the current study are available at the following repositories:
RNA-seq and small RNA-Seq data from TSC and control patients: Sequence data has been deposited at the European Genome-phenome Archive (EGA), which is hosted by the EBI and the CRG, under the accession number: EGAS00001002485.
Further information about EGA can be found on https://ega- archive.org “The European Genome-phenome Archive of human data consented for biomedical research”(http://www.nature.com/ng/journal/v47/n7/full/ng.3312.html).
Single cell RNA-seq data: NCBI’s Gene Expression Omnibus (GEO) under the accession number: GSE67835 Web link: www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE67835.
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This work was supported by European Union’s Seventh Framework Programme (FP7/2007-2013) under the grant agreement no. 602391 (project acronym EPISTOP; A.I., J.v.S., A.M., E.A., F.I., K.K., S.K., A.J., L.L., P.C., D.K.); Epilepsiefonds (WAR 15-05; RJP); European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 642881 (ECMED; A.E., J.G.). None of the authors has any conflict of interest to disclose. We confirm that we have read the Journal’s position on issues involved in ethical publication and affirm that this report is consistent with those guidelines.
The authors declare that they have no competing interests.
Accession codes: Primary RNA-Seq: EGAS00001002485 Secondary RNA-Seq: GSE67835.
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Mills, J.D., Iyer, A.M., van Scheppingen, J. et al. Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment. Sci Rep 7, 8089 (2017). https://doi.org/10.1038/s41598-017-06145-8
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