Grabole et al. 2016 (PRJNA314508)
General Details
| Title | Modeling the Neuropathology of Tuberous Sclerosis with Human Stem Cells Reveals a Role for Inflammation and Angiogenic Growth Factors [Cell Model] |
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| Organism | |
| Number of Samples | 12 |
| Release Date | 2016/03/07 00:00 |
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| Protocol Details |
Study Links
| GWIPS-viz | Trips-Viz |
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Repository Details
| SRA | SRP071232 |
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| ENA | SRP071232 |
| GEO | GSE78959 |
| BioProject | PRJNA314508 |
Publication
| Title | |
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| Authors | Grabole N, Zhang JD, Aigner S, Ruderisch N, Costa V, Weber FC, Theron M, Berntenis N, Spleiss O, Ebeling M, Yeo GW, Jagasia R, Kiialainen A |
| Journal | Genome medicine |
| Publication Date | 2016 Sep 21 |
| Abstract | Tuberous sclerosis complex (TSC) is a genetic disease characterized by benign tumor growths in multiple organs and neurological symptoms induced by mTOR hyperfunction. Because the molecular pathology is highly complex and the etiology poorly understood, we employed a defined human neuronal model with a single mTOR activating mutation to dissect the disease-relevant molecular responses driving the neuropathology and suggest new targets for treatment. We investigate the disease phenotype of TSC by neural differentiation of a human stem cell model that had been deleted for TSC2 by genome editing. Comprehensive genomic analysis was performed by RNA sequencing and ribosome profiling to obtain a detailed genome-wide description of alterations on both the transcriptional and translational level. The molecular effect of mTOR inhibitors used in the clinic was monitored and comparison to published data from patient biopsies and mouse models highlights key pathogenic processes. TSC2-deficient neural stem cells showed severely reduced neuronal maturation and characteristics of astrogliosis instead. Transcriptome analysis indicated an active inflammatory response and increased metabolic activity, whereas at the level of translation ribosomal transcripts showed a 5'UTR motif-mediated increase in ribosome occupancy. Further, we observed enhanced protein synthesis rates of angiogenic growth factors. Treatment with mTOR inhibitors corrected translational alterations but transcriptional dysfunction persisted. Our results extend the understanding of the molecular pathophysiology of TSC brain lesions, and suggest phenotype-tailored pharmacological treatment strategies. |
| PMC | PMC5031259 |
| PMID | 27655340 |
| DOI |
| Run Accession | Study Accession | Scientific Name | Cell Line | Library Type | Treatment | GWIPS-viz | Trips-Viz | Reads | BAM | BigWig (F) | BigWig (R) | ||
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| SRR3208864 | PRJNA314508 | Homo sapiens | 0.0 | Ribo-Seq | Cycloheximide |  |
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| SRR3208865 | PRJNA314508 | Homo sapiens | 0.0 | Ribo-Seq | Cycloheximide | |
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| SRR3208866 | PRJNA314508 | Homo sapiens | 0.0 | Ribo-Seq | Cycloheximide | |
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| SRR3208867 | PRJNA314508 | Homo sapiens | 0.0 | Ribo-Seq | Cycloheximide | |
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| SRR3208868 | PRJNA314508 | Homo sapiens | 0.0 | Ribo-Seq | Cycloheximide | |
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| SRR3208869 | PRJNA314508 | Homo sapiens | 0.0 | Ribo-Seq | Cycloheximide | |
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| SRR3208870 | PRJNA314508 | Homo sapiens | 0.0 | Ribo-Seq | Cycloheximide | |
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| SRR3208871 | PRJNA314508 | Homo sapiens | 0.0 | Ribo-Seq | Cycloheximide | |
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| SRR3208872 | PRJNA314508 | Homo sapiens | 0.0 | Ribo-Seq | Cycloheximide | |
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| SRR3208873 | PRJNA314508 | Homo sapiens | 0.0 | Ribo-Seq | Cycloheximide | |
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| SRR3208874 | PRJNA314508 | Homo sapiens | 0.0 | Ribo-Seq | Cycloheximide | |
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| SRR3208875 | PRJNA314508 | Homo sapiens | 0.0 | Ribo-Seq | Cycloheximide | |
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| Run Accession | Study Accession | Scientific Name | Cell Line | Library Type | Treatment | GWIPS-viz | Trips-Viz | Reads | BAM | BigWig (F) | BigWig (R) |
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