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Status |
Public on Aug 18, 2017 |
Title |
ChIP-sequencing of histone marks in WT and Fmr1-/- (KO) neurons and mice |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Widespread misregulation of histone modifcations occur in FXS, most notably increases in marks associated with active transcription.
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Overall design |
7DIV cultured cortical neurons from WT or Fmr1 KO mice were processed for H3K4me3 and H3K27ac ChIP. In addition, neurons sorted from cerebellar tissue from WT and Fmr1 KO BAC-TRAP NeuroD1 P15 mice were used for H3K4me3 ChIP, performed in triplicate
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Contributor(s) |
Korb E |
Citation(s) |
28823556 |
NIH grant(s) |
Grant ID |
Grant title |
Affiliation |
Name |
K99 MH111836 |
The histone code of neuronal function and dysfunction |
THE ROCKEFELLER UNIVERSITY |
Erica Megan Korb |
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Submission date |
May 25, 2016 |
Last update date |
Jul 25, 2021 |
Contact name |
Erica Korb |
Organization name |
University of Pennsylvania
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Lab |
Korb Lab
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Street address |
3400 Civic Center Boulevard
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City |
Philadelphia |
State/province |
PENNSYLVANIA |
ZIP/Postal code |
19104 |
Country |
USA |
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Platforms (2) |
GPL13112 |
Illumina HiSeq 2000 (Mus musculus) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (30)
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This SubSeries is part of SuperSeries: |
GSE81912 |
Fragile X Syndrome causes epigenetic disruptions treatable with BET inhibitor Jq1 |
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Relations |
BioProject |
PRJNA323399 |
SRA |
SRP075729 |