NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE101397 Query DataSets for GSE101397
Status Public on Sep 25, 2017
Title Rapid chromatin switch in the direct reprogramming of fibroblasts to neurons
Organism Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Third-party reanalysis
Summary How transcription factors (TFs) reprogram one cell lineage to another remains unclear. Here, we define chromatin accessibility changes induced by the proneural TF Ascl1 throughout conversion of fibroblasts into induced neuronal (iN) cells. Thousands of genomic loci are affected as early as 12 hours after Ascl1 induction. Surprisingly, over 80% of the accessibility changes occur between days 2 and 5 of the 3-week reprogramming process. This chromatin switch coincides with robust activation of endogenous neuronal TFs and nucleosome phasing of neuronal promoters and enhancers. Subsequent morphological and functional maturation of iN cells are accomplished with relatively little chromatin reconfiguration. Integrating chromatin accessibility and transcriptome changes, we built a network model of dynamic TF regulation during iN cell reprogramming, and identified Zfp238, Sox8 and Dlx3 as key TFs downstream of Ascl1. These results reveal a singular, coordinated epigenomic switch during direct reprogramming, in contrast to step-wise cell fate transitions in development.
 
Overall design Examination of changes of the chromatin accessibility landscape during Ascl1-mediated reprogramming of mouse embryonic fibroblasts (MEFs) into neurons, at distinct timepoints during the reprogramming process. Chromatin changes were correlated with previously published RNA-seq data for control rtTA 48hr and Ascl1 48hr (GSE43916: GSM1074345-8), and newly generated RNA-seq data for Ascl1 7d.
 
Contributor(s) Wapinski OL, Lee QY, Chen AC, Wernig M, Chang HY
Citation(s) 28954238
NIH grant(s)
Grant ID Grant title Affiliation Name
P50 HG007735 Center for Personal Dynamic Regulomes STANFORD UNIVERSITY HOWARD Y CHANG
Submission date Jul 13, 2017
Last update date May 15, 2019
Contact name Qian Yi Lee
E-mail(s) qianyi@stanford.edu
Organization name Stanford University
Department Bioengineering
Lab Wernig Lab
Street address 265 Campus Drive
City Stanford
State/province CA
ZIP/Postal code 94305
Country USA
 
Platforms (2)
GPL13112 Illumina HiSeq 2000 (Mus musculus)
GPL19057 Illumina NextSeq 500 (Mus musculus)
Samples (41)
GSM2701947 MEF
GSM2701948 MEF+rtTA_B1_rep1
GSM2701949 MEF+rtTA_B1_rep2
Relations
Reanalysis of GSM1074345
Reanalysis of GSM1074346
Reanalysis of GSM1074347
Reanalysis of GSM1074348
BioProject PRJNA394116
SRA SRP111819

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
GSE101397_GSE43916_samples_and_new_merged.genes.fpkm.txt.gz 495.7 Kb (ftp)(http) TXT
GSE101397_merged_macspeaks_all_wo.new.rtta_RPKM.quantile.filtered.stepminer.annotated.txt.gz 3.7 Mb (ftp)(http) TXT
GSE101397_merged_macspeaks_early_wo.new.rtta_RPKM.quantile.filtered.stepminer.reordered.annotated.txt.gz 592.8 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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