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Series GSE240435 Query DataSets for GSE240435
Status Public on Aug 09, 2023
Title Global mapping of RNA-chromatin contacts reveals a proximity-dominated connectivity model for ncRNA-gene interactions
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Other
Summary Non-coding RNAs (ncRNAs) are transcribed throughout the genome and provide regulatory inputs to gene expression through their interaction with chromatin. Yet, the genomic targets and functions of most ncRNAs are unknown. Here we use chromatin-associated RNA sequencing (ChAR-seq) to map the global network of ncRNA interactions with chromatin in human embryonic stem cells, and the dynamic changes in interactions during differentiation into definitive endoderm. We uncover general principles governing the organization of the RNA-chromatin interactome, demonstrating that nearly all ncRNAs exclusively interact with genes in close three-dimensional proximity to their locus, and provide a model predicting the interactome. We uncover RNAs that interact with many loci across the genome, and unveil thousands of unannotated RNAs that dynamically interact with chromatin. By relating the dynamics of the interactome to changes in gene expression, we demonstrate that activation or repression of individual genes is unlikely to be controlled by a single ncRNA.
 
Overall design To map chromatin interacting RNAs during cell differentiation we performed ChAR-seq on human ES cells and after differentiation into definitive endoderm (DE). We generated two datasets for each cell state. We also performed RNA-seq in quadruplicate on these samples to characterize changes in transcriptional output.
 
Contributor(s) Limouse C, Smith OK, Jukam D, Fryer KA, Greenleaf WJ, Straight AF
Citation(s) 37770513
NIH grant(s)
Grant ID Grant title Affiliation Name
R01 HG009909 Genome wide identification and functional analysis of chromatin regulatory RNAs STANFORD UNIVERSITY Aaron F Straight
Submission date Aug 09, 2023
Last update date Nov 08, 2023
Contact name Aaron F Straight
E-mail(s) astraigh@stanford.edu
Organization name Stanford University
Department Biochemistry
Street address 279 Campus Drive, B409A
City Stanford
State/province CA
ZIP/Postal code 94305
Country USA
 
Platforms (2)
GPL20301 Illumina HiSeq 4000 (Homo sapiens)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
Samples (22)
GSM7697939 ChAR-seq ES replicate 1
GSM7697940 ChAR-seq ES replicate 2
GSM7697941 ChAR-seq DE replicate 1
Relations
BioProject PRJNA1003796

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
GSE240435_DE-ATAC.bw 703.5 Mb (ftp)(http) BW
GSE240435_DE_rna.negativeStrand.bw 125.8 Mb (ftp)(http) BW
GSE240435_DE_rna.positiveStrand.bw 126.2 Mb (ftp)(http) BW
GSE240435_ES-ATAC.bw 554.7 Mb (ftp)(http) BW
GSE240435_ES_rna.negativeStrand.bw 117.4 Mb (ftp)(http) BW
GSE240435_ES_rna.positiveStrand.bw 124.0 Mb (ftp)(http) BW
GSE240435_RAW.tar 31.2 Gb (http)(custom) TAR (of BED)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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