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Status |
Public on Jan 24, 2018 |
Title |
ATACseq in primary pituitary cells |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
|
Summary |
Deployment of a cell-specifying enhancer repertoire by the pioneer factor Pax7 The establishment and maintenance of cell identity depends on implementation of stable cell-specific chromatin landscapes. Pioneer transcription factors establish new cell fate competences by triggering chromatin remodeling during development. Here, we used pituitary cell specification to define the salient features of pioneer action. Comparison of purified pituitary cells of different lineages showed that chromatin accessibility differs at enhancers rather than promoters. The pioneer factor Pax7 specifies one pituitary lineage identity by opening a specific repertoire of enhancers that are distinct from the myogenic targets of Pax7. Pax7 binds its pioneer targets rapidly and days before chromatin remodeling and gene activation. Finally, enhancers opened by Pax7-dependent chromatin remodeling exhibit loss of DNA methylation and they acquire long term epigenetic memory. The present work identifies enhancer pioneering as a critical feature for cell fate specification and maintenance.
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Overall design |
Transposase assay followed by high throughput sequencing (ATACseq)
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Contributor(s) |
Mayran A, Hariri F, Drouin J |
Citation(s) |
29358650, 34197620 |
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Submission date |
Sep 21, 2016 |
Last update date |
Jul 28, 2021 |
Contact name |
ALEXANDRE MAYRAN |
E-mail(s) |
alexandre.mayran@epfl.ch
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Organization name |
EPFL
|
Street address |
Station 19
|
City |
LAUSANNE |
State/province |
Waadt |
ZIP/Postal code |
1015 |
Country |
Switzerland |
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Platforms (3) |
GPL9185 |
Illumina Genome Analyzer (Mus musculus) |
GPL11002 |
Illumina Genome Analyzer IIx (Mus musculus) |
GPL13112 |
Illumina HiSeq 2000 (Mus musculus) |
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Samples (8)
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This SubSeries is part of SuperSeries: |
GSE87185 |
Pioneer factor Pax7 deploys a stable enhancer repertoire for specification of cell fate |
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Relations |
BioProject |
PRJNA343796 |
SRA |
SRP090244 |