Nodal signaling maintains H3K18ac landscape to promote mesendodermal differentiation through TRIM33
UID: 10394
- Description
- ATAC-seq, RNA-seq, and ChIP-seq datasets supporting the article "H3K18ac Primes Mesendodermal Differentiation upon Nodal Signaling". From GEO authors' summary: "The epigenome of a cell is established and maintained by chromatin modifiers and remodelers, which are recruited to the chromatin by specific transcription factors. In this report, we show that nodal cross-talks with the epigenome through TRIM33-H3K18ac to mediate mesendodermal genes expression. The chromatin accessibility at mesendodermal genes depends on TRIM33. Moreover, histone acetylation is essential for TRIM33 recruitment to many nodal target genes involved in mesendodermal differentiation. The distribution pattern of the H3K18ac mark changes from foci to expanded domains at the mesendodermal genes promoter during embryonic stem cells (ESCs) differentiation to embryoid bodies (EBs). This could be the cue to facilitate TRIM33 colocalized with Smad2/3 at chromatin in EBs but not in ESCs. TRIM33 interacts with the H3K18ac “writer” p300 dependent on nodal signaling, providing a positive feedback to promote activation of mesendodermal genes and association with HDAC1 plays a negative role in activation of mesendodermal genes."
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Access via GEO
ATAC-seq, RNA-seq, and ChIP-seq data
Accession #: GSE115169Access via SRARNA and ATAC Sequence reads for 23 samples
Accession #: SRP149451Access via BioProjectAdditional information about overall initiative.
Accession #: PRJNA473998 - Access Restrictions
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Free to All
- Access Instructions
- The NCBI Gene Expression Omnibus database provides open access to these files. SRA and/or tar files can be downloaded directly from the site or viewed in the NCBI SRA Run Selector (link at bottom of page).
- Associated Publications
- Data Type
- Equipment Used
- Dataset Format(s)
- SRA, TAR, XLSX, WIG
- Dataset Size
- 494.8 Mb MB (TAR of WIG), 3.0 Mb (XLSX), 91.11 Gb (SRA)
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