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Series GSE241701 Query DataSets for GSE241701
Status Public on Sep 29, 2023
Title Investigating the effect of Daxx deletion on gene and repeat expression in embryonic stem cells and their differentiated neural derivatives
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Genomes comprise a large fraction of repetitive sequences folded into constitutive heterochromatin to protect genome integrity and cell identity. De novo formation of heterochromatin during preimplantation development is essential to preserve the ground-state of pluripotency and the self-renewal capacity of embryonic stem cells (ESCs). In this study we find that DAXX, an H3.3 chaperone, is essential for ESCs maintenance in the ground-state of pluripotency. DAXX accumulates at pericentromeric regions, and recruits PML and SETDB1, thereby promoting heterochromatin formation. In the absence of DAXX, the 3D-architecture and physical properties of pericentric and peripheral heterochromatin are disrupted, resulting in derepression of major satellite DNA, transposable elements and genes associated with the nuclear lamina. Our data reveal that DAXX is crucial for the maintenance and 3D-organization of the heterochromatin compartment and protects ESCs viability.
 
Overall design To investigate the function of DAXX we generated a transgenic mouse ESC line lacking a functional copy of the Daxx gene (Daxx-/-). We cultured wildtype parental (WT; E14Tg2a) and Daxx-/- ESCs in three conditions: 1). Serum + LIF (ESCs), 2). 2i + Vitamin C (ground state pluripotency) and 3). Retinoic Acid -LIF (Neural differentiated). We isolated total RNA from each of these samples across three independent replicates and, following rRNA depletion, performed RNA-seq on each sample. We performed comparative gene and repeat expression analysis between WT and Daxx-/- cells cultured under each of these three conditions.
 
Contributor(s) Canat A, Veillet A, Batrin R, Dubourg C, Illingworth R, Fabre E, Therizols P
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Submission date Aug 24, 2023
Last update date Sep 30, 2023
Contact name Rob S Illingworth
E-mail(s) robert.illingworth@ed.ac.uk
Phone 01316519640
Organization name The University of Edinburgh
Department Centre for regenerative Medicine
Lab Illingworth
Street address Centre for Regenerative Medicine
City Edinburgh
State/province Midlothian
ZIP/Postal code EH16 4UU
Country United Kingdom
 
Platforms (1)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
Samples (18)
GSM7734031 DaxxKO_Diff_1
GSM7734032 DaxxKO_Diff_2
GSM7734033 DaxxKO_Diff_3
Relations
BioProject PRJNA1009138

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
GSE241701_Normalised_Gene_Expression.txt.gz 2.9 Mb (ftp)(http) TXT
GSE241701_RAW.tar 4.4 Gb (http)(custom) TAR (of BIGWIG, TXT)
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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