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Epigenetic and transcriptional regulation of mouse oocytes and early embryos

GSE241246 Mus musculus (mouse) ChIP-seq / ATAC-seq (genome binding and open chromatin) 51 samples Submitted 2025/01/20 Platform GPL21493
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 51 samples

What it is
ChIP-seq / ATAC-seq (genome binding and open chromatin)Where proteins bind the genome, or which regions are open and active.
Organism
Mus musculus (mouse)
Samples
51 samples: 22 conditions, mostly in duplicateGroups are read from the sample names, not from the paper. Check the list below.
Data you can get
A processed table (series matrix) and supplementary files from NCBI; the raw sequencing reads from ENA. Which of these hold counts depends on the study, so check the file list.
Paper
Deciphering transcription activity of mammalian early embryos unveils on/off of zygotic genome activation by protein translation/degradationCell reports · 2025
Summary (written by the submitters)
In this study, we performed ChIP-seq of RNA polymerase II, phosphorylated RNA polymerase II and related epigenetic modifications to elucidate transcriptional activities of mouse oocytes and preimplantation embryos. Through analyzing epigenetic alterations of transgenically-modified growing oocytes, early embryos from aged female, and early embryos treated with drugs disturbing proteostasis, we identified critical roles of proteostasis in transcriptional regulation of mouse oocytes and early embryos.
Published in
Deciphering transcription activity of mammalian early embryos unveils on/off of zygotic genome activation by protein translation/degradation
Zhang YR, Guo SM, Shi XY et al. · Cell reports 2025 · PMID 39823229 · doi:10.1016/j.celrep.2024.115215
This dataset
Download · which file do I need?

Direct links to NCBI and ENA, no account and no request form. Pick by what you want to do: take the small processed table to look, the supplementary files to re-analyse, or the original raw data to start over.

1 · Just have a look

Processed table

The series matrix: one table of values per sample as the submitters processed it. The smallest download, and it opens in Excel or R. Start here to see what the data look like.

2 · Re-analyse it

Supplementary files

The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE241246_RAW.tar (it can run to tens of gigabytes).

3 · Start from the raw reads

Raw sequencing reads

The original FASTQ files, straight from the sequencer, held at ENA. Large, and you align them yourself, so only choose this if you need to re-process the study from scratch.

What the files usually look like: Look for peak files (.bed, .narrowPeak) and signal tracks (.bigWig) among the supplementary files; the raw reads are on ENA.

Also filed as BioProject PRJNA1006508 and SRA study SRP455894. Searching any of these in the dataset finder brings you back here.

Study design
22 conditions, mostly in duplicate
APH_IVF_H3K4me3 ×3 2C_IVF_DRB_PolII ×2 2C_IVF_DRB_PolII_Ps ×2 Mla_IVF_RNaseA_PolII_Ps ×2 K4M_P14_H3K27ac ×2 K4M_P14_PolII_Ps ×2 WT_P14_H3K27ac ×2 WT_P14_PolII_Ps ×2 +20 more

Supports a between-group comparison across 45 samples.

How we read this: 22 replicated groups read from 51 sample titles; they account for 45 of them. These groups are guessed from the sample names, not taken from the paper, so check them against the sample list below before relying on them.

Samples in this study

+ 11 more — browse all 51 samples with per-sample file links →

Datasets on a similar topic

Search all mouse ChIP / ATAC / CUT&Tag datasets in GEO →

Share this dataset

Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.