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Status |
Public on Feb 29, 2016 |
Title |
Chromatin Remodeler CHD7 mutated in CHARGE Syndrome Interacts with Sox10 to Regulate Timing of CNS Myelination and Remyelination [ChIP-seq] |
Organism |
Rattus norvegicus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Mutations in CHD7, encoding ATP-dependent chromodomain-helicase-DNA-binding protein 7, in CHARGE syndrome leads to multiple congenital anomalies including growth retardation, craniofacial malformations and neurological dysfunction. Currently, mechanisms underlying the CNS phenotypes remain poorly understood. Here, we show that Chd7 is a direct transcriptional target of oligodendrogenesis-promoting factors Olig2 and Brg1 and required for proper timing of CNS myelination and remyelination. Genome-occupancy analyses coupled with transcriptome profiling reveal that Chd7 cooperates with Sox10 to target the enhancers of key myelinogenic genes, and identify novel Chd7 target.
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Overall design |
Examination of Chd7 and Sox10 genomewide occupancy in differentiating oligodendrocytes
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Contributor(s) |
He D, Zhao C, Lu R |
Citation missing |
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Submission date |
Sep 04, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Richard Lu |
Organization name |
Cincinnati Children's Hospital Medical Center
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Department |
CBDI
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Lab |
Lu Lab,T6.525
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Street address |
3333 Burnet Ave
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City |
Cincinnati |
State/province |
OH |
ZIP/Postal code |
45229 |
Country |
USA |
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Platforms (1) |
GPL14844 |
Illumina HiSeq 2000 (Rattus norvegicus) |
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Samples (2) |
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This SubSeries is part of SuperSeries: |
GSE72727 |
Chromatin Remodeler CHD7 mutated in CHARGE Syndrome Interacts with Sox10 to Regulate Timing of CNS Myelination and Remyelination. |
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Relations |
BioProject |
PRJNA294770 |
SRA |
SRP063347 |