NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE185774 Query DataSets for GSE185774
Status Public on Sep 29, 2022
Title Promoter repression and 3D-restructuring resolves divergent developmental gene expression in TADs [ATAC-Seq]
Organisms Gallus gallus; Mus musculus; Monodelphis domestica
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Cohesin loop extrusion facilitates precise gene expression by continuously driving promoters to sample all enhancers located within the same topologically-associated domain (TAD). However, many TADs contain multiple genes with divergent expression patterns, thereby indicating additional forces further refine how enhancer activities are utilised. Here, we unravel the mechanisms enabling a new gene, Rex1, to emerge with divergent expression within the ancient Fat1 TAD in placental mammals. We show that such divergent expression is not determined by a strict enhancer-promoter compatibility code, intra-TAD position or nuclear envelope-attachment. Instead, TAD-restructuring in embryonic stem cells (ESCs) separates Rex1 and Fat1 with distinct proximal enhancers that independently drive their expression. By contrast, in later embryonic tissues, DNA methylation renders the inactive Rex1 promoter profoundly unresponsive to Fat1 enhancers within the intact TAD. Combined, these features adapted an ancient regulatory landscape during evolution to support two entirely independent Rex1 and Fat1 expression programs. Thus, rather than operating only as rigid blocks of co-regulated genes, TAD-regulatory landscapes can orchestrate complex divergent expression patterns in evolution.
 
Overall design We mapped accessible chromatin in morphologically stage-matched limb buds from mouse (E11.5), opossum (Stage 30) and chicken (HH22) embryos using ATAC-seq as described in Paliou et al, 2019.
 
Contributor(s) Robson MI, Ringel AR
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date Oct 12, 2021
Last update date Oct 02, 2022
Contact name Michael I Robson
E-mail(s) robson@molgen.mpg.de
Organization name Max Planck Institute for Molecular Genetics
Street address Max Planck Institut für molekulare Genet, Ihnestrasse 63-73
City Berlin
ZIP/Postal code 14195
Country Germany
 
Platforms (3)
GPL17021 Illumina HiSeq 2500 (Mus musculus)
GPL26853 Illumina NovaSeq 6000 (Gallus gallus)
GPL30856 Illumina NovaSeq 6000 (Monodelphis domestica)
Samples (5)
GSM5623634 ATAC-seq__limb_HH22_wt_chicken_Rep-1
GSM5623635 ATAC-seq__limb_stg30_wt_opossum_Rep-1
GSM5623636 ATAC-seq__limb_stg30_wt_opossum_Rep-2
This SubSeries is part of SuperSeries:
GSE185775 Repression and 3D-restructuring resolves regulatory conflicts in evolutionarily rearranged genomes
Relations
BioProject PRJNA770728
SRA SRP341073

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE185774_RAW.tar 1.9 Gb (http)(custom) TAR (of BW)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap