NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE171803 Query DataSets for GSE171803
Status Public on Mar 16, 2022
Title DUX4 is a multifunctional factor priming human embryonic genome activation
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Summary Double homeobox 4 (DUX4) is expressed in at the early preimplantation stage in human embryos. Here we show that induced human DUX4 expression substantially alters the non-coding chromatin accessibility of non-coding DNA and activates thousands of newly identified putative transcribed enhancer-like regions, preferentially located within ERVL-MaLR repeat elements. CRISPR activation of transcribed enhancers by C-terminal DUX4 motifs results in the increased expression of target embryonic genome activation (EGA) genes ZSCAN4 and KHDC1P1. We show that DUX4 is markedly enriched in human zygotes, followed by intense nuclear DUX4 localization preceding and coinciding with minor EGA. DUX4 knockdown in human zygotes led to changes in the EGA transcriptome but did not terminate the embryos. We also show that the DUX4 protein interacts with the Mediator complex via the C-terminal KIX binding motif. Our findings contribute to the understanding of DUX4 as a regulator of the non-coding genome.
 
Overall design This study contains 40 samples (ATAC-seq: 8 samples; CAGE: 4 samples; NET-CAGE: 4 samples; bulk STRT: 24 samples) comprising of controls (dox minus) and Doxycycline treated (dox plus). All experiments were performed in DUX4 TetOn H1 and H9 human embryonic stem cell (hESC) lines. The DUX4 TetOn hESCs have been treated with 1μg/ml of Doxycycline for 4 hours. For ATAC-seq, 4 samples were controls and 4 samples were Doxycycline teated. For CAGE, 2 samples were controls and 2 samples were Doxycycline teated, and same was done also for the NET-CAGE samples. For bulk STRT, 12 samples were controls and 12 samples were Doxycycline teated.
 
Contributor(s) Bhagat S, Yoshihara M, Damdimopoulos A, Katayama S, Vuoristo S
Citation(s) 35402882
Submission date Apr 09, 2021
Last update date Apr 19, 2022
Contact name Shruti Bhagat
E-mail(s) shruti.bhagat@riken.jp
Organization name RIKEN, Yokohama
Department RIKEN Center for Integrative Medical Sciences
Lab Preventive Medicine and Applied Genomics Unit
Street address W424, RIKEN Yokohama Campus, 1-7-22 Suehiro-cho, Tsurumi-ku
City Yokohama
State/province Kanagawa
ZIP/Postal code 230-0045
Country Japan
 
Platforms (2)
GPL18573 Illumina NextSeq 500 (Homo sapiens)
GPL21697 NextSeq 550 (Homo sapiens)
Samples (40)
GSM5234440 ATAC-seq_H1hESC_control_biologicalRep1
GSM5234441 ATAC-seq_H1hESC_control_biologicalRep2
GSM5234442 ATAC-seq_H9hESC_control_biologicalRep1
Relations
BioProject PRJNA720936
SRA SRP314242

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
GSE171803_RAW.tar 480.6 Mb (http)(custom) TAR (of BED)
GSE171803_STRT_H1_H9_hESC_19_BO4855_TFE_RawNormCounts_Diffexp.csv.gz 15.2 Mb (ftp)(http) CSV
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