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Status |
Public on Jan 29, 2021 |
Title |
Defective metabolic programming impairs early neuronal morphogenesis in neural cultures and an organoid model of Leigh syndrome [polyA RNA-seq] |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Mutations in the mitochondrial complex IV assembly factor SURF1 represent a major cause of Leigh syndrome (LS), a fatal neurological disorder. SURF1-deficient animals failed to recapitulate the neuronal failure of LS, which is considered an early-onset neurodegeneration. Using patient induced pluripotent stem cells (iPSCs) and genetically corrected cells, we discovered aberrant bioenergetics initiating in neural progenitor cells (NPCs) leading to impaired neuronal differentiation and maturation. iPSC-derived cerebral organoids recapitulated the neurogenesis defects and appeared smaller with reduced cortical thickness. We suggest defective neurogenesis as a central mechanism in LS pathogenesis and propose NPC function as an interventional target, which allowed us to identify SURF1 gene augmentation as a strategy for restoring neural function in this fatal disease.
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Overall design |
polyA-selected RNA sequencing of neuronal cultures enriched for dopaminergic neurons, derived from two control and two patient-derived hESC/iPSC cell lines, each in three replicates at two time points (4 and 8 weeks of differentiation)
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Contributor(s) |
Inak G, Rybak-Wolf A, Lisowski P, Glažar P, Rajewsky N, Schuelke M, Prigione A |
Citation(s) |
33771987 |
Submission date |
Feb 11, 2019 |
Last update date |
Apr 20, 2021 |
Contact name |
Petar Glazar |
Organization name |
Max Delbrück Center for Molecular Medicine
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Department |
Systems Biology of Gene Regulatory Elements
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Lab |
Rajewsky lab
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Street address |
Robert Rössle Str. 10 (H. 87)
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City |
Berlin |
ZIP/Postal code |
13092 |
Country |
Germany |
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Platforms (1) |
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Samples (24)
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GSM3597145 |
H1 hESC, 8w, rep1 |
GSM3597146 |
H1 hESC, 8w, rep2 |
GSM3597147 |
H1 hESC, 8w, rep3 |
GSM3597148 |
S1 iPSC, 4w, rep1 |
GSM3597149 |
S1 iPSC, 4w, rep2 |
GSM3597150 |
S1 iPSC, 4w, rep3 |
GSM3597151 |
S1 iPSC, 8w, rep1 |
GSM3597152 |
S1 iPSC, 8w, rep2 |
GSM3597153 |
S1 iPSC, 8w, rep3 |
GSM3597154 |
S2 iPSC, 4w, rep1 |
GSM3597155 |
S2 iPSC, 4w, rep2 |
GSM3597156 |
S2 iPSC, 4w, rep3 |
GSM3597157 |
S2 iPSC, 8w, rep1 |
GSM3597158 |
S2 iPSC, 8w, rep2 |
GSM3597159 |
S2 iPSC, 8w, rep3 |
GSM3597160 |
C1 iPSC, 4w, rep1 |
GSM3597161 |
C1 iPSC, 4w, rep2 |
GSM3597162 |
C1 iPSC, 4w, rep3 |
GSM3597163 |
C1 iPSC, 8w, rep1 |
GSM3597164 |
C1 iPSC, 8w, rep2 |
GSM3597165 |
C1 iPSC, 8w, rep3 |
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This SubSeries is part of SuperSeries: |
GSE126360 |
Defective metabolic programming impairs early neuronal morphogenesis in neural cultures and an organoid model of Leigh syndrome |
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Relations |
BioProject |
PRJNA521701 |
SRA |
SRP185425 |
Supplementary file |
Size |
Download |
File type/resource |
GSE126358_RAW.tar |
5.5 Mb |
(http)(custom) |
TAR (of TXT) |
SRA Run Selector![Help](/coreweb/images/long_help4.gif) |
Raw data are available in SRA |
Processed data provided as supplementary file |
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