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Nuclear respiratory factor 1 (NRF1) serves as a transcription factor that activates the expression of a wide range of nuclear genes essential for mitochondrial biogenesis and function, including mitochondrial respiratory complex subunits, heme biosynthetic enzymes, and regulatory factors involved in the replication and transcription of mitochondrial DNA. Increasing evidence indicates that mitochondrial function is severely compromised in the brains of aging-related neurodegenerative diseases. To identify the comprehensive set of human NRF1 target genes potentially relevant to the pathogenesis of neurodegenerative diseases, we analyzed the NRF1 chromatin immunoprecipitation followed by deep sequencing (ChIP-Seq) dataset retrieved from the Encyclopedia of DNA Elements (ENCODE) project. Overall, we identified 2,470 highly stringent ChIP-Seq peaks on protein-coding genes in SK-N-SH human neuroblastoma cells. They were accumulated in the proximal promoter regions with an existence of the NRF1-binding consensus sequence. The set of ChIP-Seq-based NRF1 target genes included known NRF1 targets such as EIF2S1, EIF2S2, CYCS, FMR1, FXR2, E2F6, CD47, and TOMM34. By pathway analysis, the molecules located in the core pathways related to mitochondrial respiratory function were determined to be highly enriched in NRF1 target genes. Furthermore, we found that NRF1 target genes play a pivotal role in regulation of extra-mitochondrial biological processes, including RNA metabolism, splicing, cell cycle, DNA damage repair, protein translation initiation, and ubiquitin-mediated protein degradation. We identified a panel of neurodegenerative disease-related genes, such as PARK2 (Parkin), PARK6 (Pink1), PARK7 (DJ-1), and PAELR (GPR37) for Parkinson’s disease, as well as PSENEN (Pen2) and MAPT (tau) for Alzheimer’s disease, as previously unrecognized NRF1 targets. These results suggest a logical hypothesis that aberrant regulation of NRF1 and its targets might contribute to the pathogenesis of human neurodegenerative diseases via perturbation of diverse mitochondrial and extra-mitochondrial functions.
Mitochondria play a pivotal role in adenosine triphosphate (ATP) synthesis by oxidative phosphorylation in nearly all eukaryotic cells. Mitochondrial function is severely compromised in the brains of aging-related neurodegenerative diseases, such as Parkinson’s disease (PD), Alzheimer’s disease (AD), and Huntington’s disease (HD).1,2 The precise genetic and molecular mechanisms accounting for mitochondrial dysfunction in human neurodegenerative diseases, however, remain largely unknown. Mitochondrial DNA (mtDNA), a small circular DNA, encodes only 13 respiratory chain subunits, 22 transfer RNAs, and 2 ribosomal RNAs. In contrast, all proteins essential for mitochondrial transcription, translation, replication, and protein import and assembly are coded by a series of nuclear genes.3 Nuclear respiratory factor 1 (NRF1), alternatively named alpha-palindromic-binding protein (α-PAL), serves as a basic region-leucine zipper (bZIP) transcription factor which activates the expression of nuclear genes essential for mitochondrial biogenesis and function.3
NRF1 target genes include a wide range of genes coding for five mitochondrial respiratory complex subunits, heme biosynthetic enzymes, and regulatory factors involved in the replication and transcription of mtDNA.3 NRF1 is composed of the N-terminal serine phosphorylation domain and the nuclear localization signal (NLS), the C-terminal transactivation domain, and the central DNA binding domain which recognizes the palindromic sequence defined as YGCGCAYGCGCR, where Y and R indicate a pyrimidine or purine nucleotide, respectively.3 A homodimer of NRF1 binds to target gene promoters.4 Phosphorylation of NRF1 at the N-terminal serine residues induced in response to the serum enhances DNA binding and transactivation abilities.4
The human NRF1 gene shows a substantial homology to developmental transcription factors, such as P3A2 expressed in sea urchins, the erect wing (ewg) protein in Drosophila, not really finished (nrf) in Zebrafish, and Nrf1 in mice.5–8 The homozygous Nrf1 knockout mice revealed an embryonic lethal phenotype and NRF1−/− blastocysts exhibited reduced levels of mtDNA.7 Disruption of NRF1 ortholog functions causes a severe neurological defect in Drosophila and Zebrafish, suggesting a crucial role of NRF1 in maintenance of the nervous system function.6,8
Because mitochondria contain a number of enzymes pivotal for redox homeostasis, even a subtle defect in oxidative phosphorylation causes not only fatal energy failure in neurons but also generates a large amount of reactive oxygen species (ROS) highly toxic to vulnerable neurons in the central nervous system (CNS).1 Therefore, defective mitochondrial physiology plays a crucial role in the pathogenesis of neurodegenerative diseases, such as PD, AD and HD in which mitochondrial function is compromised at the early stage of the diseases.1,2 With respect to a crucial role of NRF1 in the maintenance of mitochondrial function, it is highly important to characterize the comprehensive set of NRF1 target genes in human neural cells involved in mitochondrial function relevant to the pathogenesis of human neurodegenerative diseases.
Recently, the next-generation sequencing (NGS) technology has rapidly advanced the genome research. Chromatin immunoprecipitation followed by deep sequencing (ChIP-Seq), an NGS application, provides a highly efficient method for global profiling of DNA-binding proteins, histone modifications, and nucleosomes on a genome-wide scale.9 ChIP-Seq endowed with higher resolution, less noise, and greater coverage of the genome, compared with microarray-based ChIP-Chip, provides an invaluable tool for characterizing the comprehensive gene regulatory networks.9,10 Since ChIP-Seq produces large amounts of high-throughput data, it is often hampered by the difficulty in interpretation of biologically meaningful implications. To overcome this problem, we could illustrate the cell-wide map of the complex molecular interactions with the help of the knowledgebase of well-annotated molecular pathways to establish a logical hypothesis accounting for cellular biological processes.11
No previous studies have characterized the comprehensive set of ChIP-Seq-based NRF1 target genes in human neural cells. At present, only one study is available, which determined the genome-wide NRF1 target genes by ChIP-Chip in T98G human glioblastoma cells.12 Recently, the Encyclopedia of DNA Elements (ENCODE) project based on an international collaborative research was established to identify a comprehensive list of functional elements in the human genome, including genes, transcripts, and transcriptional regulatory elements (encodeproject.org/ENCODE).13 A panel of high-throughput functional genomic data produced by the ENCODE project are currently available through a freely accessible database following the ENCODE Consortium Data Release restriction. They serve as a high-quality resource for the scientific community to find novel biological insights into the complex gene regulation in the human genome. In the present study, we attempted to analyze the NRF1 ChIP-Seq dataset retrieved from the database of the ENCODE project. Overall, we identified 2,470 ChIP-Seq-based reliable NRF1 targets in SK-N-SH human neuroblastoma cells, including the genes essential for mitochondrial function and those closely related to neurodegeneration. Based on these observations, we would propose an original hypothesis that deregulation of NRF1 target genes are potentially involved in the pathogenesis of human neurodegenerative diseases.
To identify a comprehensive set of NRF1 target genes, we investigated a ChIP-Seq dataset retrieved from DDBJ Sequence Read Archive (DRA) under the accession number of SRP007993. The ChIP-Seq experiments were performed for the ENCODE project (encodeproject.org/ENCODE) by researchers in Dr. Michel Snyder’s Laboratory, Stanford University. The data were opened to public on September 13, 2012. In these experiments, SK-N-SH human neuroblastoma cells (ATCC HTB-11) cultured in Eagle’s Minimum Essential Medium supplemented with 10% fetal bovine serum without any special treatments (encodeproject.org/ENCODE/cellTypes.html) were fixed with formaldehyde to crosslink NRF1-DNA complexes. Sonicated nuclear lysates were processed for immunoprecipitation with a mouse monoclonal anti-NRF1 antibody (ab55744; Abcam) (SRX186635) or normal IgG for input signal (SRX186629). NGS libraries constructed from size-selected and adapter-ligated ChIP DNA fragments were processed for deep sequencing at a 36 bp read length on Genome Analyzer (Illumina).
First, we evaluated the quality of NGS short reads by searching them on the FastQC program (http://www.bioinformatics.babraham.ac.uk/projects/fastqc). Then, we mapped them on the human genome reference sequence version hg19 by using a mapping tool of AvadisNGS (Agilent Technologies) or by the Bowtie 0.12.7 program (bowtie-bio.sourceforge.net). Subsequently, we identified statistically significant peaks of mapped reads by using the Model-based Analysis of ChIP-Seq (MACS) program under the highly stringent condition of fold enrichment (FE) ≥20 and the false discovery rate (FDR) ≤0.01, according to the methods described previously.14 The genes corresponding to MACS peaks were determined by a neighboring gene analysis tool of AvadisNGS within a distance of 5000 bp from peaks to genes. Next, we identified more detailed genomic locations of MACS peaks by importing the processed data composed of individual peaks one by one into a novel genome viewer named GenomeJack v1.4 (Mitsubishi Space Software).15 The genomic locations of the peaks were categorized into the following: the promoter region defined by the location within 5,000 bp upstream from the 5′ end of genes, the 5′ untranslated region (5′UTR), the exon, the intron, the 3′UTR, the location within 5,000 bp downstream from the 3′ end of genes (3′down), and intergenic regions outside these. In the technical aspects, we defined NRF1 target genes as those having ChIP-Seq peaks within the distance of 5,000 bp upstream or downstream from 5′ or 3′ ends of the genes whose sequences are defined by RefSeqGene (http://www.ncbi.nlm.nih.gov/refseq/rsg). The consensus motif sequences surrounding a 400 bp-length sequence of the peak summits, extracted from the hg19 sequence track of GenomeJack, were identified by the MEME-ChIP program.
To identify the pathways biologically relevant to ChIP-Seq-based NRF1 target genes, we imported the corresponding Entrez Gene IDs into the Functional Annotation tool of Database for Annotation, Visualization and Integrated Discovery (DAVID) v6.7 (david.abcc.ncifcrf.gov).16 DAVID identifies the most relevant pathway constructed by Kyoto Encyclopedia of Genes and Genomes (KEGG), composed of the genes enriched in the given set with an output of statistical significance evaluated by the modified Fisher’s exact test and corrected by Benjamini-Hochberg multiple comparison test. KEGG (http://www.kegg.jp) is a publicly accessible knowledgebase containing manually curated reference pathways that cover a wide range of metabolic, genetic, environmental, and cellular processes, as well as human diseases. It is currently composed of 271,665 pathways generated from 451 reference pathways.17
We also imported Entrez Gene IDs into Ingenuity Pathways Analysis (IPA) (Ingenuity Systems; http://www.ingenuity.com) in the setting of 140 molecules per net for greater than 1,000 imported genes and 70 molecules per net for smaller than 1,000 imported genes. IPA is a commercial knowledgebase that contains approximately 3,000,000 biological and chemical interactions and functional annotations with definite scientific evidence. By uploading the list of Gene IDs, the network-generation algorithm identifies focused genes integrated in global molecular pathways and networks. IPA calculates the score P-value that reflects the statistical significance of association between the genes and the pathways or networks by the Fisher’s exact test.
First, we evaluated the quality of short read NGS data derived from NRF1 ChIP-treated DNA, composed of 50,295,303 reads, and IgG ChIP-treated DNA, composed of 39,245,635 reads. The quality scores across all bases exceeded 30 on FastQC, indicating that these data showed an acceptable quality for downstream analysis (Supplementary Fig. 1, panels a and b). After mapping them on hg19 by AvadisNGS, we identified all 2,792 stringent ChIP-Seq peaks that met the highly stringent criteria of fold enrichment (FE) ≥20 and false discovery rate (FDR) ≤0.01 by MACS in order to reduce the detection of false positive binding sites, if at all possible.14 To process them for the pathway analysis, we omitted the peaks located in non-coding genes and uncategorized genes (n = 322). Finally, we identified 2,470 ChIP-Seq peaks on protein-coding genes. The genomic locations of the peaks were determined by using GenomeJack. Fragile X mental retardation protein 1 (FMR1) (Fig. 1, panels a and b) represents an example of well-known NRF1 target genes.18
The summits of the peaks of top 200 genes were located in the promoter (68.0%), 5′UTR (18.5%), exon (2.0%), intron (7.5%), 3′UTR (0.5%), and 3′down (3.5%) by GenomeJack, suggesting that the binding regions are accumulated in the proximal promoter regions. The comprehensive list of 2,470 NRF1 target genes is shown in Supplementary Table 1. The top 10 most significant genes are listed in Table 1. Importantly, among 691 NRF1 target genes reported by a previous ChIP-Chip study of T98G human glioblastoma cells,12 the set of 495 genes (71.6%) (Supplementary Table 1, underline), including eukaryotic translation initiation factor 2, subunit 1 alpha (EIF2S1), ataxia telangiectasia mutated (ATM), cyclin B1 (CCNB1), and proliferating cell nuclear antigen (PCNA), were overlapped with the set of 2,470 ChIP-Seq-based NRF1 target genes, supporting the validity of our results. However, a panel of neurodegenerative disease-related genes identified in SK-N-SH cells, such as PARK2 (Parkin), PARK7 (DJ-1), PAELR (GPR37), MAPT (tau), and TAF4 (TAFII130), were not included in ChIP-chip-based NRF1 targets of T98G cells.
By motif analysis using MEME-ChIP, 99 genes (99%) among top 100 genes exhibited an existence of the NRF1-binding element comprising (T/C)GCGCA(C/T)GCGC(A/G/C) (E-value = 2.6e-195) (Fig. 2), validating the specificity of mapping of ChIP-Seq short reads to genomic regions with the NRF1-binding consensus sequence motif.
Next, we studied molecular pathways of the set of 2,470 NRF1 target genes by using pathway analysis tools of bioinformatics. By using DAVID, we identified functionally associated gene ontology (GO) terms (Supplementary Table 2). The most significant GO terms included “RNA processing” (GO:0006396; P = 6.59E-12) for biological process, “intracellular organelle lumen” (GO:0070013; P = 1.08E-38) for cellular component, and “nucleotide binding” (GO:0000166; P = 3.86E-10) for molecular function.
By using KEGG, NRF1 target genes showed top 3 closest associations with “RNA degradation” (hsa03018; P = 0.00032 corrected by multiple comparison test), “Cell cycle” (hsa04110; P = 0.00041) (Fig. 3), and “Splicesome” (hsa03040; P = 0.00238), suggesting that NRF1 target genes play a key role in RNA metabolism, splicing, and cell cycle control (Table 2). Importantly, KEGG pathways defined by “Aminoacyl-tRNA biosynthesis” (hsa00970; P = 0.01104) involved in protein translation, “Oxidative phosphorylation” (hsa00190; P = 0.01545) involved in mitochondrial respiratory chain, “Base excision repair” (hsa03410; P = 0.01947) involved in DNA damage repair, and “Ubiquitin mediated proteolysis” (hsa04120; P = 0.04020) involved in protein degradation were also listed as significant pathways (Table 2). We also found that the set of 495 genes overlapped between T98G cells by ChIP-Seq and SK-N-SH cells by ChIP-Seq showed a significant relationship with “Aminoacyl-tRNA biosynthesis” (hsa00970; P = 0.01597), “Splicesome” (hsa03040; P = 0.02612), and “Oxidative phosphorylation” (hsa00190; P = 0.02917), whereas the set of 196 genes identified only in T98G did not show significant relationship with KEGG pathways.
Importantly, NRF1 target genes showed a significant relationship with “Parkinson’s disease” pathway on KEGG (hsa05012; P = 0.03561) (Fig. 2, Table 2). where PARK2 (Parkin), PARK6 (Pink1), PARK7 (DJ-1), and PAELR (GPR37) were matched with the previously unrecognized set of NRF1 target genes. We also found that the set of 28 genes (16.5%) among 170 Alzheimer’s disease-related genes (Supplementary Fig. 2) and 36 genes (21.2%) among 183 Huntington’s disease-related genes (Supplementary Fig. 3) on KEGG pathways represented ChIP-Seq-based NRF1 target genes, although the enrichment did not reach the statistical significance. However, these observations raise the possibility that aberrant regulation of NRF1 and its targets might contribute to neurodegenerative processes not only of PD but also of AD and HD.
Finally, we studied molecular pathways of 2,470 ChIP-Seq-based NRF1 target genes by using the core analysis tool of IPA (Table 3). We identified “Mitochondrial dysfunction” (P = 2.80E-06) (Fig. 5) and “Regulation of eIF4 and p70S6K signaling” (P = 7.50E-06) (Fig. 6) as the most significant canonical pathways associated with the set of imported genes. Again, these results indicate that NRF1 target genes play a key role in maintenance of mitochondrial function and protein translation initiation. Furthermore, the canonical pathways defined as “Protein ubiquitination pathway” (P = 2.85E-05), “DNA double-strand break repair by non-homologous end joining” (P = 3.28E-05), and “EIF2 signaling” (P = 3.55E-05) were also listed as significant pathways. This supports the notion that NRF1 target genes regulate a wide range of extra-mitochondrial biological processes, including protein translation, degradation, and DNA damage repair. The set of 495 genes overlapped between T98G and SK-N-SH cells showed a highly significant relationship with “Mitochondrial dysfunction” (P = 9.53E-07), while the set of 196 genes identified only in T98G were less significantly related to “Mitochondrial dysfunction” (P = 3.90E-03).
Mitochondrial function is severely compromised in the brains of aging-related neurodegenerative diseases, such as PD, AD, and HD.1,2 However, at present, the precise genetic and molecular mechanisms and causes responsible for mitochondrial dysfunction in human neurodegenerative diseases remain mostly unknown. NRF1 which activates transcription of nuclear-encoded mitochondrial proteins plays an integrative role in nuclear-mitochondrial interactions.3 ChIP-Seq showed a great advantage over ChIP-chip in resolution and coverage of the genome when we characterize the comprehensive gene regulatory networks.9,10 We, for the first time, characterized the comprehensive set of 2,470 ChIP-Seq-based NRF1 target genes in SK-N-SH human neuroblastoma cells. The binding sites were concentrated in the promoter and 5′UTR regions with an existence of the NRF1-binding consensus sequence.
The set of ChIP-Seq-based NRF1 target genes included a battery of known NRF1 targets, such as eukaryotic translation initiation factor 2, subunit 1 alpha (EIF2S1),19 eukaryotic translation initiation factor 2, subunit 2 beta (EIF2S2),20 cytochrome c, somatic (CYCS),21 fragile X mental retardation 1 (FMR1),18 fragile X mental retardation, autosomal homolog 2 (FXR2),22 E2F transcription factor 6 (E2F6),23 CD47,24 and translocase of outer mitochondrial membrane 34 (TOMM34).25 By GO analysis with DAVID, the most significant GO terms of 2,470 NRF1 target genes were “RNA processing,” “intracellular organelle lumen,” and “nucleotide binding.” By using pathway analysis with KEGG and IPA, we found that the molecules located in the core pathways related to mitochondrial respiratory function, designated as “Oxidative phosphorylation” in KEGG and “Mitochondrial dysfunction” in IPA, are enriched in NRF1 target genes. They include a panel of cytochrome c oxidase (COX), NADH dehydrogenase, succinate dehydrogenase, and ubiquinol-cytochrome c reductase genes. Furthermore, we found that NRF1 target genes play a pivotal role in regulation of extra-mitochondrial biological processes, such as RNA metabolism, splicing, cell cycle, DNA damage repair, protein translation initiation, and ubiquitin-mediated protein degradation, all of which are pivotal for neuronal and non-neuronal cell growth, differentiation, and survival. However, these biological processes are most remarkably deregulated in neurons in humans affected by neurodegenerative diseases closely associated with mitochondrial dysfunction.26,27 It is worthy to note that stable expression of NRF1 induces neurite outgrowth in IMR32 human neuroblastoma cells.28
Accumulating evidence indicated that NRF1 target genes are not restricted to the genes involved in mitochondrial function.3 Previous studies with a non-comprehensive approach identified several NRF1-binding genes encoding components of signaling pathways, and metabolic enzymes, along with the genes essential for chromosome maintenance and nuclei acid metabolism.5,29 More recently, a ChIP-chip study of T98G cells showed that a number of NRF1 target genes, particularly related to DNA replication, mitosis, and cytokinesis, were also recognized by the growth regulatory transcription factor E2F, suggesting that NRF1 plays an active role in regulation of a subset of E2F-responsive genes.12 The small interfering RNA targeting NRF1 reduced expression of a panel of NRF1 targets and E2F targets, indicating that NRF1 generally functions as a transcriptional activator.3,12
We found that a subset of NRF1 target genes show a significant relationship with the “Parkinson’s disease” pathway on KEGG where PARK2 (Parkin), PARK6 (Pink1), PARK7 (DJ-1), and PAELR (GPR37), along with numerous mitochondrial respiratory complex components, are located in the PD pathway. PD clinically causes progressive motor and autonomic dysfunction, and is pathologically characterized by a loss of nigral dopaminergic neurons linked with accumulation of cytoplasmic inclusions named Lewy bodies immunoreactive for α-synuclein. Approximately 10% of PD patients are derived from genetic mutations.30 Mutations in PARK2, PARK6, and PARK7, all of which are closely associated with mitochondrial dysfunction, cause autosomal recessive juvenile PD. Parkin plays a pivotal role in clearance of damaged mitochondria by mitophagy.31 Pink1 attaches to the outer mitochondrial membrane, where it facilitates recruitment of Parkin.32 DJ-1 capable of interacting with α-synuclein, Parkin, and Pink1 acts as a central regulator of anti-oxidant defense.33 GPR37, alternatively named Parkin-associated endothelin-like receptor (PAELR), encodes an orphan G protein-coupled receptor which serves as a substrate for an E3 ubiquitin-protein ligase Parkin when PAELR is expressed in an unfolded and insoluble form.34
We also found that a substantial subset of NRF1 target genes, mostly those related to mitochondrial respiratory function, are accumulated on “Alzheimer’s disease” and “Huntington’s disease” pathways of KEGG. AD is the most common cause of dementia worldwide. It affects the elderly population and is characterized by the hallmark pathology of widespread deposition of amyloid-β (Aβ) on senile plaques and formation of neurofibrillary tangles (NFT) containing hyperphosphorylated tau in degenerating neurons. Importantly, Aβ, produced via sequential cleavage of amyloid precursor protein (APP) by β-secretase and γ-secretase, often accumulates on mitochondria and inhibits respiratory complex IV, thereby increasing ROS production and the frequency of mtDNA mutation.35 We identified PSENEN (PEN2), a component of the γ-secretase complex and MAPT (tau) as two principal NRF1 target genes. Furthermore, a recent study showed that enhanced phosphorylation of eukaryotic initiation factor 2 α-subunit (eIF2α; EIF2S1), a prototype of NRF1 targets, inhibits protein translation, being responsible for defective synaptic plasticity in AD brains.36
HD, an intractable disease causing chorea and psychiatric disturbances due to expansion of a CAG trinucleotide repeat in the huntingtin (HTT) gene, is characterized by a loss of long projection neurons in the striatum and the cortex. Decreased activities of mitochondrial respiratory complexes II, III, and IV are found in the caudate nucleus of HD brains.37 HTT interacts with a battery of transcription factors and coactivators important for diverse biological functions, such as p53, CREB-binding protein, and Sp1. We identified HTT-interacting TAF4 (TAFII130) as one of NRF1 targets, which are involved in the dopamine D2 receptor expression in cooperation with Sp1.38 Notably, mutant HTT causes disruption of mitochondrial function by inhibiting expression of peroxisome proliferator-activated receptor gamma, coactivator 1 alpha (PGC-1α) which serves as a principal coactivator of NRF1.39
The present study has a major limitation in the interpretation of the results as we analyzed only a single ChIP-Seq dataset without experimental validation, retrieved from the ENCODE project, in which no biological replicates are currently available. However, by intensive in silico data mining from the pilot study, we could raise a logical hypothesis suggesting that aberrant regulation of NRF1 and its targets might contribute to neurodegenerative processes underlying PD, AD, and HD via perturbation of diverse mitochondrial and extra-mitochondrial functions. To evaluate this hypothesis, it is highly important to investigate a heretofore unrecognized role of NRF1 and NRF1 targets in PD, AD, and HD brains and model animals.
We identified 2,470 ChIP-Seq-based NRF1 target genes in SK-N-SH human neuroblastoma cells. The molecular pathways of these genes involve regulation of RNA metabolism, splicing, cell cycle, DNA damage repair, protein translation initiation, and ubiquitin-mediated protein degradation, along with mitochondrial respiratory function. We identified a panel of neurodegenerative disease-related genes, such as PARK2 (Parkin), PARK6 (Pink1), PARK7 (DJ-1), PAELR (GPR37), PSENEN (Pen2), and MAPT (tau) as previously unrecognized NRF1 targets. These results would suggest an original hypothesis of involvement of NRF1 and target genes in the pathogenesis of human neurodegenerative diseases.
Supplementary Figure 1
FastQC analysis of ChIP-Seq data. FASTQ format files are derived from short read NGS data of NRF1 ChIP-treated DNA (panel a) and IgG ChIP-treated DNA (panel b). They were imported into the FastQC program. The per base sequence quality score is shown with the median (red line), the mean (blue line), and the interquatile range (yellow box).
Supplementary Figure 2
KEGG “Alzheimer’s disease” pathway. Entrez Gene IDs of 2,470 NRF1 target genes were imported into the Functional Annotation tool of DAVID. The set of 28 genes (16.5%) among 170 genes located in the KEGG “Alzheimer’s disease” pathway (hsa05010) corresponded to ChIP-Seq-based NRF1 target genes highlighted by orange.
Supplementary Figure 3
KEGG “Huntington’s disease” pathway. Entrez Gene IDs of 2,470 NRF1 target genes were imported into the Functional Annotation tool of DAVID. The set of 36 genes (21.2%) among 183 genes located in the KEGG “Huntington’s disease” pathway (hsa05016) corresponded to ChIP-Seq-based NRF1 target genes highlighted by orange.
Supplementary Table 1
The comprehensive set of 2,470 ChIP-Seq-based NRF1 target genes.
Supplementary Table 2
Top 10 GO terms relevant to 2,470 ChIP-Seq-based NRF1 target genes genes.
The authors thank Ms. Mutsumi Motouri for her invaluable help.
Author(s) disclose no potential conflicts of interest.
JS designed the methods, analyzed the data, and drafted the manuscript. NK and YY helped with the data analysis. All authors have read and approved the final manuscript.
Disclosures and Ethics
As a requirement of publication the authors have provided signed confirmation of their compliance with ethical and legal obligations including but not limited to compliance with ICMJE authorship and competing interests guidelines, that the article is neither under consideration for publication nor published elsewhere, of their compliance with legal and ethical guidelines concerning human and animal research participants (if applicable), and that permission has been obtained for reproduction of any copyrighted material. This article was subject to blind, independent, expert peer review. The reviewers reported no competing interests.
This work was supported by grants from the JSPS KAKENHI (C22500322, C25430054), Japan.